摘要:肿瘤内注射novyi- nt梭菌孢子治疗难治性晚期实体瘤患者的首次临床试验:安全性、活性和免疫反应

F. Janku, M. Gounder, A. Pezeshki, R. Murthy, A. Wang-Gillam, D. Shepard, D. Hong, S. Piha-Paul, Anjali Raina, A. Leontovich, G. Decrescenzo, B. Kreider, David Tung, M. Varterasian, H. Zhang, K. Khazaie
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In this first-in-man phase 1 study, patients with injectable treatment-refractory solid tumors received a single intratumoral injection of C. novyi-NT spores across 6 dose cohorts (spore concentrations of 104, 3x104, 105, 3x105, 106, 3x106) using a 3+3 trial design. The primary endpoints were to assess the safety profile, the dose limiting toxicity, and the maximum tolerated dose of C. novyi-NT. Key secondary endpoints included assessments of the preliminary antitumor activity of the injected tumor, an overall response evaluated by RECIST v. 1.1, and the host immune and inflammatory response to C. novyi-NT. Twenty-four patients were enrolled between November, 2013 and April, 2017. A single intratumoral injection of C. novyi-NT led to germination and resultant tumor lysis of injected tumor masses in 46% of patients across all dosing cohorts. The cohort 5 dose of 106 spores was defined as the maximum tolerated dose. Dose-limiting toxicities were grade 4 sepsis and grade 4 gas gangrene (n=1), all in patients with germination. In the 22 evaluable patients, 21 (95%) had stable disease (SD) as the best response for the injected lesion (tumor shrinkage of > 10% was observed in 21% of patients) and 19 (86%) had overall SD as the best response per RECIST 1.1. C. novyi-NT injection resulted in transient serum cytokine responses consistent with inflammasome activity, activation of innate immunity, tissue remodeling, and angiogenesis. Tumor antigen specific ELISPOT assays pre- and post- treatment documented enhanced secretion of IFNγ and TNFα by circulating T-cells, indicating improved systemic tumor specific T-cell responses. Multiparametric in situ immunostaining of core biopsies suggested improved immune cell infiltration in metastatic lesions. 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引用次数: 0

摘要

溶菌策略提供了独特的优势,以对抗广泛的癌症,通常是传统化疗和/或放疗的屈光度。新梭菌nt是新梭菌的减毒菌株,是一种芽孢形成的革兰氏阳性专性厌氧菌,缺乏致命的α -毒素,由亲本菌株表达。当静脉注射或经皮注射肿瘤内时,C. novyi-NT在肿瘤的缺氧区定植和复制,引发强大的肿瘤局限性细胞溶解。在这项首次在人体内进行的1期研究中,采用3+3试验设计,可注射治疗难治性实体瘤患者接受了6个剂量队列(孢子浓度为104、3x104、105、3x105、106、3x106)的单次瘤内注射C. novyi-NT孢子。主要终点是评估C. novyi-NT的安全性、剂量限制性毒性和最大耐受剂量。关键次要终点包括注射肿瘤的初步抗肿瘤活性评估,RECIST v. 1.1评估的总体反应,以及宿主对C. novyi-NT的免疫和炎症反应。24名患者于2013年11月至2017年4月入组。在所有给药队列中,46%的患者单次肿瘤内注射C. novyi-NT导致肿瘤萌发并导致肿瘤溶解。队列5的106个孢子剂量被定义为最大耐受剂量。剂量限制性毒性为4级败血症和4级气性坏疽(n=1),均发生在萌发患者中。在22例可评估的患者中,21例(95%)的疾病稳定(SD)是注射病变的最佳缓解(21%的患者观察到肿瘤缩小> 10%),19例(86%)的总体SD是RECIST 1.1的最佳缓解。注射C. novyi-NT导致短暂的血清细胞因子反应,与炎性小体活性、先天免疫激活、组织重塑和血管生成一致。肿瘤抗原特异性ELISPOT检测显示,治疗前后循环t细胞分泌IFNγ和TNFα增强,表明全身肿瘤特异性t细胞反应改善。核心活检的多参数原位免疫染色提示转移性病变中免疫细胞浸润改善。这些早期迹象表明晚期实体瘤患者的抗肿瘤活性有所改善,这鼓励了C. novyi-NT联合免疫检查点抑制剂的新试验。引文格式:philip Janku, Mrinal Gounder, Abdul Mohammad Pezeshki, Ravi Murthy, Andrea Wang-Gillam, Dale Shepard, David S. Hong, Sarina A. Piha-Paul, Anjali Raina, Alexey A. Leontovich, Gary DeCrescenzo, Brent L. Kreider, David Tung, Mary Varterasian, Halle H. Zhang, Khashayarsha Khazaie。难治性晚期实体瘤患者瘤内注射Clostridiumnovyi-NT孢子的首次人体临床试验:安全性、活性和免疫反应[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;癌症免疫学杂志2019;7(2增刊):摘要nr A011。
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Abstract A011: First-in-man clinical trial of intratumoral injection of Clostridiumnovyi-NT spores in patients with treatment-refractory advanced solid tumors: Safety, activity, and immune responses
Bacteriolytic strategies offer unique advantages to combat a broad range of cancers often refractive to conventional chemotherapies and/or radiotherapies. C. novyi-NT is an attenuated strain of Clostridium novyi, a spore-forming, gram-positive, obligate anaerobe that lacks a lethal alpha- toxin, expressed by the parental strain. When administered intravenously or intratumorally with percutaneous injection, C. novyi-NT colonizes and replicates within the hypoxic region of the tumors, eliciting robust, tumor-confined cell lysis. In this first-in-man phase 1 study, patients with injectable treatment-refractory solid tumors received a single intratumoral injection of C. novyi-NT spores across 6 dose cohorts (spore concentrations of 104, 3x104, 105, 3x105, 106, 3x106) using a 3+3 trial design. The primary endpoints were to assess the safety profile, the dose limiting toxicity, and the maximum tolerated dose of C. novyi-NT. Key secondary endpoints included assessments of the preliminary antitumor activity of the injected tumor, an overall response evaluated by RECIST v. 1.1, and the host immune and inflammatory response to C. novyi-NT. Twenty-four patients were enrolled between November, 2013 and April, 2017. A single intratumoral injection of C. novyi-NT led to germination and resultant tumor lysis of injected tumor masses in 46% of patients across all dosing cohorts. The cohort 5 dose of 106 spores was defined as the maximum tolerated dose. Dose-limiting toxicities were grade 4 sepsis and grade 4 gas gangrene (n=1), all in patients with germination. In the 22 evaluable patients, 21 (95%) had stable disease (SD) as the best response for the injected lesion (tumor shrinkage of > 10% was observed in 21% of patients) and 19 (86%) had overall SD as the best response per RECIST 1.1. C. novyi-NT injection resulted in transient serum cytokine responses consistent with inflammasome activity, activation of innate immunity, tissue remodeling, and angiogenesis. Tumor antigen specific ELISPOT assays pre- and post- treatment documented enhanced secretion of IFNγ and TNFα by circulating T-cells, indicating improved systemic tumor specific T-cell responses. Multiparametric in situ immunostaining of core biopsies suggested improved immune cell infiltration in metastatic lesions. These early signs of improved antitumor activity in patients with advanced solid tumors have encouraged a new trial of C. novyi-NT in combination with immune checkpoint inhibitors. Citation Format: Filip Janku, Mrinal Gounder, Abdul Mohammad Pezeshki, Ravi Murthy, Andrea Wang-Gillam, Dale Shepard, David S. Hong, Sarina A. Piha-Paul, Anjali Raina, Alexey A. Leontovich, Gary DeCrescenzo, Brent L. Kreider, David Tung, Mary Varterasian, Halle H. Zhang, Khashayarsha Khazaie. First-in-man clinical trial of intratumoral injection of Clostridiumnovyi-NT spores in patients with treatment-refractory advanced solid tumors: Safety, activity, and immune responses [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 A011.
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