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Journal of Clinical Oncology· 2013Q1· Kılavuz

Meme Kanserinde HER2 Testi İçin Güncellenmiş Öneriler

Recommendations for Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Update

Antonio C. Wolff, M. Elizabeth Hammond, David G. Hicks, Mitch Dowsett ve diğerleri

Kısa özet

Güncellenmiş ASCO/CAP kılavuzları, meme kanserinde HER2 testi için kriterleri güncellemekte, tümör hücrelerinin >%10'unda protein aşırı ekspresyonu (IHC) veya gen amplifikasyonu (ISH) ile HER2-pozitif durumu tanımlamakta ve belirsiz sonuçlar için yansıtma testi önermektedir.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • İnvaziv meme kanseri olan tüm hastalar için HER2 durumu belirlenmesi önerilmektedir.
  • HER2-pozitif durumu, tümör hücrelerinin >%10'unda protein aşırı ekspresyonu (IHC) veya gen amplifikasyonu (ISH) kanıtı gerektirir.
  • Belirsiz test sonuçları, alternatif bir test (IHC veya ISH) ile yansıtma testi yapılmasını zorunlu kılar.
  • Laboratuvarlar, doğrulanmış HER2 testleriyle yüksek uyum göstermeli ve akredite olmalıdır.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (abstract)

PURPOSE: To update the American Society of Clinical Oncology (ASCO)/College of American Pathologists (CAP) guideline recommendations for human epidermal growth factor receptor 2 (HER2) testing in breast cancer to improve the accuracy of HER2 testing and its utility as a predictive marker in invasive breast cancer. METHODS: ASCO/CAP convened an Update Committee that included coauthors of the 2007 guideline to conduct a systematic literature review and update recommendations for optimal HER2 testing. RESULTS: The Update Committee identified criteria and areas requiring clarification to improve the accuracy of HER2 testing by immunohistochemistry (IHC) or in situ hybridization (ISH). The guideline was reviewed and approved by both organizations. RECOMMENDATIONS: The Update Committee recommends that HER2 status (HER2 negative or positive) be determined in all patients with invasive (early stage or recurrence) breast cancer on the basis of one or more HER2 test results (negative, equivocal, or positive). Testing criteria define HER2-positive status when (on observing within an area of tumor that amounts to > 10% of contiguous and homogeneous tumor cells) there is evidence of protein overexpression (IHC) or gene amplification (HER2 copy number or HER2/CEP17 ratio by ISH based on counting at least 20 cells within the area). If results are equivocal (revised criteria), reflex testing should be performed using an alternative assay (IHC or ISH). Repeat testing should be considered if results seem discordant with other histopathologic findings. Laboratories should demonstrate high concordance with a validated HER2 test on a sufficiently large and representative set of specimens. Testing must be performed in a laboratory accredited by CAP or another accrediting entity. The Update Committee urges providers and health systems to cooperate to ensure the highest quality testing. This guideline was developed through a collaboration between the American Society of Clinical Oncology and the College of American Pathologists and has been published jointly by invitation and consent in both Journal of Clinical Oncology and the Archives of Pathology & Laboratory Medicine.

Yazarların özeti; kaynağından alınmıştır. Journal of Clinical Oncology, 2013 · DOI ↗

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