Published 2024
| Version v1
Journal article
Safety and Patient-Reported outcomes of atezolizumab plus chemotherapy with or without bevacizumab in stage IIIB/IV non-squamous non-small cell lung cancer with EGFR mutation, ALK rearrangement or ROS1 fusion progressing after targeted therapies (GFPC 06-2018 study)
Creators
- Amari, Lyria
- Tomasini, Pascale
- Dantony, Emmanuelle
- Rousseau-Bussac, Gaëlle
- Ricordel, Charles
- Bigay Game, Laurence
- Arpin, Dominique
- Morel, Hugues
- Veillon, Remi
- Justeau, Grégoire
- Huchot, Eric
- Fournel, Pierre
- Vergnenègre, Alain
- Bizeux, Acya
- Subtil, Fabien
- Clarisse, Benedicte
- Decroisette, Chantal
- Chouaïd, Christos
- Greillier, Laurent
- Bylicki, Olivier
Contributors
Others:
- Hopital d'instruction des armées Sainte-Anne [Toulon] (HIA)
- Aix Marseille Université (AMU)
- Multidisciplinary Oncology and Therapeutic Innovations Unit / Service d'Oncologie Multidisciplinaire et d'Innovations Thérapeutiques (OMIT) ; Hôpital Nord [CHU - APHM]
- Centre de Recherche en Cancérologie de Marseille (CRCM) ; Aix Marseille Université (AMU)-Institut Paoli-Calmettes (IPC) ; Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
- Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE) ; Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon-Université de Lyon-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)
- Hospices Civils de Lyon (HCL)
- CHI Créteil
- Oncogenesis, Stress, Signaling (OSS) ; Université de Rennes (UR)-CRLCC Eugène Marquis (CRLCC) ; UNICANCER-UNICANCER-Institut National de la Santé et de la Recherche Médicale (INSERM)
- Centre Hospitalier Universitaire de Rennes [CHU Rennes] = Rennes University Hospital [Pontchaillou]
- CRLCC Eugène Marquis (CRLCC) ; UNICANCER
- Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)
- Hôpital Nord-Ouest [Villefranche sur Saône]
- Hôpital La Source [Orléans] (HLSO)
- Centre Hospitalier Universitaire de Bordeaux (CHU Bordeaux)
- Centre Hospitalier Universitaire d'Angers (CHU Angers) ; PRES Université Nantes Angers Le Mans (UNAM)
- CHU Sud Saint Pierre [Ile de la Réunion]
- Centre Hospitalier Universitaire de Saint-Etienne [CHU Saint-Etienne] (CHU ST-E)
- CHU Limoges
- Centre Hospitalier Départemental - Hôpital de La Roche-sur-Yon (CHD Vendée)
- Centre Régional de Lutte contre le Cancer François Baclesse [Caen] (UNICANCER/CRLC) ; Normandie Université (NU)-UNICANCER-Tumorothèque de Caen Basse-Normandie (TCBN)
- Centre Hospitalier Annecy-Genevois [Saint-Julien-en-Genevois]
- Hôpital Nord [CHU - APHM]
- Méthodes computationnelles pour la prise en charge thérapeutique en oncologie : Optimisation des stratégies par modélisation mécaniste et statistique (COMPO) ; Centre Inria d'Université Côte d'Azur (CRISAM) ; Institut National de Recherche en Informatique et en Automatique (Inria)-Institut National de Recherche en Informatique et en Automatique (Inria)-Centre de Recherche en Cancérologie de Marseille (CRCM) ; Aix Marseille Université (AMU)-Institut Paoli-Calmettes (IPC) ; Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU)-Institut Paoli-Calmettes (IPC) ; Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
- This trial was granted by financial support and drug supply (atezolizumab, bevacizumab) from Roche S.A.S which was not involved in the design and conduct of the study, nor in the collection, management, analysis and interpretation of the data. It was not involved in the writing of the manuscript.
Description
Background: In an open-label multicenter non-randomized non-comparative phase II study in patients with stage IIIB/IV non-squamous non -small cell lung cancer (NSCLC), oncogenic addiction (EGFR mutation or ALK/ROS1 fusion), with disease progression after tyrosine-kinase inhibitor and no prior chemotherapy (NCT04042558), atezolizumab, carboplatin, pemetrexed with or without bevacizumab showed some promising result. Beyond the clinical evaluation, we assessed safety and patient-reported outcomes (PROs) to provide additional information on the relative impact of adding atezolizumab to chemotherapy with and without bevacizumab in this population. Materials: Patients received platinum-pemetrexed-atezolizumab-bevacizumab (PPAB cohort) or, if not eligible, platinum-pemetrexed-atezolizumab (PPA cohort). The incidence, nature, and severity of adverse events (AEs) were assessed. PROs were evaluated using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-Core 30 and EORTC QLQ-Lung Cancer 13). Result: Overall, 68 (PPAB) and 72 (PPA) patients were evaluable for safety. Grade 3 -4 AEs occurred in 83.8% (PPAB) and 63.9% (PPA). Grade 3 -4 atezolizumab-related AEs occurred in 29.4% and 19.4%, respectively. Grade 3 -4 bevacizumab-related AEs occurred in 36.8% (PPAB). Most frequent grade 3 -4 AEs were neutropenia (19.1% in PPAB; 23.6% in PPA) and asthenia (16.2% in PPAB; 9.7% in PPA). In PPAB, we observed a global stability in global health security (GHS) score, fatigue and dyspnea with a constant tendency of improvement, and a significant improvement in cough. In PPA, we observed a significant improvement in GHS score with a significant improvement in fatigue, dyspnea and cough. At week 54, we observed an improvement from baseline in GHS score for 49.2% of patients. In both cohorts, patients reported on average no clinically significant worsening in their overall health or physical functioning scores. Conclusion: PPAB and PPA combinations seem tolerable and manageable in patients with stage IIIB/IV nonsquamous NSCLC with oncogenic addiction (EGFR mutation or ALK/ROS1 fusion) after targeted therapies.
Abstract
International audienceAdditional details
Identifiers
- URL
- https://hal.science/hal-04652518
- URN
- urn:oai:HAL:hal-04652518v1
Origin repository
- Origin repository
- UNICA