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Introduction: Ablation therapy (AT) and partial nephrectomy (PN) are primary treatment options for renal cell carcinoma (RCC). This study aimed to perform a systematic review and meta-analysis to compare the efficacy and safety of AT and PN in treating RCC. Methods: This study was performed in accordance with the PRISMA guidelines. A comprehensive literature search of PubMed, Embase, Cochrane Library, and Web of Science was conducted for studies published up to February 1, 2025. Statistical analyses were performed using Stata16 software. Results: A total of 32 studies involving 6,030 patients were included. The analysis demonstrated that AT was associated with significantly shorter operative time (OT), less estimated blood loss (EBL), a shorter length of hospital stay (LOS), and a lower overall complication rate (CR) compared to PN. Compared with AT, PN has more advantages in overall survival and recurrence-free survival. There were no statistically significant differences between the two interventions in cancer-specific survival. Conclusion: For selected patients with RCC, AT represents a minimally invasive alternative that offers advantages over PN in perioperative outcomes, including reduced OT, EBL, LOS, and CR, while preserving renal function. However, no significant differences were found in long-term oncological survival outcomes.

The prevalence of renal cell carcinoma (RCC) is rising at an annual rate of 3–5%, and it is estimated that approximately 140,000 fatalities per year are attributed to renal cancer [1, 2]. The therapeutic strategies for RCC encompass radical nephrectomy, partial nephrectomy (PN), and active surveillance [3]. PN serves as the primary treatment for localized RCC due to its ability to effectively preserve renal function [4]. However, for patients who are unsuitable for surgical intervention, ablation therapy (AT) has emerged as a valuable alternative. These techniques can precisely destroy tumor tissues without open surgery, offering a less invasive approach with improved patient tolerance [2].

In recent years, significant advancements have been made in AT for RCC. Technologically, AT now encompasses multiple modalities including cryoablation (CA), radiofrequency ablation (RFA), and microwave ablation (MWA) [5]. In terms of surgical access, there has been a shift from traditional laparoscopic ablation therapy (LAT) toward the less invasive percutaneous ablation therapy (PAT) [6, 7]. A recent meta-analysis involving 2,011 patients compared CA and PN for RCC and found comparable perioperative outcomes and renal function preservation between the two techniques [8]. However, another study indicated that patients selected for RFA, CA, or MWA tended to be older and have more comorbidities than those undergoing PN. Although cancer-specific survival (CSS) was similar across groups, the rate of local recurrence was consistently higher after any ablative treatment compared to PN [9].

There remains considerable controversy in the current literature. Some meta-analyses are limited by an insufficient number of included studies [10], while others compare ablation technologies (such as RFA, CA, and MWA) with PN without adequately accounting for differences between ablation modalities or distinguishing between laparoscopic and percutaneous approaches [11]. Therefore, this study aimed to systematically review a broad range of clinical evidence to clarify the safety and efficacy profiles of various ablation techniques, different surgical access routes, and AT in the management of RCC.

In February 2025, we conducted a systematic review and cumulative meta-analysis of the primary outcomes of interest. This study was performed through a comprehensive search of multiple scientific databases, adhering strictly to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and Assessing the Methodological Quality of Systematic Reviews (AMSTAR) guidelines. The literature search and screening process was conducted independently by two researchers. In the event of disagreements that could not be resolved through consensus, a third reviewer was enlisted to make the final determination. Four databases were searched: Embase, PubMed, the Cochrane Library, and Web of Science. The search strategy was designed to encompass three key concepts: (1) RCC, (2) AT, and (3) PN. These concepts were combined using the Boolean operator “AND.” Within each concept, relevant Medical Subject Headings (MeSH) and Emtree terms were utilized, along with a comprehensive list of free-text terms and synonyms (e.g., “RFA,” “cryoablation,” “nephron-sparing surgery”) connected by “OR” to maximize retrieval. The search was restricted to studies published in English. No other filters were applied. The search was restricted to studies published in English. No other filters were applied.

Eligibility Criteria

The following inclusion criteria will be applied for the selection of reports to be included in our systematic review: (1) the study subjects are diagnosed with renal cancer; (2) intervention (I): AT; (3) comparison (C): PN; (4) the study includes at least one of the following outcomes: operative time (OT), length of stay (LOS), estimated blood loss (EBL), and overall survival (OS), recurrence-free survival (RFS), CSS, estimated glomerular filtration rate (eGFR), complications, body mass index. The exclusion criteria are as follows: inability to extract relevant data; studies presented in the form of editorials, conference proceedings, or expert opinions; reports with overlapping study populations that present identical outcomes; studies involving non-human subjects; and studies that do not compare AT with PN. Systematic reviews and meta-analyses were excluded from quantitative data synthesis. These publications were consulted only for background information, contextual discussion, and identification of potential primary studies that might have been missed in the initial search, but data were never extracted from them for pooling.

Data Extraction

Data extraction was conducted by two independent reviewers who independently selected the articles to be included and extracted data in accordance with a pre-established data collection form. The data extracted comprised the following elements: author, year of publication, sample size, age, body mass index, tumor size, OT, length of stay (LOS), EBL, complications, eGFR, OS, RFS, CSS.

Study Quality Assessment

The Newcastle-Ottawa Scale (NOS) was employed to evaluate the quality of retrospective studies 9. The NOS scoring system is on a scale of 0–9, with a score exceeding 6 indicating high-quality studies.

Risk of Bias Assessment

The evaluation of the risk of bias within the included studies was independently undertaken by the same two authors.

Data Analysis

For the purpose of data analysis, we utilized the Stata version 16.0 software (StataCorp LLC, 4905 Lakeway Dr., College Station, TX, USA). In the context of our meta-analysis, the log relative risk along with its variance was employed as the summary outcome measure to synthesize information from all the trials under consideration. Specifically, for each individual trial, we calculated the hazard ratio and its corresponding 95% confidence interval (CI) for the survival rate. The choice between the fixed-effects model and the random-effects model was made based on the specific characteristics and data structure of each trial.

Statistical Analysis

The threshold for statistical significance was set at p < 0.05. WMD represented continuous variables, OR/relative risk represented dichotomous variables, and 95% CI were calculated. To assess the heterogeneity among the included studies, heterogeneity was assessed using the Q-test and the I2 statistic. If the I2 statistic exceeded 50% or the p value <0.10, it was interpreted as an indication of significant heterogeneity between the studies.

Description of Study

The authors conducted a comprehensive search across four databases, yielding a total of 680 records. Utilizing Endnote software, they identified and removed 298 duplicate studies. A further 248 studies were excluded after reviewing their titles and abstracts. Additionally, 44 studies could not be retrieved, 32 were systematic reviews, 18 did not meet the inclusion criteria, and 8 were excluded due to incomplete data. Ultimately, 32 studies involving 6,030 patients were included in this meta-analysis. The sample sizes of these studies ranged from 27 to 2,276. All 32 studies were retrospective in nature. The screening process is illustrated in Figure 1, while the baseline characteristics of the included studies are detailed in Table 1. The 32 publications were released between the years 2007 and 2025. The PRISMA checklist is included in the online supplementary document (for all online suppl. material, see https://doi.org/10.1159/000550133).

Quality Assessment

The quality assessment of the cohort studies was performed utilizing the modified NOS, with the scores ranging from 6 to 8 points. A total of 32 studies were incorporated into this evaluation, and each of them achieved a score of at least six, as detailed in Table 2.

Operative Time

A total of 18 studies reported on the outcome of OT [12‒19, 26, 27, 30, 31, 35‒37, 39, 40]. Given the presence of substantial heterogeneity among these studies (I2 = 97.9%, p = 0.000), a random-effects model was employed for the meta-analysis. The pooled analysis revealed a significant difference between the groups with PN and AT (WMD = 76.70, 95% CI: [51.50–101.90], p < 0.05, I2 = 97.9%) (Fig. 2). PN is inherently more complex, leading to significantly longer OT compared to AT [43]. However, ablative technologies are continually advancing. In this study, we conducted subgroup analyses to compare different ablative methods (RFA, CA, MWA) and surgical approaches (LAT and PAT).

Subgroup analyses were conducted by the authors based on different ablative technologies. The pooled meta-analysis revealed a significant difference between PN and different AT (Fig. 3). The 5 studies [12‒16] show that the OT for PN is longer than that for RAF (WMD = 62.16, 95% CI: [12.72–111.61], p < 0.05, I2 = 96.4%).

The 5 results showed [15, 18, 19, 30, 31] that the OT of PN was longer than MWA (WMD = 78.30, 95% CI: [30.99, 125.60], p < 0.05). High heterogeneity between studies (I2 = 56.1%, p < 0.05, I2 = 98.8%) (Fig. 3). The 5 results [35‒37, 39, 40] showed that the OT of PN was longer than CA (WMD = 83.99, 95% CI: [8.2, 159.78], p < 0.05, I2 = 98.6%) (Fig. 3).

Subgroup analyses were conducted by the authors based on different surgical approaches (LAT and PAT). The pooled meta-analysis revealed a significant difference between PN and different surgical approaches of AT (Fig. 4). The 15 studies [12‒14, 16‒19, 26, 27, 35‒37, 39, 40] involving LAT and PAT have confirmed that the OT of AT is shorter compared to PN. LAT had a shorter OT compared to PN (WMD = 62.28, 95% CI: [30.78–99.79], p < 0.05, I2 = 95.7%). Additionally, another 7 studies also showed a significant difference in OT between PAT and PN (WMD = 82.71, 95% CI: [51.81–113.62], p < 0.05, 96.6%).

LOS (Days)

A total of 26 studies [12‒21, 23‒27, 30‒37, 39, 40] reported the length of stay (LOS). The pooled meta-analysis indicated significant difference in LOS between PN and AT (WMD = 2.01, 95% CI: [1.55–2.47], p < 0.05, I2 = 91.0%) as illustrated in Figure 5. Our findings suggest that AT is associated with shorter LOS compared to PN. This is likely due to the reduced trauma and quicker postoperative recovery associated with AT. To elucidate the differences in LOS across different ablative methods and surgical approaches, we conducted subgroup analyses.

The 10 results [12‒14, 16, 17, 20, 21, 23, 31, 32] showed that the LOS of PN was longer than RAF (WMD = 2.25, 95% CI: [1.68, 2.82], p < 0.05, I2 = 84.5%) (Fig. 6). The 4 results [15, 18, 19, 30] showed that the LOS of PN was longer than MWA (WMD = 3.66, 95% CI: [1.26, 6.07], p < 0.05, I2 = 88.6%) (Fig. 6).

The 7 results [33‒37, 39, 40] showed that the LOS of PN was longer than CA (WMD = 1.48, 95% CI: [0.81, 2.15], p < 0.05, I2 = 77.0%) (Fig. 6). The 25 studies [12‒14, 16‒21, 23‒27, 30‒37, 39, 40] involving LAT and PAT have confirmed that the LOS of AT is shorter compared to PN (Fig. 7). There was high heterogeneity among the eleven studies, which showed that LAT had a shorter LOS compared to PN (WMD = 1.53, 95% CI: [0.98–2.07], p < 0.05, I2 = 78.9%). Additionally, another 14 studies also showed a significant difference in LOS between PAT and PN (WMD = 2.25, 95% CI: [1.52–2.98], p < 0.05, I2 = 93.8%).

EBL (mL)

A total of 9 studies [12‒15, 18, 34‒37, 40] reported the EBL (mL). The results showed that PN had more EBL (WMD = 112.7, 95% CI: [69.12–156.28], p < 0.05, I2 = 90.0%), as illustrated in Figure 8.

Estimated Glomerular Filtration Rate

The 10 studies reported [14‒16, 18‒20, 23‒25, 32, 40] the eGFR, a key indicator of renal function. The pooled meta-analysis indicated that compared with AT, the eGFR declines more rapidly after PN (WMD = 3.71, 95% CI: [1.29–6.13], p > 0.05, I2 = 83.7%), as illustrated in Figure 9.

Overall Complication Rate

The 17 studies [12‒15, 17, 21‒23, 26, 27, 30, 31, 33‒36] reported the overall complication rate (OCR). Results showed that significant difference in OCR between PN and AT (OR = 1.70 95% CI: [1.13–2.55], p < 0.05, I2 = 41.1%) (Fig. 10).

Major Complication Rate

A total of 19 studies [13‒18, 22‒25, 27, 30, 31, 35‒37, 39, 41] reported the major complication rate (MCR) of PN vs. AT. Results showed that difference in MCR between PN and AT (OR = 1.73, 95% CI: [1.10–2.74], p > 0.05, I2 = 0.0%) (Fig. 11).

To explore the differences in MCR between different ablative methods and surgical approaches of AT versus PN, we conducted subgroup analyses. These seven findings show no significant difference in MCR between PN and RAF (OR = 1.78, 95% CI: [0.63, 4.99], p > 0.05, I2 = 32.1%) (Fig. 12). The 4 results show significant difference in MCR between PN and MWA (OR = 3.19, 95% CI: [1.19, 8.57], p < 0.05, I2 = 0.0%) (Fig. 12). The 5 results indicated that the MCR of PN was not significantly different from that of CA (OR = 1.04, 95% CI: [0.48, 2.23], p > 0.05, I2 = 0.0%) (Fig. 12).

The 18 studies [13‒18, 22‒25, 27, 30, 31, 35‒37, 39, 41] involving LAT and PAT have confirmed that the MCR of AT is not significantly different from that of PN (Fig. 13). The 8 studies show significant difference in MCR between PN and LAT (OR = 1.98, 95% CI: [1.09–3.62], p > 0.05, I2 = 31.6%). Additionally, another 10 studies also showed significant difference in MCR between PAT and PN (OR = 2.05, 95% CI: [1.06–3.94], p > 0.05, I2 = 0.0%).

Overall Survival

The 10 studies [7, 14, 18, 19, 26, 28, 32, 39‒41] reported OS of AT vs. PN. Results showed that significant difference in OS between PN and AT (OR = 1.37, 95% CI: [1.13–1.66], p > 0.05, I2 = 34.7%) (Fig. 14).

This study performed subgroup analyses stratified by the different ablative methods, providing a clearer illustration of the OS differences between each ablation and PN. The 3 studies demonstrated that there was significant difference in OS between PN and RAF (OR = 1.69, 95% CI: [1.29, 2.22], p > 0.05, I2 = 0.0%) (Fig. 15).

The 3 studies demonstrated that there was no significant difference in OS between PN and MWA (OR = 1.19, 95% CI: [0.95, 1.51], p > 0.05, I2 = 43.8%) (Fig. 15). The 4 studies demonstrated that there was significant difference in OS between PN and CA (OR = 1.32, 95% CI: [0.68, 2.58], p > 0.05, I2 = 0.0%) (Fig. 15).

Our analysis indicates that the AT group does not have an advantage over the PN group in terms of OS. We anticipate that future well-designed clinical studies will provide more compelling evidence.

Recurrence-Free Survival

RFS is an essential time-to-event endpoint for assessing tumor treatment efficacy and prognosis, offering vital evidence for clinical decision-making and research design. Our pooled analysis of 15 included studies showed significant difference RFS between the PN and AT [7, 14, 15, 18, 22, 23, 26, 28, 29, 32, 38‒42] (OR = 1.32, 95% CI: [1.09–1.58], p > 0.05, I2 = 0.0%) (Fig. 16).

This study performed subgroup analyses stratified by the different ablative methods. The 5 studies demonstrated that there was no significant difference in RFS between RAF and PN (OR = 1.27, 95% CI: [0.69, 2.23], p > 0.05, I2 = 0.0%) (Fig. 17). The 4 studies demonstrated that there was no significant difference in RFS between PN and MWA (OR = 1.56, 95% CI: [0.75, 3.23], p > 0.05, I2 = 57.8%) (Fig. 17). The 4 studies demonstrated that there was significant difference in RFS between PN and CA (OR = 1.52, 95% CI: [1.03, 2.24], p > 0.05, I2 = 0.0%) (Fig. 17).

This study performed subgroup analyses stratified by the different surgical approaches. LAT was reported in 2 studies. The pooled meta-analysis demonstrated no significant difference in RFS between PN and LAT (OR = 0.92, 95% CI: [0.28–3.07], p > 0.05, I2 = 0.0%) (Fig. 18). PAT was reported in 9 studies. The pooled meta-analysis demonstrated significant difference in RFS between PN and PAT (OR = 1.45, 95% CI: [1.11–1.90], p < 0.05, I2 = 19.8%) (Fig. 18).

Cancer-Specific Survival

The 6 studies [7, 14, 18, 26, 39, 40] reported CSS of PN vs. AT. Results showed that no significant difference in CSS between PN and AT (OR = 1.37, 95% CI: [0.75–2.50], p > 0.05, I2 = 0.0%) (Fig. 19).

Our meta-analysis of 32 studies revealed that patients undergoing PN experienced longer OT, prolonged LOS, higher complication rate, and greater declines in postoperative eGFR. However, our analysis indicates that the AT group does not have an advantage over the PN group in terms of OS and RFS. These findings underscore the need for additional well-designed, high-quality studies to confirm these conclusions.

The incidence of RCC continues to rise annually [1, 2]. Currently, nephron-sparing PN remains the standard treatment for small RCC [44]; nevertheless, AT represents a viable alternative for patients who are unable to tolerate PN [44‒46].

Our results demonstrate that AT offers significant advantages in several short-term outcomes. Specifically, AT was associated with shorter OT, reduced LOS, lower EBL, and better preservation of renal function, as reflected by higher postoperative eGFR. These benefits are consistent with the minimally invasive nature of AT, which avoids the complex dissection and reconstruction often required in PN [27, 45]. However, this advantage did not extend to long-term oncological outcomes.

A notable finding of this study is the considerable heterogeneity observed across multiple outcome measures, such as OT (I2 = 97.9%) and LOS (I2 = 91.0%). This variability likely arises from differences in surgical expertise, institutional protocols, patient selection criteria, and technological evolution over the study period [43]. Unlike previous meta-analyses [47, 48], this study conducted detailed subgroup analyses not only across ablation modalities (RFA, MWA, CA) but also between surgical approaches (laparoscopic vs. percutaneous). These analyses consistently demonstrated that AT – regardless of technique or access – was associated with shorter OT compared to PN. This difference likely stems from the inherently more complex nature of PN, which often requires renal vascular control and parenchymal reconstruction, whereas AT involves minimally invasive tissue destruction without the need for extensive dissection [27, 45].

The superior renal functional outcomes associated with AT are particularly noteworthy. The smaller decline in eGFR following AT is likely attributable to its tissue-preserving mechanism, which selectively destroys tumor tissue while minimizing damage to adjacent healthy parenchyma [49]. In contrast, PN inevitably removes a margin of normal kidney tissue, which may impair renal function to a greater extent [50]. Nevertheless, the clinical significance of this difference remains uncertain due to significant heterogeneity (I2 = 83.7%) and the limited number of studies reporting functional outcomes.

With regard to safety, our analysis revealed that PN did not offer advantages in terms of overall complications or major complications. This aligns with previous reports indicating that AT is a safe procedure with a morbidity profile comparable to that of surgery [8, 51]. Subgroup analyses further revealed no significant differences when AT modalities or approaches were considered separately, reinforcing the general safety of ablative techniques. However, variations in complication definitions and reporting standards across studies may have introduced additional heterogeneity, limiting the strength of this conclusion.

In the AT group, significant differences were observed in OS and RFS; nevertheless, these results must be interpreted with caution. The data suggest that AT is effective in controlling cancer-specific mortality, yet they may also reflect disparities in baseline patient characteristics – such as age and comorbidity burden – or technical factors including the completeness of ablation and the management of recurrences [52]. Notably, in contrast to earlier reports, a single-center study encompassing 1,798 patients demonstrated longer CSS with PCA than with PN, underscoring the potential influence of evolving surgical techniques [7]. Another recent retrospective study analysis also indicates that the risk of surgical-related complications for CA is extremely low [53]. These findings emphasize the imperative for meticulous patient selection and the establishment of standardized procedural protocols to optimize oncological outcomes.

Several limitations must be acknowledged. First, the predominance of retrospective studies introduces potential selection and reporting biases. Second, the high and largely unexplained heterogeneity across outcomes limits the robustness of our conclusions. Third, publication bias was not assessed, which may affect the validity of the results. Finally, rapid advancements in ablative technology mean that older studies may not reflect current practice.

AT demonstrates clear advantages over PN in perioperative and functional outcomes, supporting its role as a less invasive alternative for managing small renal masses. However, its association with inferior OS and RFS highlights the need for careful patient selection and long-term monitoring. Future prospective, well-designed studies are essential to better define the role of AT, standardize its application, and evaluate its long-term efficacy relative to surgical standards.

The original studies included in this meta-analysis were ethically reviewed. The author thanks Professor Zongping Zhang for his continued support and encouragement.

A statement of ethics and consent to participate is not applicable because this study is based exclusively on published literature.

There are no conflicts of interest involved in this study.

Zongping Zhang presided over the “Ten Thousand People Plan of Guozhou (ZX-W2201-4)” fund in Guizhou. Not only did he cover the expenses for article publication but he also participated in the design and revision.

Ran Deng and Yunxiang Li participated in data analysis and validation. Zongping Zhang secured the funding for the research.

The materials used in this study are openly available and can be accessed at PubMed, Embase, Cochrane, and Web of Science databases.

1.
Sun
Z
,
Li
T
,
Xiao
C
,
Zou
S
,
Zhang
M
,
Zhang
Q
, et al
.
Prediction of overall survival based upon a new ferroptosis-related gene signature in patients with clear cell renal cell carcinoma
.
World J Surg Oncol
.
2022
;
20
(
1
):
120
.
2.
Leyderman
M
,
McElree
IM
,
Nepple
KG
,
Zakharia
Y
,
Ghodoussipour
S
,
Packiam
VT
.
Management of renal cell carcinoma with supradiaphragmatic inferior vena cava thrombus diagnosed during acute COVID-19 infection
.
Cureus
.
2024
;
16
(
3
):
e55565
.
3.
Plekhanova
OAP
,
Mono
PM
,
Martov
AGM
,
Golubev
MYG
,
Grigoriev
NAG
,
Kyzlasov
PSK
, et al
.
[Comparative analysis of clinical features of robotic-assisted and laparoscopic partial nephrectomy]
.
Urologiia
.
2021
(
3
):
92
7
.
4.
Nishimura
K
,
Sawada
Y
,
Sugihara
N
,
Funaki
K
,
Koyama
K
,
Noda
T
, et al
.
A low RENAL nephrometry score can avoid the need for the intraoperative insertion of a ureteral catheter in robot-assisted partial nephrectomy
.
World J Surg Oncol
.
2021
;
19
(
1
):
40
.
5.
Ge
S
,
Wang
Z
,
Li
Y
,
Zheng
L
,
Gan
L
,
Zeng
Z
, et al
.
Is ablation suitable for small renal masses? A meta-analysis
.
Acad Radiol
.
2025
;
32
(
1
):
218
35
.
6.
Stroup
SP
,
Kopp
RP
,
Derweesh
IH
.
Laparoscopic and percutaneous cryotherapy for renal neoplasms
.
Panminerva Med
.
2010
;
52
(
4
):
331
8
.
7.
Andrews
JR
,
Atwell
T
,
Schmit
G
,
Lohse
CM
,
Kurup
AN
,
Weisbrod
A
, et al
.
Oncologic outcomes following partial nephrectomy and percutaneous ablation for cT1 renal masses
.
Eur Urol
.
2019
;
76
(
2
):
244
51
.
8.
Gao
H
,
Zhou
L
,
Zhang
J
,
Wang
Q
,
Luo
Z
,
Xu
Q
, et al
.
Comparative efficacy of cryoablation versus robot-assisted partial nephrectomy in the treatment of cT1 renal tumors: a systematic review and meta-analysis
.
BMC Cancer
.
2024
;
24
(
1
):
1150
.
9.
Uhlig
J
,
Strauss
A
,
Rücker
G
,
Seif Amir Hosseini
A
,
Lotz
J
,
Trojan
L
, et al
.
Partial nephrectomy versus ablative techniques for small renal masses: a systematic review and network meta-analysis
.
Eur Radiol
.
2018
;
29
(
3
):
1293
307
.
10.
Dan
W
,
Ya
L
,
Yang
L
,
Dong
L
.
A systematic review and meta-analysis of laparoscopic partial nephrectomy versus laparoscopic focal therapy for small renal masses
.
Medicine
.
2025
;
104
(
33
):
e44048
.
11.
Hans-Jonas
M
,
Timo Christian
M
,
Manuel Florian
S
,
Silke
Z
.
Efficacy and safety of percutaneous thermal ablation in Bosniak III and IV cystic renal masses: a systematic review and meta-analysis
.
Diagn Interv Radiol
.
2025
;
31
(
6
):
605
11
.
12.
Bensalah
K
,
Zeltser
I
,
Tuncel
A
,
Cadeddu
J
,
Lotan
Y
.
Evaluation of costs and morbidity associated with laparoscopic radiofrequency ablation and laparoscopic partial nephrectomy for treating small renal tumours
.
BJU Int
.
2007
;
101
(
4
):
467
71
.
13.
Huang
J
,
Zhang
J
,
Wang
Y
,
Kong
W
,
Xue
W
,
Liu
D
, et al
.
Comparing zero ischemia laparoscopic radio frequency ablation assisted tumor enucleation and laparoscopic partial nephrectomy for clinical T1a renal tumor: a randomized clinical trial
.
J Urol
.
2016
;
195
(
6
):
1677
83
.
14.
Ji
C
,
Zhao
X
,
Zhang
S
,
Liu
G
,
Li
X
,
Zhang
G
, et al
.
Laparoscopic radiofrequency ablation versus partial nephrectomy for cT1a renal tumors: long-term outcome of 179 patients
.
Urol Int
.
2016
;
96
(
3
):
345
53
.
15.
Guan
W
,
Bai
J
,
Liu
J
,
Wang
S
,
Zhuang
Q
,
Ye
Z
, et al
.
Microwave ablation versus partial nephrectomy for small renal tumors: intermediate-term results
.
J Surg Oncol
.
2012
;
106
(
3
):
316
21
.
16.
Park
JM
,
Yang
SW
,
Shin
JH
,
Na
YG
,
Song
KH
,
Lim
JS
.
Oncological and functional outcomes of laparoscopic radiofrequency ablation and partial nephrectomy for T1a renal masses: a retrospective single-center 60 month follow-up cohort study
.
Urol J
.
2018
;
16
(
1
):
44
49
.
17.
Acosta Ruiz
V
,
Ladjevardi
S
,
Brekkan
E
,
Häggman
M
,
Lönnemark
M
,
Wernroth
L
, et al
.
Periprocedural outcome after laparoscopic partial nephrectomy versus radiofrequency ablation for T1 renal tumors: a modified R.E.N.A.L nephrometry score adjusted comparison
.
Acta Radiol
.
2019
;
60
(
2
):
260
8
.
18.
Yu
J
,
Liang
P
,
Yu
XL
,
Cheng
ZG
,
Han
ZY
,
Zhang
X
, et al
.
US-guided percutaneous microwave ablation versus open radical nephrectomy for small renal cell carcinoma: intermediate-term results
.
Radiology
.
2014
;
270
(
3
):
880
7
.
19.
Anglickis
M
,
Anglickienė
G
,
Andreikaitė
G
,
Skrebūnas
A
.
Microwave thermal ablation versus open partial nephrectomy for the treatment of small renal tumors in patients over 70 years old
.
Med Kaunas
.
2019
;
55
(
10
):
664
.
20.
Kim
S
,
Lee
E
,
Kim
H
,
Kwak
C
,
Ku
J
,
Lee
S
, et al
.
A propensity-matched comparison of perioperative complications and of chronic kidney disease between robot-assisted laparoscopic partial nephrectomy and radiofrequency ablative therapy
.
Asian J Surg
.
2015
;
38
(
3
):
126
33
.
21.
Chung
D
,
Hwang
H
,
Sohn
D
.
Radiofrequency ablation using real-time ultrasonography-computed tomography fusion imaging improves treatment outcomes for T1a renal cell carcinoma: comparison with laparoscopic partial nephrectomy
.
Investig Clin Urol
.
2022
;
63
(
2
):
159
67
.
22.
Stern
JM
,
Svatek
R
,
Park
S
,
Hermann
M
,
Lotan
Y
,
Sagalowsky
AI
, et al
.
Intermediate comparison of partial nephrectomy and radiofrequency ablation for clinical T1a renal tumours
.
BJU Int
.
2007
;
100
(
2
):
287
90
.
23.
Pantelidou
M
,
Challacombe
B
,
McGrath
A
,
Brown
M
,
Ilyas
S
,
Katsanos
K
, et al
.
Percutaneous radiofrequency ablation versus robotic-assisted partial nephrectomy for the treatment of small renal cell carcinoma
.
Cardiovasc Interv Radiol
.
2016
;
39
(
11
):
1595
603
.
24.
Cazalas
G
,
Klein
C
,
Piana
G
,
De Kerviler
E
,
Gangi
A
,
Puech
P
, et al
.
A multicenter comparative matched-pair analysis of percutaneous tumor ablation and robotic-assisted partial nephrectomy of T1b renal cell carcinoma (AblatT1b study-UroCCR 80)
.
Eur Radiol
.
2023
;
33
(
9
):
6513
21
.
25.
Klein
C
,
Cazalas
G
,
Margue
G
,
Piana
G
,
DE Kerviler
E
,
Gangi
A
, et al
.
Percutaneous tumor ablation versus image guided robotic-assisted partial nephrectomy for cT1b renal cell carcinoma: a comparative matched-pair analysis (UroCCR 80)
.
Minerva Urol Nephrol
.
2023
;
75
(
5
):
559
68
.
26.
Lehrer
R
,
Cornelis
F
,
Bernhard
JC
,
Bigot
P
,
Champy
C
,
Bruyère
F
, et al
.
Minimally invasive nephron-sparing treatments for T1 renal cell cancer in patients over 75 years: a comparison of outcomes after robot-assisted partial nephrectomy and percutaneous ablation
.
Eur Radiol
.
2023
;
33
(
12
):
8426
35
.
27.
Pandolfo
SD
,
Loizzo
D
,
Beksac
AT
,
Derweesh
I
,
Celia
A
,
Bianchi
L
, et al
.
Percutaneous thermal ablation for cT1 renal mass in solitary kidney: a multicenter trifecta comparative analysis versus robot-assisted partial nephrectomy
.
Eur J Surg Oncol
.
2023
;
49
(
2
):
486
90
.
28.
Chlorogiannis
DD
,
Kratiras
Z
,
Efthymiou
E
,
Moulavasilis
N
,
Kelekis
N
,
Chrisofos
M
, et al
.
Percutaneous microwave ablation versus robot-assisted partial nephrectomy for stage I renal cell carcinoma: a propensity-matched cohort study focusing upon long-term Follow-Up of oncologic outcomes
.
Cardiovasc Interv Radiol
.
2024
;
47
(
5
):
573
82
.
29.
Qiu
J
,
Ballantyne
C
,
Lange
M
,
Kennady
E
,
Yeaman
C
,
Culp
S
, et al
.
Comparison of microwave ablation and partial nephrectomy for T1a small renal masses
.
Urol Oncol
.
2023
;
41
(
10
):
434.e9
16
.
30.
Kula
O
,
Ateş
Y
,
Çek
HM
,
Tozsin
A
,
Günay
B
,
Akgül
B
, et al
.
Comparison of the efficacy of percutaneous microwave ablation therapy versus laparoscopic partial nephrectomy for early-stage renal tumors
.
Diagnostics
.
2024
;
14
(
14
):
1574
.
31.
Lucignani
G
,
De Lorenzis
E
,
Ierardi
AM
,
Silvani
C
,
Marmiroli
A
,
Nizzardo
M
, et al
.
Perioperative and survival outcomes of patients treated with robot-assisted partial nephrectomy and percutaneous microwave ablation for small renal masses: a single center experience
.
Clin Genitourin Cancer
.
2024
;
22
(
2
):
8426
35
.
32.
Pedraza-Sánchez
JP
,
Chaves-Marcos
R
,
Mazuecos-Quirós
J
,
Bisonó-Castillo
ÁL
,
Osmán-García
I
,
Gutiérrez-Marín
CM
, et al
.
Percutaneous radiofrequency ablation is an effective treatment option for small renal masses, comparable to partial nephrectomy
.
Eur Radiol
.
2023
;
33
(
11
):
7371
9
.
33.
Haramis
G
,
Graversen
JA
,
Mues
AC
,
Korets
R
,
Rosales
JC
,
Okhunov
Z
, et al
.
Retrospective comparison of laparoscopic partial nephrectomy versus laparoscopic renal cryoablation for small (<3.5 cm) cortical renal masses
.
J Laparoendosc Adv Surg Tech
.
2012
;
22
(
2
):
152
7
.
34.
Lin
YC
,
Turna
B
,
Frota
R
,
Aron
M
,
Haber
GP
,
Kamoi
K
, et al
.
Laparoscopic partial nephrectomy versus laparoscopic cryoablation for multiple ipsilateral renal tumors
.
Eur Urol
.
2008
;
53
(
6
):
1210
6
.
35.
Liu
HY
,
Kang
CH
,
Wang
HJ
,
Chen
CH
,
Luo
HL
,
Chen
YT
, et al
.
Comparison of robot-assisted laparoscopic partial nephrectomy with laparoscopic cryoablation in the treatment of localised renal tumours: a propensity score-matched comparison of long-term outcomes
.
Diagnostics
.
2021
;
11
(
5
):
759
.
36.
O’Malley
RL
,
Berger
AD
,
Kanofsky
JA
,
Phillips
CK
,
Stifelman
M
,
Taneja
SS
.
A matched-cohort comparison of laparoscopic cryoablation and laparoscopic partial nephrectomy for treating renal masses
.
BJU Int
.
2006
;
99
(
2
):
395
8
.
37.
Guillotreau
J
,
Haber
GP
,
Autorino
R
,
Miocinovic
R
,
Hillyer
S
,
Hernandez
A
, et al
.
Robotic partial nephrectomy versus laparoscopic cryoablation for the small renal mass
.
Eur Urol
.
2012
;
61
(
5
):
899
904
.
38.
Fraisse
G
,
Colleter
L
,
Peyronnet
B
,
Khene
ZE
,
Mandoorah
Q
,
Soorojebally
Y
, et al
.
Peri-operative and local control outcomes of robot-assisted partial nephrectomy vs percutaneous cryoablation for renal masses: comparison after matching on radiological stage and renal score
.
BJU Int
.
2019
;
123
(
4
):
632
8
.
39.
Yanagisawa
T
,
Miki
J
,
Shimizu
K
,
Fukuokaya
W
,
Urabe
F
,
Mori
K
, et al
.
Functional and oncological outcome of percutaneous cryoablation versus laparoscopic partial nephrectomy for clinical T1 renal tumors: a propensity score-matched analysis
.
Urol Oncol
.
2020
;
38
(
12
):
938.e1
7
.
40.
Haber
G
,
Lee
MC
,
Crouzet
S
,
Kamoi
K
,
Gill
IS
.
Tumour in solitary kidney: laparoscopic partial nephrectomy vs laparoscopic cryoablation
.
BJU Int
.
2011
;
109
(
1
):
118
24
.
41.
Uemura
T
,
Kato
T
,
Nagahara
A
,
Kawashima
A
,
Hatano
K
,
Ujike
T
, et al
.
Therapeutic and clinical outcomes of robot-assisted partial nephrectomy versus cryoablation for T1 renal cell carcinoma
.
In Vivo
.
2021
;
35
(
3
):
1573
9
.
42.
Millan
B
,
Breau
RH
,
Bhindi
B
,
Mallick
R
,
Tanguay
S
,
Finelli
A
, et al
.
A comparison of percutaneous ablation therapy to partial nephrectomy for cT1a renal cancers: results from the Canadian kidney cancer information system
.
J Urol
.
2022
;
208
(
4
):
804
12
.
43.
Long
X
,
Du
X
,
Wang
Y
,
Qiu
Q
,
Wu
J
,
Huang
Y
, et al
.
Evidence-based practice and future development of enhanced recovery after surgery (ERAS) in urology: a multidimensional assessment based on the GRADE system
.
J Robot Surg
.
2025
;
19
(
1
):
358
.
44.
Antonelli
A
,
Ficarra
V
,
Bertini
R
,
Carini
M
,
Carmignani
G
,
Corti
S
, et al
.
Elective partial nephrectomy is equivalent to radical nephrectomy in patients with clinical T1 renal cell carcinoma: results of a retrospective, comparative, multi-institutional study
.
BJU Int
.
2011
;
109
(
7
):
1013
8
.
45.
Higgins
LJ
,
Hong
K
.
Renal ablation techniques: state of the art
.
AJR Am J Roentgenol
.
2015
;
205
(
4
):
735
41
.
46.
Carbonara
U
,
Ditonno
F
,
Beksac
AT
,
Derweesh
I
,
Cerrato
C
,
Celia
A
, et al
.
Percutaneous cryotherapy and radiofrequency ablation of renal masses: multicenter comparative analysis with minimum 3-year follow-up
.
Int Braz J Urol
.
2025
;
51
(
2
):
e20240565
.
47.
Wu
J
,
Sami
S
,
Lajkosz
K
,
Kishibe
T
,
Ordon
M
.
An updated systematic review and meta-analysis on the technical, oncologic, and safety outcomes of microwave ablation in patients with renal cell carcinoma
.
J Endourol
.
2023
;
37
(
12
):
1314
30
.
48.
Li
KP
,
Chen
SY
,
Wan
S
,
Wang
CY
,
Li
XR
,
Yang
L
.
Percutaneous ablation versus robotic-assisted partial nephrectomy for cT1 renal cell carcinoma: an evidence-based analysis of comparative outcomes
.
J Robot Surg
.
2024
;
18
(
1
):
301
.
49.
Alenezi
AN
,
Karim
O
.
Role of intra-operative contrast-enhanced ultrasound (CEUS) in robotic-assisted nephron-sparing surgery
.
J Robot Surg
.
2015
;
9
(
1
):
1
10
.
50.
Guo
RQ
,
Zhao
PJ
,
Sun
J
,
Li
YM
.
Comparing the oncologic outcomes of local tumor destruction vs. local tumor excision vs. partial nephrectomy in T1a solid renal masses: a population-based cohort study from the SEER database
.
Int J Surg
.
2024
;
110
(
8
):
4571
80
.
51.
Chan
VW
,
Abul
A
,
Osman
FH
,
Ng
HH
,
Wang
K
,
Yuan
Y
, et al
.
Ablative therapies versus partial nephrectomy for small renal masses - a systematic review and meta-analysis
.
Int J Surg
.
2022
;
97
:
106194
.
52.
Aveta
A
,
Iossa
V
,
Spena
G
,
Conforti
P
,
Pagano
G
,
Dinacci
F
, et al
.
Ablative treatments for small renal masses and management of recurrences: a comprehensive review
.
Life
.
2024
;
14
(
4
):
450
.
53.
Iossa
V
,
Pandolfo
SD
,
Buonopane
R
,
Di Girolamo
A
,
Fiore
F
,
Sessa
G
, et al
.
Robot-assisted partial nephrectomy vs. percutaneous cryoablation for T1a renal tumors: a single-center retrospective analysis of outcomes and costs
.
Int Urol Nephrol
.
2024
;
57
(
4
):
1097
104
.

Data & Figures

Fig. 1.

Flow diagram of study selection process.

Fig. 1.

Flow diagram of study selection process.

Close modal
Fig. 2.

Forest plot and meta-analysis of operative time (OT) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 2.

Forest plot and meta-analysis of operative time (OT) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Fig. 3.

Forest plot and meta-analysis of operative time (OT) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Fig. 3.

Forest plot and meta-analysis of operative time (OT) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Close modal
Fig. 4.

Forest plot and meta-analysis of operative time (OT) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Fig. 4.

Forest plot and meta-analysis of operative time (OT) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Close modal
Fig. 5.

Forest plot and meta-analysis of length of stay (LOS) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 5.

Forest plot and meta-analysis of length of stay (LOS) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Fig. 6.

Forest plot and meta-analysis of length of stay (LOS) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Fig. 6.

Forest plot and meta-analysis of length of stay (LOS) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Close modal
Fig. 7.

Forest plot and meta-analysis of length of stay (LOS) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Fig. 7.

Forest plot and meta-analysis of length of stay (LOS) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Close modal
Fig. 8.

Forest plot and meta-analysis of estimated blood loss (EBL) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 8.

Forest plot and meta-analysis of estimated blood loss (EBL) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Fig. 9.

Forest plot and meta-analysis of estimated glomerular filtration rate (eGFR) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 9.

Forest plot and meta-analysis of estimated glomerular filtration rate (eGFR) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Fig. 10.

Forest plot and meta-analysis of overall complication rate (OCR) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 10.

Forest plot and meta-analysis of overall complication rate (OCR) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Fig. 11.

Forest plot and meta-analysis of major complication rate (MCR) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 11.

Forest plot and meta-analysis of major complication rate (MCR) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Fig. 12.

Forest plot and meta-analysis of major complication rate (MCR) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Fig. 12.

Forest plot and meta-analysis of major complication rate (MCR) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Close modal
Fig. 13.

Forest plot and meta-analysis of major complication rate (MCR) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Fig. 13.

Forest plot and meta-analysis of major complication rate (MCR) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Close modal
Fig. 14.

Forest plot and meta-analysis of overall survival (OS) between ablation therapy (AT) and partial nephrectomy (PN).

Fig. 14.

Forest plot and meta-analysis of overall survival (OS) between ablation therapy (AT) and partial nephrectomy (PN).

Close modal
Fig. 15.

Forest plot and meta-analysis of overall survival (OS) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Fig. 15.

Forest plot and meta-analysis of overall survival (OS) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Close modal
Fig. 16.

Forest plot and meta-analysis of recurrence-free survival (RFS) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 16.

Forest plot and meta-analysis of recurrence-free survival (RFS) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Fig. 17.

Forest plot and meta-analysis of recurrence-free survival (RFS) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Fig. 17.

Forest plot and meta-analysis of recurrence-free survival (RFS) between partial nephrectomy (PN) and different types of ablation therapy (AT).

Close modal
Fig. 18.

Forest plot and meta-analysis of recurrence-free survival (RFS) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Fig. 18.

Forest plot and meta-analysis of recurrence-free survival (RFS) between partial nephrectomy (PN) and different surgical approaches of ablation therapy (AT).

Close modal
Fig. 19.

Forest plot and meta-analysis of cancer-specific survival (CSS) between partial nephrectomy (PN) and ablation therapy (AT).

Fig. 19.

Forest plot and meta-analysis of cancer-specific survival (CSS) between partial nephrectomy (PN) and ablation therapy (AT).

Close modal
Table 1.

Baseline data for studies included in the meta-analysis

AuthorYearStudy typeSample (PN/ablation)Age, yearsStageBMI, kg/m2Tumor size, cmOperative methods
Bensalah et al. [122007 Retrospective study 40/14 56.5/62 T1a 31.1/29.6 2.6/2.3 LPNc/LRFAd 
Huang et al. [132016 RCT 45/44 52/51 T1a 24.4/24.8 3.0/2.65 LPN/LRFA 
Ji et al. [142016 Retrospective study 74/105 57.3/64.2 T1a NA 2.9/2.2 LPN/LRFA 
Guan et al. [152012 Retrospective study 54/48 46.4/45.5 T1a 23.1/23/5 2.8/3.1 PN/MWAe 
Park et al. [162019 Retrospective study 53/62 53/58 T1a 24.9/26 2.75/2.14 LPN/LRFA 
Acosta Ruiz et al. [172018 Retrospective study 49/84 63/66 T1 NA 3.2/2.6 LPN/LRFA 
Yu et al. [182020 Retrospective study 185/185 50.9/63.2 T1a NA 2.3/2.3 LPN/PMWA 
Anglickis et al. [192019 Retrospective study 18/15 71.5/75 T1 25/25 3/3.2 OPNf/PMWA 
Kim et al. [202014 Retrospective study 27/27 25.9/26.6 T1-3 25.9/26.6 1.77/1.8 RALPNg/PRFA 
Chung et al. [212022 Retrospective study 46/39 59.4/61.6 T1a NA 2.4/2.2 LPN/PRFA 
Stern et al. [222007 Retrospective study 37/40 56.4/60.5 T1a NA 2.43/2.41 PN/RFA 
Pantelidou et al. [232015 Retrospective study 63/63 54/61 T1 NA 2.88/2.11 RALPN/PRFA 
Cazalas et al. [242023 Retrospective study 75/75 61.1/76.9 T1b 27.9/30.5 NA RALPN/PTAh 
Klein et al. [252023 Retrospective study 112/86 60.7/70.3 T2b 27.9/29.6 NA RALPN/PTA 
Lehrer et al. [262023 Retrospective study 142/66 79/80.4 T1 26.8/27.1 3.2/2.7 RPN/PTA 
Pandolfo et al. [272023 Retrospective study 60/92 56.4/63.4 T1 28/28 NA RAPN/PTA 
Chlorogiannis et al. [282024 Retrospective study 87/71 56/70 T1 NA 3.2/3.0 RPN/PMWA 
Qiu et al. [292023 Retrospective study 80/126 54/67 T1a NA 3.4/3.5 PN/MWA 
Kula et al. [302024 Retrospective study 55/55 56/64 T1a NA 3.0/2.3 LPN/MWA 
Lucignani et al. [312024 Retrospective study 109/62 65/73 T1 25/26 NA RAPN/MWA 
Pedraza-Sánchez et al. [322023 Retrospective study 180/111 57.47/64.49 T1 NA 3.2/2.1 PN/PRFA 
Haramis et al. [332012 Retrospective study 92/75 58.8/69.2 T1a NA 1.9/2.0 LPN/LCAi 
Lin et al. [342008 Retrospective study 14/13 58/69 T1a 28.1/25.9 3.6/2.5 LPN/LCA 
Liu et al. [352021 Retrospective study 55/55 52.3/69.4 T1-T2 25.29/25.0 4.06/3.86 RAPN/LCA 
O’Malley et al. [362006 Retrospective study 15/15 75.7/76.1 T1 27.1/29.1 2.5/2.7 LPN/LCA 
Guillotreau et al. [372012 Retrospective study 210/226 57.8/67.4 T1 30.1/29.3 2.4/2.2 RPN/LCA 
Fraisse et al. [382017 Retrospective study 177/177 59.9/69.9 T1 26.4/27.9 2.8/2.6 RPN/LCA 
Yanagisawa et al. [392020 Retrospective study 90/90 69.5/68.5 T1 NA 2.9/2.8 LPN/PCA 
Haber et al. [402011 Retrospective study 48/30 60.6/60.9 T2 30.1/31.5 3.2/2.6 LPN/PCA 
Uemura et al. [412021 Retrospective study 78/48 61/78 T1 23/23 NA RAPN/PCA 
Pandolfo et al. [272022 Retrospective study 50/119 65/61 T1 26.6/29.6 NA RAPN/PTA 
Millan et al. [422022 Retrospective study 2,001/275 60/67 T1 NA 2.6/2.6 PN/TA 
AuthorYearStudy typeSample (PN/ablation)Age, yearsStageBMI, kg/m2Tumor size, cmOperative methods
Bensalah et al. [122007 Retrospective study 40/14 56.5/62 T1a 31.1/29.6 2.6/2.3 LPNc/LRFAd 
Huang et al. [132016 RCT 45/44 52/51 T1a 24.4/24.8 3.0/2.65 LPN/LRFA 
Ji et al. [142016 Retrospective study 74/105 57.3/64.2 T1a NA 2.9/2.2 LPN/LRFA 
Guan et al. [152012 Retrospective study 54/48 46.4/45.5 T1a 23.1/23/5 2.8/3.1 PN/MWAe 
Park et al. [162019 Retrospective study 53/62 53/58 T1a 24.9/26 2.75/2.14 LPN/LRFA 
Acosta Ruiz et al. [172018 Retrospective study 49/84 63/66 T1 NA 3.2/2.6 LPN/LRFA 
Yu et al. [182020 Retrospective study 185/185 50.9/63.2 T1a NA 2.3/2.3 LPN/PMWA 
Anglickis et al. [192019 Retrospective study 18/15 71.5/75 T1 25/25 3/3.2 OPNf/PMWA 
Kim et al. [202014 Retrospective study 27/27 25.9/26.6 T1-3 25.9/26.6 1.77/1.8 RALPNg/PRFA 
Chung et al. [212022 Retrospective study 46/39 59.4/61.6 T1a NA 2.4/2.2 LPN/PRFA 
Stern et al. [222007 Retrospective study 37/40 56.4/60.5 T1a NA 2.43/2.41 PN/RFA 
Pantelidou et al. [232015 Retrospective study 63/63 54/61 T1 NA 2.88/2.11 RALPN/PRFA 
Cazalas et al. [242023 Retrospective study 75/75 61.1/76.9 T1b 27.9/30.5 NA RALPN/PTAh 
Klein et al. [252023 Retrospective study 112/86 60.7/70.3 T2b 27.9/29.6 NA RALPN/PTA 
Lehrer et al. [262023 Retrospective study 142/66 79/80.4 T1 26.8/27.1 3.2/2.7 RPN/PTA 
Pandolfo et al. [272023 Retrospective study 60/92 56.4/63.4 T1 28/28 NA RAPN/PTA 
Chlorogiannis et al. [282024 Retrospective study 87/71 56/70 T1 NA 3.2/3.0 RPN/PMWA 
Qiu et al. [292023 Retrospective study 80/126 54/67 T1a NA 3.4/3.5 PN/MWA 
Kula et al. [302024 Retrospective study 55/55 56/64 T1a NA 3.0/2.3 LPN/MWA 
Lucignani et al. [312024 Retrospective study 109/62 65/73 T1 25/26 NA RAPN/MWA 
Pedraza-Sánchez et al. [322023 Retrospective study 180/111 57.47/64.49 T1 NA 3.2/2.1 PN/PRFA 
Haramis et al. [332012 Retrospective study 92/75 58.8/69.2 T1a NA 1.9/2.0 LPN/LCAi 
Lin et al. [342008 Retrospective study 14/13 58/69 T1a 28.1/25.9 3.6/2.5 LPN/LCA 
Liu et al. [352021 Retrospective study 55/55 52.3/69.4 T1-T2 25.29/25.0 4.06/3.86 RAPN/LCA 
O’Malley et al. [362006 Retrospective study 15/15 75.7/76.1 T1 27.1/29.1 2.5/2.7 LPN/LCA 
Guillotreau et al. [372012 Retrospective study 210/226 57.8/67.4 T1 30.1/29.3 2.4/2.2 RPN/LCA 
Fraisse et al. [382017 Retrospective study 177/177 59.9/69.9 T1 26.4/27.9 2.8/2.6 RPN/LCA 
Yanagisawa et al. [392020 Retrospective study 90/90 69.5/68.5 T1 NA 2.9/2.8 LPN/PCA 
Haber et al. [402011 Retrospective study 48/30 60.6/60.9 T2 30.1/31.5 3.2/2.6 LPN/PCA 
Uemura et al. [412021 Retrospective study 78/48 61/78 T1 23/23 NA RAPN/PCA 
Pandolfo et al. [272022 Retrospective study 50/119 65/61 T1 26.6/29.6 NA RAPN/PTA 
Millan et al. [422022 Retrospective study 2,001/275 60/67 T1 NA 2.6/2.6 PN/TA 

BMI, body mass index.

Table 2.

Quality score of included studies based on the NOS scale

StudySelectionComparabilityExposureTotal stars
RECSNECAEDOSCAFAOFUAFU
Bensalah et al. [12​ ​ 
Huang et al. [13​ ​ 
Ji et al. [14​ ​ 
Guan et al. [15​ ​ 
Park et al. [16​ ​ 
Acosta Ruiz et al. [17​ ​ ​ 
Yu et al. [18​ ​ 
Anglickis et al. [19​ ​ ​ 
Kim et al. [20​ ​ 
Chung et al. [21​ ​ 
Stern et al. [22​ ​ 
Pantelidou et al. [23​ 
Cazalas et al. [24​ ​ 
Klein et al. [25​ ​ 
Lehrer et al. [26​ ​ 
Pandolfo et al. [27​ ​ 
Chlorogiannis et al. [28​ ​ ​ 
Qiu et al. [29​ ​ 
Kula et al. [30​ ​ ​ 
Lucignani et al. [31​ ​ 
Pedraza-Sánchez et al. [32​ ​ 
Haramis et al. [33​ ​ 
Lin et al. [34​ ​ 
Liu et al. [35​ ​ ​ 
O’Malley et al. [36​ ​ 
Guillotreau et al. [37​ ​ ​ 
Fraisse et al. [38​ ​ ​ 
Yanagisawa et al. [39​ 
Haber et al. [40​ ​ ​ 
Uemura et al. [41​ ​ ​ 
Pandolfo et al. [27​ ​ ​ 
Millan et al. [42​ ​ 
StudySelectionComparabilityExposureTotal stars
RECSNECAEDOSCAFAOFUAFU
Bensalah et al. [12​ ​ 
Huang et al. [13​ ​ 
Ji et al. [14​ ​ 
Guan et al. [15​ ​ 
Park et al. [16​ ​ 
Acosta Ruiz et al. [17​ ​ ​ 
Yu et al. [18​ ​ 
Anglickis et al. [19​ ​ ​ 
Kim et al. [20​ ​ 
Chung et al. [21​ ​ 
Stern et al. [22​ ​ 
Pantelidou et al. [23​ 
Cazalas et al. [24​ ​ 
Klein et al. [25​ ​ 
Lehrer et al. [26​ ​ 
Pandolfo et al. [27​ ​ 
Chlorogiannis et al. [28​ ​ ​ 
Qiu et al. [29​ ​ 
Kula et al. [30​ ​ ​ 
Lucignani et al. [31​ ​ 
Pedraza-Sánchez et al. [32​ ​ 
Haramis et al. [33​ ​ 
Lin et al. [34​ ​ 
Liu et al. [35​ ​ ​ 
O’Malley et al. [36​ ​ 
Guillotreau et al. [37​ ​ ​ 
Fraisse et al. [38​ ​ ​ 
Yanagisawa et al. [39​ 
Haber et al. [40​ ​ ​ 
Uemura et al. [41​ ​ ​ 
Pandolfo et al. [27​ ​ ​ 
Millan et al. [42​ ​ 

REC, representativeness of the cohort; SNEC, selection of the none posed cohort; AE, ascertainment of exposure; DO, demonstration that outcome of interest was not present at start of study; SC, study controls most important factors; AF, study controls for other important factors; AO, assessment of outcome; FU, follow-up long enough for outcomes to occur; AFU, adequacy of follow-up of cohort (≥80%).

Supplements

References

1.
Sun
Z
,
Li
T
,
Xiao
C
,
Zou
S
,
Zhang
M
,
Zhang
Q
, et al
.
Prediction of overall survival based upon a new ferroptosis-related gene signature in patients with clear cell renal cell carcinoma
.
World J Surg Oncol
.
2022
;
20
(
1
):
120
.
2.
Leyderman
M
,
McElree
IM
,
Nepple
KG
,
Zakharia
Y
,
Ghodoussipour
S
,
Packiam
VT
.
Management of renal cell carcinoma with supradiaphragmatic inferior vena cava thrombus diagnosed during acute COVID-19 infection
.
Cureus
.
2024
;
16
(
3
):
e55565
.
3.
Plekhanova
OAP
,
Mono
PM
,
Martov
AGM
,
Golubev
MYG
,
Grigoriev
NAG
,
Kyzlasov
PSK
, et al
.
[Comparative analysis of clinical features of robotic-assisted and laparoscopic partial nephrectomy]
.
Urologiia
.
2021
(
3
):
92
7
.
4.
Nishimura
K
,
Sawada
Y
,
Sugihara
N
,
Funaki
K
,
Koyama
K
,
Noda
T
, et al
.
A low RENAL nephrometry score can avoid the need for the intraoperative insertion of a ureteral catheter in robot-assisted partial nephrectomy
.
World J Surg Oncol
.
2021
;
19
(
1
):
40
.
5.
Ge
S
,
Wang
Z
,
Li
Y
,
Zheng
L
,
Gan
L
,
Zeng
Z
, et al
.
Is ablation suitable for small renal masses? A meta-analysis
.
Acad Radiol
.
2025
;
32
(
1
):
218
35
.
6.
Stroup
SP
,
Kopp
RP
,
Derweesh
IH
.
Laparoscopic and percutaneous cryotherapy for renal neoplasms
.
Panminerva Med
.
2010
;
52
(
4
):
331
8
.
7.
Andrews
JR
,
Atwell
T
,
Schmit
G
,
Lohse
CM
,
Kurup
AN
,
Weisbrod
A
, et al
.
Oncologic outcomes following partial nephrectomy and percutaneous ablation for cT1 renal masses
.
Eur Urol
.
2019
;
76
(
2
):
244
51
.
8.
Gao
H
,
Zhou
L
,
Zhang
J
,
Wang
Q
,
Luo
Z
,
Xu
Q
, et al
.
Comparative efficacy of cryoablation versus robot-assisted partial nephrectomy in the treatment of cT1 renal tumors: a systematic review and meta-analysis
.
BMC Cancer
.
2024
;
24
(
1
):
1150
.
9.
Uhlig
J
,
Strauss
A
,
Rücker
G
,
Seif Amir Hosseini
A
,
Lotz
J
,
Trojan
L
, et al
.
Partial nephrectomy versus ablative techniques for small renal masses: a systematic review and network meta-analysis
.
Eur Radiol
.
2018
;
29
(
3
):
1293
307
.
10.
Dan
W
,
Ya
L
,
Yang
L
,
Dong
L
.
A systematic review and meta-analysis of laparoscopic partial nephrectomy versus laparoscopic focal therapy for small renal masses
.
Medicine
.
2025
;
104
(
33
):
e44048
.
11.
Hans-Jonas
M
,
Timo Christian
M
,
Manuel Florian
S
,
Silke
Z
.
Efficacy and safety of percutaneous thermal ablation in Bosniak III and IV cystic renal masses: a systematic review and meta-analysis
.
Diagn Interv Radiol
.
2025
;
31
(
6
):
605
11
.
12.
Bensalah
K
,
Zeltser
I
,
Tuncel
A
,
Cadeddu
J
,
Lotan
Y
.
Evaluation of costs and morbidity associated with laparoscopic radiofrequency ablation and laparoscopic partial nephrectomy for treating small renal tumours
.
BJU Int
.
2007
;
101
(
4
):
467
71
.
13.
Huang
J
,
Zhang
J
,
Wang
Y
,
Kong
W
,
Xue
W
,
Liu
D
, et al
.
Comparing zero ischemia laparoscopic radio frequency ablation assisted tumor enucleation and laparoscopic partial nephrectomy for clinical T1a renal tumor: a randomized clinical trial
.
J Urol
.
2016
;
195
(
6
):
1677
83
.
14.
Ji
C
,
Zhao
X
,
Zhang
S
,
Liu
G
,
Li
X
,
Zhang
G
, et al
.
Laparoscopic radiofrequency ablation versus partial nephrectomy for cT1a renal tumors: long-term outcome of 179 patients
.
Urol Int
.
2016
;
96
(
3
):
345
53
.
15.
Guan
W
,
Bai
J
,
Liu
J
,
Wang
S
,
Zhuang
Q
,
Ye
Z
, et al
.
Microwave ablation versus partial nephrectomy for small renal tumors: intermediate-term results
.
J Surg Oncol
.
2012
;
106
(
3
):
316
21
.
16.
Park
JM
,
Yang
SW
,
Shin
JH
,
Na
YG
,
Song
KH
,
Lim
JS
.
Oncological and functional outcomes of laparoscopic radiofrequency ablation and partial nephrectomy for T1a renal masses: a retrospective single-center 60 month follow-up cohort study
.
Urol J
.
2018
;
16
(
1
):
44
49
.
17.
Acosta Ruiz
V
,
Ladjevardi
S
,
Brekkan
E
,
Häggman
M
,
Lönnemark
M
,
Wernroth
L
, et al
.
Periprocedural outcome after laparoscopic partial nephrectomy versus radiofrequency ablation for T1 renal tumors: a modified R.E.N.A.L nephrometry score adjusted comparison
.
Acta Radiol
.
2019
;
60
(
2
):
260
8
.
18.
Yu
J
,
Liang
P
,
Yu
XL
,
Cheng
ZG
,
Han
ZY
,
Zhang
X
, et al
.
US-guided percutaneous microwave ablation versus open radical nephrectomy for small renal cell carcinoma: intermediate-term results
.
Radiology
.
2014
;
270
(
3
):
880
7
.
19.
Anglickis
M
,
Anglickienė
G
,
Andreikaitė
G
,
Skrebūnas
A
.
Microwave thermal ablation versus open partial nephrectomy for the treatment of small renal tumors in patients over 70 years old
.
Med Kaunas
.
2019
;
55
(
10
):
664
.
20.
Kim
S
,
Lee
E
,
Kim
H
,
Kwak
C
,
Ku
J
,
Lee
S
, et al
.
A propensity-matched comparison of perioperative complications and of chronic kidney disease between robot-assisted laparoscopic partial nephrectomy and radiofrequency ablative therapy
.
Asian J Surg
.
2015
;
38
(
3
):
126
33
.
21.
Chung
D
,
Hwang
H
,
Sohn
D
.
Radiofrequency ablation using real-time ultrasonography-computed tomography fusion imaging improves treatment outcomes for T1a renal cell carcinoma: comparison with laparoscopic partial nephrectomy
.
Investig Clin Urol
.
2022
;
63
(
2
):
159
67
.
22.
Stern
JM
,
Svatek
R
,
Park
S
,
Hermann
M
,
Lotan
Y
,
Sagalowsky
AI
, et al
.
Intermediate comparison of partial nephrectomy and radiofrequency ablation for clinical T1a renal tumours
.
BJU Int
.
2007
;
100
(
2
):
287
90
.
23.
Pantelidou
M
,
Challacombe
B
,
McGrath
A
,
Brown
M
,
Ilyas
S
,
Katsanos
K
, et al
.
Percutaneous radiofrequency ablation versus robotic-assisted partial nephrectomy for the treatment of small renal cell carcinoma
.
Cardiovasc Interv Radiol
.
2016
;
39
(
11
):
1595
603
.
24.
Cazalas
G
,
Klein
C
,
Piana
G
,
De Kerviler
E
,
Gangi
A
,
Puech
P
, et al
.
A multicenter comparative matched-pair analysis of percutaneous tumor ablation and robotic-assisted partial nephrectomy of T1b renal cell carcinoma (AblatT1b study-UroCCR 80)
.
Eur Radiol
.
2023
;
33
(
9
):
6513
21
.
25.
Klein
C
,
Cazalas
G
,
Margue
G
,
Piana
G
,
DE Kerviler
E
,
Gangi
A
, et al
.
Percutaneous tumor ablation versus image guided robotic-assisted partial nephrectomy for cT1b renal cell carcinoma: a comparative matched-pair analysis (UroCCR 80)
.
Minerva Urol Nephrol
.
2023
;
75
(
5
):
559
68
.
26.
Lehrer
R
,
Cornelis
F
,
Bernhard
JC
,
Bigot
P
,
Champy
C
,
Bruyère
F
, et al
.
Minimally invasive nephron-sparing treatments for T1 renal cell cancer in patients over 75 years: a comparison of outcomes after robot-assisted partial nephrectomy and percutaneous ablation
.
Eur Radiol
.
2023
;
33
(
12
):
8426
35
.
27.
Pandolfo
SD
,
Loizzo
D
,
Beksac
AT
,
Derweesh
I
,
Celia
A
,
Bianchi
L
, et al
.
Percutaneous thermal ablation for cT1 renal mass in solitary kidney: a multicenter trifecta comparative analysis versus robot-assisted partial nephrectomy
.
Eur J Surg Oncol
.
2023
;
49
(
2
):
486
90
.
28.
Chlorogiannis
DD
,
Kratiras
Z
,
Efthymiou
E
,
Moulavasilis
N
,
Kelekis
N
,
Chrisofos
M
, et al
.
Percutaneous microwave ablation versus robot-assisted partial nephrectomy for stage I renal cell carcinoma: a propensity-matched cohort study focusing upon long-term Follow-Up of oncologic outcomes
.
Cardiovasc Interv Radiol
.
2024
;
47
(
5
):
573
82
.
29.
Qiu
J
,
Ballantyne
C
,
Lange
M
,
Kennady
E
,
Yeaman
C
,
Culp
S
, et al
.
Comparison of microwave ablation and partial nephrectomy for T1a small renal masses
.
Urol Oncol
.
2023
;
41
(
10
):
434.e9
16
.
30.
Kula
O
,
Ateş
Y
,
Çek
HM
,
Tozsin
A
,
Günay
B
,
Akgül
B
, et al
.
Comparison of the efficacy of percutaneous microwave ablation therapy versus laparoscopic partial nephrectomy for early-stage renal tumors
.
Diagnostics
.
2024
;
14
(
14
):
1574
.
31.
Lucignani
G
,
De Lorenzis
E
,
Ierardi
AM
,
Silvani
C
,
Marmiroli
A
,
Nizzardo
M
, et al
.
Perioperative and survival outcomes of patients treated with robot-assisted partial nephrectomy and percutaneous microwave ablation for small renal masses: a single center experience
.
Clin Genitourin Cancer
.
2024
;
22
(
2
):
8426
35
.
32.
Pedraza-Sánchez
JP
,
Chaves-Marcos
R
,
Mazuecos-Quirós
J
,
Bisonó-Castillo
ÁL
,
Osmán-García
I
,
Gutiérrez-Marín
CM
, et al
.
Percutaneous radiofrequency ablation is an effective treatment option for small renal masses, comparable to partial nephrectomy
.
Eur Radiol
.
2023
;
33
(
11
):
7371
9
.
33.
Haramis
G
,
Graversen
JA
,
Mues
AC
,
Korets
R
,
Rosales
JC
,
Okhunov
Z
, et al
.
Retrospective comparison of laparoscopic partial nephrectomy versus laparoscopic renal cryoablation for small (<3.5 cm) cortical renal masses
.
J Laparoendosc Adv Surg Tech
.
2012
;
22
(
2
):
152
7
.
34.
Lin
YC
,
Turna
B
,
Frota
R
,
Aron
M
,
Haber
GP
,
Kamoi
K
, et al
.
Laparoscopic partial nephrectomy versus laparoscopic cryoablation for multiple ipsilateral renal tumors
.
Eur Urol
.
2008
;
53
(
6
):
1210
6
.
35.
Liu
HY
,
Kang
CH
,
Wang
HJ
,
Chen
CH
,
Luo
HL
,
Chen
YT
, et al
.
Comparison of robot-assisted laparoscopic partial nephrectomy with laparoscopic cryoablation in the treatment of localised renal tumours: a propensity score-matched comparison of long-term outcomes
.
Diagnostics
.
2021
;
11
(
5
):
759
.
36.
O’Malley
RL
,
Berger
AD
,
Kanofsky
JA
,
Phillips
CK
,
Stifelman
M
,
Taneja
SS
.
A matched-cohort comparison of laparoscopic cryoablation and laparoscopic partial nephrectomy for treating renal masses
.
BJU Int
.
2006
;
99
(
2
):
395
8
.
37.
Guillotreau
J
,
Haber
GP
,
Autorino
R
,
Miocinovic
R
,
Hillyer
S
,
Hernandez
A
, et al
.
Robotic partial nephrectomy versus laparoscopic cryoablation for the small renal mass
.
Eur Urol
.
2012
;
61
(
5
):
899
904
.
38.
Fraisse
G
,
Colleter
L
,
Peyronnet
B
,
Khene
ZE
,
Mandoorah
Q
,
Soorojebally
Y
, et al
.
Peri-operative and local control outcomes of robot-assisted partial nephrectomy vs percutaneous cryoablation for renal masses: comparison after matching on radiological stage and renal score
.
BJU Int
.
2019
;
123
(
4
):
632
8
.
39.
Yanagisawa
T
,
Miki
J
,
Shimizu
K
,
Fukuokaya
W
,
Urabe
F
,
Mori
K
, et al
.
Functional and oncological outcome of percutaneous cryoablation versus laparoscopic partial nephrectomy for clinical T1 renal tumors: a propensity score-matched analysis
.
Urol Oncol
.
2020
;
38
(
12
):
938.e1
7
.
40.
Haber
G
,
Lee
MC
,
Crouzet
S
,
Kamoi
K
,
Gill
IS
.
Tumour in solitary kidney: laparoscopic partial nephrectomy vs laparoscopic cryoablation
.
BJU Int
.
2011
;
109
(
1
):
118
24
.
41.
Uemura
T
,
Kato
T
,
Nagahara
A
,
Kawashima
A
,
Hatano
K
,
Ujike
T
, et al
.
Therapeutic and clinical outcomes of robot-assisted partial nephrectomy versus cryoablation for T1 renal cell carcinoma
.
In Vivo
.
2021
;
35
(
3
):
1573
9
.
42.
Millan
B
,
Breau
RH
,
Bhindi
B
,
Mallick
R
,
Tanguay
S
,
Finelli
A
, et al
.
A comparison of percutaneous ablation therapy to partial nephrectomy for cT1a renal cancers: results from the Canadian kidney cancer information system
.
J Urol
.
2022
;
208
(
4
):
804
12
.
43.
Long
X
,
Du
X
,
Wang
Y
,
Qiu
Q
,
Wu
J
,
Huang
Y
, et al
.
Evidence-based practice and future development of enhanced recovery after surgery (ERAS) in urology: a multidimensional assessment based on the GRADE system
.
J Robot Surg
.
2025
;
19
(
1
):
358
.
44.
Antonelli
A
,
Ficarra
V
,
Bertini
R
,
Carini
M
,
Carmignani
G
,
Corti
S
, et al
.
Elective partial nephrectomy is equivalent to radical nephrectomy in patients with clinical T1 renal cell carcinoma: results of a retrospective, comparative, multi-institutional study
.
BJU Int
.
2011
;
109
(
7
):
1013
8
.
45.
Higgins
LJ
,
Hong
K
.
Renal ablation techniques: state of the art
.
AJR Am J Roentgenol
.
2015
;
205
(
4
):
735
41
.
46.
Carbonara
U
,
Ditonno
F
,
Beksac
AT
,
Derweesh
I
,
Cerrato
C
,
Celia
A
, et al
.
Percutaneous cryotherapy and radiofrequency ablation of renal masses: multicenter comparative analysis with minimum 3-year follow-up
.
Int Braz J Urol
.
2025
;
51
(
2
):
e20240565
.
47.
Wu
J
,
Sami
S
,
Lajkosz
K
,
Kishibe
T
,
Ordon
M
.
An updated systematic review and meta-analysis on the technical, oncologic, and safety outcomes of microwave ablation in patients with renal cell carcinoma
.
J Endourol
.
2023
;
37
(
12
):
1314
30
.
48.
Li
KP
,
Chen
SY
,
Wan
S
,
Wang
CY
,
Li
XR
,
Yang
L
.
Percutaneous ablation versus robotic-assisted partial nephrectomy for cT1 renal cell carcinoma: an evidence-based analysis of comparative outcomes
.
J Robot Surg
.
2024
;
18
(
1
):
301
.
49.
Alenezi
AN
,
Karim
O
.
Role of intra-operative contrast-enhanced ultrasound (CEUS) in robotic-assisted nephron-sparing surgery
.
J Robot Surg
.
2015
;
9
(
1
):
1
10
.
50.
Guo
RQ
,
Zhao
PJ
,
Sun
J
,
Li
YM
.
Comparing the oncologic outcomes of local tumor destruction vs. local tumor excision vs. partial nephrectomy in T1a solid renal masses: a population-based cohort study from the SEER database
.
Int J Surg
.
2024
;
110
(
8
):
4571
80
.
51.
Chan
VW
,
Abul
A
,
Osman
FH
,
Ng
HH
,
Wang
K
,
Yuan
Y
, et al
.
Ablative therapies versus partial nephrectomy for small renal masses - a systematic review and meta-analysis
.
Int J Surg
.
2022
;
97
:
106194
.
52.
Aveta
A
,
Iossa
V
,
Spena
G
,
Conforti
P
,
Pagano
G
,
Dinacci
F
, et al
.
Ablative treatments for small renal masses and management of recurrences: a comprehensive review
.
Life
.
2024
;
14
(
4
):
450
.
53.
Iossa
V
,
Pandolfo
SD
,
Buonopane
R
,
Di Girolamo
A
,
Fiore
F
,
Sessa
G
, et al
.
Robot-assisted partial nephrectomy vs. percutaneous cryoablation for T1a renal tumors: a single-center retrospective analysis of outcomes and costs
.
Int Urol Nephrol
.
2024
;
57
(
4
):
1097
104
.

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