Pathological complete response with neoadjuvant pembrolizumab and chemotherapy in non-metastatic triple-negative inflammatory breast cancer

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Authors: F. Lynce, C. Valenza, S.M. Niman, F. Bertucci, M. Kai, S. Ryan, E. Troll, R.M. Layman, K.A. Fanucci, A. Giordano, Azadeh Nasrazadani, F. Nakhlis
+27 more J. Bellon, L. Warren, C. Block, S. Schumer, A. Lucci, Savitri Krishnamurthy, D. Trapani, F. Lerebours, F. Dalenc, C. Levy, T. Petit, M. Leheurteur, T. Bachelot, O. Tredan, J.M. Ribeiro, B. Pistilli, P. Zagami, S. Ladoire, L. Lopez Almeida, C. Zemmour, L.A. Carey, S.M. Tolaney, V. Valero, G. Curigliano, M.M. Regan, A. Goncalves, W.A. Woodward
Cited by: 1
References: 9

Abstract

BACKGROUND: The efficacy of neoadjuvant chemoimmunotherapy in patients with non-metastatic triple-negative inflammatory breast cancer (TN-IBC) remains unclear, as patients with IBC have been poorly represented in pivotal clinical trials. PATIENTS AND METHODS: We conducted an observational, retrospective/prospective, multicenter cohort study from 2023 to 2024 of patients with non-metastatic TN-IBC who received at least one cycle of neoadjuvant pembrolizumab plus multi-agent chemotherapy from September 2018 to April 2023. The median follow-up was 1.4 years [95% confidence interval (CI) 1.2-1.7 years]. The primary endpoint was pathological complete response (pCR). RESULTS: Overall, 63 female patients with TN-IBC were included from four cohorts. The most common regimen was pembrolizumab, taxane/carboplatin, and anthracycline/cyclophosphamide (61.9%). Among all patients, 59 (94%) underwent surgery and 4 (6.4%) experienced local and/or distant disease progression during the neoadjuvant treatment. The pCR rate was 31.7% (20/63; 95% CI 20.6% to 44.7%). CONCLUSIONS: The combination of neoadjuvant chemotherapy and pembrolizumab resulted in a pCR rate of 31.7% in patients with non-metastatic TN-IBC. Compared with triple-negative non-IBC, the lower pCR rate with this combination regimen highlights the need for biomarkers for better patient selection and more active treatment options for this rare and aggressive breast cancer subtype.

Fields of Study & Subjects

Cancer Immunotherapy and Biomarkers Breast Cancer Treatment Studies HER2/EGFR in Cancer Research

Publication details

Journal / source
ESMO Open
Publisher
Elsevier BV
Volume
11
Issue
2
Pages
106050–106050
Publication date
19 January 2026
Language
EN