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2026 conference-abstract

Abstract PS1-09-19: Real world outcomes of sacituzumab govitecan in hormone receptor-positive and triple-negative breast cancer: Impact of prior therapy

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Abstract Background: The antibody-drug conjugate sacituzumab govitecan (SG) is approved for patients with metastatic triple-negative breast cancer (mTNBC) and hormone receptor (HR)+/Human epidermal growth factor receptor 2 (HER2)- metastatic breast cancer (mBC). The impact of HER2-low status on treatment outcomes remains unclear. This study examines overall survival by subtype and prior therapies, explores HER2-low as a predictor of time to next treatment (TTNT), and evaluates TTNT as a potential surrogate for SG benefit. Methods: We identified 472 patients who received SG for HR+/HER2- mBC or mTNBC between 2020 and 2024. We compared overall survival (OS) by breast cancer subtype, treatment history, TTNT, and HER2-low status (1-2+ ISH neg) and investigated factors associated with OS. Results: The median age was 51 years (range, 24-85). Of the 472 patients, 292 (62%) had HER2-low status at any time and 184 (39%) had HER2-0 tumors. The median follow-up time was 9.1 months. Most (84%, n=396) received ≥1 prior therapy in the metastatic setting including chemotherapy (95%) while 34% (n=160) received ≥3 lines of therapy. Among HR+/HER2- mBC patients (n=118), 74% (n=87) received ≥3 lines of prior therapy. Among mTNBC patients (n=354), 38% (n=133) received prior ICI while 21% (n=73) received ≥3 lines of prior therapy. The median overall survival (mOS) duration was 15.3 months (95% CI: 13.5-17.5) for all patients, 12.1 months (95% CI: 8.6-14.9) for HR+/HER2- mBC patients, and 16.5 months (95% CI: 113.6-21.3) for mTNBC patients. Factors associated with worse OS were primary HR+ status (hazard ratio [HR], 1.31; 95% CI, 1.00-1.71; p=0.052), anthracycline therapying metastatic setting (HR, 1.51; 95% CI, 1.05-2.18; p=0.027), and ≥3 prior lines of treatment (HR, 1.49; 95% CI, 1.13-1.96; p=0.004). There were no significant differences in survival based on race, age, or prior ICI therapy. Among 223 patients who were evaluable for TTNT, median TTNT was 5.9 months (range, 0.8-47.8 months), and 49.3% had a TTNT ≥6 months. Patients with a TTNT ≥6 months were more likely than those with a TTNT <6 months to have received ADCs as a subsequent line of treatment (30% vs 14%; p<0.001). For the 223 patients evaluable for TTNT, the mOS was 16.4 months (95% CI, 13.7-20.3) for all patients, 19.9 months (95% CI, 10.2-not estimable) for HR+/HER2- mBC patients, and 16.4 months (95% CI, 13.6-20.3) for mTNBC patients, and HER2-low status at any time point was associated with better OS (HR, 0.68; 95% CI, 0.48-0.98; p=0.036). Conclusions: The survival outcomes in this real-world study were consistent with those reported for clinical trials. Among mTNBC patients, those who received fewer lines of prior chemotherapy had longer OS, and HER2-low status was significantly associated with OS. Prior ICI therapy did not significantly impact outcomes, but patients with >3 lines of prior therapy had worse outcomes, suggesting that earlier utilization of SG may be beneficial. Citation Format: A. Raghavendra, Z. Wang, R. Bssett Jr, S. Damodaran, C. Yam, V. Valero, P. Pohlmann, J. Litton, F. Meric-Bernstam, D. Tripathy, T. Adesoye. Real world outcomes of sacituzumab govitecan in hormone receptor-positive and triple-negative breast cancer: Impact of prior therapy [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS1-09-19.

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DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Abstract PS1-09-19: Real world outcomes of sacituzumab govitecan in hormone receptor-positive and triple-negative breast cancer: Impact of prior therapy
Date Crossref
17/02/2026
Éditeur
American Association for Cancer Research (AACR)
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

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Les sujets associés

Advanced Breast Cancer TherapiesHER2/EGFR in Cancer ResearchPARP inhibition in cancer therapy

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