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dc.contributor.authorGarcía Campelo, María del Rosario *
dc.contributor.authorZhou, C.*
dc.contributor.authorRamalingam, S.S.*
dc.contributor.authorLin, H.M.*
dc.contributor.authorKim, T.M.*
dc.contributor.authorRiely, G.J.*
dc.contributor.authorMekhail, T.*
dc.contributor.authorNguyen, D.*
dc.contributor.authorGoodman, E.*
dc.contributor.authorMehta, M.*
dc.contributor.authorPopat, S.*
dc.contributor.authorJänne, P.A.*
dc.date.accessioned2025-09-12T11:49:16Z
dc.date.available2025-09-12T11:49:16Z
dc.date.issued2023
dc.identifier.citationGarcia Campelo MR, Zhou C, Ramalingam SS, Lin HM, Kim TM, Riely GJ, et al. Mobocertinib (TAK-788) in EGFR Exon 20 Insertion+ Metastatic NSCLC: Patient-Reported Outcomes from EXCLAIM Extension Cohort. Journal of Clinical Medicine. 2023;12(1).
dc.identifier.issn2077-0383
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/63cc8c99ab05b07b66656778
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21829
dc.description.abstractMobocertinib, an oral, first-in-class epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor selective for EGFR exon 20 insertions (ex20ins), achieved durable responses in adults with previously treated EGFR ex20ins+ metastatic non-small cell lung cancer (mNSCLC) in the EXCLAIM extension cohort of a phase 1/2 study (N = 96; NCT02716116). We assessed patient-reported outcomes (PROs) with mobocertinib 160 mg once daily (28-day cycles) in EXCLAIM (N = 90) with the European Organisation for Research and Treatment of Cancer Core Quality-of-Life Questionnaire (EORTC QLQ-C30) v3.0, lung cancer module (QLQ-LC13), EuroQol-5 Dimensions-5 Levels (EQ-5D-5L) questionnaire, and selected PRO Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) questionnaire. Median treatment duration was 6.8 (range, 0.0-18.8) months (median follow-up: 13.0 [0.7-18.8] months; data cutoff: 1 November 2020). Clinically meaningful improvements in lung cancer symptoms measured by EORTC QLQ-LC13 were observed for dyspnea (54.4% of patients), cough (46.7%), and chest pain (38.9%), evident at cycle 2 and throughout treatment (least-squares mean [LSM] changes from baseline: dyspnea, ?3.2 [p = 0.019]; cough, ?9.3 [p < 0.001]; chest pain, ?8.2 [p < 0.001]). EORTC QLQ-C30 results indicated no statistically significant changes in global health status/quality of life (LSM change from baseline: ?1.8 [p = 0.235]). On symptom scores, significant worsening from baseline was observed for diarrhea (LSM change from baseline: +34.1; p < 0.001) and appetite loss (+6.6; p = 0.004), while improvements were observed for dyspnea (LSM change from baseline: ?5.1 [p = 0.002]), insomnia (?6.5 [p = 0.001]), and constipation (?5.7 [p < 0.001]). EQ-5D-5L health status was maintained. Common PRO-CTCAE symptoms were diarrhea, dry skin, rash, and decreased appetite (mostly low grade); in the first 24 weeks of treatment, 64.4% of patients had worsening diarrhea frequency and 67.8% had worsening dry skin severity. Overall, PROs with mobocertinib showed clinically meaningful improvement in lung cancer-related symptoms, with health-related quality of life maintained despite changes in some adverse event symptom scales.
dc.description.sponsorshipThis analysis was sponsored by Takeda Development Center Americas, Inc., Lexington, MA, USA. Employees of Takeda designed the study at the direction of the clinical study investigators. Huamao M. Lin and Erin Goodman are employees of Takeda. Minal Mehta was an employee of Takeda at the time the study was conducted. Maria Rosario Garcia Campelo, Caicun Zhou, Suresh S. Ramalingam, Tae Min Kim, Gregory J. Riely, Tarek Mekhail, Danny Nguyen, Sanjay Popat, and Pasi A. Jaenne led recruitment of study participants and data collection. All authors had full access to all of the data in the study, participated in the analysis and interpretation of the data, contributed to the writing and critical revision of all drafts, and agreed to submit the paper for publication.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleMobocertinib (TAK-788) in EGFR Exon 20 Insertion+ Metastatic NSCLC: Patient-Reported Outcomes from EXCLAIM Extension Cohort
dc.typeArtigo
dc.authorsophosGarcia Campelo, M.R.; Zhou, C.; Ramalingam, S.S.; Lin, H.M.; Kim, T.M.; Riely, G.J.; Mekhail, T.; Nguyen, D.; Goodman, E.; Mehta, M.; Popat, S.; Jänne, P.A.
dc.identifier.doi10.3390/jcm12010112
dc.identifier.sophos63cc8c99ab05b07b66656778
dc.issue.number1
dc.journal.titleJournal of Clinical Medicine*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario A Coruña::Oncoloxía médica
dc.relation.projectIDTakeda Development Center Americas, Inc., Lexington, MA, USA
dc.relation.publisherversionhttps://doi.org/10.3390/jcm12010112
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS A Coruña
dc.subject.keywordCHUAC
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number12


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)