Metronomic chemotherapy for patients with metastatic breast cancer: Review of effectiveness and potential use during pandemics.


Journal

Cancer treatment reviews
ISSN: 1532-1967
Titre abrégé: Cancer Treat Rev
Pays: Netherlands
ID NLM: 7502030

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 13 05 2020
revised: 23 06 2020
accepted: 24 06 2020
pubmed: 10 8 2020
medline: 29 8 2020
entrez: 10 8 2020
Statut: ppublish

Résumé

Metronomic chemotherapy (M-CT) is defined as dose dense administration of chemotherapy at lower doses than maximum tolerated dose but at shorter free intervals, to obtain a near continuous exposure of cancer cells to those potentially effective drugs. M-CT is a useful strategy to obtain response, overcome resistance and reduce side effects, with low costs. This review will focus on the use of M-CT in advanced breast cancer (ABC). Cytostatic and cytotoxic effect on cancer cells, the anti-angiogenic and the immunomodulatory effects are its main mechanisms of actions. Many clinical trials proved the efficacy and tolerability of different monotherapies and combinations of chemotherapeutic agents administered in metronomic doses and frequencies in ABC. M-CT is a reasonable option for second and later lines of chemotherapy in metastatic breast cancer including those with prior anthracycline or taxane exposure, older patients and patients with comorbidities, and even as first-line in certain groups of patients. The acceptable efficacy and low toxicity of oral metronomic chemotherapy makes it a reasonable option during COVID-19 pandemic as well as in the post-COVID era which is projected to last for some time.

Identifiants

pubmed: 32769038
pii: S0305-7372(20)30104-3
doi: 10.1016/j.ctrv.2020.102066
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

102066

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Johny E Fares (JE)

Department of Internal Medicine, Lankenau Medical Center, 18 E Lancaster Avenue, Wynnewood, PA 19096, United States. Electronic address: faresj@mlhs.org.

Paul El Tomb (P)

Department of Internal Medicine, Mount Sinai West, 1000 10th Ave, New York, NY 10019, United States. Electronic address: paul.eltomb@mountsinai.org.

Lana E Khalil (LE)

Division of Hematology Oncology, Department of Internal Medicine, American University of Beirut Medical Center, PO Box: 11-0236, Riad El Solh, 1107 2020 Beirut, Lebanon.

Rula W Atwani (RW)

Division of Hematology Oncology, Department of Internal Medicine, American University of Beirut Medical Center, PO Box: 11-0236, Riad El Solh, 1107 2020 Beirut, Lebanon.

Hiba A Moukadem (HA)

Division of Hematology Oncology, Department of Internal Medicine, American University of Beirut Medical Center, PO Box: 11-0236, Riad El Solh, 1107 2020 Beirut, Lebanon.

Ahmad Awada (A)

Department of Oncology Medicine, Institut Jules Bordet, Université Libre de Bruxelles, Institut Jules Bordet, 121-125, boulevard de Waterloo, 1000 Brussels, Belgium.

Nagi S El Saghir (NS)

Division of Hematology Oncology, Department of Internal Medicine, American University of Beirut Medical Center, PO Box: 11-0236, Riad El Solh, 1107 2020 Beirut, Lebanon. Electronic address: ns23@aub.edu.lb.

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Classifications MeSH