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https://hdl.handle.net/20.500.13003/19787 Randomized phase II study of fulvestrant plus palbociclib or placebo in endocrine-sensitive, hormone receptor- positive/HER2-advanced breast cancer: GEICAM/2014-12 (FLIPPER)
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Identifiers
eISSN: 1879-0852
ISSN: 0959-8049
WOS ID: 791945800004
Scopus EID: 2-s2.0-85121004899
PMID: 34902765
Embase PUI: L2015918313
Authors
Albanell, Joan
Martinez, M. T.
Ramos, M.
O'Connor, M.
De la Cruz-Merino, Luis
Santaballa, Ana
Martinez-Janez, N.
Moreno, F.
Fernandez, I
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Date of defense
Publication date
2022-01
Document type
research article
Citation
Albanell J, Martinez MT, Ramos M, O'Connor M, de la Cruz-Merino L, Santaballa A, et al. Randomized phase II study of fulvestrant plus palbociclib or placebo in endocrine-sensitive, hormone receptor- positive/HER2-advanced breast cancer: GEICAM/2014-12 (FLIPPER). Eur J Cancer. 2022 Jan;161:26-37.
Volume Title
Abstract
Background: The potential benefit of adding palbociclib to fulvestrant as first-line treatment in hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative endocrine-sensitive advanced breast cancer (ABC) patients remains uncharacterized.& nbsp;Patients and methods: In this randomized (1:1), double-blind, phase II study, postmenopausal women with HR-positive, HER2-negative ABC with de novo metastatic disease or those who relapsed after > 12 months of adjuvant endocrine therapy received palbociclib/fulvestrant or placebo/fulvestrant. Stratification was based on recurrent versus de novo metastatic disease and visceral involvement. The primary objective was one-year progression-free survival (PFS-1y) rate. The sample size was 190 patients. The two-sided alpha of 0.2, 80% of power to detect a difference between the arms, assuming PFS rates of 0.695 and 0.545 for palbociclib/fulvestrant and placebo/fulvestrant, respectively.& nbsp;Results: In total, 189 patients were randomized to palbociclib/fulvestrant ([n = 94] or placebo/ fulvestrant [n = 95]). 45.5% and 60.3% of patients had de novo metastatic disease and visceral involvement, respectively. PFS-1y rates were 83.5% and 71.9% in the palbociclib/fulvestrant and placebo/fulvestrant arms, (HR 0.55, 80% CI 0.36-0.83, P = 0.064). The median PFS were 31.8 and 22.0 months for the palbociclib/fulvestrant and placebo/fulvestrant arms (aHR 0.48, 80% CI 0.37-0.64, P = 0.001).& nbsp;The most frequent grade 3-4 adverse events were neutropenia (68.1% vs. 0%), leucopenia (26.6% vs. 0%), anemia (3.2% vs. 0%), and lymphopenia (14.9% vs. 2.1%) for the palbociclib/fulvestrant and placebo/fulvestrant, respectively.The most frequent non-hematologic grade 3-4 adverse event was fatigue (4.3% vs. 0%).& nbsp;Conclusions: Palbociclib/fulvestrant demonstrated better PFS-1y rates and median PFS than placebo/fulvestrant in HR-positive/HER2-negative endocrine-sensitive ABC patients. (C) 2021 The Author(s). Published by Elsevier Ltd.
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Keywords
Breast cancer Metastatic First-line Endocrine-sensitive Fulvestrant Palbociclib CDK 4/6
MeSH
Breast Neoplasms
Aged, 80 and over
Aged
Adult
Female
Piperazines
Pyridines
Humans
Fulvestrant
Middle Aged
Double-Blind Method
Aged, 80 and over
Aged, 80 and over
Aged
Adult
Female
Piperazines
Pyridines
Humans
Fulvestrant
Middle Aged
Double-Blind Method
Aged, 80 and over
DeCS
Método Doble Ciego
Piperazinas
Fulvestrant
Piridinas
Humanos
Persona de Mediana Edad
Anciano
Anciano de 80 o más Años
Femenino
Neoplasias de la Mama
Adulto
Piperazinas
Fulvestrant
Piridinas
Humanos
Persona de Mediana Edad
Anciano
Anciano de 80 o más Años
Femenino
Neoplasias de la Mama
Adulto











