Review of Bone Modifying Agents in Metastatic Breast Cancer.

bone modifying agents metastatic breast cancer

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
13 Feb 2021
Historique:
entrez: 19 3 2021
pubmed: 20 3 2021
medline: 20 3 2021
Statut: epublish

Résumé

Bone is the most common site for distant metastases in breast cancer and can cause significant morbidity and mortality. Bone modifying agents (BMAs) that include bisphosphonates (BPAs) and denosumab help in decreasing and delaying skeletal-related events (SREs) associated with metastatic breast cancer. BPAs approved for use by the Food and Drug Administration (FDA) in bone metastases (BM) in the United States are pamidronate and zolendronic acid, while clodronate and ibandronate are licensed for use in other countries. Current American Society of Clinical Oncology (ASCO) guidelines recommend denosumab 120 mg subcutaneously every four weeks, or zolendronic acid 4 mg every four weeks or every 12 weeks, or intravenous pamidronate 90 mg every four weeks. Current guidelines do not recommend one BMA over another, however, zolendronic acid and denosumab were the most commonly used BMAs in population-based studies. Side effects of BMAs include acute phase reactions, hypocalcemia, nephrotoxicity, osteonecrosis of jaw, etc. While other side effects are common with both BPAs and denosumab, the latter has less nephrotoxic potential and is preferred for use in patients with renal failure. Current ASCO guidelines recommend continuing BMAs indefinitely, however, in clinical practice, this decision needs to be individualized, especially since there is no data on the impact of long-term use of BMAs. Further studies would need to be developed to develop an algorithm of SRE risk assessment and to determine which patients would benefit from BMAs.

Identifiants

pubmed: 33738175
doi: 10.7759/cureus.13332
pmc: PMC7960030
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

e13332

Informations de copyright

Copyright © 2021, Raghu Subramanian et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Charumathi Raghu Subramanian (C)

Department of Medicine, Washington Hospital Healthcare System, Fremont, USA.

Swapna Talluri (S)

Department of Medicine, Guthrie Robert Packer Hospital, Sayre, USA.

Sanjana Mullangi (S)

Department of Medicine, Hillcrest Medical Center, Tulsa, USA.

Manidhar R Lekkala (MR)

Department of Hematology/Oncology, James P Wilmot Cancer Institute, University of Rochester School of Medicine and Dentistry, Rochester, USA.

Bahar Moftakhar (B)

Department of Hematology/Oncology, James P Wilmot Cancer Institute, University of Rochester School of Medicine and Dentistry, Rochester, USA.

Classifications MeSH