摘 要 目的:應(yīng)用R.E.N.A.L.腎功能評(píng)分系統(tǒng)進(jìn)行配對(duì)分析,比較腹膜后腹腔鏡腎部分切除術(shù)(Laparoscopic Partial Nephrectomy,LPN)與機(jī)器人腎部分切除術(shù)(Robot-assisted Partial Nephrectomy,RPN)的圍手術(shù)期療效。方法:對(duì)2016年1月—2020年3月543例于浙江大學(xué)醫(yī)學(xué)院附屬第一醫(yī)院泌尿外科行腹腔鏡及機(jī)器人輔助腎部分切除術(shù)患者的相關(guān)臨床資料進(jìn)行分析。根據(jù)R.E.N.A.L.腎功能評(píng)分、性別和年齡進(jìn)行1∶1配對(duì)(112對(duì)配對(duì)),通過(guò)統(tǒng)計(jì)分析對(duì)圍手術(shù)期結(jié)果進(jìn)行比較。結(jié)果:LPN組和RPN組在年齡、性別、體重指數(shù)(Body Mass Index,BMI)、腫瘤大小、美國(guó)麻醉學(xué)家協(xié)會(huì)(American Society of Anesthesiologists,ASA)評(píng)分和術(shù)前估算腎小球?yàn)V過(guò)率(Estimated Glomerular Filtration Rate,eGFR)方面均無(wú)顯著差異。接受LPN的患者左側(cè)腫瘤所占比例略高(51.7% Vs"42.9%,P=0.032)。兩組在手術(shù)時(shí)間、術(shù)中出血量、術(shù)后住院時(shí)間(Length of Stay,LOS)、術(shù)后eGFR、輸血量和/或術(shù)后并發(fā)癥等方面均無(wú)顯著差異。RPN組熱缺血時(shí)間(Warm Ischemia Time,WIT)明顯比LPN組短(18.9 min Vs"22.6 min,P=0.032)。以復(fù)雜性為特點(diǎn)的亞集分析顯示,復(fù)雜腫瘤RPN的WIT顯著短于LPN(21.1 min Vs 26.3 min,P=0.012),而單純性腫瘤RPN與LPN的WIT差異無(wú)統(tǒng)計(jì)學(xué)意義(16.4 min Vs 18.3 min,P=0.085)。結(jié)論:經(jīng)腹膜后RPN手術(shù)時(shí)間較經(jīng)腹膜后LPN短,但二者圍手術(shù)期效果基本相同。在有限的腹膜后工作空間內(nèi)進(jìn)行復(fù)雜的腫瘤切除和修補(bǔ),機(jī)器人輔助手術(shù)可能比傳統(tǒng)的腹腔鏡術(shù)更具優(yōu)勢(shì)。
關(guān)鍵詞 腎細(xì)胞癌;腎部分切除術(shù);腹腔鏡手術(shù);機(jī)器人輔助手術(shù)
中圖分類號(hào) R608 R737 文獻(xiàn)標(biāo)識(shí)碼 A 文章編號(hào) 2096-7721(2023)04-0333-10
Retroperitoneal robotic versus laparoscopic partial nephrectomy for renal tumors: a matched comparison of perioperative outcomes of a single surgeon
XU Yifan, XIA Dan, MENG Hongzhou, QIN Jie, KONG Debo, JING Taile, YE Sunyi, LAI Chong,
WANG Shuo, WANG Ping
(Department of Urology, the First Affiliated Hospital, Medical College of Zhejiang University, Hangzhou 310003, China)
Abstract Objective: To compare the perioperative outcomes of patients undergoing retroperitoneal laparoscopic partial nephrectomy(LPN) and retroperitoneal robot-assisted partial nephrectomy (RPN) by matched analysis using R.E.N.A.L. nephrometry scoring system. Methods: Relevant clinical data of 543 case of laparoscopic and robot-assisted partial nephrectomy performed by a single surgeon via the RP approach from January 2016 to March 2020 from our database were screened and analyzed. Two groups were matched 1:1 (112 matched pairs) by R.E.N.A.L. nephrometry score, gender, and age. Statistical analysis was done to compare perioperative outcomes. Results: There was no significant difference between the LPN group and RPN group in terms of age, gender, body mass index (BMI), tumor size, American Society of Anesthesiologists (ASA) score or preoperative estimated glomerular filtration rate (eGFR). Patients undergoing LPN had a slightly higher proportion of the left side tumor (51.7% Vs 42.9%, P=0.032). No significant differences regarding to operative time, estimated blood loss, postoperative LOS, postoperative eGFR, transfusion or postoperative complications were found between the two groups. However, Warm ischemia times (WIT) in the RPN group were significantly shorter than that in the LPN group (18.9 min Vs 22.6 min, P=0.032). Subset analysis based on complexity indicated that WIT of complex tumors in the RPN group was significantly shorter than that in the LPN group (21.1 min Vs 26.3 min, P=0.012), but no difference of WIT was found on simple tumors between the RPN group and LPN group (16.4 min Vs 18.3 min, P=0.085). Conclusion: Retroperitoneal RPN showed shorter WIT and generally equivalent perioperative results to retroperitoneal LPN. Robotic surgery may have advantages over the traditional laparoscopic surgery on complex tumor excision and renorrhaphy in the limited retroperitoneal space.
Key words Renal cell cancer; Partial nephrectomy; Laparoscopic surgery; Robot-assisted surgery Partial nephrectomy (PN) currently represents the standard of care for small renal tumors, as it can provide oncologic outcomes equivalent to those of radical nephrectomy (RN)[1]. Although open PN (OPN) is an efficacious procedure, progress in technology has recently led to effective minimally invasive surgical approaches for PN, including laparoscopic PN (LPN) and robot-assisted PN (RPN)[2].
LPN or RPN may be performed via a transperitoneal (TP) or retroperitoneal (RP) approach. Compared with TP approach, the main advantage of the RP approach is that it could pass renal artery directly and quickly. However, due to the smaller and limited working space, the RP approach may be more technically challenging[3].The Da Vinci Surgical System mitigates the disadvantages of the retroperitoneal laparoscopic approach because of increased degrees of freedom of movement and enhanced reconstructive capabilities, which make it possible to operate easily in confined spaces[3-4]. However, as so far, few studies on comparison of surgical outcomes between retroperitoneal LPN and retroperitoneal RPN. In this article, perioperative outcomes for retroperitoneal LPN and retroperitoneal RPN performed by a single experienced laparoscopic surgeon using R.E.N.A.L. nephrometry scoring were compared and reported[5].
1 Materials and Methods
1.1 Study population
All patients treated with LPN and RPN via retroperitoneal approach by a single surgeon (WANG S) for renal tumor from January 2016 to March 2020 were identified in our institution and were maintained prospectively in a database approved by the Institutional Review Board. Patients who had solitary kidneys, multifocal tumors, or radiological evidence of locally advanced disease or metastases were excluded. Medial renal masses were also not included in this study since they are very difficult to remove via the retroperitoneal approach. For our RPN cases, the 15 initial cases were excluded to avoid the influence on learning curve. RPN was performed using the da Vinci? SiTM Surgical System (Intuitive Surgical, Sunnyvale, CA, USA). All patients underwent computed tomography angiogram (CTA) prior to surgery to determine tumor characteristics, renal vascular anatomy and R.E.N.A.L nephrometry score.
Patient demographics, tumor characteristics, perioperative information and pathologic findings were abstracted from the database. The R.E.N.A.L nephrometry score was determined as previously described by Kutikov A and Uzzo R G[5]. The complex tumor was defined as the tumor with R.E.N.A.L score ≥7, the simple tumor was defined as the tumor with"R.E.N.A.L scorelt;7. The operative time was considered to be started from the initial carbon dioxide insufflation to gas discharge, which could avoid biases caused by setup time or anesthesia time. Renal function was assessed by the estimated glomerular filtration rate (eGFR), which was calculated using the modification of diet in renal disease (MDRD) formula[6]. The eGFR results was obtained preoperatively, and the last available value (obtained at least 3 months before surgery) was used to calculate the change in renal function. Preservation of eGFR was defined as a ratio of postoperative eGFR to preoperative eGFR. Surgical complications were graded according to the Clavien classification system[7]. Hemorrhagic complications were defined as those requiring blood transfusion for intraoperative or postoperative bleeding, or those involving clinically significant bleeding requiring further management, such as 1 aneurysm, arteriovenous fistula, hematuria et al. One-to-one matching was done between the LPN and RPN groups based on R.E.N.A.L. nephrometry score, gender, and age (within 10 years).
1.2 Surgical techniques
Patients were placed in full flank position with the ipsilateral side up. Retroperitoneal working space establishment and Trocar placement for LPN has been described previously[8]. Trocar placement for RPN was performed according to UCLA mode[9]. The fourth robotic arm was not used due to the limited retroperitoneal working space. Intracorporeal operation of RPN was similar to LPN. Generally, the Gerota fascia paralleled to the psoas major was incised after the paranephric fat being cleared. The ureter could be easily identified anterior to the psoas major and dissection towards to the hilum was then performed. The renal artery is skeletonized to allow for adequate closing pressure with bulldog clamps. The renal vein is rarely clamped and only if a tumor in a very central location encroaching on the venous vasculature. The capsular borders of the tumor were defatted circumferentially to obtain clear visualization of the dissection margin and provide a clear view of the capsule for subsequent reconstruction. The fat overlying the tumor was left and attached to the capsule for retraction. The laparoscopic ultrasound probe was used to identify and confirm tumor location and resection margins scored by electrocautery. Tumor excision was performed by cold scissors dissection in all cases. Renorrhaphy was performed in 2 layers, 3-0 V-Loc suture was used on the deep layer for the closure of vascular structures and any collecting system injury, and 2-0 V-Loc suture was used for the closure of the outer cortical layer. All tumors were sent to pathology for frozen section analysis.
1.3 Statistical analysis
Patient demographics, perioperative parameters and complications were compared using SPSS version 19. Continuous variables were presented as mean ±"standard deviation (SD), nonparametric variables were presented as median and interquartile range (IQR), and categorical variables were reported as frequencies and proportions. The Student’s t test and Mann-Whitney U-test were used to compare continuous variables, as appropriate. Categorical variables were compared using the Chi-square (χ2) test. All tests were considered statistically significant at Plt;0.05.
2 Results
A total of 365 cases of retroperitoneal LPN and 178 cases of retroperitoneal RPN were performed by a single surgeon (Wang S) at our institution from January 2016 to February 2020, of which 16 cases of LPN and 3 cases of RPN were excluded from this study due to incomplete clinical or image data. 2 cases of LPN converted to nephrectomy for oncological control were also excluded. Acceptable matches were obtained for the remaining 112 patients in each group.
There was no difference in terms of age, gender, body mass index (BMI), American Society of Anesthesiologists (ASA) score, tumor size, tumor location, nephrometry score and preoperative eGFR between the LPN and RPN groups (Table 1). Left side tumors were more common in the LPN group while more right tumors in the RPN group. No patient with solitary kidney was found in either group.
Operative time, estimated blood loss (EBL), oral resumption, postoperative length of hospital stay (LOS) and Transfusion were not significantly different between the two groups (Table 2). Warm ischemia time (WIT) was significantly shorter in the RPN group than that in the LPN group[ (22.6±5.2)min Vs (18.9±4.1) min, P= 0.032]. However, no significant difference for postop eGFR [(71.3±21.5) mL/min/1.73 m2 Vs (72.2±20.2) mL/min/1.73 m2, P= 0.096), postoperative drainage time, change of eGFR and eGFR reserved (85.2% Vs 86.6%, P=0.205) was found between the RPN group and the LPN group.
In terms of subset analysis based on tumor complexity, as defined by the R.E.N.A.L score, there were 54 simple and 58 complex tumors in both the LPN group and RPN group (Table 3). After further analysis, we found that the tumor complexity had a rather significant effect on WIT. The WIT of complex tumors in the LPN group was longer than that in the RPN group (26.3 min Vs 21.1 min, P=0.012). However, the WIT for simple tumors in the LPN group and RPN group was not significantly different (18.3 min Vs 16.4 min, P=0.085). With respect to renal function outcomes, there were no significant differences on postop eGFR, change of eGFR and preservation of eGFR between the LPN group and RPN group for both simple and complex tumors.
Postoperative complications were graded by the Clavien classification system (Table 4). There were no significant differences on overall, minor (Clavien grade 1 and 2) and major (Clavien grade 3 and 4) postoperative complications between the LPN group and RPN group. Postoperative complications occurred in 19 patients who underwent LPN (17.0%), including 2 major complications, of which 1 case of bleeding(1 aneurysm) was managed by super-selective angioembolization. There were 17 (15.2%) complications in the RPN group, including 3 major complications, of which 2 cases of bleeding (1 arteriovenous fistula and 1 1 aneurysm) were also managed by angioembolization.
The definitive pathological examination showed 11(9.8%) benign tumors (oncocytomas or angiomyolipomas) in the LPN group and 9 (8.0%) in the RPN group (P=0.312 )(Table 5). There were no significant differences on Fuhrman nuclear grade and pathological stage between the two groups.
PSM (Positive surgical margin, PSM) was found in 1(0.9%) patient in the LPN group and 2 (1.8%) patients in the RPN group (Table 6). Clear cell renal cell carcinoma was found in 2 cases of patients with PSM and chromophobe cancer in 1 patient with PSM by final pathological diagnosis. All patients with PSM were managed with active surveillance. With a mean follow-up of 32 months for the LPN grou and 12.5 months for the RPN group, no local recurrence or distant metastasis were found during the follow-up.
3 Discussion
The majority of published reports on less-invasive nephron-sparing surgery described the transperitoneal approach, which probably be due to larger working space and more anatomic landmarks provided by the transperitoneal laparoscopic approach. Retroperitoneal LPN or RPN is less commonly used, although it has advantages on early exposure and renal vasculature isolation, which could reach posteriorly located tumors directly with less manipulation of abdominal organs and quicker recovery. Because the traditional LPN remains technically challenging, RPN has emerged as an attractive option for both naive and experienced laparoscopic surgeons[10].To date, although several studies on retroperitoneal RPN have been reported[9, 11-17],"no study on the comparison of surgical outcomes between retroperitoneal LPN and retroperitoneal RPN has been reported. Thus, our study aims to evaluate of the outcomes of retroperitoneal LPN and retroperitoneal RPN in treating renal tumor.
A study on the comparison of LPN and RPN shows that RPN is a safe and viable alternative to LPN, and RPN appears to decrease LOS, significantly reduce intraoperative EBL and shorten WIT[10]. In a similar analysis, 102 cases of comparison study between LPN and RPN for the treatment of suspected RCC of a single-surgeon experience was reported by WANG S[18], whose results showed that the mean operative time (140 min Vs 156 min, P=0.04), WIT (19 min Vs 25 min, P=0.03), and LOS (2.5 d Vs 2.9 d,"P=0.03) of RPN were significantly shorter than LPN. However, these studies mentioned above were performed through the transperitoneal laparoscopic approach.
In this study, a matched-pair analysis with R.E.N.A.L. nephrometry scores was used to compare retroperitoneal LPN and retroperitoneal RPN performed by a single surgeon. No significant difference was found between the retroperitoneal RPN and the retroperitoneal LPN group in terms of operative parameters, except that the RPN group had significantly less WIT. Then, renal tumors in our study were divided into simple tumors (lt; 7) and complex tumors (≥ 7) according to the R.E.N.A.L. nephrometry score[5]. The results showed that WIT of the retroperitoneal LPN and retroperitoneal RPN both increased with increasing complexity of tumors. Furthermore, WIT was not significantly different between the LPN and RPN in the excision of simple tumor (18.3 min Vs 16.4 min, P=0.085), however, the WIT of the RPN group was significantly less than the LPN group in the excision of complex tumor (26.3 min Vs 21.1 min, P=0.012). This result is different with the study reported by Long J A et al, who retrospectively compared the LPN and RPN in treating single renal mass with moderate or high complexity[19], and the results showed that there was no difference in WIT between moderate and high R.E.N.A.L. score subgroups. We believe that surgeon experience and tumor anatomical characteristics are important factors influencing WIT. Furthermore, a large working space is greatly facilitated to intracorporeal suturing, but robotic technology make it possible to perform renorrhaphy within confined retroperitoneal space.
One of the most important aims of NSS (Nephron Sparing Surgery, NSS) is to preserve renal function. Declining renal function after PN is usually caused by 2 independent factors: WIT[20] and the percentage of functional volume preservation[21]. The importance of WIT is well known, every minute matters was proposed by Eggener S E, who emphasized that the shorter WIT, the higher possibility of better recovery of renal function after PN[22]. However, some researchers believe that limited WIT in minimally invasive PN has only a marginal impact on postoperative renal functional outcomes, despite the clear cutoff value still being debatable[23-24]. In our study, the RPN group had a shorter WIT comparing with the LPN group, but the decreasing of eGFR was not statistically significant. There are several reasons that might explain this result. Firstly, the GFR was estimated based on the measurement of serum creatinine, which may not accurately reflect the degree of renal dysfunction in the clamped kidney. Secondly, in our unilateral minimally invasive PN study, WIT occurs unilaterally and the real function could be compensated by improving the function of the normal contralateral kidney. In addition, Simmons M N et al[21] reported that the degree of renal volume reduction was the primary determinants of the long-term functional outcome in patients who had acceptable ischemia time. Unfortunately, the volume of resected renal was not calculated for our patients in our study.
Despite a PSM rarely progressing to local recurrence[25], every effort should be taken to ensure complete gross and microscopic removal of the tumor in PN. Based on different surgical approaches, PSM rates are 0 to 7% after open PN, 0.7% to 4% after LPN, and 3.9% to 5.7% after RPN[26]. PSMs were detected in 1 (0.99%) patient after LPN and in 2 (1.94%) after RPN, the PSM rate was lower in our study than that in the other reported studies[25-26]. In our experience, less intraoperative blood loss could provide a clear operative field, which could help us to improve visualization of the resection margin. In our study, all patients underwent CTA examination to understand the variations exactly in renal vascular anatomy preoperatively. The variations in the origin of renal arteries are very common, such as accessory renal arteries, double renal arteries and early dividing renal artery. During resection the tumor, we underline the role of complete vascular occlusion to improve visualization of the resection margin.
The limitations of our study must be noted. This study was not a randomized trial, which may lead to possible bias. Moreover, surgeon experience was higher in the LPN group. The initial 15 RPN cases were excluded to minimize the effect of a learning curve, but it was impossible to adequately control for variable surgeon experience. Additionally, we also could not evaluate the oncologic outcomes duo to limited time of follow-up, especially in the RPN group.
4 Conclusion
Robotic surgical systems help to overcome the obstacles caused by the limited retroperitoneal working space in LPN. Our study indicates that retroperitoneal RPN could bring equivalent perioperative outcomes to the retroperitoneal LPN with a significantly shorter WIT. In terms of subset analysis based on tumor complexity, RPN has shorter WIT than LPN in the excision of complex tumors. However, the WITs of RPN and LPN in treating simple tumors are equivalent.
References
[1] Patard J J, Shvarts O, Pantuck A, et al. 281 Safety and efficacy of partial nephrectomy for all T1 tumours based on an international multicentre experience[J]. European Urology Supplements, 2004, 2(3): 73.
[2] Bukavina L, Mishra K, Calaway A, et al. robotic partial nephrectomy: update on techniques[J]. Urol Clin North Am, 2021, 48(1): 81-90.
[3] Patel M, Porter J. Robotic retroperitoneal surgery: a contemporary review[J]. Current Opinion in Urology, 2013, 23(1): 51-56.
[4] Crisan N, Neiculescu C, Matei D V, et al. Robotic retroperitoneal approach-a new technique for the upper urinary tract and adrenal gland[J]. The International Journal of Medical Robotics and Computer Assisted Surgery, 2013, 9(4): 492-496.
[5] Kutikov A, Uzzo R G. The R.E.N.A.L. nephrometry score: a comprehensive standardized system for quantitating renal tumor size, location and depth[J]. The Journal of Urology, 2009, 182(3): 844-853.
[6] Levey A S, Bosch J P, Lewis J B, et al. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation[J]. Annals of Internal Medicine, 1999, 130(6): 461-470.
[7] Dindo D, Demartines N, Clavien P A. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey[J]. Annals of Surgery, 2004, 240(2): 205.
[8] WANG P, XIA D, MA Q, et al. Retroperitoneal laparoscopic management of ureteropelvic junction obstruction in patients with horseshoe kidney[J]. Urology, 2014, 84(6): 1351-1354.
[9] Hu J C, Treat E, Filson C P, et al. Technique and outcomes of robot-assisted retroperitoneoscopic partial nephrectomy: a multicenter study[J]. European Urology, 2014, 66(3): 542-549.
[10] Benway B M, Bhayani S B, Rogers C G, et al. Robot assisted partial nephrectomy versus laparoscopic partial nephrectomy for renal tumors: a multi-institutional analysis of perioperative outcomes[J]. The Journal of Urology, 2009, 182(3): 866-873.
[11] Gin G E, Maschino A C, Spaliviero M, et al. Comparison of perioperative outcomes of retroperitoneal and transperitoneal minimally invasive partial nephrectomy after adjusting for tumor complexity[J]. Urology, 2014, 84(6): 1355-1360.
[12] Choo S H, Lee S Y, Sung H H, et al. Transperitoneal versus retroperitoneal robotic partial nephrectomy: matched-pair comparisons by nephrometry scores[J]. World Journal of Urology, 2014, 32(6): 1523-1529.
[13] Ghani K R, Porter J, Menon M, et al. Robotic retroperitoneal partial nephrectomy: a step-by-step guide[J]. BJU International, 2014, 114(2): 311-313.
[14] Tanaka K, Shigemura K, Furukawa J, et al. Comparison of the transperitoneal and retroperitoneal approach in robot-assisted partial nephrectomy in an initial case series in Japan[J]. Journal of Endourology, 2013, 27(11): 1384-1388.
[15] Hughes-Hallett A, Patki P, Patel N, et al. Robot-assisted partial nephrectomy: a comparison of the transperitoneal and retroperitoneal approaches[J]. Journal of Endourology, 2013, 27(7): 869-874.
[16] Patel M, Porter J. Robotic retroperitoneal partial nephrectomy[J]. World Journal of Urology, 2013, 31(6): 1377-1382.
[17] Socarrás M R, Elbers J R, Rivas J G, et al. Retroperitoneal robot-assisted partial nephrectomy (rrapn): surgical technique and review[J]. Current Urology Reports, 2021, 22(6): 1-6.
[18] Wang A J, Bhayani S B. Robotic partial nephrectomy versus laparoscopic partial nephrectomy for renal cell carcinoma: single-surgeon analysis of gt; 100 consecutive procedures[J]. Urology, 2009, 73(2): 306-310.
[19] Long J A, Yakoubi R, Lee B, et al. Robotic versus laparoscopic partial nephrectomy for complex tumors: comparison of perioperative outcomes[J]. European Urology, 2012, 61(6): 1257-1262.
[20] Thompson R H, Lane B R, Lohse C M, et al. Every minute counts when the renal hilum is clamped during partial nephrectomy[J]. European Urology, 2010, 58(3): 340-345.
[21] Simmons M N, Fergany A F, Campbell S C. Effect of parenchymal volume preservation on kidney function after partial nephrectomy[J]. The Journal of Urology, 2011, 186(2): 405-410.
[22] Patel A R, Eggener S E. Warm ischemia less than 30 minutes is not necessarily safe during partial nephrectomy: every minute matters[C]//Urologic Oncology: Seminars and Original Investigations. Elsevier, 2011, 29(6): 826-828.
[23] Lane B R, Gill I S, Fergany A F, et al. Limited warm ischemia during elective partial nephrectomy has only a marginal impact on renal functional outcomes[J]. The Journal of Urology, 2011, 185(5): 1598-1603.
[24] Godoy G, Ramanathan V, Kanofsky J A, et al. Effect of warm ischemia time during laparoscopic partial nephrectomy on early postoperative glomerular filtration rate[J]. The Journal of Urology, 2009, 181(6): 2438-2445.
[25] Yossepowitch O, Thompson R H, Leibovich B C, et al."Positive surgical margins at partial nephrectomy: predictors and oncological outcomes[J]. The Journal of Urology, 2008, 179(6): 2158-2163.
[26] Marszalek M, Carini M, Chlosta P, et al. Positive surgical margins after nephron-sparing surgery[J]. European Urology, 2012, 61(4): 757-763.