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Breast cancer research and treatment · 2026

Risk of CNS relapse following pathological complete response to neoadjuvant chemotherapy in early breast cancer.

СтатьяНазвание и аннотация: Перевод в очереди
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de Moura Leite Luciana, de Almeida Guilherme Rossato, Tavares Monique Celeste, Cesca Marcelle Goldner, Campos Fernando Augusto Batista, de Oliveira Fernanda Alves, Dornellas Debora Maciel Santana, Saldanha Erick F, Guimarães Paula Tavares, de Arruda Daniella Dias Sá, de Held Maria Fernanda Simões Devides, Viana Rafael Lima, Moura Francisca Giselle Rocha, Loose Simone Klug, Silva Sinara Figueiredo, Pirolli Rafaela, Fogassa Camilla Albina Zanco, Mattos Bruna Raphaeli Silva, Sanches Solange Moraes, de Lima Vladmir C Cordeiro

Аннотация

PURPOSE: Pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) improves outcomes in breast cancer (BC); however it may not prevent brain metastases. We evaluated central nervous system (CNS) recurrence patterns in early-stage BC following NAC according to pCR.

METHODS: All consecutive stage I-III BC treated with NAC and surgery at a single center between 2007 and 2018 were analyzed. Endpoints included the impact of pCR on CNS recurrence across BC subtypes-hormone receptor-positive(HR)/HER2-negative, HER2-positive and triple-negative (TNBC), CNS recurrence patterns and overall survival (OS) after CNS relapse. Statistical comparisons included Fisher's Exact test, Chi-square, Kaplan-Meier, and regression analyses.

RESULTS: Among 1147 patients, 537 had HR-positive/HER2-negative, 301 HER2-positive, 309 TNBC, mostly stage III, treated with anthracycline + taxane NAC, and trastuzumab if HER2-positive. Three hundred sixty-five achieved pCR (59/537 HR-positive/HER2-negative, 158/301 HER2-positive, 148/309 TNBC). CNS recurrence occurred in 72 (6.2%) patients, with no difference between pCR and non-pCR (4.7 vs. 7.0%, p = 0.15). Across subtypes, there was no difference for HR-positive/HER2-negative (3.4 vs. 4%, p = 1.0), TNBC (5.4 vs. 9.3%, p = 0.2), however there was a reduction in HER2-positive (4.4 vs. 14.7%, p = 0.003) after pCR. Isolated CNS relapse was the predominant pattern of CNS metastasis (82.4%) in pCR, particularly in HER2-positive. Median OS after CNS relapse was 12 months. Multivariate analysis identified HER2-positive, TNBC, and cN2-3 status as independent predictors of CNS recurrence.

CONCLUSION: Although pCR was not associated with a lower overall risk of CNS recurrence, it predicted a reduced risk in HER2-positive disease. Isolated CNS relapse predominated, suggesting a sanctuary effect.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты