Cancers (Apr 2023)

Perioperative Cetuximab with Cisplatin and 5-Fluorouracil in Esogastric Adenocarcinoma: A Phase II Study

  • Caroline Gronnier,
  • Christophe Mariette,
  • Come Lepage,
  • Carole Monterymard,
  • Marine Jary,
  • Aurélie Ferru,
  • Mathieu Baconnier,
  • Xavier Adhoute,
  • David Tavan,
  • Hervé Perrier,
  • Véronique Guerin-Meyer,
  • Cédric Lecaille,
  • Nathalie Bonichon-Lamichhane,
  • Didier Pillon,
  • Oana Cojocarasu,
  • Joëlle Egreteau,
  • Xavier Benoit D’journo,
  • Laétitia Dahan,
  • Christophe Locher,
  • Patrick Texereau,
  • Denis Collet,
  • Pierre Michel,
  • Meher Ben Abdelghani,
  • Rosine Guimbaud,
  • Marie Muller,
  • Olivier Bouché,
  • Guillaume Piessen

DOI
https://doi.org/10.3390/cancers15072188
Journal volume & issue
Vol. 15, no. 7
p. 2188

Abstract

Read online

Purpose: While perioperative chemotherapy provides a survival benefit over surgery alone in gastric and gastroesophageal junction (G/GEJ) adenocarcinomas, the results need to be improved. This study aimed to evaluate the efficacy and safety of perioperative cetuximab combined with 5-fluorouracil and cisplatin. Patients and Methods: Patients received six cycles of cetuximab, cisplatin, and simplified LV5FU2 before and after surgery. The primary objective was a combined evaluation of the tumor objective response (TOR), assessed by computed tomography, and the absence of major toxicities resulting in discontinuation of neoadjuvant chemotherapy (NCT) (45% and 90%, respectively). Results: From 2011 to 2013, 65 patients were enrolled. From 64 patients evaluable for the primary endpoint, 19 (29.7%) had a morphological TOR and 61 (95.3%) did not stop NCT prematurely due to major toxicity. Sixty patients (92.3%) underwent resection. Sixteen patients (/56 available, 28.5%) had histological responses (Mandard tumor regression grade ≤3). After a median follow-up of 44.5 months, median disease-free and overall survival were 24.4 [95% CI: 16.4-39.4] and 40.3 months [95% CI: 27.5-NA], respectively. Conclusion: Adding cetuximab to the NCT regimen in operable G/GEJ adenocarcinomas is safe, but did not show enough efficacy in the present study to meet the primary endpoint (NCT01360086).

Keywords