First-line ribociclib plus letrozole in postmenopausal women with HR+ , HER2- advanced breast cancer: Tumor response and pain reduction in the phase 3 MONALEESA-2 trial
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, randomizované kontrolované studie
PubMed
29404806
DOI
10.1007/s10549-017-4658-x
PII: 10.1007/s10549-017-4658-x
Knihovny.cz E-zdroje
- Klíčová slova
- Advanced breast cancer, CDK4/6, MONALEESA-2, Ribociclib,
- MeSH
- aminopyridiny aplikace a dávkování MeSH
- dospělí MeSH
- Kaplanův-Meierův odhad MeSH
- kvalita života MeSH
- letrozol aplikace a dávkování MeSH
- lidé středního věku MeSH
- lidé MeSH
- metastázy nádorů MeSH
- mladý dospělý MeSH
- nádorové biomarkery MeSH
- nádory prsu farmakoterapie metabolismus patologie MeSH
- protokoly protinádorové kombinované chemoterapie škodlivé účinky terapeutické užití MeSH
- puriny aplikace a dávkování MeSH
- receptor erbB-2 metabolismus MeSH
- receptory pro estrogeny metabolismus MeSH
- receptory progesteronu metabolismus MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- staging nádorů MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- aminopyridiny MeSH
- letrozol MeSH
- nádorové biomarkery MeSH
- puriny MeSH
- receptor erbB-2 MeSH
- receptory pro estrogeny MeSH
- receptory progesteronu MeSH
- ribociclib MeSH Prohlížeč
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.
Centre Léon Bérard Lyon France
Centre René Gauducheau Institut de Cancérologie de l'Ouest Saint Herblain France
Department of Internal Medicine Hematology and Oncology University Hospital Brno Brno Czech Republic
Highlands Oncology Group Fayetteville AR USA
Hospital Clínico Universitario e Instituto de Investigación Santiago CIBERONC A Coruña Spain
Hospital Universitario La Paz Madrid Spain
Hospital Universitario Virgen de la Victoria IBIMA Málaga Spain
Institut Català d'Oncologia IDIBELL L'Hospitalet de Llobregat Barcelona Spain
Minnesota Oncology Minneapolis MN USA
Novartis Pharmaceuticals Corporation East Hanover NJ USA
Oncology Hematology Associates of Southwest Virginia Roanoke VA USA
Oncology Hematology Care Kenwood OH USA
Perlmutter Cancer Center at New York University Langone Health New York NY USA
Rocky Mountain Cancer Centers Aurora CO USA
Saint Luke's Health System Kansas City MO USA
Citace poskytuje Crossref.org
ClinicalTrials.gov
NCT01958021