nextMONARCH Phase 2 randomized clinical trial: overall survival analysis of abemaciclib monotherapy or in combination with tamoxifen in patients with endocrine-refractory HR +, HER2-metastatic breast cancer

dc.contributor.authorHamilton, Erika
dc.contributor.authorCortes, Javier
dc.contributor.authorOzyilkan, Ozgur
dc.contributor.authorChen, Shin-Cheh
dc.contributor.authorPetrakova, Katarina
dc.contributor.authorManikhas, Aleksey
dc.contributor.authorJerusalem, Guy
dc.contributor.authorHegg, Roberto
dc.contributor.authorHuober, Jens
dc.contributor.authorZhang, Wei
dc.contributor.authorChen, Yanyun
dc.contributor.authorMartin, Miguel
dc.contributor.pubmedID35829935en_US
dc.date.accessioned2022-12-20T10:27:00Z
dc.date.available2022-12-20T10:27:00Z
dc.date.issued2022
dc.description.abstractPurpose Resistance to endocrine therapy poses a major clinical challenge for patients with hormone receptor-positive (HR +), human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer (MBC). We present the preplanned 24-month final overall survival (OS) results, alongside updated progression-free survival (PFS), and objective response rate (ORR) results. Methods nextMONARCH is an open-label, controlled, randomized, Phase 2 study of abemaciclib alone or in combination with tamoxifen in women with endocrine-refractory HR + , HER2- MBC previously treated with chemotherapy. Patients were randomized 1:1:1 to: abemaciclib 150 mg and tamoxifen 20 mg (A + T), abemaciclib 150 mg (A-150), or abemaciclib 200 mg and prophylactic loperamide (A-200). OS was the main prespecified secondary endpoint. PFS, ORR, and safety at 24 months were compared to previously reported primary analysis results. Results Of the 234 patients enrolled, 12 were receiving study treatment at data cutoff (28Jun2019). Median follow-up was 27.2 months. Median OS was 24.2 months in the A + T arm, 20.8 months in A-150, and 17.0 months in A-200 (A + T versus A-200: HR 0.62; 95%CI [0.40, 0.97], P = 0.03 and A-150 versus A-200: HR 0.96; 95%CI [0.64, 1.44], P = 0.83). PFS and ORR results at 24 months were consistent with the primary analysis. The safety profile corresponded with previous reports. Conclusion The addition of tamoxifen to abemaciclib demonstrated greater OS benefit than monotherapy. This study confirmed the single-agent activity of abemaciclib in heavily pretreated women with endocrine-refractory HR + , HER2- MBC, as well as the previously reported primary PFS and ORR results, with no new safety signals observed.en_US
dc.identifier.endpage64en_US
dc.identifier.issn0167-6806en_US
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-85134355712en_US
dc.identifier.startpage55en_US
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338008/pdf/10549_2022_Article_6662.pdf
dc.identifier.urihttp://hdl.handle.net/11727/8364
dc.identifier.volume195en_US
dc.identifier.wos000824437600002en_US
dc.language.isoengen_US
dc.relation.isversionof10.1007/s10549-022-06662-9en_US
dc.relation.journalBREAST CANCER RESEARCH AND TREATMENTen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCyclin-dependent kinase 4 and 6en_US
dc.subjectEndocrine therapyen_US
dc.subjectHER2-negativeen_US
dc.subjectHormone receptor-positiveen_US
dc.subjectMBCen_US
dc.subjectOverall survivalen_US
dc.titlenextMONARCH Phase 2 randomized clinical trial: overall survival analysis of abemaciclib monotherapy or in combination with tamoxifen in patients with endocrine-refractory HR +, HER2-metastatic breast canceren_US
dc.typearticleen_US

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