Systemic Therapy for Advanced Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer: ASCO Guideline Update.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
10 08 2022
Historique:
pubmed: 1 6 2022
medline: 10 8 2022
entrez: 31 5 2022
Statut: ppublish

Résumé

To update evidence-based guideline recommendations to practicing oncologists and others on systemic therapy for patients with human epidermal growth factor receptor 2 (HER2)-positive advanced breast cancer. An Expert Panel conducted a targeted systematic literature review (for both systemic treatment and CNS metastases) and identified 545 articles. Outcomes of interest included efficacy and safety. Of the 545 publications identified and reviewed, 14 were identified to form the evidentiary basis for the guideline recommendations. HER2-targeted therapy is recommended for patients with HER2-positive advanced breast cancer, except for those with clinical congestive heart failure or significantly compromised left ventricular ejection fraction, who should be evaluated on a case-by-case basis. Trastuzumab, pertuzumab, and taxane for first-line treatment and trastuzumab deruxtecan for second-line treatment are recommended. In the third-line setting, clinicians should offer other HER2-targeted therapy combinations. There is a lack of head-to-head trials; therefore, there is insufficient evidence to recommend one regimen over another. The patient and the clinician should discuss differences in treatment schedule, route, toxicities, etc during the decision-making process. Options include regimens with tucatinib, trastuzumab emtansine, trastuzumab deruxtecan (if either not previously administered), neratinib, lapatinib, chemotherapy, margetuximab, hormonal therapy, and abemaciclib plus trastuzumab plus fulvestrant, and may offer pertuzumab if the patient has not previously received it. Optimal duration of chemotherapy is at least 4-6 months or until maximum response, depending on toxicity and in the absence of progression. HER2-targeted therapy can continue until time of progression or unacceptable toxicities. For patients with HER2-positive and estrogen receptor-positive or progesterone receptor-positive breast cancer, clinicians may recommend either standard first-line therapy or, for selected patients, endocrine therapy plus HER2-targeted therapy or endocrine therapy alone.Additional information is available at www.asco.org/breast-cancer-guidelines.

Identifiants

pubmed: 35640077
doi: 10.1200/JCO.22.00519
doi:

Substances chimiques

ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2612-2635

Auteurs

Sharon H Giordano (SH)

University of Texas MD Anderson, Houston, TX.

Maria Alice B Franzoi (MAB)

Institute Gustave Roussy, Villejuif, France.

Sarah Temin (S)

American Society of Clinical Oncology, Alexandria, VA.

Carey K Anders (CK)

Duke University, Durham, NC.

Sarat Chandarlapaty (S)

Memorial Sloan Kettering Cancer Center, New York, NY.

Jennie R Crews (JR)

Seattle Cancer Care Alliance, Seattle, WA.

Jeffrey J Kirshner (JJ)

Hematology/Oncology Associates of Central New York, East Syracuse, NY.

Ian E Krop (IE)

Dana-Farber Cancer Institute, Boston, MA.

Nancy U Lin (NU)

Dana-Farber Cancer Institute, Boston, MA.

Aki Morikawa (A)

University of Michigan, Ann Arbor, MI.

Jane Perlmutter (J)

Patient Advocate, Ann Arbor, MI.

Naren Ramakrishna (N)

University of Florida Health Cancer Center at Orlando Health, Orlando, FL.

Nancy E Davidson (NE)

Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA.

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Classifications MeSH