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Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: ASCO-College of American Pathologists Guideline Update.
Wolff, Antonio C; Somerfield, Mark R; Dowsett, Mitchell; Hammond, M Elizabeth H; Hayes, Daniel F; McShane, Lisa M; Saphner, Thomas J; Spears, Patricia A; Allison, Kimberly H.
Afiliação
  • Wolff AC; Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD.
  • Somerfield MR; American Society of Clinical Oncology, Alexandria, VA.
  • Dowsett M; The Royal Marsden NHS Foundation Trust, London, United Kingdom.
  • Hammond MEH; Intermountain Healthcare and University of Utah School of Medicine, Salt Lake City, UT.
  • Hayes DF; University of Michigan, Ann Arbor, MI.
  • McShane LM; National Cancer Institute, Bethesda, MD.
  • Saphner TJ; Vince Lombardi Cancer Clinic, Two Rivers, WI.
  • Spears PA; University of North Carolina, Chapel Hill, NC.
  • Allison KH; Stanford University School of Medicine, Stanford, CA.
J Clin Oncol ; 41(22): 3867-3872, 2023 08 01.
Article em En | MEDLINE | ID: mdl-37284804
PURPOSE: To update ASCO-College of American Pathologists (CAP) recommendations for human epidermal growth factor receptor 2 (HER2) testing in breast cancer. The Panel is aware that a new generation of antibody-drug conjugates (ADCs) targeting the HER2 protein is active against breast cancers that lack protein overexpression or gene amplification. METHODS: An Update Panel conducted a systematic literature review to identify signals for updating recommendations. RESULTS: The search identified 173 abstracts. Of five potential publications reviewed, none constituted a signal for revising existing recommendations. RECOMMENDATIONS: The 2018 ASCO-CAP recommendations for HER2 testing are affirmed. DISCUSSION: HER2 testing guidelines have focused on identifying HER2 protein overexpression or gene amplification in breast cancer to identify patients for therapies that disrupt HER2 signaling. This update acknowledges a new indication for trastuzumab deruxtecan when HER2 is not overexpressed or amplified but is immunohistochemistry (IHC) 1+ or 2+ without amplification by in situ hybridization. Clinical trial data on tumors that tested IHC 0 are limited (excluded from DESTINY-Breast04), and evidence is lacking that these cancers behave differently or do not respond similarly to newer HER2 ADCs. Although current data do not support a new IHC 0 versus 1+ prognostic or predictive threshold for response to trastuzumab deruxtecan, this threshold is now relevant because of the trial entry criteria that supported its new regulatory approval. Therefore, while it is premature to create new result categories of HER2 expression (eg, HER2-Low, HER2-Ultra-Low), best practices to distinguish IHC 0 from 1+ are now clinically relevant. This Update affirms prior HER2 reporting recommendations and offers a new HER2 testing reporting comment to highlight the current relevance of IHC 0 versus 1+ results and best practice recommendations to distinguish these often subtle differences.Additional information is available at www.asco.org/breast-cancer-guidelines.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Limite: Female / Humans Idioma: En Revista: J Clin Oncol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Limite: Female / Humans Idioma: En Revista: J Clin Oncol Ano de publicação: 2023 Tipo de documento: Article