Abstract A002: Autologous Tcells transduced with the affinity enhanced NY-ESO-1c259TCR in patients with synovial sarcoma expressing low levels of the NY-ESO-1 antigen

D. Araujo, S. D’Angelo, G. Demetri, M. Druta, J. Glod, W. Chow, W. Tap, J. Senra, R. Abbott, E. V. Winkle, K. Chagin, M. Maroto, E. Norry, M. Iyengar, T. Trivedi, A. Gerry, R. Amado, C. Mackall
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引用次数: 0

Abstract

Background: NY-ESO-1c259 is an affinity optimized TCR recognizing an NY-ESO-1-derived peptide complexed with HLA-A*02 (SPEAR T-cells). NY-ESO-1c259TCR therapy induced responses in ~50% of patients whose tumors express high level NY-ESO-1 (NCT01343043). Here we report on preclinical studies of TCR activity and results from a cohort of patients whose tumors express low NY-ESO-1 levels. Methods: T-cell response against tumor-derived cell lines with differential NY-ESO-1 expression levels was assessed by ELISA. Patients had selected HLA subtypes (HLA-A*02:01, 02:05, 02:06) and advanced NY-ESO-1+ SS. In this cohort, tumors express NY-ESO-1 at ≥ 1+ in > 1% but 1×10e4 mRNA copies/10e6 reference gene transcripts. Ten patients in this cohort have been treated (as of 23Nov17). One died due to disease progression 2 days post infusion. Four have had a partial response (ORR 40%), and median duration of response was 8.5 weeks (range, 8-13). Antigen expression level by IHC (% 1+, 2+, and/or 3+), best overall response (BOR) by RECIST v1.1, and transduced cell expansion (copies/microgram DNA) are listed below for the 9 evaluable patients: Pt 264, 30% 1+/2+, PR, 86320; Pt 313, 90% 1+, PR, 45430; Pt 325, 10% 2+, PR, 13365; Pt 331, 40% 1+, 10% 2+, 10% 3+, PR, 197546; Pt 324, 50% 1+, 10% 2+, SD, 133334; Pt 305, 5% 1+, 5% 2+, 5% 3+, SD, 74855; Pt 322, 50% 1+, 10% 2+, SD, 54569; Pt 323, 20% 1+, 10% 2+, SD, 50912; Pt 211, 10% 1+, 20% 2+, 20% 3+, PD, 22627. Conclusions: In vitro assays can assess mRNA levels and protein expression of target antigen required for T-cell activation and cytotoxicity, predicting expression levels required for anti-tumor activity in vivo. The patient data suggest that affinity optimized TCRs can be used to treat tumors with low target antigen expression. Citation Format: Dejka Araujo, Sandra D9Angelo, George Demetri, Mihaela Druta, John Glod, Warren Chow, William Tap, Joana Senra, Rachel Abbott, Erin Van Winkle, Karen Chagin, Miguel Maroto, Elliot Norry, Malini Iyengar, Trupti Trivedi, Andrew Gerry, Rafael Amado, Crystal Mackall. Autologous Tcells transduced with the affinity enhanced NY-ESO-1c259TCR in patients with synovial sarcoma expressing low levels of the NY-ESO-1 antigen [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 A002.
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摘要:自体t细胞在表达低水平NY-ESO-1抗原的滑膜肉瘤患者中以亲和力增强的NY-ESO-1c259TCR转导
背景:NY-ESO-1c259是一种亲和优化的TCR,识别ny - eso -1衍生的肽与HLA-A*02 (SPEAR t细胞)络合。NY-ESO-1c259TCR治疗在约50%的肿瘤表达高水平NY-ESO-1 (NCT01343043)的患者中诱导了应答。在这里,我们报告了TCR活性的临床前研究和来自肿瘤表达低NY-ESO-1水平的患者队列的结果。方法:采用ELISA法观察t细胞对NY-ESO-1表达水平差异的肿瘤源性细胞系的反应。患者有选择的HLA亚型(HLA- a *02:01, 02:05, 02:06)和晚期NY-ESO-1+ SS,在该队列中,肿瘤表达NY-ESO-1≥1+,> 1%,但1×10e4 mRNA拷贝数/10e6参考基因转录本。该队列中已有10例患者接受治疗(截至2017年11月23日)。1例患者在输注后2天因疾病进展死亡。4例有部分缓解(ORR 40%),中位缓解持续时间为8.5周(范围8-13周)。9例可评估患者的免疫组化抗原表达水平(% 1+,2+和/或3+),RECIST v1.1的最佳总反应(BOR)和转导细胞扩增(拷贝数/微克DNA)如下:Pt 264, 30% 1+/2+, PR, 86320;Pt 313, 90% 1+, PR, 45430;Pt 325, 10% 2+, PR, 13365;Pt 331, 40% 1+, 10% 2+, 10% 3+, PR, 197546;Pt 324, 50% 1+, 10% 2+, SD, 133334;Pt 305, 5% 1+, 5% 2+, 5% 3+, SD, 74855;Pt 322, 50% 1+, 10% 2+, SD, 54569;Pt 323, 20% 1+, 10% 2+, SD, 50912;Pt 211, 10% 1+, 20% 2+, 20% 3+, PD, 22627。结论:体外检测可以评估t细胞活化和细胞毒性所需靶抗原的mRNA水平和蛋白表达,预测体内抗肿瘤活性所需的表达水平。患者数据表明,亲和性优化的tcr可用于治疗低靶抗原表达的肿瘤。引文格式:Dejka Araujo, Sandra D9Angelo, George Demetri, Mihaela Druta, John Glod, Warren Chow, William Tap, Joana Senra, Rachel Abbott, Erin Van Winkle, Karen Chagin, Miguel Maroto, Elliot Norry, Malini Iyengar, Trupti Trivedi, Andrew Gerry, Rafael Amado, Crystal Mackall。自体t细胞在表达低水平NY-ESO-1抗原的滑膜肉瘤患者中以亲和力增强的NY-ESO-1c259TCR转导[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;癌症免疫杂志2019;7(2增刊):摘要nr A002。
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