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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">MI</journal-id>
<journal-title-group>
<journal-title>Medicine International</journal-title>
</journal-title-group>
<issn pub-type="ppub">2754-3242</issn>
<issn pub-type="epub">2754-1304</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">MI-5-4-00247</article-id>
<article-id pub-id-type="doi">10.3892/mi.2025.247</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Influence of tumor-associated factors on the treatment selection between partial nephrectomy and ablation therapy for small renal tumors (Review)</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Bekku</surname><given-names>Kensuke</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
<xref rid="c1-MI-5-4-00247" ref-type="corresp"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Inoue</surname><given-names>Shota</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Yoshinaga</surname><given-names>Kasumi</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Yamanoi</surname><given-names>Tomoaki</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Mitsui</surname><given-names>Yosuke</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Kawada</surname><given-names>Tatsushi</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Tominaga</surname><given-names>Yusuke</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Sadahira</surname><given-names>Takuya</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Iwata</surname><given-names>Takehiro</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Katayama</surname><given-names>Satoshi</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Nishimura</surname><given-names>Shingo</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Edamura</surname><given-names>Kohei</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Kobayashi</surname><given-names>Tomoko</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Araki</surname><given-names>Motoo</given-names></name>
<xref rid="af1-MI-5-4-00247" ref-type="aff"/>
</contrib>
</contrib-group>
<aff id="af1-MI-5-4-00247">Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700‑8558, Japan</aff>
<author-notes>
<corresp id="c1-MI-5-4-00247"><italic>Correspondence to:</italic> Dr Kensuke Bekku, Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-chou, Kita-ku, Okayama 700-8558, Japan <email>gmd421030@s.okayama-u.ac.jp</email></corresp>
</author-notes>
<pub-date pub-type="collection"><season>Jul-Aug</season><year>2025</year></pub-date>
<pub-date pub-type="epub"><day>04</day><month>06</month><year>2025</year></pub-date>
<volume>5</volume>
<issue>4</issue>
<elocation-id>48</elocation-id>
<history>
<date date-type="received">
<day>13</day>
<month>02</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>13</day>
<month>05</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2025 Bekku et al.</copyright-statement>
<copyright-year>2025</copyright-year>
<license license-type="open-access">
<license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.</license-p></license>
</permissions>
<abstract>
<p>For small renal tumors, nephron-preserving treatment, including partial nephrectomy or ablation therapy, is recommended. According to major guidelines, ablation therapies are advised for patients who are deemed not suitable to undergo surgery due to an advanced age or the presence of comorbidities. However, compared with surgery, ablation therapy can result in superior safety and functional outcomes. The present review discusses the factors affecting decision-making as regards treatment options for small renal tumors. When determining an appropriate treatment option, tumor locations, as well as the condition and preferences of the patient, are considered. Scoring systems, such as the RENAL Nephrometry Score can assist in guiding treatment decisions. However, surgery may be the preferred approach for tumors near major vessels and collecting systems. For endophytic tumors, partial nephrectomy can be challenging due to the difficulty in visualizing intra-parenchymal tumors during the procedure, whereas ablation therapies may be inferior to partial nephrectomy. Although treatment selection for small renal tumors can be affected by tumor location, partial nephrectomy remains the gold standard for numerous cases.</p>
</abstract>
<kwd-group>
<kwd>small renal mass</kwd>
<kwd>partial nephrectomy</kwd>
<kwd>ablation therapy</kwd>
<kwd>tumor location</kwd>
<kwd>endophytic tumor</kwd>
</kwd-group>
<funding-group>
<funding-statement><bold>Funding:</bold> Not applicable.</funding-statement>
</funding-group>
</article-meta>
</front>
<body>
<sec>
<title>1. Introduction</title>
<p>The increasing use of imaging techniques, such as computed tomography (CT), ultrasound and magnetic resonance imaging, has led to an increase in the incidental detection of small renal tumors. For small-scale cancers, a partial nephrectomy (PN) or ablation therapy (AT) is highly recommended to preserve kidney function. ATs, such as cryoablation (CA) and radiofrequency ablation (RFA), have emerged as valuable treatment options (<xref rid="b1-MI-5-4-00247" ref-type="bibr">1</xref>), whereas PN remains the gold standard for the treatment of small renal tumors, particularly for clinical T1a (cT1a, #x003C;4 cm) tumors. Based on major guidelines, ATs are recommended for selected patients deemed unfit for surgery (<xref rid="b2-MI-5-4-00247" ref-type="bibr">2</xref>,<xref rid="b3-MI-5-4-00247" ref-type="bibr">3</xref>); however, ATs can achieve favorable oncological outcomes comparable to those of PN (<xref rid="b4-MI-5-4-00247" ref-type="bibr">4</xref>,<xref rid="b5-MI-5-4-00247" ref-type="bibr">5</xref>). As ATs may provide outcomes superior to those of PN in selected patients (<xref rid="b6-MI-5-4-00247 b7-MI-5-4-00247 b8-MI-5-4-00247" ref-type="bibr">6-8</xref>), the selection between PN and AT for small renal tumors remains a topic of debate, and is affected by multiple factors, such as patient health, preoperative renal function and tumor-associated factors, such as tumor complexity. Although ATs are less invasive and suitable for patients who are deemed unfit for surgery, establishing the criteria for &#x2018;poor surgical candidates&#x2019; is challenging. The decision becomes particularly complex when considering older adults or otherwise healthy individuals or younger patients with multiple comorbidities. As regards recovery time and complications, AT is generally associated with a shorter hospitalization period, a reduced operative time, lower morbidity rates and a more rapid recovery than that observed following surgical options (<xref rid="b6-MI-5-4-00247 b7-MI-5-4-00247 b8-MI-5-4-00247" ref-type="bibr">6-8</xref>). These advantages are particularly relevant for patients who wish to minimize their downtime or have other health concerns. Although surgery remains the gold standard for numerous patients, some may prefer the less invasive nature of ATs, particularly for small renal masses, for which observation may also be a reasonable option. In some cases, the discretion and experience of the clinician, as well as patient preferences may influence treatment selection (<xref rid="b9-MI-5-4-00247" ref-type="bibr">9</xref>).</p>
<p>Tumor location also plays a critical role in determining appropriate treatment strategies. Although basing treatment decisions on tumor-associated factors can provide a holistic approach (<xref rid="b10-MI-5-4-00247" ref-type="bibr">10</xref>), their effect on the selection of nephron-sparing treatment remains uncertain. The present review discusses how tumor-associated factors affect the oncological and functional outcomes of cT1 renal cancers.</p>
</sec>
<sec>
<title>2. Scoring systems and treatment selection</title>
<p>High-complexity tumors, such as hilar or endophytic tumors, are associated with a higher risk of negative oncological outcomes and severe complications when treating small renal masses (<xref rid="b11-MI-5-4-00247" ref-type="bibr">11</xref>). The RENAL Nephrometry Score is commonly used to assess tumor complexity and to aid in treatment approaches for small renal tumors (<xref rid="b9-MI-5-4-00247 b10-MI-5-4-00247 b11-MI-5-4-00247 b12-MI-5-4-00247 b13-MI-5-4-00247" ref-type="bibr">9-13</xref>). The system consists of five factors, and is simple and practical. A previous study supported the usefulness of scoring systems for predicting the oncological and safety outcomes of ATs and PN (<xref rid="b14-MI-5-4-00247" ref-type="bibr">14</xref>). Schmit <italic>et al</italic> (<xref rid="b14-MI-5-4-00247" ref-type="bibr">14</xref>) demonstrated an association between the RENAL score and the outcomes of percutaneous ATs. Patients who experienced treatment failure had significantly higher RENAL scores than those in patients without treatment failure (mean, 7.6 vs. 6.7; P#x003C;0.001) (<xref rid="b14-MI-5-4-00247" ref-type="bibr">14</xref>). Furthermore, patients who experienced major complications had significantly higher RENAL scores than those in patients without (mean, 8.1 vs. 6.8; P#x003C;0.001) (<xref rid="b14-MI-5-4-00247" ref-type="bibr">14</xref>).</p>
<p>The Preoperative Aspects and Dimensions Used for an Anatomical (PADUA) score is another system used to assess the tumor complexity. Compared to the RENAL score, the system provides more detailed three-dimensional and anatomical information (<xref rid="b15-MI-5-4-00247" ref-type="bibr">15</xref>). Takahara <italic>et al</italic> (<xref rid="b15-MI-5-4-00247" ref-type="bibr">15</xref>) demonstrated that trifecta achievement in patients with PADUA scores &#x2265;10 was significantly lower than that in those with scores #x003C;10 (68 vs. 86&#x0025;). However, the aforementioned studies investigated the outcomes of different interventions using different scoring systems (<xref rid="b14-MI-5-4-00247" ref-type="bibr">14</xref>,<xref rid="b15-MI-5-4-00247" ref-type="bibr">15</xref>). To date, to the best of our knowledge, no scoring system has been developed to compare the outcomes of both PN and ATs. Although treatment decisions based on tumor-associated factors ensure a comprehensive approach, their effect on nephron-sparing treatment selection remains uncertain.</p>
</sec>
<sec>
<title>3. Novel scoring systems to improve prediction for the outcomes of AT</title>
<p>Several novel scoring systems have been developed or modified to predict the outcomes of each treatment more accurately (<xref rid="b16-MI-5-4-00247" ref-type="bibr">16</xref>). Gahan <italic>et al</italic> (<xref rid="b17-MI-5-4-00247" ref-type="bibr">17</xref>) proposed a modified RENAL score based on AT outcomes, primarily involving percutaneous ATs. In this scoring system, tumor size was scaled down compared to the original scale, reflecting the general trend that tumors treated with ATs are typically #x003C;4 cm (<xref rid="b17-MI-5-4-00247" ref-type="bibr">17</xref>). Their findings indicated that the modified score was significantly associated with initial ablation success and recurrence rates. However, this modified system may limit direct comparison in patients undergoing PN (<xref rid="b17-MI-5-4-00247" ref-type="bibr">17</xref>). Additionally, a previous meta-analysis assessing existing scoring systems found that although these systems could predict warm ischemic time and complications, they failed to predict a trifecta achievement in PN (<xref rid="b9-MI-5-4-00247" ref-type="bibr">9</xref>). Thus, the usefulness of these scoring systems for predicting oncological and functional outcomes of both treatments remain unclear. The ABLATE (A: Axial tumor diameter, B: Bowel proximity, L: Location within the kidney, A: Angle, T: touching, E: extra) and simplified ABLATE scores were developed to predict the probability of complications and oncological outcomes following AT (<xref rid="b16-MI-5-4-00247" ref-type="bibr">16</xref>). These scores consider the association between renal tumors and adjacent abdominal organs, particularly the colon and intestines. A previous study identified tumor depth as an independent predictor of treatment failure following AT. Compared to PN, tumor location within the body is a more critical factor in determining the feasibility of AT (<xref rid="b16-MI-5-4-00247" ref-type="bibr">16</xref>).</p>
</sec>
<sec>
<title>4. Components of scoring systems and their significance</title>
<p>It may be challenging for any single scoring system to be applied to all small renal tumors to predict outcomes and guide treatment decisions. An independent evaluation of the scoring system components can help interpret the significance of the findings. Larger tumors tend to have higher malignant potential (<xref rid="b9-MI-5-4-00247" ref-type="bibr">9</xref>). Although previous studies have applied ATs to larger tumors (&#x003E;4 cm in diameter; cT1b) (<xref rid="b18-MI-5-4-00247" ref-type="bibr">18</xref>,<xref rid="b19-MI-5-4-00247" ref-type="bibr">19</xref>), the use of ATs may be challenging, and supporting evidence remains limited. Even in cT1a tumors, larger tumor size is a predictor of poor prognosis (<xref rid="b20-MI-5-4-00247" ref-type="bibr">20</xref>,<xref rid="b21-MI-5-4-00247" ref-type="bibr">21</xref>). ATs are generally considered for tumors #x003C;3-4 cm in diameter. Optimal results are typically achieved for tumors sized #x003C;4 cm, with some guidelines supporting ablation as a primary treatment option for tumors #x003C;3 cm in size (<xref rid="b2-MI-5-4-00247" ref-type="bibr">2</xref>,<xref rid="b3-MI-5-4-00247" ref-type="bibr">3</xref>).</p>
<p>Tumor location relative to the polar line is also a component of the scoring systems (<xref rid="b11-MI-5-4-00247" ref-type="bibr">11</xref>). Owing to their proximity to major vessels and the collection system, hilar tumors require careful consideration to minimize significant complications (<xref rid="b11-MI-5-4-00247" ref-type="bibr">11</xref>). However, major vessels near tumors can undermine the effectiveness of AT. The heat sink effect can reduce the efficacy of RFA, whereas in CA, the increased temperature due to vessel flow can lead to inadequate ablation (<xref rid="b22-MI-5-4-00247" ref-type="bibr">22</xref>). Furthermore, hilar tumors often exhibit more aggressive malignant potential (<xref rid="b9-MI-5-4-00247" ref-type="bibr">9</xref>), thereby affecting oncological control.</p>
<p>Proximity to the collecting system may also affect treatment choice. Among ATs, CA appears to have a lower effect than RFA does on the urinary tract (<xref rid="b22-MI-5-4-00247" ref-type="bibr">22</xref>). However, Lagerveld <italic>et al</italic> (<xref rid="b23-MI-5-4-00247" ref-type="bibr">23</xref>) demonstrated that proximity to the collecting system significantly predicted postoperative complications following laparoscopic CA. Another study that included various AT devices identified renal sinus proximity as a risk factor of local recurrence (<xref rid="b24-MI-5-4-00247" ref-type="bibr">24</xref>). Given these findings, PN may be a preferred approach for tumors near major vessels and the collecting system, although the current evidence remains insufficient to draw definitive conclusions (<xref rid="b25-MI-5-4-00247" ref-type="bibr">25</xref>).</p>
</sec>
<sec>
<title>5. Treatment selection for endophytic tumors</title>
<p>Endophytic tumors pose additional challenges due to their location within the normal parenchyma. Theoretically, PN may cause greater damage to normal renal tissue than AT, leading to intraoperative bleeding and post-operative renal impairment. Advanced imaging may facilitate the visualization of endophytic tumors, rendering image-guided percutaneous AT a potentially superior approach (<xref rid="b26-MI-5-4-00247" ref-type="bibr">26</xref>). Percutaneous CA (PCA) is particularly effective for completely endophytic tumors due to its ability to visualize the ice-ball margins. Although several studies support the feasibility and safety of robot-assisted partial nephrectomy (RAPN) for completely endophytic tumors, available evidence is limited (<xref rid="b27-MI-5-4-00247" ref-type="bibr">27</xref>).</p>
<sec>
<title/>
<sec>
<title>RAPN for endophytic tumors</title>
<p>With the widespread use of surgical robots in the field of renal cell carcinoma, indications for PN have expanded to include the management of more complex tumors. Previous studies have shown comparable trifecta achievement in RAPN for endophytic, mesophytic and exophytic tumors (<xref rid="b28-MI-5-4-00247" ref-type="bibr">28</xref>,<xref rid="b29-MI-5-4-00247" ref-type="bibr">29</xref>). A previous multi-institutional study with the largest cohort found that RAPN for endophytic tumors resulted in longer warm ischemia times (median, 22 vs. 21 vs. 16 min, respectively; P#x003C;0.001), a greater estimated blood loss (median, 130 vs. 185 vs. 170 ml, respectively; P=0.001) and lower trifecta achievement rates (45.5 vs. 50.9 vs. 68.8&#x0025;, respectively; P#x003C;0.001), than those for mesophytic and exophytic tumors (<xref rid="b28-MI-5-4-00247" ref-type="bibr">28</xref>). However, these differences were not significant in clinical practice, and comparable positive surgical margins were observed in those cases with no significant difference (4.5 vs. 3.7 vs. 3.9&#x0025;, respectively; P=0.9) (<xref rid="b28-MI-5-4-00247" ref-type="bibr">28</xref>). Of all factors including the endophytic status, multivariate analysis identified tumor size as an independent predictor of trifecta achievement (<xref rid="b28-MI-5-4-00247" ref-type="bibr">28</xref>). Since the first report in 2014(<xref rid="b30-MI-5-4-00247" ref-type="bibr">30</xref>), several studies have demonstrated the feasibility and safety of RAPN for completely endophytic renal tumors, and the majority of studies defined endophytic tumors as scores of 3 points for the &#x2018;E&#x2019; domain in the RENAL nephrometry score, with few local recurrence and low complication rates (<xref rid="tI-MI-5-4-00247" ref-type="table">Table I</xref>) (<xref rid="b25-MI-5-4-00247" ref-type="bibr">25</xref>,<xref rid="b28-MI-5-4-00247 b29-MI-5-4-00247 b30-MI-5-4-00247 b31-MI-5-4-00247 b32-MI-5-4-00247 b33-MI-5-4-00247 b34-MI-5-4-00247" ref-type="bibr">28-34</xref>). Moreover, the post-operative loss of renal function in each study was not significant (<xref rid="b29-MI-5-4-00247 b30-MI-5-4-00247 b31-MI-5-4-00247 b32-MI-5-4-00247" ref-type="bibr">29-32</xref>). By contrast, the trifecta achievement rate varied from 37.8 to 88.5&#x0025; (<xref rid="b25-MI-5-4-00247" ref-type="bibr">25</xref>,<xref rid="b28-MI-5-4-00247 b29-MI-5-4-00247 b30-MI-5-4-00247 b31-MI-5-4-00247 b32-MI-5-4-00247 b33-MI-5-4-00247 b34-MI-5-4-00247" ref-type="bibr">28-34</xref>). This suggests that RAPN for endophytic tumors is still challenging, and performing it in centers with experienced surgeons may lead to improved results (<xref rid="b29-MI-5-4-00247" ref-type="bibr">29</xref>).</p>
</sec>
<sec>
<title>Image-guided PCA for endophytic tumors</title>
<p>Conversely, previous studies have demonstrated the efficacy of image-guided PCA for completely or partially endophytic tumors (<xref rid="tII-MI-5-4-00247" ref-type="table">Table II</xref>) (<xref rid="b35-MI-5-4-00247 b36-MI-5-4-00247 b37-MI-5-4-00247 b38-MI-5-4-00247" ref-type="bibr">35-38</xref>). Murray <italic>et al</italic> (<xref rid="b35-MI-5-4-00247" ref-type="bibr">35</xref>) evaluated imaging-guided CA in 47 patients with completely endophytic renal cancers. During a median follow-up of 54 months, 6 patients experienced local recurrence, and 5 patients (10&#x0025;) had seven major treatment-related complications. Jensen <italic>et al</italic> (<xref rid="b36-MI-5-4-00247" ref-type="bibr">36</xref>) recently reported the safety and feasibility of CT-guided PCA in 56 patients with endophytic renal cancer with a small number of major complications. Considering secondary efficacy in treating imaging-guided AT is critical, and Jensen <italic>et al</italic> (<xref rid="b36-MI-5-4-00247" ref-type="bibr">36</xref>) revealed that 5 patients received a second PCA; 4 patients were successfully controlled, although 2 of 4 (7&#x0025;) patients experienced local recurrences within 4 years following PCA and needed to undergo salvage PN (<xref rid="b36-MI-5-4-00247" ref-type="bibr">36</xref>). As regards functional outcomes, Michimoto <italic>et al</italic> (<xref rid="b38-MI-5-4-00247" ref-type="bibr">38</xref>) demonstrated a significant difference in the mean estimated glomerular filtration rate (eGFR) level between before and after (at 3 months) the procedure (58.1 and 5.35 ml/min/1.73 m<sup>2</sup>, respectively, P=0.01). In their study, transarterial embolization was performed to visualize intra-parenchymal tumors, which may exhibit significance. By contrast, the sub-analysis according to the pre-operative eGFR level (below and above 60 ml/min/1.73 m<sup>2</sup>) revealed no significance between pre- and post-operative eGFR levels (#x003C;60 group: 44.8&#x00B1;9.4 to 38.8&#x00B1;6.8 ml/min/1.73 m<sup>2</sup>, P=0.07; &#x003E;60 group: 69.6&#x00B1;7.4 to 66.0&#x00B1;8.7 ml/min/1.73 m<sup>2</sup>, P=0.12) (<xref rid="b38-MI-5-4-00247" ref-type="bibr">38</xref>). Taken together, these results suggest that ATs can preserve kidney function, even in endophytic tumors (<xref rid="b33-MI-5-4-00247" ref-type="bibr">33</xref>,<xref rid="b36-MI-5-4-00247" ref-type="bibr">36</xref>,<xref rid="b37-MI-5-4-00247" ref-type="bibr">37</xref>).</p>
</sec>
<sec>
<title>Direct comparison between RAPN and PCA for endophytic tumors</title>
<p>Despite the advancements in interventional and surgical technologies, data comparing the outcomes of PN and ATs are limited. Park <italic>et al</italic> (<xref rid="b39-MI-5-4-00247" ref-type="bibr">39</xref>) compared CT-guided RFA with RAPN for cT1a renal cancer using propensity score matching. In their study, RAPN led to superior recurrence-free survival compared with RFA; however, approximately half of the patients treated with RFA had endophytic tumors compared to 27&#x0025; of those treated with RAPN. The authors concluded that RFA was a reasonable option for treating endophytic tumors (<xref rid="b39-MI-5-4-00247" ref-type="bibr">39</xref>). A recent study demonstrated that PCA achieved oncological outcomes and superior safety compared with RAPN for completely endophytic renal tumors (<xref rid="b26-MI-5-4-00247" ref-type="bibr">26</xref>). Moreover, PCA was superior to RAPN in terms of functional outcomes, where changes in eGFR at 1 year were significantly lower. AS regards oncological outcomes, 2 (3.3&#x0025;) patients treated with RAPN and 6 (6.5&#x0025;) patients treated with PCA experienced recurrence, with no significant difference (P=0.428); 3 (3.3&#x0025;) patients treated with PCA experienced metastases, although none of the patients in the RAPN group had metastases (P=0.139). The trifecta achievement for PCA was comparable (58.8&#x0025;) to that for RAPN (65.3&#x0025;, P=0.477) (<xref rid="b26-MI-5-4-00247" ref-type="bibr">26</xref>). A significant limitation of that study was the non-matched patient group with differences in performance status and comorbidities (<xref rid="b26-MI-5-4-00247" ref-type="bibr">26</xref>). Additionally, there is no unified definition of trifecta achievement between RAPN and PCA. For RAPN, trifecta is defined as no major complications, negative surgical margins, and no significant (&#x2265;25&#x0025;) reduction in baseline eGFR values. For PCA, trifecta was defined as no major complications, no significant (&#x2265;25&#x0025;), reduction in baseline eGFR, and no residual or enhancing mass at 6 months post-treatment (<xref rid="b26-MI-5-4-00247" ref-type="bibr">26</xref>). To compare these modalities effectively, standardized criteria for treatment success are required.</p>
</sec>
</sec>
</sec>
<sec>
<title>6. Conclusion</title>
<p>Tumor size and location within the kidney are crucial for determining the feasibility and success of PN and AT, and a multidisciplinary approach that considers tumor characteristics, patient conditions and preferences is necessary. Proximity to the collecting system, renal sinus, or other critical structures affects treatment decisions. For completely endophytic tumors, image-guided AT may provide outcomes comparable to those of PN, although further investigations with matched backgrounds are required. Despite the promising results of AT, surgery remains the gold standard in numerous cases, particularly for larger tumors or when long-term oncological control is a priority. Further studies with matched backgrounds for the two treatment types, such as randomized controlled studies, are desirable.</p>
</sec>
</body>
<back>
<ack>
<title>Acknowledgements</title>
<p>Not applicable.</p>
</ack>
<sec sec-type="data-availability">
<title>Availability of data and materials</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Authors&#x0027; contributions</title>
<p>KB was involved in the conceptualization of the study. KB was also involved in the writing and preparation of the original draft. KY, SI, YM, TY, TaK, TS, YT, TI, SK, SN, KE and ToK were involved in the writing, reviewing and editing of the manuscript. MA supervised the study and was also involved in project administration. All authors have read and agreed to the published version of the manuscript. Data authentication is not applicable.</p>
</sec>
<sec>
<title>Ethics approval and consent to participants</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Patient consent for publication</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="COI-statement">
<title>Competing interests</title>
<p>The authors declare that they have no competing interests.</p>
</sec>
<sec>
<title>Use of artificial intelligence tools</title>
<p>During the preparation of this work, AI tools were used to improve the readability and language of the manuscript or to generate images, and subsequently, the authors revised and edited the content produced by the AI tools as necessary, taking full responsibility for the ultimate content of the present manuscript.</p>
</sec>
<ref-list>
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<floats-group>
<table-wrap id="tI-MI-5-4-00247" position="float">
<label>Table I</label>
<caption><p>The outcomes of RAPN for completely endophytic tumors: Overview of reported studies.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">Authors, year of publication</th>
<th align="center" valign="middle">No. of patients</th>
<th align="center" valign="middle">Tumor size</th>
<th align="center" valign="middle">Follow-up</th>
<th align="center" valign="middle">Oncological outcomes</th>
<th align="center" valign="middle">Complications</th>
<th align="center" valign="middle">Functional outcomes</th>
<th align="center" valign="middle">Trifecta<sup><xref rid="tfna-MI-5-4-00247" ref-type="table-fn">a</xref></sup> achievement (&#x0025;)</th>
<th align="center" valign="middle">(Refs.)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Autorino <italic>et al</italic>, 2014</td>
<td align="center" valign="middle">65</td>
<td align="center" valign="middle">2.5 (SD 1.1) cm</td>
<td align="center" valign="middle">12.6 (SD 1.1) months</td>
<td align="left" valign="middle">3 (4.6&#x0025;) patients had PSM; 1 (1.6&#x0025;) patient had local recurrence</td>
<td align="left" valign="middle">1 (1.6&#x0025;) patient had grade &#x2265;3 complication</td>
<td align="left" valign="middle">The mean difference in eGFR was-9.7 (SD 17.4)</td>
<td align="center" valign="middle">39(60)</td>
<td align="center" valign="middle">(<xref rid="b30-MI-5-4-00247" ref-type="bibr">30</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Komininos <italic>et al</italic>, 2014</td>
<td align="center" valign="middle">45</td>
<td align="center" valign="middle">2.6 (range, 1.3-3.7) cm</td>
<td align="center" valign="middle">48 (range, 20-59) months</td>
<td align="left" valign="middle">5 (11.1&#x0025;) patients had PSM 1 (2.2&#x0025;) patient had local recurrence</td>
<td align="left" valign="middle">2 (4.4&#x0025;) patients had grade &#x2265;3 complication</td>
<td align="left" valign="middle">No significant difference in eGFR change at the last follow-up</td>
<td align="center" valign="middle">17 (37.8)</td>
<td align="center" valign="middle">(<xref rid="b31-MI-5-4-00247" ref-type="bibr">31</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Kara <italic>et al</italic>, 2016</td>
<td align="center" valign="middle">87</td>
<td align="center" valign="middle">2.8 (range, 2.1-3.7) cm</td>
<td align="center" valign="middle">15.2 (range, 7-27.2) months</td>
<td align="left" valign="middle">No local recurrence</td>
<td align="left" valign="middle">4 (4.5&#x0025;) patients had major complications</td>
<td align="left" valign="middle">eGFR preservation rate at the last follow-up was 85.2&#x0025;</td>
<td align="center" valign="middle">NA</td>
<td align="center" valign="middle">(<xref rid="b32-MI-5-4-00247" ref-type="bibr">32</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Harke <italic>et al</italic>, 2018</td>
<td align="center" valign="middle">64</td>
<td align="center" valign="middle">2.4 (range, 1.7-3.0) cm</td>
<td align="center" valign="middle">NA</td>
<td align="left" valign="middle">No PSM</td>
<td align="left" valign="middle">10.9&#x0025; patients had grade &#x2265;3 complications</td>
<td align="left" valign="middle">eGFR preservation rate at the last follow-up was 72.5&#x0025;</td>
<td align="center" valign="middle">48(75)</td>
<td align="center" valign="middle">(<xref rid="b33-MI-5-4-00247" ref-type="bibr">33</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Raheem <italic>et al</italic>, 2019</td>
<td align="center" valign="middle">52</td>
<td align="center" valign="middle">2.8 (SD 1.3) cm</td>
<td align="center" valign="middle">59 (range, 30-73) months</td>
<td align="left" valign="middle">1 (2.3&#x0025;) patient had local recurrence</td>
<td align="left" valign="middle">2 (3.8&#x0025;) patients had grade &#x2265;3 complications</td>
<td align="left" valign="middle">eGFR preservation rate at the last follow-up was 88 (80-100)</td>
<td align="center" valign="middle">NA</td>
<td align="center" valign="middle">(<xref rid="b34-MI-5-4-00247" ref-type="bibr">34</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Carvonara <italic>et al</italic>, 2021</td>
<td align="center" valign="middle">147</td>
<td align="center" valign="middle">4.2 (SD 2.5) cm</td>
<td align="center" valign="middle">21.6 (SD 20) months</td>
<td align="left" valign="middle">3 (2.9&#x0025;) patients had local recurrence 4 (3.3&#x0025;) patients had metastases</td>
<td align="left" valign="middle">7 (17.5&#x0025;) patients had grade &#x2265;3 complications</td>
<td align="left" valign="middle">The median difference in eGFR was-10.8 (SD21.5)</td>
<td align="center" valign="middle">44 (45.4)</td>
<td align="center" valign="middle">(<xref rid="b28-MI-5-4-00247" ref-type="bibr">28</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Motoyama <italic>et al</italic>, 2022</td>
<td align="center" valign="middle">26</td>
<td align="center" valign="middle">1.9 (range, 0.5-4.5) cm</td>
<td align="center" valign="middle">NA</td>
<td align="left" valign="middle">No PSM</td>
<td align="left" valign="middle">2 (7.7&#x0025;) patients had grade &#x2265;3 complications</td>
<td align="left" valign="middle">NA</td>
<td align="center" valign="middle">23 (88.5)</td>
<td align="center" valign="middle">(<xref rid="b29-MI-5-4-00247" ref-type="bibr">29</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Ito <italic>et al</italic>, 2024</td>
<td align="center" valign="middle">76</td>
<td align="center" valign="middle">2.34 (SD 0.84) cm</td>
<td align="center" valign="middle">12 (range, 1-64) months</td>
<td align="left" valign="middle">Cancer-free rate 97.4&#x0025;</td>
<td align="left" valign="middle">1 (1.3&#x0025;) patient had grade &#x2265;3 complication</td>
<td align="left" valign="middle">NA</td>
<td align="center" valign="middle">48 (69.6)</td>
<td align="center" valign="middle">(<xref rid="b25-MI-5-4-00247" ref-type="bibr">25</xref>)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="tfna-MI-5-4-00247"><p><sup>a</sup>Trifecta was defined as a warm ischemia time #x003C;25 min, the absence of complications, and a negative surgical margin. RAPN, robot-assisted partial nephrectomy; SD, standard deviation; NA, not available; PSM, positive surgical margins; eGFR, estimated glomerular filtration rate (ml/min/1.73 m<sup>2</sup>).</p></fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="tII-MI-5-4-00247" position="float">
<label>Table II</label>
<caption><p>The outcomes of ablation therapies for endophytic tumors: Overview of reported studies.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">Authors, year of publication</th>
<th align="center" valign="middle">Intervention</th>
<th align="center" valign="middle">No. of patients</th>
<th align="center" valign="middle">Tumor size</th>
<th align="center" valign="middle">Follow-up</th>
<th align="center" valign="middle">Oncological outcomes</th>
<th align="center" valign="middle">Complications</th>
<th align="center" valign="middle">Functional outcomes</th>
<th align="center" valign="middle">(Refs.)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Park <italic>et al</italic>, 2010</td>
<td align="left" valign="middle">Laparoscopic RFA</td>
<td align="center" valign="middle">17</td>
<td align="center" valign="middle">2.8 (range 1.7-3.7) cm</td>
<td align="center" valign="middle">32.6 (range, 12-51) months</td>
<td align="left" valign="middle">1 (6.7&#x0025;) patient experienced local recurrence</td>
<td align="left" valign="middle">No major complications</td>
<td align="left" valign="middle">Pre- and post-operative (day 7) mean creatinine levels were 1.31 and 1.43 (P=0.13)</td>
<td align="center" valign="middle">(<xref rid="b39-MI-5-4-00247" ref-type="bibr">39</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Michimoto <italic>et al</italic>, 2016</td>
<td align="left" valign="middle">CT-guided PCA</td>
<td align="center" valign="middle">17 (9 completely endophytic and 8 partial endophytic)</td>
<td align="center" valign="middle">2.65 (range 1.2-3.6) cm</td>
<td align="center" valign="middle">15.4 (SD 5.1) months</td>
<td align="left" valign="middle">1 patient experienced local recurrence at 12 months</td>
<td align="left" valign="middle">No major complications</td>
<td align="left" valign="middle">Pre- and post-operative (3 months) mean eGFR levels were 58.1 and 53.5 (P=0.01)</td>
<td align="center" valign="middle">(<xref rid="b38-MI-5-4-00247" ref-type="bibr">38</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Murray <italic>et al</italic>, 2019</td>
<td align="left" valign="middle">CT-guided PCA</td>
<td align="center" valign="middle">47</td>
<td align="center" valign="middle">2.5 (SD 0.5) cm</td>
<td align="center" valign="middle">56 (range, 3-128) months</td>
<td align="left" valign="middle">6 patients had local recurrence, and 5 of 6 were successfully treated with re-PCA</td>
<td align="left" valign="middle">5 patients (10&#x0025;) had major complications</td>
<td align="left" valign="middle">The mean change in serum creatinine on the day of discharge was 0.2 (SD 0.2) mg/dl</td>
<td align="center" valign="middle">(<xref rid="b35-MI-5-4-00247" ref-type="bibr">35</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Jensen <italic>et al</italic>, 2024</td>
<td align="left" valign="middle">CT-guided PCA</td>
<td align="center" valign="middle">56</td>
<td align="center" valign="middle">2.57 (SD 0.87) cm</td>
<td align="center" valign="middle">996 (SD 559) days</td>
<td align="left" valign="middle">4 (7&#x0025;) experienced local recurrence</td>
<td align="left" valign="middle">3 patients (5.4&#x0025;) had grade &#x2265;3 complications</td>
<td align="center" valign="middle">NA</td>
<td align="center" valign="middle">(<xref rid="b36-MI-5-4-00247" ref-type="bibr">36</xref>)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn><p>RFA, radiofrequency ablation; CT, computed tomography; PCA, percutaneous cryoablation; SD. standard deviation; NA. not available.</p></fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</article>
