Single-fraction or multi-fraction stereotactic ablative body radiotherapy followed by atezolizumab in advanced triple-negative breast cancer: a randomized phase II trial

Pre-clinical evidence suggests that stereotactic ablative body radiotherapy (SABR) can enhance systemic anti-tumor responses when combined with immune checkpoint inhibition, although optimal fractionation remains uncertain. Here we conducted a phase II multi-center randomized trial (AZTEC trial; ClinicalTrials.gov identifier NCT03464942) to investigate the efficacy and safety of single-fraction (SF: 20 Gy; n = 27) or multi-fraction (MF: 24 Gy in three fractions; n = 27) SABR followed by anti-PD-L1 atezolizumab in 54 women with advanced triple-negative breast cancer (TNBC) as first or second-line treatment. The primary endpoint was progression free survival (PFS). Secondary endpoints included best overall response rate, clinical benefit rate, overall survival and safety. We observed that both treatment arms had similar efficacy: median PFS was 2.5 months (90% CI: 1.7-4.5) for SF and 3.1 months (90% CI: 1.8-3.9) for MF. The null hypothesis (PFS of 2 months) was not rejected in either arm. Clinical benefit (RECIST complete response/partial response or stable disease for ≥24 weeks) was achieved in 5 (20%) SF and 6 (25%) MF patients, all with oligometastatic disease, independent of PD-L1 expression. Adverse events were similar between arms. Prespecified exploratory analysis of peripheral blood found higher CD8 TPEX cells before and during treatment correlated with improved response duration. Combining SABR with atezolizumab is safe, however further testing is required to determine efficacy for advanced TNBC patients with oligometastatic disease. Combining radiotherapy with immune checkpoint inhibitors can amplify anti-tumor immune responses. Here the authors report the results of a randomized phase II trial of single fraction or multi-fraction stereotactic ablative body radiotherapy followed by anti-PD-L1 atezolizumab in patients with advanced triple-negative breast cancer.

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Journal
Nature Communications
Published
2026-07-27
DOI
https://doi.org/10.1038/s41467-026-75660-y
Primary Topic
Breast Cancer Treatment Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Single-fraction or multi-fraction stereotactic ablative body radiotherapy followed by atezolizumab in advanced triple-negative breast cancer: a randomized phase II trial

Sherene Loi, Steven David, Robyn Cheuk, Michelle Grogan et al.
Nature Communications
Breast Cancer Treatment Studies
article

Single-fraction or multi-fraction stereotactic ablative body radiotherapy followed by atezolizumab in advanced triple-negative breast cancer: a randomized phase II trial

Sherene Loi, Steven David, Robyn Cheuk, Michelle Grogan, Paul J. Neeson, Mathias Bressel, Peter Savas, Maria Farrell, Gavin M. Marx, Jessica Foudoulis, Shankar Siva, Bronte Nikolic, Michael W. Neeson, Shane White, Michelle White
article en

Abstract

Pre-clinical evidence suggests that stereotactic ablative body radiotherapy (SABR) can enhance systemic anti-tumor responses when combined with immune checkpoint inhibition, although optimal fractionation remains uncertain. Here we conducted a phase II multi-center randomized trial (AZTEC trial; ClinicalTrials.gov identifier NCT03464942) to investigate the efficacy and safety of single-fraction (SF: 20 Gy; n = 27) or multi-fraction (MF: 24 Gy in three fractions; n = 27) SABR followed by anti-PD-L1 atezolizumab in 54 women with advanced triple-negative breast cancer (TNBC) as first or second-line treatment. The primary endpoint was progression free survival (PFS). Secondary endpoints included best overall response rate, clinical benefit rate, overall survival and safety. We observed that both treatment arms had similar efficacy: median PFS was 2.5 months (90% CI: 1.7-4.5) for SF and 3.1 months (90% CI: 1.8-3.9) for MF. The null hypothesis (PFS of 2 months) was not rejected in either arm. Clinical benefit (RECIST complete response/partial response or stable disease for ≥24 weeks) was achieved in 5 (20%) SF and 6 (25%) MF patients, all with oligometastatic disease, independent of PD-L1 expression. Adverse events were similar between arms. Prespecified exploratory analysis of peripheral blood found higher CD8 TPEX cells before and during treatment correlated with improved response duration. Combining SABR with atezolizumab is safe, however further testing is required to determine efficacy for advanced TNBC patients with oligometastatic disease. Combining radiotherapy with immune checkpoint inhibitors can amplify anti-tumor immune responses. Here the authors report the results of a randomized phase II trial of single fraction or multi-fraction stereotactic ablative body radiotherapy followed by anti-PD-L1 atezolizumab in patients with advanced triple-negative breast cancer.

Nature Communications
Australian National University (AU), The University of Melbourne (AU), Sydney Adventist Hospital (AU), Royal Brisbane and Women's Hospital (AU), Peter MacCallum Cancer Centre (AU), Monash Medical Centre (AU), Prince of Wales Hospital (AU), Olivia Newton-John Cancer Wellness & Research Centre (AU), Monash University (AU)
Breast Cancer Research Foundation, National Breast Cancer Foundation, Medical Research Council, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 12%
Breast Cancer Treatment Studies
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