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Randomized Phase III Study Comparing Neoadjuvant Chemotherapy Followed by Surgery Versus Chemoradiation in Stage IB2-IIB Cervical Cancer: EORTC-55994

  • Gemma G. Kenter
  • , Stefano Greggi
  • , Ignace Vergote
  • , Dionyssios Katsaros
  • , Juliusz Kobierski
  • , Heleen van Doorn
  • , Fabio Landoni
  • , Jacobus van der Velden
  • , Nicholas Reed
  • , Corneel Coens
  • , Iske van Luijk
  • , Nicoletta Colombo
  • , Elzbietta van der Steen-Banasik
  • , Nelleke Ottevanger
  • , EORTC-55994 Study Group
  • Amsterdam UMC - University of Amsterdam
  • IRCCS Istituto nazionale tumori Fondazione Giovanni Pascale - Napoli
  • KU Leuven
  • University of Turin
  • Medical University of Gdańsk
  • Erasmus University Rotterdam
  • University of Milan - Bicocca
  • NHS Greater Glasgow and Clyde
  • European Organization for Research and Treatment
  • Haaglanden Medisch Centrum
  • IRCCS Istituto Europeo di Oncologia - Milano
  • Radboud University Medical Center
  • Hospital Clínico San Carlos de Madrid

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

PURPOSEThis multicenter trial by the European Organisation for Research and Treatment of Cancer Gynecological Cancer Group was motivated by conflicting evidence on the value of neoadjuvant chemotherapy before surgery compared with concomitant chemoradiotherapy (CCRT) in stage IB2-IIB cervical carcinoma.METHODSBetween May 2002 and January 2014, 626 patients with International Federation of Gynecology and Obstetrics stage IB2-IIb were randomly assigned between neoadjuvant chemotherapy followed by surgery (NACT-S; n = 314) and standard CCRT (n = 312). The primary end point was 5-year overall survival (OS) rate. Secondary end points were progression-free survival, OS, toxicity, and health-related quality of life (HRQOL).RESULTSAfter a median follow-up of 8.7 years, 198 patients (31.6%) died. Age, stage, and cell type were balanced in both arms. Protocol treatment was completed in 223 of 314 (71%) patients in NACT-S and 257 of 312(82%) in CCRT arms. Main reasons for incomplete protocol treatment were toxicity (30 of 314; 9.6%) and progressive disease (21 of 314; 6.7%) in the NACT-S arm and toxicity (23 of 312; 7.4%) and patient refusal (13 of 312; 4.2%) in the CCRT arm. Additional radiotherapy after completed NACT-S was given to 107 patients (48%), and additional surgery to 20 patients (8%) after completed CCRT. Short-term adverse events (AEs) â ‰¥grade 3 occurred more frequently with NACT-S (41% v 23%), and long-term AEs â ‰¥grade 3 more often with CCRT (21% v 15%). The 5-year OS was not significantly different between NACT-S (72%; 95% CI, 66 to 77) and CCRT (76%; 95% CI, 70 to 80).CONCLUSIONThis trial failed to demonstrate superiority in favor of the NACT-S arm but resulted in acceptable morbidity and HRQOL in both arms.

Original languageEnglish
Pages (from-to)5035-5043
Number of pages9
JournalJournal of clinical oncology
Volume41
Issue number32
DOIs
Publication statusPublished - 10 Nov 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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