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First-Line Mobocertinib Versus Platinum-Based Chemotherapy in Patients With EGFR Exon 20 Insertion-Positive Metastatic Non-Small Cell Lung Cancer in the Phase III EXCLAIM-2 Trial

DC Field Value Language
dc.contributor.author조병철-
dc.date.accessioned2025-09-02T08:15:55Z-
dc.date.available2025-09-02T08:15:55Z-
dc.date.issued2025-05-
dc.identifier.issn0732-183X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/207230-
dc.description.abstractPurpose: Mobocertinib is an oral epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor that targets EGFR exon 20 insertion (ex20ins) mutations in non-small cell lung cancer (NSCLC). This open-label, phase III trial (EXCLAIM-2, ClinicalTrials.gov identifier: NCT04129502) compared mobocertinib versus platinum-based chemotherapy as first-line treatment of EGFR ex20ins+ advanced/metastatic NSCLC. Methods: Patients with treatment-naive EGFR ex20ins+ locally advanced/metastatic NSCLC were randomly assigned 1:1 to mobocertinib 160 mg once daily or pemetrexed plus cisplatin or carboplatin every 3 weeks for four cycles followed by maintenance pemetrexed. The primary end point was progression-free survival (PFS) by blinded independent central review (BICR), with planned interim analysis (IA) after approximately 70% of 227 expected PFS events. Results: A total of 354 patients were randomly assigned (mobocertinib: n = 179; chemotherapy: n = 175). Baseline characteristics were balanced between arms. At IA (cutoff: April 4, 2023), the median PFS per BICR was 9.6 months in each treatment arm (hazard ratio [HR], 1.04 [95% CI, 0.77 to 1.39]; P = .803). The primary end point crossed the prespecified futility boundary (HR > 1). The confirmed objective response rate (95% CI) per BICR was 32% (26 to 40) with mobocertinib versus 30% (24 to 38) with chemotherapy; the median duration of response was 12.0 versus 8.4 months. Quality-of-life assessments indicated clinically meaningful delays in time to deterioration of lung cancer symptoms, cognitive function, and constipation with mobocertinib versus chemotherapy. Grade ≥3 adverse events in >5% of patients (mobocertinib, chemotherapy) were diarrhea (20%, 1%), anemia (6%, 10%), increased lipase (6%, 0%), and decreased neutrophil count (1%, 7%). Conclusion: The EXCLAIM-2 trial did not meet its primary end point. The efficacy of mobocertinib was not superior to platinum-based chemotherapy for first-line treatment of patients with EGFR ex20ins+ advanced/metastatic NSCLC.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherAmerican Society of Clinical Oncology-
dc.relation.isPartOfJOURNAL OF CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAniline Compounds-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / adverse effects-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / therapeutic use-
dc.subject.MESHCarboplatin / administration & dosage-
dc.subject.MESHCarboplatin / adverse effects-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / drug therapy-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / enzymology-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / genetics-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / pathology-
dc.subject.MESHCisplatin / administration & dosage-
dc.subject.MESHCisplatin / adverse effects-
dc.subject.MESHErbB Receptors / antagonists & inhibitors-
dc.subject.MESHErbB Receptors / genetics-
dc.subject.MESHExons-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIndoles-
dc.subject.MESHLung Neoplasms* / drug therapy-
dc.subject.MESHLung Neoplasms* / enzymology-
dc.subject.MESHLung Neoplasms* / genetics-
dc.subject.MESHLung Neoplasms* / pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPemetrexed / administration & dosage-
dc.subject.MESHPemetrexed / adverse effects-
dc.subject.MESHProgression-Free Survival-
dc.subject.MESHProtein Kinase Inhibitors* / adverse effects-
dc.subject.MESHProtein Kinase Inhibitors* / therapeutic use-
dc.subject.MESHPyrimidines-
dc.titleFirst-Line Mobocertinib Versus Platinum-Based Chemotherapy in Patients With EGFR Exon 20 Insertion-Positive Metastatic Non-Small Cell Lung Cancer in the Phase III EXCLAIM-2 Trial-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorPasi A Jänne-
dc.contributor.googleauthorBin-Chao Wang-
dc.contributor.googleauthorByoung Chul Cho-
dc.contributor.googleauthorJun Zhao-
dc.contributor.googleauthorJuan Li-
dc.contributor.googleauthorMaximilian Hochmair-
dc.contributor.googleauthorSolange Peters-
dc.contributor.googleauthorBenjamin Besse-
dc.contributor.googleauthorNick Pavlakis-
dc.contributor.googleauthorJoel W Neal-
dc.contributor.googleauthorTerufumi Kato-
dc.contributor.googleauthorYi-Long Wu-
dc.contributor.googleauthorDanny Nguyen-
dc.contributor.googleauthorJunjing Lin-
dc.contributor.googleauthorJianchang Lin-
dc.contributor.googleauthorFlorin Vranceanu-
dc.contributor.googleauthorAnnette Szumski-
dc.contributor.googleauthorHuamao M Lin-
dc.contributor.googleauthorRobert J Fram-
dc.contributor.googleauthorTony S K Mok-
dc.identifier.doi10.1200/JCO-24-01269-
dc.contributor.localIdA03822-
dc.relation.journalcodeJ01331-
dc.identifier.eissn1527-7755-
dc.identifier.pmid39879577-
dc.contributor.alternativeNameCho, Byoung Chul-
dc.contributor.affiliatedAuthor조병철-
dc.citation.volume43-
dc.citation.number13-
dc.citation.startPage1553-
dc.citation.endPage1563-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL ONCOLOGY, Vol.43(13) : 1553-1563, 2025-05-
dc.identifier.rimsid89855-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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