Abstract PS4-07-11: Analysis of patients with triple-negative breast cancer and germline BRCA mutation undergoing neoadjuvant treatment following the keynote 522 protocol in real-world. Insights from the Neo-Real/GBECAM-0123 Study

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Authors: M. Celeleste Tavares, Flávia Cavalcanti Balint, Romualdo Barroso‐Sousa, S. Moraes Sanches, Laura Testa, G. Colucci, N. C. Nunes, B. G. Giner, M. Gill, I. S. Martins, M. O. Andrade, M. C. Gouveia
+21 more Fernanda Madasi, José Bines, R. Ferreira, Daniela D. Rosa, C. Santos, M. F. Monteiro, Zenaide Silva de Souza, Daniele Xavier Assad, Carlos Henrique dos Anjos, Débora De Melo Gagliato, André Vieira Gomes, Bruna Migliavacca Zucchetti, Augusto Ferrari, M. L. Brito, M. F. Monteiro, Poliana Albuquerque Signorini, N. J. Gomes, S. Mazzotta, P. G. Hoff, Maria Del Pilar Estevez-Diz, R. Colombo Bonadio
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Abstract

Abstract Background The KEYNOTE-522 study established a new standard of care for early-stage triple-negative breast cancer (TNBC), demonstrating that the addition of pembrolizumab to neoadjuvant chemotherapy, followed by adjuvant pembrolizumab, significantly improves pathological complete response (PCR) rates, event-free survival (EFS), and overall survival (OS). BRCA1/2 mutations define a distinct molecular subgroup of TNBC, characterized by impaired DNA repair and potential differential sensitivity to platinum agents and immunotherapy. Real-world data on this subgroup remain limited. Methods Neo-Real/GBECAM-0123 is a multicenter, real-world study that included patients with early-stage TNBC treated with the KEYNOTE-522 regimen in Brazil and Argentina since July 2020. Patients were categorized as BRCA mutation carriers (mBRCA) or wild-type/unknown (wt/unkBRCA). Clinical, pathological, and treatment-related outcomes were compared using descriptive and inferential statistics. Results Among 726 patients, 104 (14.3%) were mBRCA and 622 (85.7%) were wt/unkBRCA (495 [84.2%] wild-type and 93 [15.8%] unknown). Patients with mBRCA were significantly younger at diagnosis (mean age: 40.2 vs. 45.3 years; p < 0.001). In both groups, the majority of patients had stage II (73.0% and 72.3%) and stage 3 (80.2% and 74.2%) tumors. The pCR rate was significantly higher in the mBRCA group (74.0% vs. 61.4%; p = 0.018). Mastectomy was performed more frequently in mBRCA patients (88.3% vs. 34.7%; p < 0.001), and radiation therapy was also administered less frequently (64.4% vs. 87.1%; p < 0.001). With a median follow-up of 22 months, 82 patients experienced disease recurrence or death. Two-year EFS rates were 92.3% in the mBRCA group and 86.0% in the wt/unkBRCA group (HR 0.51, 95% CI: 0.23-1.11; p = 0.091). Discussion This real-world analysis provides strong evidence that patients with triple-negative breast cancer (TNBC) with mBRCA experience distinct clinical characteristics and superior outcomes when treated with the KEYNOTE-522 regimen. The 12.3% absolute increase in the pCR rate translated into favorable EFS trends. These findings are clinically relevant and may guide future strategies for risk-adapted treatment de-escalation. Citation Format: M. C. Tavares, F. C. Balint, R. B. Barroso-Sousa, S. Sanches, L. Testa, G. Colucci, N. C. Nunes, B. G. Giner, M. Gill, I. S. Martins, M. Andrade, M. Gouveia, F. Madasi, J. Bines, R. Ferreira, D. Rosa, C. Santos, M. Monteiro, Z. S. Souza, D. Assad-Suzuki, C. Anjos, D. M. Gagliato, A. Gomes, B. Zucchetti, A. Ferrari, M. Brito, M. F. Monteiro, P. A. Signorini, N. J. Gomes, S. Mazzotta, P. M. Hoff, M. Estevez-Diz, R. R. Bonadio. Analysis of patients with triple-negative breast cancer and germline BRCA mutation undergoing neoadjuvant treatment following the keynote 522 protocol in real-world. Insights from the Neo-Real/GBECAM-0123 Study [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS4-07-11.

Fields of Study & Subjects

BRCA gene mutations in cancer Breast Cancer Treatment Studies PARP inhibition in cancer therapy

Publication details

Journal / source
Clinical Cancer Research
Volume
32
Issue
4_Supplement
Pages
PS4–07
Publication date
17 February 2026
Language
EN