Cited 4 times in

Patient-reported outcomes in CodeBreaK 200: Sotorasib versus docetaxel for previously treated advanced NSCLC with KRAS G12C mutation

Authors
 David M Waterhouse  ;  Sacha Rothschild  ;  Christophe Dooms  ;  Bertrand Mennecier  ;  Farastuk Bozorgmehr  ;  Margarita Majem  ;  Michel H van den Heuvel  ;  Helena Linardou  ;  Byoung Chul Cho  ;  Rachel Roberts-Thomson  ;  Kentaro Tanaka  ;  Normand Blais  ;  Gustavo Schvartsman  ;  Karin Holmskov Hansen  ;  Izabela Chmielewska  ;  Martin D Forster  ;  Christina Giannopoulou  ;  Björn Stollenwerk  ;  Cynthia C Obiozor  ;  Yang Wang  ;  Silvia Novello 
Citation
 LUNG CANCER, Vol.196 : 107921, 2024-10 
Journal Title
LUNG CANCER
ISSN
 0169-5002 
Issue Date
2024-10
MeSH
Adult ; Aged ; Aged, 80 and over ; Antineoplastic Agents / adverse effects ; Antineoplastic Agents / therapeutic use ; Carcinoma, Non-Small-Cell Lung* / drug therapy ; Carcinoma, Non-Small-Cell Lung* / genetics ; Docetaxel* / therapeutic use ; Female ; Humans ; Lung Neoplasms* / drug therapy ; Lung Neoplasms* / genetics ; Lung Neoplasms* / pathology ; Male ; Middle Aged ; Mutation* ; Neoplasm Staging ; Patient Reported Outcome Measures* ; Piperazines ; Proto-Oncogene Proteins p21(ras)* / genetics ; Pyridines ; Pyrimidines / therapeutic use ; Quality of Life* ; Surveys and Questionnaires ; Treatment Outcome
Keywords
Quality of life ; Side effects ; Symptom burden
Abstract
Background: In the CodeBreaK 200 phase III, open-label trial, sotorasib significantly improved efficacy versus docetaxel in previously treated KRAS G12C-mutated advanced non-small cell lung cancer (NSCLC). Patient-reported outcomes (PROs) for global health status, physical functioning, dyspnea, and cough favored sotorasib over docetaxel. Here, we report sotorasib's additional impact on quality of life (QOL).

Methods: In CodeBreaK 200, 345 patients who had progressed after prior therapy received sotorasib (960 mg orally daily) or docetaxel (75 mg/m2 intravenously every 3 weeks). Validated questionnaires captured patients' perception of their QOL and symptom burden for key secondary and exploratory PRO endpoints, including the European Organisation for Research and Treatment of Cancer Quality-of-life Questionnaire Core 30 (EORTC QLQ-C30) and Quality-of-life Questionnaire Lung Cancer 13 (EORTC QLQ-LC13), question GP5 from the Functional Assessment of Cancer Therapy Tool General Form (FACT-G GP5), PRO-Common Terminology Criteria for Adverse Events (PRO-CTCAE), and 5-level EuroQOL-5 dimensions (EQ-5D-5L) including visual analog scale (EQ-5D VAS). Change from baseline to week 12 was assessed with generalized estimating equations for ordinal outcomes.

Results: Patients receiving sotorasib were less bothered by treatment side effects than those receiving docetaxel (odds ratio [OR] 5.7) and experienced symptoms at lower severity (pain: OR 2.9; aching muscles: OR 4.4; aching joints: OR 4.2; mouth or throat sores: OR 4.3). Further, patients' symptoms interfered less with usual/daily activities (pain: OR 3.2; aching muscles: OR 3.9; aching joints: OR 10.7). QOL remained stable with sotorasib but worsened with docetaxel (change from baseline in EQ-5D VAS score: 1.5 vs -8.4 at cycle 1 day 5 and 2.2 vs -5.8 at week 12).

Conclusions: Patients receiving sotorasib reported less severe symptoms than those receiving docetaxel. In addition to improving clinical efficacy outcomes, sotorasib maintained QOL versus docetaxel, suggesting sotorasib may be a more tolerable treatment option for patients with pretreated, KRAS G12C-mutated advanced NSCLC.
Full Text
https://www.sciencedirect.com/science/article/pii/S0169500224004550
DOI
10.1016/j.lungcan.2024.107921
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/22282913/202271
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