First-Line Treatment for Endocrine-Sensitive Bone-Only Metastatic Breast Cancer: Systematic Review and Meta-analysis.


Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
12 2019
Historique:
received: 28 05 2019
accepted: 25 06 2019
pubmed: 21 8 2019
medline: 9 9 2020
entrez: 21 8 2019
Statut: ppublish

Résumé

In the last decade, several clinical trials have investigated novel endocrine combinations for the first-line treatment of hormone receptor-positive metastatic breast cancer. Nevertheless, the use of combinations for the first-line treatment of bone-only disease is widely discussed as a result of its indolent natural history. We performed a comprehensive search of phase 3 randomized clinical trials published in the literature through September 2018. Our aim was to explore the role of the new endocrine approaches in bone-only metastatic breast cancer, suggesting a possible strategy for their selection. In particular, we evaluated the comparative risk of adverse event occurrence during these treatments. A total of 6 studies were deemed suitable for meta-analysis: the Monaleesa-2, Monaleesa-7, Monarch-3, Paloma-2, SWOG, and Alliance trials. Overall, the novel strategies were shown to improve progression-free survival in bone-only disease (hazard ratio = 0.65; 95% confidence interval, 0.49-0.86; P = .003). Combinations with cyclin-dependent kinase inhibitors improved progression-free survival (hazard ratio = 0.54; 95% confidence interval, 0.39-0.75; P < .001) with an acceptable toxicity profile. Abemaciclib was associated with increased anemia and gastrointestinal toxicity (especially diarrhea), whereas palbociclib was associated with increased leukopenia (but not neutropenia) compared to the other compounds. Increased aspartate aminotransferase levels were reported for both ribociclib and abemaciclib. The combination of cyclin-dependent kinase 4/6 inhibitors and endocrine therapy represents an effective and well-tolerated approach for first-line treatment in bone-only disease settings. Because no direct comparison between the 3 cyclin-dependent kinase 4/6 inhibitors is available, the selection of the most appropriate treatment should be based on toxicity profile as well as patient preference and copathologies.

Identifiants

pubmed: 31427171
pii: S1526-8209(19)30418-5
doi: 10.1016/j.clbc.2019.06.011
pii:
doi:

Substances chimiques

Antineoplastic Agents, Hormonal 0

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e701-e716

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Angela Toss (A)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy. Electronic address: angela.toss@unimore.it.

Marta Venturelli (M)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Isabella Sperduti (I)

Department of Biostatistics, RCCS Regina Elena National Cancer Institute, Rome, Italy.

Eleonora Molinaro (E)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Chrystel Isca (C)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Elena Barbieri (E)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Federico Piacentini (F)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Claudia Omarini (C)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Laura Cortesi (L)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Stefano Cascinu (S)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Luca Moscetti (L)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

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