Abstract 1381: BCL-2 selective inhibitor venetoclax combined with topoisomerase I inhibitor irinotecan is effective in small cell lung cancer (SCLC)

伊立替康 威尼斯人 癌症研究 拓扑异构酶 肺癌 医学 拓扑异构酶抑制剂 癌症 生物 肿瘤科 内科学 结直肠癌 DNA 白血病 遗传学 慢性淋巴细胞白血病
作者
Yanli Xing,Krista M. Dalton,Jane L. Roberts,Anthony C. Faber
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:85 (8_Supplement_1): 1381-1381
标识
DOI:10.1158/1538-7445.am2025-1381
摘要

Abstract Background: Lung cancer is the third most common cancers globally, and small cell lung cancer (SCLC) accounts for 10-15% of all lung cancer cases. Extensive stage (ES)-SCLC has an overall five-year survival rate of ∼5%. Although ES-SCLC initially responds well to platinum-based combination chemotherapy, it almost invariably develops resistance over time. Immunotherapy can induce some responses in ES-SCLC, and arlatamab-dlle, a DLL3 targeted bi-specific T-cell engager, was recently given advanced approval to treat relapsed ES-SCLC. However, ES-SCLC remains a dismal prognosis. Venetoclax is a Bcl-2 selective inhibitor that induces apoptosis by binding to the hydrophobic groove of BCL-2. We previously demonstrated that venetoclax is effective in SCLC with high BCL-2 expression (Lochmann et al., Clinical Cancer Research 2018). Irinotecan is an antineoplastic enzyme inhibitor that blocks the topoisomerase I-DNA complex, preventing DNA repair and causing double-strand breaks that lead to cell death. It is often given in the relapsed setting as second-line therapy for ES-SCLC. Aims: We aimed to determine if venetoclax could enhance responses to irinotecan in SCLC preclinical models, and vice versa. Methods: Venetoclax was combined with irinotecan and SCLC cell viability was evaluated including CellTiter-Glo (CTG), immunoblotting, and in mouse models, including patient-derived xenografts, in vivo. Results: Our data showed that combining the BCL-2 selective inhibitor venetoclax with irinotecan demonstrated in many SCLC models, enhanced activity over single-agent alone. In vivo, the combination enhanced survival compared to either single-agent. Conclusion: We demonstrate that combining the BCL-2 selective inhibitor venetoclax with irinotecan could enhance responses and survival in the refractory SCLC setting. Citation Format: Yanli Xing, Krista M. Dalton, Jane L. Roberts, Anthony C. Faber. BCL-2 selective inhibitor venetoclax combined with topoisomerase I inhibitor irinotecan is effective in small cell lung cancer (SCLC) [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 1381.

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