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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorde Andrea, Carlos E
dc.contributor.authorDíez García, Marc
dc.contributor.authorGuardeño, Raquel
dc.contributor.authorCALVO, MARIONA
dc.contributor.authorBugés, Cristina
dc.contributor.authorGarcía-Galea, Eduardo
dc.contributor.authorGros, Alena
dc.contributor.authorVila-Casadesús, Maria
dc.contributor.authorLópez García, Darío
dc.contributor.authorMuñoz, Susana
dc.contributor.authorAlsina, Maria
dc.contributor.authorVillacampa Javierre, Guillermo
dc.contributor.authorVivancos, Ana
dc.contributor.authorPonz-Sarvise, Mariano
dc.contributor.authorArrazubi, Virginia
dc.contributor.authorTabernero, Josep
dc.contributor.authorNavarro Garces, Victor
dc.date.accessioned2025-09-09T08:59:11Z
dc.date.available2025-09-09T08:59:11Z
dc.date.issued2025-07-15
dc.identifier.citationAlsina M, Villacampa G, de Andrea C, Vivancos A, Ponz-Sarvise M, Arrazubi V, et al. Phase II study of perioperative Avelumab plus chemotherapy for patients with resectable gastric cancer or gastroesophageal junction cancer – the MONEO Study. Clin Cancer Res. 2025 Jul 15;31(14):2890–8.
dc.identifier.issn1557-3265
dc.identifier.urihttp://hdl.handle.net/11351/13628
dc.descriptionPerioperative avelumab; Resectable gastric cancer; Gastroesophageal junction cancer
dc.description.abstractPurpose: 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.
dc.language.isoeng
dc.publisherAmerican Association for Cancer Research
dc.relation.ispartofseriesClinical Cancer Research;31(14)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectQuimioteràpia combinada
dc.subjectAnticossos monoclonals - Ús terapèutic
dc.subjectEsòfag - Càncer - Tractament
dc.subjectEstómac - Càncer - Tractament
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshEsophageal Neoplasms
dc.subject.meshStomach Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshEsophagogastric Junction
dc.subject.meshAntibodies, Monoclonal, Humanized
dc.titleA Phase II Study of Perioperative Avelumab plus Chemotherapy for Patients with Resectable Gastric Cancer or Gastroesophageal Junction Cancer - The MONEO Study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1158/1078-0432.CCR-25-0369
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsneoplasias del esófago
dc.subject.decsneoplasias gástricas
dc.subject.decs/farmacoterapia
dc.subject.decsunión esofagogástrica
dc.subject.decsanticuerpos monoclonales humanizados
dc.relation.publishversionhttps://doi.org/10.1158/1078-0432.CCR-25-0369
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Alsina M] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Medical Oncology Department, Hospital Universitario de Navarra, Pamplona, Spain. Translational Medical Oncology Unit, Navarrabiomed – IdiSNA, Pamplona, Spain. [Villacampa G, Navarro V, García-Galea E] Statistics Unit, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [de Andrea C] Cínica Universidad de Navarra, University of Navarra, Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Pamplona, Spain. [Vivancos A, Vila-Casadesús M] Cancer Genomics, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Ponz-Sarvise M] Department of Medical Oncology and Program in Solid Tumors, CIMAIdiSNA-Universidad de Navarra, Cancer Center Clínica Universidad de Navarra (CCUN), Pamplona, Spain. [Arrazubi V] Medical Oncology Department, Hospital Universitario de Navarra, Pamplona, Spain. [Gros A, Tabernero J] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [López D, Muñoz S] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Diez M, Calvo M] Institut Catala d'Oncologia (ICO), l'Hospitalet de Llobregat, Spain. Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), l'Hospitalet de Llobregat, Spain. [Guardeño R] Institut Català d'Oncologia (ICO), Girona, Spain. Hospital Universitari Dr. Josep Trueta, Girona, Spain. [Bugés C] Institut Català d'Oncologia (ICO), Badalona, Spain. Hospital Germans Trias i Pujol, Badalona, Spain
dc.identifier.pmid40388549
dc.identifier.wos001529643800004
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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