免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:NIVO-TIL: combination anti-PD-1 therapy and adoptive T-cell transfer in untreated metastatic melanoma: an exploratory open-label phase I trial.
NIVO-TIL: combination anti-PD-1 therapy and adoptive T-cell transfer in untreated metastatic melanoma: an exploratory open-label phase I trial.
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对于抗PD-1治疗有应答的转移性黑色素瘤患者,瘤内CD8+ T细胞增殖与临床应答直接相关,因此TIL(肿瘤浸润淋巴细胞)成为与PD-1抑制剂联合治疗的关注对象;PD-1抑制剂是转移性黑色素瘤治疗公认的金标准。本试验旨在评估纳武利尤单抗(一种PD-1抑制剂)与TIL过继T细胞序贯联合治疗转移性黑色素瘤患者的安全性和疗效。
我们开展了一项探索性、前瞻性、单中心、开放标签、非随机、非对照I/II期研究。纳入10例既往未接受治疗的晚期黑色素瘤患者。治疗方案为新辅助抗PD-1治疗,随后两次输注TIL,再进行第二阶段抗PD-1治疗。 结果与阐释:在4例接受自体TIL联合纳武利尤单抗治疗的患者中,3例(75%)达到客观缓解(其中研究结束时两例达到部分缓解〔PR〕、两例达到完全缓解〔CR〕);另有一例在研究结束时达到CR。在这3例患者中,纳武利尤单抗疗程结束后、接受任何TIL输注前,有1例达到PR,另2例病情稳定(SD),这进一步说明TIL输注后肿瘤应答的重要性。上述应答均持久,持续时间为9个月至3.4年。
BACKGROUND AND PURPOSE: In patients with metastatic melanoma who respond to anti-PD-1 therapy, the proliferation of intra-tumour CD8+ T cells is directly correlated with the clinical response, making tumour-infiltrating lymphocytes (TILs) a treatment of interest in combination with a PD-1 inhibitor, which is the undisputed gold standard in the management of metastatic melanoma. The aim of this trial was, therefore, to evaluate the safety and efficacy of sequential combination therapy consisting of nivolumab (a PD-1 inhibitor) and TILs adoptive T cells in patients with metastatic melanoma. MATERIALS AND METHODS: We performed an exploratory, prospective, single-centre, open-label, non-randomised, uncontrolled phase I/II study. We enrolled 10 previously untreated patients with advanced melanoma. The treatment regimen was neoadjuvant anti-PD-1 therapy followed by 2 injections of TILs and a second sequence of anti-PD-1 therapy. RESULTS AND INTERPRETATION: Among the four patients who received the autologous TILs + nivolumab combination, three (75%) achieved an objective response (two achieved a partial response [PR] at the end of the study, two achieved a complete response [CR]), and one achieved a CR at the end of the study. Among these three patients, one had a PR, and two had stable disease (SD) after the nivolumab course and before any TILs administration, reinforcing the importance of the tumour response after TILs injection. These responses were persistent, ranging from 9 months to 3.4 years.
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