Palbociclib plus endocrine therapy in HER2 negative, hormonal receptor-positive, advanced breast cancer: A real-world experience.
Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Breast
/ metabolism
Breast Neoplasms
/ metabolism
Disease-Free Survival
Female
Humans
Male
Middle Aged
Piperazines
/ pharmacology
Pyridines
/ pharmacology
Receptor, ErbB-2
/ metabolism
Receptors, Estrogen
/ drug effects
Receptors, Progesterone
/ drug effects
Treatment Outcome
advanced breast cancer, hormonal therapy
endocrine resistance
palbociclib
real-world setting
Journal
Journal of cellular physiology
ISSN: 1097-4652
Titre abrégé: J Cell Physiol
Pays: United States
ID NLM: 0050222
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
received:
10
10
2018
accepted:
06
11
2018
pubmed:
12
12
2018
medline:
9
4
2020
entrez:
12
12
2018
Statut:
ppublish
Résumé
Data from 423 human epidermal growth factor receptor 2-negative (HER2-), hormone receptor-positive (HR+) advanced breast cancer (aBC) patients treated with palbociclib and endocrine therapy (ET) were provided by 35 Italian cancer centers and analyzed for treatment outcomes. Overall, 158 patients were treated in first line and 265 in second/later lines. We observed 19 complete responses and 112 partial responses. The overall response rate (ORR) was 31% (95% confidence interval [CI], 26.6-35.4) and clinical benefit was 52.7% (95% CI, 48-57.5). ORR was negatively affected by prior exposure to everolimus/exemestane ( p = 0.002) and favorably influenced by early line-treatment ( p < 0.0001). At 6 months, median progression-free survival was 12 months (95% CI, 8-16) and median overall survival was 24 months (95% CI, 17-30). More favorable outcomes were associated with palbociclib in early lines, no visceral metastases and no prior everolimus/exemestane. The main toxicity reported was neutropenia. Our results provide further support to the use of palbociclib with ET in HER2-, HR+ aBC. Differences in outcomes across patients subsets remain largely unexplained.
Substances chimiques
Piperazines
0
Pyridines
0
Receptors, Estrogen
0
Receptors, Progesterone
0
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
palbociclib
G9ZF61LE7G
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
7708-7717Informations de copyright
© 2018 Wiley Periodicals, Inc.