Incidence of brain metastases in patients with early HER2-positive breast cancer receiving neoadjuvant chemotherapy with trastuzumab and pertuzumab

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作者
Emanuela Ferraro
Jasmeet Singh
Sujata Patil
Pedram Razavi
Shanu Modi
Sarat Chandarlapaty
Andrea V. Barrio
Rachna Malani
Ingo K. Mellinghoff
Adrienne Boire
Hannah Y. Wen
Edi Brogi
Andrew D. Seidman
Larry Norton
Mark E. Robson
Chau T. Dang
机构
[1] Memorial Sloan Kettering Cancer Center,Breast Cancer Service, Department of Medicine
[2] Memorial Sloan Kettering Cancer Center,Breast Cancer Service, Department of Medicine
[3] Weill Cornell Medicine College,Breast Cancer Service, Department of Surgery
[4] Memorial Sloan Kettering Cancer Center,Brain Tumor Center, Department of Neurology
[5] Memorial Sloan Kettering Cancer Center,Brain Tumor Center, Human Oncology and Pathogenesis Program, Department of Neurology
[6] Memorial Sloan Kettering Cancer Center,Department of Pathology
[7] Memorial Sloan Kettering Cancer Center,Department of Quantitative Health Sciences
[8] Cleveland Clinic,undefined
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The addition of pertuzumab (P) to trastuzumab (H) and neoadjuvant chemotherapy (NAC) has decreased the risk of distant recurrence in early stage HER2-positive breast cancer. The incidence of brain metastases (BM) in patients who achieved pathological complete response (pCR) versus those who do not is unknown. In this study, we sought the incidence of BM in patients receiving HP-containing NAC as well as survival outcome. We reviewed the medical records of 526 early stage HER2-positive patients treated with an HP-based regimen at Memorial Sloan Kettering Cancer Center (MSKCC), between September 1, 2013 to November 1, 2019. The primary endpoint was to estimate the cumulative incidence of BM in pCR versus non-pCR patients; secondary endpoints included disease free-survival (DFS) and overall survival (OS). After a median follow-up of 3.2 years, 7 out of 286 patients with pCR had a BM while 5 out of 240 non-pCR patients had a BM. The 3-year DFS was significantly higher in the pCR group compared to non-pCR group (95% vs 91 %, p = 0.03) and the same trend was observed for overall survival. In our cohort, despite the better survival outcomes of patients who achieved pCR, we did not observe appreciable differences in the incidence of BM by pCR/non-pCR status. This finding suggests that the BM incidence could not be associated with pCR. Future trials with new small molecules able to cross the blood brain barrier should use more specific biomarkers rather than pCR for patients’ selection.
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