Neoadjuvant stereotactic body radiation therapy with durvalumab and oleclumab in ER+HER2− breast cancer: a randomized phase 2 trial
Abstract Patients with estrogen receptor-positive (ER + ), HER2-negative, early breast cancer (BC) have low pathologic complete response (pCR) rates following neoadjuvant chemotherapy. Immune checkpoint inhibitors (ICIs) provide limited benefit in programmed death-ligand 1 (PD-L1)-negative tumors, characterized by an immune-cold tumor microenvironment. Here we hypothesized that immune-modulating stereotactic body radiation therapy (iSBRT; 3 × 8 Gy) could enhance response through tumor microenvironment reprogramming, and that CD73 blockade could further improve efficacy. We conducted a phase 2, randomized, multicenter trial (Neo-CheckRay) in 147 female patients with high-risk, ER + HER2 − early BC. Patients received neoadjuvant chemotherapy plus iSBRT alone (No_ICI), with anti-PD-L1 durvalumab (Single_ICI) or with durvalumab plus anti-CD73 oleclumab (Double_ICI). In the intention-to-treat population, the primary endpoint, residual cancer burden 0/1 rate, was 35.4% with No_ICI, 45.1% with Single_ICI and 47.9% with Double_ICI, without statistically significant differences. pCR rates were 16.7%, 29.4% and 33.3%, respectively ( P = 0.059). In the per-protocol population (MammaPrint High Risk, n = 131), pCR rates were 16.3%, 32.6% and 35.6%, respectively ( P = 0.040). Among PD-L1-negative tumors ( n = 91), pCR rates were 3.4%, 28.1% and 30.0%, respectively. No new safety signals were observed. Baseline transcriptomic analysis showed low immune signature expression in PD-L1-negative tumors. Paired baseline and on-treatment biopsies obtained 1 week after iSBRT demonstrated tumor microenvironment reprogramming toward an inflamed phenotype in the iSBRT + anti-PD-L1 arms. These findings suggest that iSBRT + anti-PD-L1 may convert immune-cold ER + HER2 − BC into more inflamed tumors and improve response, particularly in PD-L1-negative disease. ClinicalTrials.gov registration: NCT03875573 .
Authors
- Roberto Salgado (ORCID: https://orcid.org/0000-0002-1110-3801)
- Luca Arecco (ORCID: https://orcid.org/0000-0002-3818-0364)
- Laurence Buisseret (ORCID: https://orcid.org/0000-0002-3751-0819)
- Guilherme Nader Marta (ORCID: https://orcid.org/0000-0001-7864-3637)
- Isabelle Desmoulins (ORCID: https://orcid.org/0000-0002-1251-5648)
- Paulus Kristanto (ORCID: https://orcid.org/0000-0002-1657-5250)
- E. Longton
- David Venet (ORCID: https://orcid.org/0000-0001-9038-5271)
- Christos Sotiriou (ORCID: https://orcid.org/0000-0002-5745-9977)
- Xavier Catteau (ORCID: https://orcid.org/0000-0003-3031-5719)
- Adinda Baten (ORCID: https://orcid.org/0000-0001-7104-7808)
- Alex De Caluwé (ORCID: https://orcid.org/0000-0001-5989-7017)
- Michail Ignatiadis (ORCID: https://orcid.org/0000-0002-4493-3748)
- Emanuela Romano (ORCID: https://orcid.org/0000-0002-1574-5545)
- Elisa Agostinetto (ORCID: https://orcid.org/0000-0003-0295-7511)
- Kim Cao (ORCID: https://orcid.org/0000-0003-2475-1821)
- Jennifer Dhont (ORCID: https://orcid.org/0000-0003-1296-4627)
- Zoë Denis
- Karine Peignaux
- J. C. A. Stagg
- Andrea Joaquin Garcia
- Vincent Remouchamps
- Denis Larsimont
- Philip Poortmans
- Martine Piccart
Institutions
- Cliniques Universitaires Saint-Luc (BE)
- Université Libre de Bruxelles (BE)
- University of Antwerp (BE)
- Universitair Ziekenhuis Leuven (BE)
- Peter MacCallum Cancer Centre (AU)
- Institut Jules Bordet (BE)
- St. Elisabeth Hospital (CW)
- Centre Georges François Leclerc (FR)
- Institute for Research in Immunology and Cancer (CA)
- Iridium Kankernetwerk (BE)
- McGill University (CA)
- Institut Curie (FR)
Publication Details
- Journal
- Nature Medicine
- Published
- 2026-06-25
- DOI
- https://doi.org/10.1038/s41591-026-04453-z
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Stichting Tegen Kanker