UK real-world evidence on pembrolizumab and neoadjuvant chemotherapy for early-stage triple-negative breast cancer

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Authors: J. McKeon, E. Daniels, A. Halstead, C. Machado, S. Potter, T. Strawson-Smith, A. Okines, S. Mcintosh, H. Tovey, Tim Robinson, H. Abdallah, Syed Salahuddin Ahmed
+71 more N. Ainsworth, A. Akhtar, M. Amaya, C. Archer, A. Armstrong, O. Ayodele, A. Ayyad, M. Azhar, K. Ball, B. Baraka, H. Barot, U. Barthakur, A. Borley, Rebecca Bowen, F. Britton, H. Chapman, H. Cook, E. Copson, K. Crawford, N. Cresti, B. Crook, R. Cutress, L. Drewett, K.H. El-Shakankery, L. Glanville, R. Gul, A. Guppy, L. Gurung, V. Harding, C. Harper-Wynne, L. Hennah, S. Ho, J. Howells, T. Irfan, C. Iwu, E. Johnston, S. Khan, J. King, P. Koliou, A. Konstantis, C. Kruppa, A. Lewis, P. Lowdon, T. Lucas, A.L. Smith, K. McAdams, H. McKenzie, C. Michie, T. Nawarathna, D. Nelmes, O. Oikonomidou, O. Omokhodion, C. O’Neill, A. Percival, C. Pow, S. Rana, D. Rea, S. Rehman, Rizwan Sarwar, S. Seymour, A. Shaheen, A. Sheri, R. Simcock, S. Spensley, M.H. Syed Khaja, A. Thomson, L. Uden, L. Walkington, L. Watts, H. Whydle, H. Yusof
Cited by: 5
References: 17

Abstract

Background: The KEYNOTE-522 trial showed that use of pembrolizumab-chemotherapy for stage 2-3 triple-negative breast cancer improved pathological complete response (pCR) rates and event-free and overall survival compared with chemotherapy alone. This retrospective multicentre cohort study collated real-world-evidence (RWE) of the efficacy and safety of neoadjuvant pembrolizumab-chemotherapy. Patients and methods: Patients treated with pembrolizumab-chemotherapy who completed pembrolizumab treatment before 1 July 2024 were included in the study. Data were collected on safety and efficacy of treatment. pCR rates were compared between subgroups using chi-square and tests for trend (where appropriate), no adjustment was made for multiplicity. Results: Five hundred and forty-five patients were recruited from 34 UK centres (median age 50 years, range 21-79 years). Neoadjuvant treatment delays and discontinuations were reported by 59% [95% confidence interval (CI) 55% to 63%] and 47% (95% CI 42% to 51%) respectively. Immune-related adverse events (irAEs) were experienced by 65% (95% CI 61% to 69%); 20% of patients (95% CI 16% to 23%) experienced grade ≥3 irAEs. A total of 83% (95% CI 80% to 86%) and 45% (95% CI 41% to 50%) of patients had unplanned medical contacts and admissions. pCR rate was 56% (95% CI 52% to 60%). IrAEs were associated with increased pCR rates, but steroid use and pembrolizumab-chemotherapy discontinuation did not adversely affect rates of pCR. Conclusions: This large, national RWE study demonstrates pCR rate was lower compared with that observed in KEYNOTE-522. High rates of dose reductions, discontinuations and unplanned medical contacts (with significant health care resource use) suggests that patient selection is important for this regimen. Collection of long-term outcomes will be important to better evaluate the benefit/risks of pembrolizumab, especially in certain subgroups.

Fields of Study & Subjects

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

Publication details

Journal / source
ESMO Real World Data and Digital Oncology
Publisher
Elsevier BV
Volume
11
Pages
100664–100664
Publication date
6 January 2026
Language
EN