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Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

2934 - Ribociclib (RIBO) + letrozole (LET) in premenopausal patients (pts) with hormone receptor-positive (HR+), human epidermal growth factor receptor-2–negative (HER2–) advanced breast cancer (ABC) with no prior endocrine therapy (ET) for ABC: Preliminary subgroup results from the phase 3b CompLEEment-1 trial

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Cytotoxic Therapy;  Breast Cancer

Presenters

Hikmat Abdel-Razeq

Citation

Annals of Oncology (2018) 29 (suppl_8): viii90-viii121. 10.1093/annonc/mdy272

Authors

H. Abdel-Razeq1, P.H. Cottu2, A. Ring3, M. De Laurentiis4, J. Lu5, H.A. Azim6, C. Zamagni7, K. Zhou8, J. Wu8, L. Menon8, M. Martín9

Author affiliations

  • 1 Department Of Internal Medicine, King Hussein Cancer Center, 11941 - Amman/JO
  • 2 Department Of Medical Oncology, Institut Curie, 75248 cedex5 - Paris/FR
  • 3 Medical Oncology, The Royal Marsden NHS Foundation Trust, Surrey/GB
  • 4 Dept. Breast And Thoracic Oncology, Istituto Nazionale Tumori, Napoli/IT
  • 5 Keck School Of Medicine, Division Of Medical Oncology, University of Southern California, Los Angeles/US
  • 6 Clinical Oncology, Cairo Oncology Center Cairo University-CairoCure, Cairo/EG
  • 7 Head Breast And Gynaecological Medical Oncology Unit, Policlinico S. Orsola-Malpighi-"F.Addarii", 40138 - Bologna/IT
  • 8 Novartis Pharmaceuticals, Novartis Pharmaceuticals, East Hanover/US
  • 9 Instituto De Investigación Sanitaria Gregorio Marañón, Ciberonc, Geicam, Universidad Complutense, Madrid/ES
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Resources

Abstract 2934

Background

CDK4/6 inhibitor RIBO significantly improved progression-free survival in combination with ET versus placebo + ET in pre- and postmenopausal women with HR+, HER2– ABC and no prior therapy for advanced disease in the pivotal phase 3 MONALEESA-7 and MONALEESA-2 trials (Tripathy et al. SABCS 2018; Hortobagyi et al. NEJM 2016). Here, we report additional safety data for RIBO+LET in premenopausal female pts enrolled in CompLEEment-1, an open-label, phase 3b trial evaluating RIBO+LET as first-line therapy in an expanded pt population.

Methods

Premenopausal pts with HR+, HER2– ABC, ≤1 line of prior chemotherapy, and no prior ET for ABC received RIBO (600 mg/day, 3 wk on/1 wk off) + LET (2.5 mg/day) and goserelin (3.6-mg subcutaneous implant every 28 days). The primary outcome was safety and tolerability. A pre-planned interim analysis was conducted ∼15 months after first pt first visit.

Results

Of the first 1,008 pts enrolled who completed 56 days of follow-up or discontinued before data cut-off, 153 were premenopausal women. Median age was 45.0 years and the majority of pts (99.3%) had an Eastern Cooperative Oncology Group performance status ≤1; 40.5% had stage IV disease at diagnosis. Bone (73.9%), lung (31.4%), and liver (30.7%) were the most common metastatic sites. The most frequent adverse events (AEs) were neutropenia (53.6%), nausea (30.1%), hot flush (20.9%), headache (17.0%), and asthenia (16.3%). The most frequent grade ≥3 AE was neutropenia (34.0%). QT prolongation was infrequent (2.0%). Dose adjustment/treatment interruption due to AEs was required for 48.4% of pts. Four patients (2.6%) discontinued treatment due to AEs.

Conclusions

Initial safety results from CompLEEment-1 demonstrate the tolerability of RIBO+LET + ovarian functional suppression in premenopausal women, consistent with previous reports. NCT02941926.

Clinical trial identification

NCT02941926.

Legal entity responsible for the study

Novartis Pharmaceuticals.

Funding

Novartis Pharmaceuticals.

Editorial Acknowledgement

Financial support for medical editorial assistance was provided by Novartis Pharmaceuticals. We thank Elise Blankenship, PhD, ProEd Communications, Inc., for her medical editorial assistance with this abstract.

Disclosure

P.H. Cottu: Consulting or advisory role: Novartis and Pfizer; Travel, accommodations, expenses: Novartis, Pfizer, Roche; Honoraria: AstraZeneca, NanoString Technologies, Novartis, Pfizer, Roche; Research funding: AstraZeneca, Genentech/Roche, Novartis, Pierre Fabre, and Pfizer. A. Ring: Consulting or advisory role: Pfizer and Roche; Honoraria: AstraZeneca, Lilly, Novartis, Pfizer, Roche; Research funding: AstraZeneca. M. De Laurentiis: Consulting or advisory role: AstraZeneca, Celgene, Lilly, Novartis, Pfizer, Roche Honoraria: AstraZeneca, Celgene, Novartis, Pfizer, and Roche. J. Lu: Personal fees: Novartis; Personal fees from outside the submitted work; Syndex. H.A. Azim: Employment: Innate, France (immediate family member); Consulting or advisory role: AstraZeneca, Bristol-Myers Squibb, Janssen, MSD, Novartis, Pfizer, Roche; Honoraria: Amgen, AstraZeneca, Bristol-Myers Squibb, MSD, Novartis, Pfizer, Roche; Research funding: Pfizer. C. Zamagni: Consulting or advisory role: AstraZeneca, Eisai, Novartis, Pfizer, PharmaMar, Pierre Fabre, Roche; Travel, accommodations, expenses: Celgene, Novartis, Pierre Fabre, Roche; Research funding: AbbVie, Array BioPharma, AstraZeneca, Celgene, Medivation, Morphotek, Novartis, Pfizer, Roche, Roche/Genentech. K. Zhou, L. Menon: Employee: Novartis. J. Wu: Employee of Novartis; Employment: Janssen (immediate family member); Travel, accommodations, expenses: Janssen (immediate family member). M. Martín: Consulting or advisory role: Amgen, Lilly, Novartis, Pfizer, PharmaMar, Roche/Genentech; Research funding: Novartis. All other authors have declared no conflicts of interest.

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