Updated Overall Survival of Ribociclib plus Endocrine Therapy versus Endocrine Therapy Alone in Pre- and Perimenopausal Patients with HR+/HER2- Advanced Breast Cancer in MONALEESA-7: A Phase III Randomized Clinical Trial

dc.contributor.authorLu, Yen Shen
dc.contributor.authorIm, Seock Ah
dc.contributor.authorColleoni, Marco Angelo
dc.contributor.authorFranke, Fábio Andre
dc.contributor.authorBardia, Aditya
dc.contributor.authorCardoso, Fatima V.
dc.contributor.authorHarbeck, Nadia
dc.contributor.authorHurvitz, Sara Alsterlind
dc.contributor.authorChow, Louis W.C.
dc.contributor.authorSohn, Joohyuk
dc.contributor.authorLee, Keun-seok
dc.contributor.authorCampos-Gómez, Saúl
dc.contributor.authorVázquez, Rafael Villanueva
dc.contributor.authorJung, Kyung-hae
dc.contributor.authorBabu, K. Govind
dc.contributor.authorWheatley-Price, Paul F.
dc.contributor.authorDe Laurentiis, Michelino
dc.contributor.authorIm, Young-hyuck
dc.contributor.authorKuemmel, Sherko
dc.contributor.authorEl-Saghir, Nagi S.
dc.contributor.authorO'Regan, Ruth M.
dc.contributor.authorGasch, Claudia
dc.contributor.authorSolovieff, Nadia
dc.contributor.authorWang, Craig
dc.contributor.authorWang, Yongyu
dc.contributor.authorChakravartty, Arunava
dc.contributor.authorJi, Yan
dc.contributor.authorTripathy, Debu
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:14Z
dc.date.available2025-01-24T11:44:14Z
dc.date.issued2022
dc.description.abstractPurpose: Ribociclib plus endocrine therapy (ET) demonstrated a statistically significant progression-free survival and overall survival (OS) benefit in the phase III MONALEESA-7 trial of pre-/perimenopausal patients with hormone receptor (HR)- positive (HR+), HER2-negative (HER2-) advanced breast cancer (ABC). The median OS was not reached in the ribociclib arm in the protocol-specified final analysis; we hence performed an exploratory OS and additional outcomes analysis with an extended follow-up (median, 53.5 months). Patients and Methods: Patients were randomized to receive ET [goserelin plus nonsteroidal aromatase inhibitor (NSAI) or tamoxifen] with ribociclib or placebo. OS was evaluated with a stratified Cox proportional hazard model and summarized with Kaplan-Meier methods. Results: The intent-to-treat population included 672 patients. Median OS was 58.7 months with ribociclib versus 48.0 months with placebo [hazard ratio 0.76; 95% confidence interval (CI), 0.61-0.96]. Kaplan-Meier estimated OS at 48 months was 60% and 50% with ribociclib and placebo, respectively. Subgroup analyses were generally consistent with the OS benefit, including patients who received NSAI and patients aged less than 40 years. Subsequent antineoplastic therapies following discontinuation were balanced between the ribociclib (77%) and placebo (78%) groups. Use of cyclin-dependent kinase 4/6 inhibitors after discontinuation was higher with placebo (26%) versus ribociclib (13%). Time to first chemotherapy was significantly delayed with ribociclib versus placebo. No drug- drug interactions were observed between ribociclib and either NSAI. Conclusions: Ribociclib plus ET continued to show significantly longer OS than ET alone in pre-/perimenopausal patients, including patients aged less than 40 years, with HR+/HER2- ABC with 53.5 months of median follow-up. © 2021 The Authors.
dc.identifier.doihttps://doi.org/10.1158/1078-0432.CCR-21-3032
dc.identifier.eid2-s2.0-85125729661
dc.identifier.pmid34965945
dc.identifier.urihttp://hdl.handle.net/10938/30420
dc.language.isoen
dc.publisherAmerican Association for Cancer Research Inc.
dc.relation.ispartofClinical Cancer Research
dc.sourceScopus
dc.subjectAminopyridines
dc.subjectAntineoplastic combined chemotherapy protocols
dc.subjectAromatase inhibitors
dc.subjectBreast neoplasms
dc.subjectFemale
dc.subjectHumans
dc.subjectPerimenopause
dc.subjectPurines
dc.subjectReceptor, erbb-2
dc.subjectReceptors, estrogen
dc.subjectAnastrozole
dc.subjectGoserelin
dc.subjectLetrozole
dc.subjectPlacebo
dc.subjectRibociclib
dc.subjectTamoxifen
dc.subjectAminopyridine derivative
dc.subjectAntineoplastic agent
dc.subjectAromatase inhibitor
dc.subjectEpidermal growth factor receptor 2
dc.subjectEstrogen receptor
dc.subjectPurine derivative
dc.subjectAdult
dc.subjectArticle
dc.subjectCancer chemotherapy
dc.subjectCancer hormone therapy
dc.subjectCancer patient
dc.subjectCancer survival
dc.subjectClimacterium
dc.subjectConfidence interval
dc.subjectControlled study
dc.subjectDrug blood level
dc.subjectFollow up
dc.subjectHazard ratio
dc.subjectHepatobiliary disease
dc.subjectHormone receptor-positive, her2-negative breast cancer
dc.subjectHuman
dc.subjectIntention to treat analysis
dc.subjectKaplan meier method
dc.subjectMajor clinical study
dc.subjectMultiple cycle treatment
dc.subjectNeutropenia
dc.subjectOverall survival
dc.subjectPremenopause
dc.subjectProportional hazards model
dc.subjectQt prolongation
dc.subjectSide effect
dc.subjectBreast tumor
dc.subjectClinical trial
dc.subjectPhase 3 clinical trial
dc.subjectRandomized controlled trial
dc.titleUpdated Overall Survival of Ribociclib plus Endocrine Therapy versus Endocrine Therapy Alone in Pre- and Perimenopausal Patients with HR+/HER2- Advanced Breast Cancer in MONALEESA-7: A Phase III Randomized Clinical Trial
dc.typeArticle

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