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免疫基因组分析:BCG 无应答性非肌肉浸润性膀胱癌对 ALT-803(IL-15 类似物)的优异应答者:病例系列和文献复习。

Immunogenomic Analysis of Exceptional Responder to ALT-803 (IL-15 Analogue) in BCG Unresponsive Nonmuscle Invasive Bladder Cancer: A Case Series and Review of the Literature.

机构信息

University of Hawaii Cancer Center, Clinical & Translational Research Program, Honolulu, HI.

Departments of Radiation Oncology.

出版信息

J Immunother. 2019 Nov/Dec;42(9):354-358. doi: 10.1097/CJI.0000000000000269.

Abstract

The clinical validity and utility of complex biomarkers have not been extensively studied in bladder cancer. Three patients with nonmuscle invasive bladder cancer [1 patient with an exceptional response; complete response (CR) for 30 months] who failed intravesical BCG were evaluated using an NYS CLEP approved assay, Immune Report Card, which measures programmed death-ligand 1 expression, CD8 T-cell infiltration pattern, mutational burden, and gene expression of 51 immune-related transcripts using RNA-Seq. Patients were tested before being treated under our expanded access protocol for intravesical BCG with ALT-803. Subject 1 had failed his fourth line of therapy, subject 2 had failed only his first line of therapy, and subject 3 had failed his seventh line of therapy. Surprisingly, subject 1 had an unusually prolonged CR which lasted 30 months; subject 2 had the persistent and recurrent disease until 12 months when he then developed a CR; subject 3 had disease recurrence at 3 months, along with progression noted at 6 months. Immunomutational status was extensively evaluated to identify potential alterations that might play a role as predictive markers for subject 1, who had an exceptional response. Compared with subject 3, tumor in subject 1 demonstrated a high level of expression for CTLA4 (immunosuppression) and CD39 (immunosuppressive). Together, an immunosuppressive tumor environment in nonmuscle invasive bladder cancer that have failed prior BCG may respond better to interleukin-15 immunotherapy compared with tumors without an immunosuppressive environment.

摘要

在膀胱癌中,复杂生物标志物的临床有效性和实用性尚未得到广泛研究。三名非肌肉浸润性膀胱癌患者[1 名患者有异常反应;完全缓解(CR)持续 30 个月],在使用 NYS CLEP 批准的检测方法 Immune Report Card 进行评估后,他们对卡介苗的膀胱内治疗失败。该检测方法可测量程序性死亡配体 1 表达、CD8 T 细胞浸润模式、突变负担以及 51 个免疫相关转录本的基因表达,采用的是 RNA-Seq 技术。在根据我们的扩大准入方案用 ALT-803 进行膀胱内卡介苗治疗之前,对患者进行了检测。1 号患者已经接受了第四线治疗,2 号患者只接受了一线治疗,3 号患者接受了第七线治疗。令人惊讶的是,1 号患者的 CR 持续时间异常延长,持续了 30 个月;2 号患者的疾病持续存在并复发,直到 12 个月时他才出现 CR;3 号患者在 3 个月时出现疾病复发,并在 6 个月时出现进展。对免疫突变状态进行了广泛评估,以确定可能作为预测标志物发挥作用的潜在改变,该标志物可能与出现异常反应的 1 号患者有关。与 3 号患者相比,1 号患者的肿瘤 CTLA4(免疫抑制)和 CD39(免疫抑制)表达水平较高。总之,在卡介苗治疗失败的非肌肉浸润性膀胱癌中,与没有免疫抑制环境的肿瘤相比,先前存在免疫抑制环境的肿瘤可能对白细胞介素-15 免疫疗法的反应更好。

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