The Evolving Complexity of Treating Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor-2 (HER2)-Negative Breast Cancer: Special Considerations in Older Breast Cancer Patients-Part II: Metastatic Disease.


Journal

Drugs & aging
ISSN: 1179-1969
Titre abrégé: Drugs Aging
Pays: New Zealand
ID NLM: 9102074

Informations de publication

Date de publication:
05 2020
Historique:
pubmed: 1 4 2020
medline: 31 10 2020
entrez: 1 4 2020
Statut: ppublish

Résumé

Breast cancer is a disease of aging, and the incidence of breast cancer is projected to increase dramatically as the global population ages. The majority of breast cancers that occur in older adults are hormone-receptor positive, human epidermal growth factor receptor-2 (HER2)-negative phenotypes, with favorable tumor biology; yet, because of underrepresentation in clinical trials, less evidence is available to guide the complex care for this population. Providing care for older patients with metastatic breast cancer, with coexisting medical conditions, increased risk of treatment toxicity, and frailty, remains a clinical challenge in oncology. In this review, we provide an overview of the current evidence from clinical trials and subanalyses of older adults with hormone receptor-positive, HER2-negative metastatic breast cancer, highlighting data on the safety and efficacy of oral therapies, including endocrine therapy alone or in combination with cyclin-dependent kinase (CDK) 4/6 inhibitors, phosphatidylinositol 3-kinase (PI3K) inhibitors, and mammalian target of rapamycin (mTOR) inhibitors. In addition, we note the significant underrepresentation of older and frail adults in these studies. Current and future directions in research for this special population, in order to address significant knowledge gaps, include the need to improve long-term adherence to hormonal and targeted therapy, prospective clinical trials that capture clinical and biological aging endpoints, and the need for a multidisciplinary approach with integration of geriatric and oncology principles.

Identifiants

pubmed: 32227289
doi: 10.1007/s40266-020-00758-x
pii: 10.1007/s40266-020-00758-x
pmc: PMC7194122
mid: NIHMS1580351
doi:

Substances chimiques

Aromatase Inhibitors 0
Protein Kinase Inhibitors 0
Receptors, Cell Surface 0
Tamoxifen 094ZI81Y45
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
TOR Serine-Threonine Kinases EC 2.7.11.1

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

349-358

Subventions

Organisme : NCI NIH HHS
ID : K12 CA001727
Pays : United States

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Auteurs

Addie Hill (A)

Department of Medical Oncology and Therapeutics Research, City of Hope National Medical Center, 1500 East Duarte Road, Duarte, CA, 91010, USA.

Eutiquio Gutierrez (E)

Department of Internal Medicine, Harbor-UCLA Medical Center, Los Angeles, CA, USA.

Jennifer Liu (J)

Department of Medical Oncology and Therapeutics Research, City of Hope National Medical Center, 1500 East Duarte Road, Duarte, CA, 91010, USA.

Sarah Sammons (S)

Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Duke Cancer Institute, Durham, NC, USA.

Gretchen Kimmick (G)

Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Duke Cancer Institute, Durham, NC, USA.

Mina S Sedrak (MS)

Department of Medical Oncology and Therapeutics Research, City of Hope National Medical Center, 1500 East Duarte Road, Duarte, CA, 91010, USA. msedrak@coh.org.

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Classifications MeSH