Abstract A009: Forty-three week follow-up of a phase 1a clinical trial of a PSA, IL-2, GM-CSF containing prostate cancer therapeutic vaccine in PSA defined biochemical recurrent prostate cancer patients

J. Head, G. Daniels, M. McKinney, J. Wang-Rodriguez
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Abstract

While progress has occurred in both cellular and immune checkpoint therapy, the benefit of therapeutic cancer vaccines has been difficult to demonstrate. Prostate cancer may be an exception with the modest activity of Sipuleucel T. We have developed a potentially low cost and easy to administer therapeutic vaccine with the combination of tumor antigen (PSA) and biologic adjuvants (IL2 and GM-CSF). This study is a phase 1a clinical trial of a PSA/IL-2/GM-CSF vaccine in biochemically recurrent hormone-naive and hormone-independent prostate cancer patients. Major inclusion criteria include adenocarcinoma of the prostate, rising serum PSA and no measurable disease. Phase 1a examines the rate of serious adverse events (SAEs) and dose limiting adverse events (DLAEs) in an initial course of 6 vaccinations (“induction vaccination”). Twenty patients enrolled and nineteen patients completed all six intradermal injections (one patient received 5 vaccines, missed week 11 vaccine) of the PSA/IL-2/GM-CSF vaccine at weeks 1, 2, 3, 7, 11 and 15. None of the patients vaccinated in the phase 1a portion had an SAE or DLAE with the most common AE relating to grade 1 injection site reactions. Fifteen of the 18 patients who received vaccines had immune responses to PSA as demonstrated in a lymphocyte blastogenesis assay by week 31. Interestingly, after vaccination 14 of 20 patients had an increase in the doubling time of their serum PSA, suggesting a slowing of the growth of the prostate cancer. Five of 20 patients have progressed (3 PSA progression and 2 radiologic progression) at 43 weeks’ follow-up. Citation Format: Jonathan F. Head, Gregory A. Daniels, Michelle McKinney, Jessica Wang-Rodriguez. Forty-three week follow-up of a phase 1a clinical trial of a PSA, IL-2, GM-CSF containing prostate cancer therapeutic vaccine in PSA defined biochemical recurrent prostate cancer patients [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A009.
A009:一项含有PSA、IL-2、GM-CSF的前列腺癌治疗性疫苗在PSA定义的生化复发性前列腺癌患者中的临床试验进行了43周的随访
虽然在细胞和免疫检查点治疗方面都取得了进展,但治疗性癌症疫苗的益处一直难以证明。前列腺癌可能是一个例外,Sipuleucel t具有适度的活性。我们已经开发出一种潜在的低成本和易于管理的治疗性疫苗,该疫苗结合了肿瘤抗原(PSA)和生物佐剂(il - 2和GM-CSF)。这项研究是PSA/IL-2/GM-CSF疫苗在生化复发的激素初始和激素不依赖型前列腺癌患者中的1a期临床试验。主要入选标准包括前列腺腺癌、血清PSA升高和无可测量疾病。第1a期研究在最初接种6次疫苗(“诱导接种”)的过程中,严重不良事件(sae)和剂量限制性不良事件(DLAEs)的发生率。20名患者入组,19名患者在第1,2,3,7,11和15周完成了PSA/IL-2/GM-CSF疫苗的所有6次皮内注射(1名患者接种了5种疫苗,未接种第11周的疫苗)。在1a期部分接种疫苗的患者中没有发生SAE或DLAE,最常见的AE与1级注射部位反应有关。在接受疫苗的18例患者中,有15例在第31周的淋巴细胞母细胞发生试验中对PSA有免疫应答。有趣的是,接种疫苗后,20名患者中有14人的血清PSA翻倍时间增加,这表明前列腺癌的生长速度有所减缓。在43周的随访中,20例患者中有5例进展(3例PSA进展,2例放射学进展)。引用格式:Jonathan F. Head, Gregory A. Daniels, Michelle McKinney, Jessica Wang-Rodriguez。一项含有PSA、IL-2、GM-CSF的前列腺癌治疗性疫苗在PSA定义的生化复发前列腺癌患者中的1a期临床试验的43周随访[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫,2019;7(2增刊):摘要nr A009。
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