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ATIM-26. IMMUNOLOGIC TRENDS ASSOCIATED WITH PATIENT OUTCOMES IN A PHASE 1 CLINICAL TRIAL OF TOCA 511 AND TOCA FC IN RECURRENT HIGH GRADE GLIOMA

机译:ATIM-26。复发性高度胶质瘤TOCA 511和TOCA FC一期临床试验中与患者结果相关的免疫学趋势

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摘要

Toca 511 (vocimagene amiretrorepvec) is a cancer selective, retroviral replicating vector encoding a codon optimized, heat stabilized cytosine deaminase that converts Toca FC (extended-release 5- fluorocytosine, 5-FC) into the anticancer agent 5-fluorouracil. Preclinical evidence demonstrates that the Toca 511 & Toca FC regimen kills cancer cells and immunosuppressive myeloid cells in the tumor microenvironment, leading to durable antitumor immune responses that can be adoptively transferred to untreated animals. In an ascending dose trial () in patients with recurrent high grade glioma (rHGG), Toca 511 was injected into the resection cavity walls at the time of resection, and then multiple courses of oral Toca FC were administered. Multiyear durable and complete responses by independent radiology review have been reported. Human immune monitoring results support an immunologic mechanism of action and identify potential biomarkers related to patient outcomes. Measurements included the quantification of peripheral blood and tumor infiltrating leukocyte subsets by flow cytometry, immunohistochemistry, and deconvolution of DNA and RNA sequencing data. In addition, systemic cytokine levels were assessed in peripheral blood serum by multiplex digital ELISA. Univariate comparisons and multivariate models revealed immunologic trends associated with patient outcomes. Pre-treatment tumor infiltrating cell subsets, quantified via deconvolution of RNA sequencing data, were associated with both objective responses and survival. Subsequent exploratory models applied to selected patient data indicate that a combined biomarker using mRNA signatures from multiple leukocyte subsets may predict patient outcomes with high sensitivity and selectivity. In addition, post-treatment serum cytokine time-course results suggest that differences and temporal modulations are associated with both objective response and survival. These results support an immune-related mechanism of action for the Toca 511 & Toca FC regimen. Potentially predictive and/or prognostic biomarkers of patient outcomes will be evaluated in the ongoing randomized Phase 3 Toca 5 trial in patients with rHGG ().
机译:Toca 511(vocimagene amiretrorepvec)是一种癌症选择性逆转录病毒复制载体,编码经过密码子优化,热稳定的胞嘧啶脱氨酶,可将Toca FC(缓释5-氟胞嘧啶,5-FC)转化为抗癌剂5-氟尿嘧啶。临床前证据表明,Toca 511和Toca FC方案可杀死肿瘤微环境中的癌细胞和免疫抑制性髓样细胞,从而导致持久的抗肿瘤免疫反应,可以过继转移至未经治疗的动物。在复发性高级别神经胶质瘤(rHGG)患者的递增剂量试验()中,在切除时将Toca 511注入切除腔壁,然后进行多疗程的口服Toca FC。据报道,经过独立的放射学审查,多年耐用和完整的反应。人体免疫监测结果支持免疫作用机制,并确定与患者预后相关的潜在生物标志物。测量包括通过流式细胞术,免疫组织化学以及DNA和RNA测序数据的解卷积来量化外周血和肿瘤浸润的白细胞亚群。另外,通过多重数字ELISA评估外周血血清中的全身细胞因子水平。单变量比较和多变量模型揭示了与患者预后相关的免疫学趋势。通过对RNA测序数据进行反卷积量化,对治疗前的肿瘤浸润细胞亚群与客观反应和生存率相关。随后应用于选定患者数据的探索性模型表明,使用来自多个白细胞亚群的mRNA签名的组合生物标志物可以高灵敏度和选择性地预测患者预后。此外,治疗后血清细胞因子的时程结果表明,差异和时间调节与客观反应和生存相关。这些结果支持了Toca 511和Toca FC方案的免疫相关作用机制。在正在进行的rHGG患者的随机3期Toca 5试验中,将评估患者预后的潜在预测和/或预后生物标志物()。

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