Minimally invasive post-chemotherapy retroperitoneal lymph node dissection for nonseminoma

Can J Urol. 2015 Aug;22(4):7882-9.

Abstract

Introduction: We present our experience with minimally-invasive retroperitoneal lymph node dissection (MI-RPLND) in the post-chemotherapy (PC) setting for residual masses in patients with nonseminoma.

Materials and methods: Nineteen men who underwent PC MI-RPLND (14--laparoscopic, 5--robotic) for low-volume residual disease (no more than 5 clinically enlarged retroperitoneal masses, size < 5 cm, no adjacent organ or vascular invasion) between 2006 and 2011 were identified. Clinicodemographic information and pathological outcomes were reported.

Results: Median age of our study population was 32 (interquartile range [IQR]: 28-39). Most patients presented with clinical stage II disease (63%) and were categorized as good risk (90%) by the International Germ Cell Consensus Classification. Median size of residual masses on PC imaging was 2.1 cm (IQR: 1.7-3). Full-template bilateral RPLND was completed in 53% of cases, and modified left-sided RPLND in 47%. Median operative time was 370 minutes (IQR: 320-420), and median estimated blood loss was 300 cc (IQR: 150-450). Median length of stay was 3 days (IQR: 2-3). Five patients (26%) experienced a postoperative 30 day complication, but none were higher than Clavien grade II. On final pathology, median number of lymph nodes removed was 12 (IQR: 8-23), and 8 patients (42%) had residual teratoma. No patient experienced a recurrence at median follow up of 24 months (IQR: 5-76).

Conclusions: PC MI-RPLND is a feasible option in a select group of patients with acceptable patient morbidity and short-term outcomes. Longer follow up is required to determine the oncologic efficacy of this approach.

MeSH terms

  • Adult
  • Antineoplastic Agents / therapeutic use
  • Blood Loss, Surgical
  • Disease-Free Survival
  • Humans
  • Laparoscopy / adverse effects
  • Length of Stay
  • Lymph Node Excision* / adverse effects
  • Lymphatic Metastasis
  • Male
  • Neoplasm, Residual
  • Neoplasms, Germ Cell and Embryonal / drug therapy
  • Neoplasms, Germ Cell and Embryonal / secondary*
  • Neoplasms, Germ Cell and Embryonal / surgery*
  • Operative Time
  • Retroperitoneal Space
  • Retrospective Studies
  • Robotic Surgical Procedures / adverse effects
  • Testicular Neoplasms / drug therapy
  • Testicular Neoplasms / pathology*
  • Testicular Neoplasms / secondary
  • Testicular Neoplasms / surgery*
  • Tumor Burden

Substances

  • Antineoplastic Agents

Supplementary concepts

  • Nonseminomatous germ cell tumor