4.7 Article

Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases

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BRITISH JOURNAL OF CANCER
卷 124, 期 11, 页码 1836-1842

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DOI: 10.1038/s41416-021-01351-8

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  1. Nottingham Health Science Biobank
  2. PathLAKE project
  3. AIRC [22850]
  4. Birmingham Cancer Research UK Centre [C17422/A25154]

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The ASCO/CAP guidance on HER2 testing in breast cancer has changed recently, leading to the re-classification of Group 2 tumors with specific characteristics. This study examined the response of Group 2 tumors to neoadjuvant chemotherapy. Results showed a higher pCR rate in Group 2 compared to combined Groups 4 + 5, indicating the need for further evaluation of HER2 Group 2 carcinomas for targeted therapy eligibility.
Background The ASCO/CAP guidance on HER2 testing in breast cancer (BC) has recently changed. Group 2 tumours with immunohistochemistry score 2+ and HER2/CEP17 ratio >= 2.0 and HER2 copy number <4.0 signals/cell were re-classified as HER2 negative. This study aims to examine the response of Group 2 tumours to neoadjuvant chemotherapy (NACT). Methods 749 BC cases were identified from 11 institutions. The association between HER2 groups and pathological complete response (pCR) was assessed. Results 54% of immunohistochemistry HER2 positive (score 3+) BCs showed pCR, compared to 19% of immunohistochemistry 2+ FISH amplified cases. 27% of Group 2 treated with HER2 targeted therapy achieved pCR, compared to 19 and 11% in the combined Groups 1 + 3 and Groups 4 + 5, respectively. No difference in pCR rates was identified between Group 2 and Group 1 or combined Groups 1 + 3. However, Group 2 response rate was higher than Groups 4 + 5 (p = 0.017). Conclusion No difference in pCR was detected in tumours with a HER2/CEP17 ratio >= 2.0 and a HER2 score 2+ by IHC when stratified by HER2 gene copy number. Our data suggest that ASCO/CAP HER2 Group 2 carcinomas should be evaluated further with respect to eligibility for HER2 targeted therapy.

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