Literature DB >> 29860922

Phase III Randomized Study of Ribociclib and Fulvestrant in Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Advanced Breast Cancer: MONALEESA-3.

Dennis J Slamon1, Patrick Neven1, Stephen Chia1, Peter A Fasching1, Michelino De Laurentiis1, Seock-Ah Im1, Katarina Petrakova1, Giulia Val Bianchi1, Francisco J Esteva1, Miguel Martín1, Arnd Nusch1, Gabe S Sonke1, Luis De la Cruz-Merino1, J Thaddeus Beck1, Xavier Pivot1, Gena Vidam1, Yingbo Wang1, Karen Rodriguez Lorenc1, Michelle Miller1, Tetiana Taran1, Guy Jerusalem1.   

Abstract

Purpose This phase III study evaluated ribociclib plus fulvestrant in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer who were treatment naïve or had received up to one line of prior endocrine therapy in the advanced setting. Patients and Methods Patients were randomly assigned at a two-to-one ratio to ribociclib plus fulvestrant or placebo plus fulvestrant. The primary end point was locally assessed progression-free survival. Secondary end points included overall survival, overall response rate, and safety. Results A total of 484 postmenopausal women were randomly assigned to ribociclib plus fulvestrant, and 242 were assigned to placebo plus fulvestrant. Median progression-free survival was significantly improved with ribociclib plus fulvestrant versus placebo plus fulvestrant: 20.5 months (95% CI, 18.5 to 23.5 months) versus 12.8 months (95% CI, 10.9 to 16.3 months), respectively (hazard ratio, 0.593; 95% CI, 0.480 to 0.732; P < .001). Consistent treatment effects were observed in patients who were treatment naïve in the advanced setting (hazard ratio, 0.577; 95% CI, 0.415 to 0.802), as well as in patients who had received up to one line of prior endocrine therapy for advanced disease (hazard ratio, 0.565; 95% CI, 0.428 to 0.744). Among patients with measurable disease, the overall response rate was 40.9% for the ribociclib plus fulvestrant arm and 28.7% for placebo plus fulvestrant. Grade 3 adverse events reported in ≥ 10% of patients in either arm (ribociclib plus fulvestrant v placebo plus fulvestrant) were neutropenia (46.6% v 0%) and leukopenia (13.5% v 0%); the only grade 4 event reported in ≥ 5% of patients was neutropenia (6.8% v 0%). Conclusion Ribociclib plus fulvestrant might represent a new first- or second-line treatment option in hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer.

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Year:  2018        PMID: 29860922     DOI: 10.1200/JCO.2018.78.9909

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  205 in total

1.  Safety and efficacy of everolimus (EVE) plus exemestane (EXE) in postmenopausal women with locally advanced or metastatic breast cancer: final results from EVEREXES.

Authors:  Young-Hyuck Im; Bulent Karabulut; Keun Seok Lee; Byeong-Woo Park; Aditya Adhav; Havva Yesil Cinkir; Hikmat Abdel-Razeq; Yuan-Ching Chang; Sercan Aksoy; Seock-Ah Im; Joon Jeong; Yeesoo Chae; James Bowles; Khemaies Slimane; Hongling Xue; Sung-Bae Kim
Journal:  Breast Cancer Res Treat       Date:  2021-03-16       Impact factor: 4.872

Review 2.  The Role of CDK4/6 Inhibitors in Breast Cancer.

Authors:  Conleth G Murphy
Journal:  Curr Treat Options Oncol       Date:  2019-05-18

3.  Cyclin E mRNA: Assessing Cyclin-Dependent Kinase (CDK) Activation State to Elucidate Breast Cancer Resistance to CDK4/6 Inhibitors.

Authors:  Sarat Chandarlapaty; Pedram Razavi
Journal:  J Clin Oncol       Date:  2019-03-28       Impact factor: 44.544

4.  Prognosis Varies by Intrinsic Tumor Subtype in Patients Treated with Ribociclib.

Authors: 
Journal:  Oncologist       Date:  2021-01-05

Review 5.  Strategies for Early Prediction and Timely Recognition of Drug-Induced Liver Injury: The Case of Cyclin-Dependent Kinase 4/6 Inhibitors.

Authors:  Emanuel Raschi; Fabrizio De Ponti
Journal:  Front Pharmacol       Date:  2019-10-24       Impact factor: 5.810

Review 6.  Mechanisms of resistance to cyclin-dependent kinase 4/6 inhibitors.

Authors:  Georgia Gomatou; Ioannis Trontzas; Stephanie Ioannou; Maria Drizou; Nikolaos Syrigos; Elias Kotteas
Journal:  Mol Biol Rep       Date:  2021-01-07       Impact factor: 2.316

Review 7.  QT Interval Prolongation Associated With Cytotoxic and Targeted Cancer Therapeutics.

Authors:  Sanjay Chandrasekhar; Michael G Fradley
Journal:  Curr Treat Options Oncol       Date:  2019-05-25

8.  Estrogen Down-regulator Fulvestrant Potentiates Antitumor Activity of Fluoropyrimidine in Estrogen-responsive MCF-7 Human Breast Cancer Cells.

Authors:  Mamoru Nukatsuka; Hitoshi Saito; Shinzaburo Noguchi; Teiji Takechi
Journal:  In Vivo       Date:  2019 Sep-Oct       Impact factor: 2.155

Review 9.  Advances in Endocrine-Based Therapies for Estrogen Receptor-Positive Metastatic Breast Cancer.

Authors:  Vassilis Aggelis; Stephen R D Johnston
Journal:  Drugs       Date:  2019-11       Impact factor: 9.546

Review 10.  An Update on the Clinical Use of CDK4/6 Inhibitors in Breast Cancer.

Authors:  Marie Robert; Jean-Sébastien Frenel; Emmanuelle Bourbouloux; Dominique Berton Rigaud; Anne Patsouris; Paule Augereau; Carole Gourmelon; Mario Campone
Journal:  Drugs       Date:  2018-09       Impact factor: 9.546

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