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Enhanced Versus Standard Dermatologic Management With Amivantamab-Lazertinib in EGFR-Mutated Advanced NSCLC: The COCOON Global Randomized Controlled Trial

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dc.contributor.authorChul, Byoung-
dc.contributor.authorLi, Weimin-
dc.contributor.authorSpira, Alexander I.-
dc.contributor.authorSauder, Maxwell-
dc.contributor.authorFeldman, Jill-
dc.contributor.authorBozorgmehr, Farastuk-
dc.contributor.authorMak, Milena-
dc.contributor.authorSmith, Janellen-
dc.contributor.authorVoon, Pei Jye-
dc.contributor.authorLiu, Baogang-
dc.contributor.authorTian, Panwen-
dc.contributor.authorTan, Jiunn-Liang-
dc.contributor.authorYang, Cheng-Ta-
dc.contributor.authorShih, Jin-Yuan-
dc.contributor.authorKaradurmus, Nuri-
dc.contributor.authorCundom, Juan Esteban-
dc.contributor.authorBertollo, Glaucio-
dc.contributor.authorCicin, Irfan-
dc.contributor.authorNieva, Jorge-
dc.contributor.authorOrtega-Granados, Ana Laura-
dc.contributor.authorTomasini, Pascale-
dc.contributor.authorNguyen, Danny-
dc.contributor.authorFelip, Enriqueta-
dc.contributor.authorSchuchard, Julia-
dc.contributor.authorMurphy, Sean P.-
dc.contributor.authorAnderson, Bailey G.-
dc.contributor.authorRomero, Tonatiuh-
dc.contributor.authorXia, Yichuan-
dc.contributor.authorSheng, Shubin-
dc.contributor.authorBauml, Joshua M.-
dc.contributor.authorMahadevia, Parthiv J.-
dc.contributor.authorKam, Julian-
dc.contributor.authorNematian-Samani, Mehregan-
dc.contributor.authorSimoes, Jairo-
dc.contributor.authorWildgust, Mark-
dc.contributor.authorGirard, Nicolas-
dc.date.accessioned2026-01-16T08:21:23Z-
dc.date.available2026-01-16T08:21:23Z-
dc.date.created2026-01-02-
dc.date.issued2025-10-
dc.identifier.issn1556-0864-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/209850-
dc.description.abstractIntroduction: Amivantamab plus lazertinib significantly improved progression-free and overall survival versus osimertinib in patients with previously untreated, EGFR-mutant advanced NSCLC. EGFR-targeted therapies are associated with dermatologic adverse events (AEs), which can affect quality of life (QoL). COCOON was conducted to assess prophylactic management and improve treatment experience. Methods: In the phase 2 COCOON study (NCT06120140), participants with previously untreated, EGFR-mutant, locally advanced or metastatic NSCLC received intravenous amivantamab plus oral lazertinib and were randomized 1:1 to enhanced dermatologic management (COCOON DM) or standard of care (SoC DM) per local guidelines. COCOON DM included oral doxycycline or minocycline (100 mg twice daily; weeks 1-12), clindamycin 1% (on scalp daily; weeks 13-52), chlorhexidine 4% (on fingernails and toenails daily), and ceramide-based moisturizer (on body and face at least daily). Primary end point was incidence of grade 2 or higher dermatologic AEs of interest (DAEIs) by week 12. Results: In total, 201 participants were randomized (99 to COCOON DM and 102 to SoC DM). At a median follow-up of 7.1 months, COCOON DM demonstrated significant reduction in the primary end point versus SoC DM (42% versus 75%; OR, 0.24; 95% confidence interval, 0.13-0.45; p < 0.0001). By week 12, the largest benefit with COCOON DM was observed in DAEIs involving the face and body (excludes paronychia; 26% versus 60%; p < 0.0001) and DAEIs involving the scalp (10% versus 26%; p = 0.0049). This benefit was maintained at 6 months, with significant reductions of DAEIs involving face, body, and scalp (excluding paronychia). Patient-reported outcomes favored COCOON DM, indicating reduced impact of dermatologic symptoms on QoL. Conclusion: An uncomplicated, widely available, prophylactic regimen (COCOON DM) reduced the incidence of DAEIs with amivantamab-lazertinib and the impact of symptoms on QoL. (c) 2025 The Author(s). Published by Elsevier Inc. on behalf of International Association for the Study of Lung Cancer. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfJOURNAL OF THORACIC ONCOLOGY-
dc.relation.isPartOfJOURNAL OF THORACIC ONCOLOGY-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / therapeutic use-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / drug therapy-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / genetics-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / pathology-
dc.subject.MESHErbB Receptors / genetics-
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.MESHQuality of Life-
dc.subject.MESHQuinolines* / pharmacology-
dc.subject.MESHQuinolines* / therapeutic use-
dc.titleEnhanced Versus Standard Dermatologic Management With Amivantamab-Lazertinib in EGFR-Mutated Advanced NSCLC: The COCOON Global Randomized Controlled Trial-
dc.typeArticle-
dc.contributor.googleauthorChul, Byoung-
dc.contributor.googleauthorLi, Weimin-
dc.contributor.googleauthorSpira, Alexander I.-
dc.contributor.googleauthorSauder, Maxwell-
dc.contributor.googleauthorFeldman, Jill-
dc.contributor.googleauthorBozorgmehr, Farastuk-
dc.contributor.googleauthorMak, Milena-
dc.contributor.googleauthorSmith, Janellen-
dc.contributor.googleauthorVoon, Pei Jye-
dc.contributor.googleauthorLiu, Baogang-
dc.contributor.googleauthorTian, Panwen-
dc.contributor.googleauthorTan, Jiunn-Liang-
dc.contributor.googleauthorYang, Cheng-Ta-
dc.contributor.googleauthorShih, Jin-Yuan-
dc.contributor.googleauthorKaradurmus, Nuri-
dc.contributor.googleauthorCundom, Juan Esteban-
dc.contributor.googleauthorBertollo, Glaucio-
dc.contributor.googleauthorCicin, Irfan-
dc.contributor.googleauthorNieva, Jorge-
dc.contributor.googleauthorOrtega-Granados, Ana Laura-
dc.contributor.googleauthorTomasini, Pascale-
dc.contributor.googleauthorNguyen, Danny-
dc.contributor.googleauthorFelip, Enriqueta-
dc.contributor.googleauthorSchuchard, Julia-
dc.contributor.googleauthorMurphy, Sean P.-
dc.contributor.googleauthorAnderson, Bailey G.-
dc.contributor.googleauthorRomero, Tonatiuh-
dc.contributor.googleauthorXia, Yichuan-
dc.contributor.googleauthorSheng, Shubin-
dc.contributor.googleauthorBauml, Joshua M.-
dc.contributor.googleauthorMahadevia, Parthiv J.-
dc.contributor.googleauthorKam, Julian-
dc.contributor.googleauthorNematian-Samani, Mehregan-
dc.contributor.googleauthorSimoes, Jairo-
dc.contributor.googleauthorWildgust, Mark-
dc.contributor.googleauthorGirard, Nicolas-
dc.identifier.doi10.1016/j.jtho.2025.07.117-
dc.relation.journalcodeJ01909-
dc.identifier.eissn1556-1380-
dc.identifier.pmid40923969-
dc.subject.keywordAmivantamab-
dc.subject.keywordDermatologic adverse events-
dc.subject.keywordDermatologic management-
dc.subject.keywordLazertinib-
dc.subject.keywordNon-small cell lung cancer-
dc.contributor.affiliatedAuthorChul, Byoung-
dc.identifier.scopusid2-s2.0-105017873500-
dc.identifier.wosid001592074500010-
dc.citation.volume20-
dc.citation.number10-
dc.citation.startPage1517-
dc.citation.endPage1530-
dc.identifier.bibliographicCitationJOURNAL OF THORACIC ONCOLOGY, Vol.20(10) : 1517-1530, 2025-10-
dc.identifier.rimsid90642-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorAmivantamab-
dc.subject.keywordAuthorDermatologic adverse events-
dc.subject.keywordAuthorDermatologic management-
dc.subject.keywordAuthorLazertinib-
dc.subject.keywordAuthorNon-small cell lung cancer-
dc.subject.keywordPlusINDUCED-SKIN TOXICITIES-
dc.subject.keywordPlusBISPECIFIC ANTIBODY-
dc.subject.keywordPlusTREATMENT REGIMEN-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusPHASE-II-
dc.subject.keywordPlusIMPACT-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryRespiratory System-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaRespiratory System-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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