A randomized trial of lymphadenectomy in patients with advanced ovarian neoplasms

Philipp Harter, Jalid Sehouli, Domenica Lorusso, Alexander Reuss, Ignace Vergote, Christian Marth, Jae-Weon Kim, Fran-Cesco Raspagliesi, Björn Lampe, Giovanni Aletti, Werner Meier, David Cibula, Alexander Mustea, Sven Mahner, Ingo B. Runnebaum, Barbara Schmalfeldt, Alexander Burges, Rainer Kimmig, Giovanni Scambia, Stefano GreggiFelix Hilpert, Annette Hasenburg, Peter Hillemanns, Giorgio Giorda, Ingo Von Leffern, Carmen Schade-Brittinger, Uwe Wagner, Andreas Du Bois

Risultato della ricerca: Contributo in rivistaArticolo in rivista

137 Citazioni (Scopus)

Abstract

BACKGROUND Systematic pelvic and paraaortic lymphadenectomy has been widely used in the surgical treatment of patients with advanced ovarian cancer, although supporting evidence from randomized clinical trials has been limited. METHODS We intraoperatively randomly assigned patients with newly diagnosed advanced ovarian cancer (International Federation of Gynecology and Obstetrics stage IIB through IV) who had undergone macroscopically complete resection and had normal lymph nodes both before and during surgery to either undergo or not undergo lymphadenectomy. All centers had to qualify with regard to surgical skills before participation in the trial. The primary end point was overall survival. RESULTS A total of 647 patients underwent randomization from December 2008 through January 2012, were assigned to undergo lymphadenectomy (323 patients) or not undergo lymphadenectomy (324), and were included in the analysis. Among patients who underwent lymphadenectomy, the median number of removed nodes was 57 (35 pelvic and 22 paraaortic nodes). The median overall survival was 69.2 months in the no-lymphadenectomy group and 65.5 months in the lymphadenectomy group (hazard ratio for death in the lymphadenectomy group, 1.06; 95% confidence interval [CI], 0.83 to 1.34; P=0.65), and median progression-free survival was 25.5 months in both groups (hazard ratio for progression or death in the lymphadenectomy group, 1.11; 95% CI, 0.92 to 1.34; P=0.29). Serious postoperative complications occurred more frequently in the lymphadenectomy group (e.g., incidence of repeat laparotomy, 12.4% vs. 6.5% [P=0.01]; mortality within 60 days after surgery, 3.1% vs. 0.9% [P=0.049]). CONCLUSIONS Systematic pelvic and paraaortic lymphadenectomy in patients with advanced ovarian cancer who had undergone intraabdominal macroscopically complete resection and had normal lymph nodes both before and during surgery was not associated with longer overall or progression-free survival than no lymphadenectomy and was associated with a higher incidence of postoperative complications.
Lingua originaleEnglish
pagine (da-a)822-832
Numero di pagine11
RivistaTHE NEW ENGLAND JOURNAL OF MEDICINE
Volume380
DOI
Stato di pubblicazionePubblicato - 2019

Keywords

  • Adult
  • Aged
  • Aged, 80 and over
  • CA-125 Antigen
  • Female
  • Humans
  • Kaplan-Meier Estimate
  • Lymph Node Excision
  • Lymphatic Metastasis
  • Medicine (all)
  • Middle Aged
  • Operative Time
  • Ovarian Neoplasms
  • Postoperative Complications
  • Progression-Free Survival
  • Proportional Hazards Models
  • Survival Rate
  • Treatment Failure
  • Young Adult

Fingerprint

Entra nei temi di ricerca di 'A randomized trial of lymphadenectomy in patients with advanced ovarian neoplasms'. Insieme formano una fingerprint unica.

Cita questo