Wolfgang Janni1, Emilio Alba2, Thomas Bachelot3, Sami Diab4, Miguel Gil-Gil5, Thaddeus J Beck6, Larisa Ryvo7, Rafael Lopez8, Michaela Tsai9, Francisco J Esteva10, Pilar Zamora Auñón11, Zdenek Kral12, Patrick Ward13, Paul Richards14, Timothy J Pluard15, Santosh Sutradhar16, Michelle Miller16, Mario Campone17. 1. University of Ulm, Helmholtzstraße 18, 89081, Ulm, Germany. Wolfgang.Janni@uniklinik-ulm.de. 2. Hospital Universitario Virgen de la Victoria, IBIMA, Málaga, Spain. 3. Centre Léon Bérard, Lyon, France. 4. Rocky Mountain Cancer Centers, Aurora, CO, USA. 5. Institut Català d'Oncologia, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain. 6. Highlands Oncology Group, Fayetteville, AR, USA. 7. Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 8. Hospital Clínico Universitario e Instituto de Investigación Santiago-CIBERONC, A Coruña, Spain. 9. Minnesota Oncology, Minneapolis, MN, USA. 10. Perlmutter Cancer Center at New York University Langone Health, New York, NY, USA. 11. Hospital Universitario La Paz, Madrid, Spain. 12. Department of Internal Medicine, Hematology and Oncology, University Hospital Brno, Brno, Czech Republic. 13. Oncology Hematology Care, Kenwood, OH, USA. 14. Oncology Hematology Associates of Southwest Virginia, Roanoke, VA, USA. 15. Saint Luke's Health System, Kansas City, MO, USA. 16. Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA. 17. Centre René Gauducheau, Institut de Cancérologie de l'Ouest, Saint-Herblain, France.
Abstract
PURPOSE: The phase 3 MONALEESA-2 study demonstrated that addition of ribociclib (RIB) to letrozole (LET) significantly improved progression-free survival (PFS) in patients (pts) with hormone receptor-positive (HR+), HER2-negative (HER2-) advanced breast cancer (ABC). Here, we evaluated duration of response (DoR), tumor shrinkage, PFS by treatment-free interval (TFI), and health-related quality of life (HRQoL). METHODS:Postmenopausal women (N = 668) with HR+ , HER2- ABC and no prior systemic therapy for ABC were randomized to RIB (600 mg/day; 3 weeks on/1 week off) plus LET (2.5 mg/day; continuous) or placebo (PBO) plus LET. Primary end point was PFS; HRQoL was the secondary end point; DoR was exploratory end point and PFS by TFI was post hoc analysis. RESULTS: Of 501 pts with measurable disease and confirmed complete or partial response, median DoR was 26.7 months (95% CI, 24.0-NR) in the RIB arm versus 18.6 months (95% CI, 14.8-23.1) in the PBO arm. At 8 weeks, more pts in the RIB arm (32%) versus the PBO arm (17%) experienced best percentage change ≥ 60%. The average pain reduction was greater in the RIB arm (26%) versus the PBO arm (15%). PFS benefit was seen with RIB vs PBO, irrespective of TFI. CONCLUSION: RIB plus LET versus PBO plus LET is associated with earlier and more durable tumor response, greater degree of tumor shrinkage and pain reduction, and PFS benefit irrespective of TFI. These data further support RIB plus LET as a first-line treatment option for postmenopausal women with HR+ , HER2- ABC.
RCT Entities:
PURPOSE: The phase 3 MONALEESA-2 study demonstrated that addition of ribociclib (RIB) to letrozole (LET) significantly improved progression-free survival (PFS) in patients (pts) with hormone receptor-positive (HR+), HER2-negative (HER2-) advanced breast cancer (ABC). Here, we evaluated duration of response (DoR), tumor shrinkage, PFS by treatment-free interval (TFI), and health-related quality of life (HRQoL). METHODS: Postmenopausal women (N = 668) with HR+ , HER2- ABC and no prior systemic therapy for ABC were randomized to RIB (600 mg/day; 3 weeks on/1 week off) plus LET (2.5 mg/day; continuous) or placebo (PBO) plus LET. Primary end point was PFS; HRQoL was the secondary end point; DoR was exploratory end point and PFS by TFI was post hoc analysis. RESULTS: Of 501 pts with measurable disease and confirmed complete or partial response, median DoR was 26.7 months (95% CI, 24.0-NR) in the RIB arm versus 18.6 months (95% CI, 14.8-23.1) in the PBO arm. At 8 weeks, more pts in the RIB arm (32%) versus the PBO arm (17%) experienced best percentage change ≥ 60%. The average pain reduction was greater in the RIB arm (26%) versus the PBO arm (15%). PFS benefit was seen with RIB vs PBO, irrespective of TFI. CONCLUSION: RIB plus LET versus PBO plus LET is associated with earlier and more durable tumor response, greater degree of tumor shrinkage and pain reduction, and PFS benefit irrespective of TFI. These data further support RIB plus LET as a first-line treatment option for postmenopausal women with HR+ , HER2- ABC.
Entities:
Keywords:
Advanced breast cancer; CDK4/6; MONALEESA-2; Ribociclib
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