Stereotactic Ablative Body Radiotherapy for Oligoprogressive Estrogen Receptor–Positive Breast Cancer (TROG 20.03 AVATAR): A Phase II Prospective Multicenter Trial

PURPOSE AVATAR (trial registration: ACTRN 12620001212943) is a multicenter phase II single-arm trial to evaluate whether stereotactic ablative body radiotherapy (SABR) for oligoprogressive estrogen receptor (ER)–positive human epidermal growth factor receptor 2 (HER2)–negative breast cancer can delay a change from combination cyclin-dependent kinase 4 and 6 inhibitor (CDK4/6i) and an aromatase inhibitor (AI) to next-line systemic therapy. METHODS Patients received SABR to all sites of oligoprogressive disease while continuing CDK 4/6i and AI therapy. SABR was permitted for further oligoprogression without altering systemic therapy. The primary end point was event-free survival defined as the time from SABR to either (1) a change in systemic therapy, (2) any progression within 6 months, or (3) the appearance of >3 new progressing lesions. A key secondary end point was modified progression-free survival (mPFS), defined as oligoprogression not amenable to further SABR, or death due to any cause. RESULTS Thirty-two eligible patients were recruited between August 2020 and November 2022, with a median follow-up of 24 months. The primary end point was met, with 47% (95% CI, 29 to 63) of patients remaining event-free for ≥6 months. The median mPFS was 9.9 months (95% CI, 4.1 to not reached), with an estimated 44% (95% CI, 26 to 60) and 36% (95% CI, 20 to 53) of patients maintaining systemic therapy unchanged for 12 and 24 months, respectively. Median PFS was 5.2 months (95% CI, 3.1 to 6.8), with 11 (34%) and two (6%) of patients receiving second and third courses of SABR, respectively. No grade 3 or higher toxicities were reported. CONCLUSION In patients with oligoprogressive ER-positive, HER2-negative breast cancer, these findings suggest that SABR is a viable strategy to maintain treatment with CDK 4/6i in lieu of a change in systemic therapy.

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Journal
JCO oncology advances.
Published
2025-03-01
DOI
https://doi.org/10.1200/oa-25-00031
Citations
7
Primary Topic
Breast Cancer Treatment Studies
Type
article
Field-Weighted Citation Impact
6.55
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article

Stereotactic Ablative Body Radiotherapy for Oligoprogressive Estrogen Receptor–Positive Breast Cancer (TROG 20.03 AVATAR): A Phase II Prospective Multicenter Trial

Reem Alomran, Michelle White, Steven David, E. M. Connolly et al.
7 citations
JCO oncology advances.
Breast Cancer Treatment Studies
6.55
article

Stereotactic Ablative Body Radiotherapy for Oligoprogressive Estrogen Receptor–Positive Breast Cancer (TROG 20.03 AVATAR): A Phase II Prospective Multicenter Trial

Reem Alomran, Michelle White, Steven David, E. M. Connolly, Mathias Bressel, Jennifer Pei-Ling Tan, Catherine Morton, Gerard G. Hanna, Shankar Siva, E. Yip
article en
7 citations

Abstract

PURPOSE AVATAR (trial registration: ACTRN 12620001212943) is a multicenter phase II single-arm trial to evaluate whether stereotactic ablative body radiotherapy (SABR) for oligoprogressive estrogen receptor (ER)–positive human epidermal growth factor receptor 2 (HER2)–negative breast cancer can delay a change from combination cyclin-dependent kinase 4 and 6 inhibitor (CDK4/6i) and an aromatase inhibitor (AI) to next-line systemic therapy. METHODS Patients received SABR to all sites of oligoprogressive disease while continuing CDK 4/6i and AI therapy. SABR was permitted for further oligoprogression without altering systemic therapy. The primary end point was event-free survival defined as the time from SABR to either (1) a change in systemic therapy, (2) any progression within 6 months, or (3) the appearance of >3 new progressing lesions. A key secondary end point was modified progression-free survival (mPFS), defined as oligoprogression not amenable to further SABR, or death due to any cause. RESULTS Thirty-two eligible patients were recruited between August 2020 and November 2022, with a median follow-up of 24 months. The primary end point was met, with 47% (95% CI, 29 to 63) of patients remaining event-free for ≥6 months. The median mPFS was 9.9 months (95% CI, 4.1 to not reached), with an estimated 44% (95% CI, 26 to 60) and 36% (95% CI, 20 to 53) of patients maintaining systemic therapy unchanged for 12 and 24 months, respectively. Median PFS was 5.2 months (95% CI, 3.1 to 6.8), with 11 (34%) and two (6%) of patients receiving second and third courses of SABR, respectively. No grade 3 or higher toxicities were reported. CONCLUSION In patients with oligoprogressive ER-positive, HER2-negative breast cancer, these findings suggest that SABR is a viable strategy to maintain treatment with CDK 4/6i in lieu of a change in systemic therapy.

JCO oncology advances.(2)
The University of Melbourne (AU), Walter and Eliza Hall Institute of Medical Research (AU), Trinity College Dublin (IE), Peter MacCallum Cancer Centre (AU), Monash Medical Centre (AU), King Fahd Medical City (SA), Monash University (AU)
Openalex Percentile: Top 3%
Breast Cancer Treatment Studies
6.55
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