来自PORTER的临床和转化结果,PORTER是一项多队列联合免疫治疗转移性去势抵抗性前列腺癌的1期平台试验

IF 10.9 1区 医学 Q1 ONCOLOGY Clinical Cancer Research Pub Date : 2025-04-14 DOI:10.1158/1078-0432.CCR-24-3693
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 O Chen, Jennifer Lata, Jeffrey Skolnik, Tibor Keler, Michael J Yellin, Theresa M LaVallee, Justin Fairchild, Silvia Boffo, Jill O'Donnell-Tormey, Ute Dugan, Nina Bhardwaj, Sumit K Subudhi, Lawrence Fong
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引用次数: 0

摘要

目的:目前的免疫检查点疗法对转移性去势抵抗性前列腺癌(mCRPC)的疗效有限。新的组合可能会提高免疫治疗的疗效。患者和方法:我们在mCRPC中进行了一项开放标签、非比较平台试验(NCT03835533),以评估基于尼沃单抗的联合用药。队列为:A)苯甲galdesleukin 0.006 mg/kg和nivolumab 360 mg Q3W静脉注射;B)立体定向体放射治疗30-50 Gray, CDX-301 75 μg/kg皮下注射5天,polyiclc 1 mg肌肉注射,每周两次,连续3周,nivolumab 480 mg Q4W; C) CDX-301 75 μg/kg连续10天,INO-5151 3 mg肌肉注射,在引入第8天,第1-3周期第1天,然后Q12W, nivolumab 480 mg Q4W。主要终点是安全性;次要终点包括复合缓解率(放射学、PSA或循环肿瘤细胞反应)、6个月疾病控制率、无进展生存期和总生存期。分析了一系列血液和组织样本的药效学和与疾病控制的关系。结果:纳入43例患者(N = 14、15、14,A、B、C组)。3-4级治疗相关不良事件(TRAE)分别发生在10例(71%)、2例(13%)和2例(14%)患者中,其中A组1例发生5级TRAE,综合有效率分别为7%(1/14)、33%(5/15)和7%(1/14)。在所有队列中,6个月的疾病控制与预先存在的记忆/调节性T细胞、TNFα和其他炎症途径有关。结论:B队列联合CDX-301、poly-ICLC和纳武单抗显示出令人鼓舞的临床活性。在所有队列中,预先存在的免疫激活而不是治疗诱导的免疫激活与临床获益相关,这突出了基线免疫适应性的重要性。
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Clinical and Translational Results from PORTER, a Multicohort Phase I Platform Trial of Combination Immunotherapy in Metastatic Castration-Resistant Prostate Cancer.

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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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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