Abstract LB012: Efficacy of atezolizumab in the treatment of solid tumors with high tumor mutational burden (TMB): A MyPathway study cohort

J. Hainsworth, C. Friedman, R. Kurzrock, D. Spigel, H. Burris, C. Sweeney, F. Meric-Bernstam, Yong Wang, Jonathan Levy, D. Shames, K. Schulze, Arisha Patel, C. Swanton
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引用次数: 1

Abstract

Purpose Data suggest that TMB is correlated with response to checkpoint blockade. We present an analysis of atezolizumab treatment of patients (pts) with advanced solid tumors and high TMB from MyPathway (NCT02091141), a multi-basket study assessing activity of FDA-approved therapies in non-indicated tumors with targetable alterations. Methods Eligible pts were ≥18 years old with previously treated advanced solid tumors with TMB ≥10 mut/Mb by any CLIA-certified assay. Pts received atezolizumab 1200 mg IV q3w. The pre-planned primary endpoint was objective response rate (ORR) in pts with TMB ≥16 mut/Mb by FoundationOne CDx (F1CDx), a threshold determined by a retrospective study that showed TMB ≥16 mut/Mb is associated with improved ORR and duration of response (DOR) for various tumor types. Other endpoints in this group included disease control rate (DCR), DOR, progression-free survival (PFS), and overall survival (OS). Separate analyses were performed in pts with TMB ≥10 and Results Enrollment closed on 7-9-20. By the 12-11-20 data cutoff, 118 pts with 20 tumor types and TMB ≥10 mut/Mb by any CLIA assay were evaluable for efficacy. In the primary efficacy population of 42 pts with TMB ≥16 mut/Mb by F1CDx, confirmed investigator-assessed ORR was 38.1% vs 2.1% in 48 pts with TMB ≥10 mut/Mb and Conclusions Atezolizumab had durable activity against diverse solid tumor types with TMB ≥16 mut/Mb, independent of MSI status. Limited activity was observed in tumors with TMB ≥10 and Citation Format: John Hainsworth, Claire F. Friedman, Razelle Kurzrock, David R. Spigel, Howard Burris, Christopher J. Sweeney, Funda Meric-Bernstam, Yong Wang, Jonathan Levy, David Shames, Katja Schulze, Arisha Patel, Charles Swanton. Efficacy of atezolizumab in the treatment of solid tumors with high tumor mutational burden (TMB): A MyPathway study cohort [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr LB012.
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摘要:atezolizumab治疗高肿瘤突变负荷(TMB)实体瘤的疗效:一项MyPathway研究队列
目的:数据表明TMB与对检查点阻断的反应相关。我们对来自MyPathway (NCT02091141)的atezolizumab治疗晚期实体瘤和高TMB患者(pts)进行了分析,这是一项多筐研究,评估fda批准的治疗具有靶向改变的非适应症肿瘤的活性。方法符合条件的患者为≥18岁,既往治疗过的晚期实体瘤,经任何clia认证的检测,TMB≥10 mut/Mb。患者接受atezolizumab 1200mg IV q3w。预先计划的主要终点是FoundationOne CDx (F1CDx)测试中TMB≥16 mut/Mb的患者的客观缓解率(ORR),该阈值由一项回顾性研究确定,该研究显示TMB≥16 mut/Mb与各种肿瘤类型的改善ORR和反应持续时间(DOR)相关。该组的其他终点包括疾病控制率(DCR)、DOR、无进展生存期(PFS)和总生存期(OS)。TMB≥10的患者进行单独分析,结果入组截止日期为2020-7-9。截至2012年12月11日数据截止,有118例患者(20种肿瘤类型,TMB≥10 mut/Mb)通过任何CLIA检测可评估疗效。在F1CDx检测的42例TMB≥16 mut/Mb患者的主要疗效人群中,研究者评估的确诊ORR为38.1%,而48例TMB≥10 mut/Mb患者的ORR为2.1%。结论:Atezolizumab对TMB≥16 mut/Mb的多种实体肿瘤类型具有持久的活性,与MSI状态无关。在TMB≥10的肿瘤中观察到有限的活性,引文形式:John Hainsworth, Claire F. Friedman, Razelle Kurzrock, David R. Spigel, Howard Burris, Christopher J. Sweeney, Funda Meric-Bernstam, Yong Wang, Jonathan Levy, David Shames, Katja Schulze, Arisha Patel, Charles Swanton。atezolizumab治疗高肿瘤突变负荷(TMB)实体瘤的疗效:一个MyPathway研究队列[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要nr LB012。
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