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Patient-reported outcomes with durvalumab, with or without tremelimumab, plus chemotherapy as first-line treatment for metastatic non-small-cell lung cancer (POSEIDON)

Authors
 Edward B Garon  ;  Byoung Chul Cho  ;  Alexander Luft  ;  Jorge Alatorre-Alexander  ;  Sarayut Lucien Geater  ;  Sang-We Kim  ;  Grygorii Ursol  ;  Maen Hussein  ;  Farah Louise Lim  ;  Cheng-Ta Yang  ;  Luiz Henrique Araujo  ;  Haruhiro Saito  ;  Niels Reinmuth  ;  Nenad Medic  ;  Helen Mann  ;  Xiaojin Shi  ;  Solange Peters  ;  Tony Mok  ;  Melissa Johnson 
Citation
 LUNG CANCER, Vol.186 : 107422, 2023-12 
Journal Title
LUNG CANCER
ISSN
 0169-5002 
Issue Date
2023-12
MeSH
Antineoplastic Combined Chemotherapy Protocols / therapeutic use ; Carcinoma, Non-Small-Cell Lung* / pathology ; Diarrhea ; Dyspnea ; Humans ; Lung Neoplasms* / pathology ; Nausea ; Pain / drug therapy ; Patient Reported Outcome Measures ; Quality of Life ; Vomiting
Keywords
Durvalumab ; Health-related quality of life ; Metastatic non-small-cell lung cancer ; POSEIDON ; Patient-reported outcomes ; Tremelimumab
Abstract
Objectives: In the phase 3 POSEIDON study, first-line tremelimumab plus durvalumab and chemotherapy significantly improved overall survival and progression-free survival versus chemotherapy in metastatic non-small-cell lung cancer (NSCLC). We present patient-reported outcomes (PROs). Patients and methods: Treatment-naïve patients were randomized 1:1:1 to tremelimumab plus durvalumab and chemotherapy, durvalumab plus chemotherapy, or chemotherapy. PROs (prespecified secondary endpoints) were assessed using the European Organisation for Research and Treatment of Cancer 30-item core quality of life questionnaire version 3 (QLQ-C30) and its 13-item lung cancer module (QLQ-LC13). We analyzed time to deterioration (TTD) of symptoms, functioning, and global health status/quality of life (QoL) from randomization by log-rank test and improvement rates by logistic regression. Results: 972/1013 (96 %) patients randomized completed baseline QLQ-C30 and QLQ-LC13 questionnaires, with scores comparable between treatment arms. Patients receiving tremelimumab plus durvalumab and chemotherapy versus chemotherapy had longer median TTD for all PRO items. Hazard ratios for TTD favored tremelimumab plus durvalumab and chemotherapy for all items except diarrhea; 95 % confidence intervals did not cross 1.0 for global health status/QoL, physical functioning, cognitive functioning, pain, nausea/vomiting, insomnia, constipation, hemoptysis, dyspnea, and pain in other parts. For durvalumab plus chemotherapy, median TTD was longer versus chemotherapy for all items except nausea/vomiting and diarrhea. Hazard ratios favored durvalumab plus chemotherapy for all items except appetite loss; 95 % confidence intervals did not cross 1.0 for global health status/QoL, physical functioning, role functioning, dyspnea, and pain in other parts. For both immunotherapy plus chemotherapy arms, improvement rates in all PRO items were numerically higher versus chemotherapy, with odds ratios > 1. Conclusions: Tremelimumab plus durvalumab and chemotherapy delayed deterioration in symptoms, functioning, and global health status/QoL compared with chemotherapy. Together with significant improvements in survival, these results support tremelimumab plus durvalumab and chemotherapy as a first-line treatment option in metastatic NSCLC. © 2023 The Authors
Files in This Item:
T202400914.pdf Download
DOI
10.1016/j.lungcan.2023.107422
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Cho, Byoung Chul(조병철) ORCID logo https://orcid.org/0000-0002-5562-270X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/198103
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