Clinical and Translational Results from PORTER, a Multicohort Phase I Platform Trial of Combination Immunotherapy in Metastatic Castration-Resistant Prostate Cancer

医学 无容量 前列腺癌 临床终点 内科学 队列 肿瘤科 免疫疗法 临床试验 不利影响 癌症 醋酸阿比特龙酯 雄激素剥夺疗法
作者
Matthew D. Galsky,Karen A. Autio,Christopher R. Cabanski,Kristopher Wentzel,Julie N. Graff,Terence W. Friedlander,Timothy R. Howes,Kristin M. Shotts,Julie Densmore,Marko Spasic,Diane M. Da Silva,Richard Chen,Jennifer Lata,Jeffrey Skolnik,Tibor Keler,Michael Yellin,Theresa LaVallee,Justin Fairchild,Silvia Boffo,Jill O’Donnell-Tormey
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:31 (8): 1463-1475 被引量:8
标识
DOI:10.1158/1078-0432.ccr-24-3693
摘要

Abstract Purpose: Current immune checkpoint therapies offer limited benefits for metastatic castration-resistant prostate cancer. Novel combinations may enhance immunotherapy efficacy. Patients and Methods: We conducted an open-label, noncomparative platform trial (NCT03835533) in metastatic castration-resistant prostate cancer to assess nivolumab-based combinations. The cohorts were as follows: (A) bempegaldesleukin 0.006 mg/kg and nivolumab 360 mg i.v. every 3 weeks; (B) stereotactic body radiotherapy 30 to 50 Gy, CDX-301 75 μg/kg s.c. for 5 days, poly-ICLC 1 mg intramuscularly weekly twice for 3 weeks, and nivolumab 480 mg every 4 weeks; and (C) CDX-301 75 μg/kg for 10 days, INO-5151 3 mg intramuscularly on lead-in day 8, day 1 of cycles 1 to 3, and then every 12 weeks, and nivolumab 480 mg every 4 weeks. The primary endpoint was safety; secondary endpoints included composite response rate (radiographic, PSA, or circulating tumor cell responses), 6-month disease control rate, progression-free survival, and overall survival. Serial blood and tissue samples were analyzed for pharmacodynamics and association with disease control. Results: A total of 43 patients were enrolled (n = 14, 15, and 14 in cohorts A, B, and C, respectively). Grade 3 to 4 treatment-related adverse events occurred in 10 (71%), 2 (13%), and 2 (14%) patients, respectively, with one grade 5 treatment-related adverse event in cohort A. Composite response rates were 7% (1/14), 33% (5/15), and 7% (1/14). Across cohorts, 6-month disease control was associated with preexisting memory/regulatory T cells, TNFα, and other inflammatory pathways. Conclusions: Cohort B, which combined radiotherapy with CDX-301, poly-ICLC, and nivolumab, demonstrated encouraging clinical activity. Preexisting rather than treatment-induced immune activation was associated with clinical benefit across cohorts, highlighting the importance of baseline immune fitness.
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