HER2 amplification level by in situ hybridization predicts survival outcome in advanced HER2-positive breast cancer treated with pertuzumab, trastuzumab, and docetaxel regardless of HER2 IHC results

Bibliographic Details
Title: HER2 amplification level by in situ hybridization predicts survival outcome in advanced HER2-positive breast cancer treated with pertuzumab, trastuzumab, and docetaxel regardless of HER2 IHC results
Authors: Jeongmin Seo, Jiwon Koh, Dae-Won Lee, Jinyong Kim, Han Suk Ryu, Kyung-Hun Lee, Tae-Yong Kim, Seock-Ah Im
Source: Breast Cancer Research, Vol 25, Iss 1, Pp 1-10 (2023)
Publisher Information: BMC, 2023.
Publication Year: 2023
Collection: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Subject Terms: HER2 positive breast cancer, HER2/CEP17 ratio, HER2 copy number, HER2 in situ hybridization, Dual HER2 blockade, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
More Details: Abstract Background The role of HER2 amplification level in predicting the effectiveness of HER2-directed therapies has been established. However, its association with survival outcomes in advanced HER2-positive breast cancer treated with dual HER2-blockade remains unexplored. Methods This is a single-center retrospective study of patients with advanced HER2-positive breast cancer treated with first-line pertuzumab, trastuzumab, and docetaxel. The primary objective was to ascertain the relationship between treatment outcomes and the level of HER2 amplification by in situ hybridization (ISH). Results A total of 152 patients were included with a median follow-up duration of 50.0 months. Among the 78 patients who received ISH, a higher HER2/CEP17 ratio correlated significantly with longer PFS (HR 0.50, p = 0.022) and OS (HR 0.28, p = 0.014) when dichotomized by the median. A higher HER2 copy number also correlated significantly with better PFS (HR 0.35, p
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1465-542X
Relation: https://doaj.org/toc/1465-542X
DOI: 10.1186/s13058-023-01746-w
Access URL: https://doaj.org/article/3baff563765d491e86fc3d30af39cc2a
Accession Number: edsdoj.3baff563765d491e86fc3d30af39cc2a
Database: Directory of Open Access Journals
More Details
ISSN:1465542X
DOI:10.1186/s13058-023-01746-w
Published in:Breast Cancer Research
Language:English