Neutrophil-to-Eosinophil Ratio Predicts the Efficacy of Avelumab in Patients With Advanced Urothelial Carcinoma Enrolled in the MALVA Study (Meet-URO 25).

Biomarker Eosinophilia Predictive factors Prognostic factors

Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
24 Apr 2024
Historique:
received: 28 02 2024
revised: 18 04 2024
accepted: 20 04 2024
medline: 23 5 2024
pubmed: 23 5 2024
entrez: 22 5 2024
Statut: aheadofprint

Résumé

Neutrophil-to-eosinophil ratio (NER) has been described to be associated with outcomes to immune checkpoint inhibitors (ICI) in several tumor types, but less is known about its role of in the response to avelumab in advanced urothelial cancer (aUC). Thus, we reported outcomes by NER of aUC patients treated with avelumab as maintenance after initial response to platinum-based chemotherapy and enrolled in the Maintenance with AVeLumAb ([MALVA] in advanced urothelial neoplasms in response to first-line chemotherapy: an observational retrospective study) study (Meet-URO 25). Median NER at baseline and after 3 cycles of avelumab were calculated. Progression-free survival (PFS) and overall survival (OS) by NER were reported. At the cutoff date (April 15, 2023), a total of 109 patients were included. The median NER was 28.05 at baseline and 24.46 after 3 cycles of avelumab, respectively. Median PFS was not reached for patients with baseline NER less than the median (<median) compared to 5.1 months for patients with baseline NER greater than the median (≥median) (P = .0005). Median OS was significantly longer for patients with baseline NER <median compared with patients with baseline NER ≥median (not reached vs. 11.7 months, respectively; P = .0016). Significantly better PFS and OS were confirmed for NER after 3 cycles of avelumab <median compared with NER ≥median at the same timepoint. NER <median may be predictive of PFS in aUC patients treated with avelumab, and prognostic for OS regardless of treatment. Prospective studies are warranted to validate NER as a readily available and reproducible laboratory-biomarker for efficacy outcomes of avelumab in aUC.

Sections du résumé

BACKGROUND BACKGROUND
Neutrophil-to-eosinophil ratio (NER) has been described to be associated with outcomes to immune checkpoint inhibitors (ICI) in several tumor types, but less is known about its role of in the response to avelumab in advanced urothelial cancer (aUC). Thus, we reported outcomes by NER of aUC patients treated with avelumab as maintenance after initial response to platinum-based chemotherapy and enrolled in the Maintenance with AVeLumAb ([MALVA] in advanced urothelial neoplasms in response to first-line chemotherapy: an observational retrospective study) study (Meet-URO 25).
PATIENTS AND METHODS METHODS
Median NER at baseline and after 3 cycles of avelumab were calculated. Progression-free survival (PFS) and overall survival (OS) by NER were reported.
RESULTS RESULTS
At the cutoff date (April 15, 2023), a total of 109 patients were included. The median NER was 28.05 at baseline and 24.46 after 3 cycles of avelumab, respectively. Median PFS was not reached for patients with baseline NER less than the median (<median) compared to 5.1 months for patients with baseline NER greater than the median (≥median) (P = .0005). Median OS was significantly longer for patients with baseline NER <median compared with patients with baseline NER ≥median (not reached vs. 11.7 months, respectively; P = .0016). Significantly better PFS and OS were confirmed for NER after 3 cycles of avelumab <median compared with NER ≥median at the same timepoint.
CONCLUSION CONCLUSIONS
NER <median may be predictive of PFS in aUC patients treated with avelumab, and prognostic for OS regardless of treatment. Prospective studies are warranted to validate NER as a readily available and reproducible laboratory-biomarker for efficacy outcomes of avelumab in aUC.

Identifiants

pubmed: 38776583
pii: S1558-7673(24)00070-3
doi: 10.1016/j.clgc.2024.102099
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102099

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Elisabetta Gambale (E)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Careggi University Hospital, Clinical Oncology, Florence, Italy.

Marco Maruzzo (M)

Oncology Unit 1, Istituto Oncologico Veneto, IOV - IRCCS, Padova, Italy.

Carlo Messina (C)

Ospedale Arnas Civico, Clinical Oncology, Palermo, Italy.

Irene De Gennaro Aquino (I)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Careggi University Hospital, Clinical Oncology, Florence, Italy.

Ismaela Anna Vascotto (IA)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Careggi University Hospital, Clinical Oncology, Florence, Italy.

Virginia Rossi (V)

Careggi University Hospital, Clinical Oncology, Florence, Italy.

Davide Bimbatti (D)

Oncology Unit 1, Istituto Oncologico Veneto, IOV - IRCCS, Padova, Italy.

Nicolò Cavasin (N)

Oncology Unit 1, Istituto Oncologico Veneto, IOV - IRCCS, Padova, Italy.

Marco Messina (M)

Ospedale Arnas Civico, Clinical Oncology, Palermo, Italy.

Alessia Mennitto (A)

University Hospital Maggiore della Carità, Division of Oncology, Novara, Italy.

Sara Elena Rebuzzi (SE)

Ospedale San Paolo, Medical Oncology Unit, Savona, Italy; Department of Internal Medicine and Medical Specialties (Di.M.I.), University of Genoa, Genoa, Italy.

Cecilia Nasso (C)

Medical Oncology, Ospedale Santa Corona, 17027 Pietra Ligure, Italy.

Chiara Mercinelli (C)

Azienda Ospedaliero-Universitaria Pisana, Medical Oncology Unit 2, Pisa, Italy; Department of Medical Oncology, IRRCS San Raffaele Hospital, Milan, Italy.

Brigida Anna Maiorano (BA)

Department of Medical Oncology, IRRCS San Raffaele Hospital, Milan, Italy; Oncology Unit, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo.

Martina Fanelli (M)

University Hospital of Udine, Department of Oncology, Udine, Italy.

Mariella Sorarù (M)

Ospedale di Camposampiero, U.O. Oncologia, Camposampiero, Italy.

Federico Scolari (F)

Department of Biomedical, Experimental and Clinical Sciences, University of Florence, Florence, Italy.

Marinella Micol Mela (MM)

Careggi University Hospital, Clinical Oncology, Florence, Italy.

Luca Galli (L)

Azienda Ospedaliero-Universitaria Pisana, Medical Oncology Unit 2, Pisa, Italy.

Alessia Salfi (A)

Azienda Ospedaliero-Universitaria Pisana, Medical Oncology Unit 2, Pisa, Italy.

Mimma Rizzo (M)

Oncologia Medica Universitaria Azienda Ospedaliera Universitaria Consorziale Policlinico di Bari piazza Giulio Cesare, 11, 70124 Bari.

Silvia Puglisi (S)

IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Valentina Orlando (V)

Department of Oncology, Ospedale Maggiore, Trieste, Italy.

Giuseppe Fornarini (G)

IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Alessandro Rametta (A)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Giacomo Venezian 1, Milan, Italy.

Patrizia Giannatempo (P)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Giacomo Venezian 1, Milan, Italy.

Linda Cerbone (L)

Department of Medical Oncology, San Camillo Forlanini Hospital, Rome, Italy.

Laura Doni (L)

Careggi University Hospital, Clinical Oncology, Florence, Italy.

Giandomenico Roviello (G)

Department of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Viale Pieraccini, 6, 50139 Florence, Italy.

Serena Pillozzi (S)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Careggi University Hospital, Clinical Oncology, Florence, Italy.

Lorenzo Antonuzzo (L)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Careggi University Hospital, Clinical Oncology, Florence, Italy.

Classifications MeSH