Department of Urology, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.
BJU Int. 2013 Jun;111(7):1068-74. doi: 10.1111/j.1464-410X.2012.11729.x. Epub 2013 Apr 2.
WHAT'S KNOWN ON THE SUBJECT? AND WHAT DOES THE STUDY ADD?: Several lymph node staging strategies have been proposed as a response to the high morbidity seen after standard inguinal lymphadenectomy for penile cancer. A video-endoscopic (laparoscopic and robotic) approach has been proposed as a less morbid procedure in several retrospective studies. To date, none has evaluated the oncological adequacy with regard to whether all relevant nodes have been removed. To the authors' knowledge this is the first prospective study of a robotic or laparoscopic inguinal lymphadenectomy that evaluates the oncological adequacy of this approach for penile cancer. The study shows that robotic inguinal lymphadenectomy allowed adequate staging of disease in the inguinal region by removing all relevant lymph nodes as assessed by an independent evaluating urological oncologist.
To prospectively determine the oncological adequacy of robotic assisted video-endoscopic inguinal lymphadenectomy (RAVEIL).
Patients with T1-3N0 penile cancer were enrolled into a prospective phase I trial at a tertiary care institution from March 2010 to January 2012. All patients underwent an initial RAVEIL approach. Verification of adequacy of dissection was performed by an independent surgeon via a separate open incision at the conclusion of the RAVEIL procedure. Out of 10 patients, if more than two superficial inguinal fields with ≥2 nodes or more than four with ≥1 node remained within the superficial dissection field, the study would not proceed to phase II.
Of 10 enrolled patients two had inguinal metastases and all positive nodes were detected by RAVEIL. The remaining eight patients had no metastases, with a mean of nine (range 5-21) left and nine (range 6-17) right nodes removed. One inguinal field RAVEIL was converted to an open dissection. The verifying surgeon confirmed that 18 of 19 inguinal fields (94.7% in nine patients) had an adequate dissection. Two benign nodes were found just beneath Scarpa's fascia above the inguinal dissection field. Limitations of the study include an inability to determine decisively what specific wound complications were related to RAVEIL because of the protocol-specified creation of a small inguinal incision for verification of adequate dissection.
RAVEIL allowed adequate staging of disease in the inguinal region among patients with penile cancer at risk for inguinal metastases.
前瞻性确定机器人辅助视频内镜腹股沟淋巴结清扫术(RAVEIL)的肿瘤学充分性。
2010 年 3 月至 2012 年 1 月,在一家三级医疗机构,对 T1-3N0 阴茎癌患者进行了一项前瞻性 I 期试验。所有患者均接受初始 RAVEIL 方法。在 RAVEIL 手术结束时,由独立外科医生通过单独的开放性切口进行充分性验证。如果 10 例患者中超过 2 例浅层腹股沟区有≥2 个淋巴结或超过 4 例有≥1 个淋巴结仍留在浅层解剖区,则研究将不会进入 II 期。
10 例入组患者中有 2 例腹股沟转移,所有阳性淋巴结均通过 RAVEIL 检测到。其余 8 例患者无转移,左侧平均切除 9 个(范围 5-21),右侧切除 9 个(范围 6-17)个淋巴结。1 例腹股沟区域 RAVEIL 转为开放解剖。验证外科医生确认 19 个腹股沟区域中的 18 个(9 名患者中有 18 个,94.7%)有足够的解剖。在腹股沟解剖区上方 Scarpa 筋膜下方发现了 2 个良性淋巴结。该研究的局限性包括由于方案规定为验证充分性而创建一个小的腹股沟切口,因此无法确定特定的伤口并发症与 RAVEIL 有何具体关系。
RAVEIL 可使有腹股沟转移风险的阴茎癌患者腹股沟区域的疾病得到充分分期。