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

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dc.contributor.author조병철-
dc.date.accessioned2025-02-03T09:11:23Z-
dc.date.available2025-02-03T09:11:23Z-
dc.date.issued2024-10-
dc.identifier.issn0169-5002-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/202271-
dc.description.abstractBackground: 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.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier Scientific Publishers-
dc.relation.isPartOfLUNG CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAntineoplastic Agents / adverse effects-
dc.subject.MESHAntineoplastic Agents / therapeutic use-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / drug therapy-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / genetics-
dc.subject.MESHDocetaxel* / therapeutic use-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLung Neoplasms* / drug therapy-
dc.subject.MESHLung Neoplasms* / genetics-
dc.subject.MESHLung Neoplasms* / pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMutation*-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHPatient Reported Outcome Measures*-
dc.subject.MESHPiperazines-
dc.subject.MESHProto-Oncogene Proteins p21(ras)* / genetics-
dc.subject.MESHPyridines-
dc.subject.MESHPyrimidines / therapeutic use-
dc.subject.MESHQuality of Life*-
dc.subject.MESHSurveys and Questionnaires-
dc.subject.MESHTreatment Outcome-
dc.titlePatient-reported outcomes in CodeBreaK 200: Sotorasib versus docetaxel for previously treated advanced NSCLC with KRAS G12C mutation-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorDavid M Waterhouse-
dc.contributor.googleauthorSacha Rothschild-
dc.contributor.googleauthorChristophe Dooms-
dc.contributor.googleauthorBertrand Mennecier-
dc.contributor.googleauthorFarastuk Bozorgmehr-
dc.contributor.googleauthorMargarita Majem-
dc.contributor.googleauthorMichel H van den Heuvel-
dc.contributor.googleauthorHelena Linardou-
dc.contributor.googleauthorByoung Chul Cho-
dc.contributor.googleauthorRachel Roberts-Thomson-
dc.contributor.googleauthorKentaro Tanaka-
dc.contributor.googleauthorNormand Blais-
dc.contributor.googleauthorGustavo Schvartsman-
dc.contributor.googleauthorKarin Holmskov Hansen-
dc.contributor.googleauthorIzabela Chmielewska-
dc.contributor.googleauthorMartin D Forster-
dc.contributor.googleauthorChristina Giannopoulou-
dc.contributor.googleauthorBjörn Stollenwerk-
dc.contributor.googleauthorCynthia C Obiozor-
dc.contributor.googleauthorYang Wang-
dc.contributor.googleauthorSilvia Novello-
dc.identifier.doi10.1016/j.lungcan.2024.107921-
dc.contributor.localIdA03822-
dc.relation.journalcodeJ02174-
dc.identifier.eissn1872-8332-
dc.identifier.pmid39303400-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0169500224004550-
dc.subject.keywordQuality of life-
dc.subject.keywordSide effects-
dc.subject.keywordSymptom burden-
dc.contributor.alternativeNameCho, Byoung Chul-
dc.contributor.affiliatedAuthor조병철-
dc.citation.volume196-
dc.citation.startPage107921-
dc.identifier.bibliographicCitationLUNG CANCER, Vol.196 : 107921, 2024-10-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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