Atezolizumab for Alveolar Soft Part Sarcoma: A Clinical Trial Update

阿替唑单抗 医学 贝伐单抗 临床试验 外科 软组织肉瘤 临床研究阶段 内科学 药品 肺泡软组织肉瘤 完全响应 肿瘤科 化疗 疾病 癌症 总体生存率 护理标准
作者
Alice P. Chen,Christina L. Rosenberger,Nancy Moore,Jared C. Foster,Abdul Rafeh Naqash,Elad Sharon,Geraldine O'Sullivan Coyne,Gary K. Schwartz,Richard F. Riedel,John Glod,James Hu,Anthony P. Conley,William L. Read,Melissa Burgess,Elizabeth J. Davis,Priscilla Merriam,Hari A. Deshpande,Brian H. Ladle,Scott H. Okuno,Jill C. Beck
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:44 (16): 1490-1497
标识
DOI:10.1200/jco-25-02811
摘要

We previously reported initial results of the pivotal phase II trial of atezolizumab for patients with alveolar soft part sarcoma (ASPS; ClinicalTrials.gov identifier: NCT03141684). Here, we report on three additional years of observation. Fifty-three patients with ASPS received atezolizumab. Median duration of response increased to 37.0 months. Objective response rate (ORR) and median progression-free survival (mPFS) remained essentially as previously reported (35.8% [95% CI, 23.1 to 50.2] and 20.8 months [IQR, 7.6-not reached], respectively). ASPSCR1::TFE3 fusion type was determined for 47/53 patients; ORR and mPFS were higher among the 41 patients expressing type 1 (43.9% [95% CI, 28.5 to 60.2] and 28.3 months [IQR, 9.2-not reached], respectively) than the six patients expressing type 2 (0% [95% CI, 0 to 45.9] and 7.5 months [IQR, 3.9-not reached], respectively, PFS HR, 3.2 [95% CI, 1.01 to 10.2]). Eleven patients chose a per-protocol drug holiday (range, 3.5-26.4 months) after ≥2 years of treatment; two experienced disease progression during the holiday. Nine eligible patients elected to receive bevacizumab plus atezolizumab after progressing on monotherapy; ORR was 0% and mPFS was 18.5 months (IQR, 7.9-21.1) in this small cohort. Long-term results support using atezolizumab to treat ASPS, even for several years; a drug holiday with careful monitoring may be an option for some patients.

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