Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/222810
Title: | A Phase II Study of Perioperative Avelumab plus Chemotherapy for Patients with Resectable Gastric Cancer or Gastroesophageal Junction Cancer – The MONEO Study |
Author: | Alsina, Maria Villacampa, Guillermo De Andrea, Carlos Vivancos, Ana Ponz-sarvise, Mariano Arrazubi, Virginia Jimenez-fonseca, Paula Diez, Marc Sanz-garcia, Enrique Martínez, Eva Guardeño, Raquel Calvo, Mariona Bugés, Cristina Longo, Federico Navarro, Víctor García-galea, Eduardo Gros, Alena C. Ochoa, Maria Lopez-janeiro, Alvaro Sanchez-gregorio, Sandra Herrero, Claudia Labiano, Ibone Vila-casadesús, Maria López, Dario Alexandru, Raluca Muñoz, Susana Tabernero, Josep Melero, Ignacio |
Issue Date: | 19-May-2025 |
Publisher: | American Association for Cancer Research (AACR) |
Abstract: | Purpose: Immune checkpoint inhibitors combined with chemotherapy have provided successful results in patients with gastric and gastroesophageal junction (G/GEJ) cancers in the metastatic setting. Similar strategies have been explored in earlier stages. In this study, we present the final results of the phase II MONEO trial, which evaluated the addition of avelumab to neoadjuvant chemotherapy.Patients and Methods: Patients with untreated, resectable G/GEJ adenocarcinoma received neoadjuvant treatment with four cycles of avelumab plus the FLOT4 regimen, followed by surgery. Upon postoperative recovery, patients underwent four additional adjuvant cycles of the same combination, followed by avelumab monotherapy for up to 1 year. The primary endpoint was pathologic complete response rate. Sequential flow cytometry and cytokine determination were performed in peripheral blood, along with multiplex tissue immunofluorescence and RNA sequencing in tumor specimens.Results: Forty patients were enrolled, achieving a pathologic complete response rate of 21.1% (95% confidence interval, 10.0-37.0). The major pathologic response rate was 28.9%, more pronounced in patients with tumors expressing PD-L1 before treatment as measured by the combined positive score (cutoff, 10; 33.3% vs. 21.1%). The results propose several potential biomarkers considering tumor immune infiltrate, circulating immune cells, and cytokines. Eighty percent of patients experienced treatment-related grade >= 3 adverse events.Conclusions: The combination of avelumab plus the FLOT4 regimen showed relatively modest efficacy in resectable G/GEJ adenocarcinoma. Better results were observed in PD-L1 combined positive score >= 10% tumors. Exploratory biomarker analyses provide insights that may help to identify candidates most likely to benefit from chemoimmunotherapy as a neoadjuvant treatment. |
Note: | Reproducció del document publicat a: https://doi.org/10.1158/1078-0432.CCR-25-0369 |
It is part of: | Clinical Cancer Research, 2025, vol. 31, issue. 14, p. 2890-2898 |
URI: | https://hdl.handle.net/2445/222810 |
Related resource: | https://doi.org/10.1158/1078-0432.CCR-25-0369 |
Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
ccr-25-0369.pdf | 2.77 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.