Center for Cancer Immune Therapy, Department of Hematology, Herlev Hospital, University of Copenhagen, Herlev, Denmark. Department of Oncology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.
Department of Plastic Surgery, Herlev Hospital, University of Copenhagen, Herlev, Denmark.
Clin Cancer Res. 2016 Aug 1;22(15):3734-45. doi: 10.1158/1078-0432.CCR-15-1879. Epub 2016 Mar 22.
PURPOSE: Adoptive cell transfer therapy (ACT) based on autologous tumor-infiltrating lymphocytes (TIL) has achieved impressive clinical results in several phase I and II trials performed outside of Europe. Although transient, the toxicities associated with high-dose (HD) bolus IL2 classically administered together with TILs are severe. To further scrutinize whether similar results can be achieved with lower doses of IL2, we have carried out a phase I/II trial of TIL transfer after classical lymphodepleting chemotherapy followed by an attenuated IL2 regimen. EXPERIMENTAL DESIGN: Twenty-five patients with progressive treatment-refractory metastatic melanoma, good clinical performance, age < 70 years, and at least one resectable metastasis were eligible. TIL infusion was preceded by standard lymphodepleting chemotherapy and followed by attenuated doses of IL2 administered in an intravenous, continuous decrescendo regimen (ClinicalTrials.gov Identifier: NCT00937625). RESULTS: Classical IL2-related toxicities were observed but patients were manageable in a general oncology ward without the need for intervention from the intensive care unit. RECIST 1.0 evaluation displayed three complete responses and seven partial responses (ORR 42%). Median overall survival was 21.8 months. Tumor regression was associated with a higher absolute number of infused tumor-reactive T cells. Moreover, induction and persistence of antimelanoma T-cell responses in the peripheral blood was strongly correlated to clinical response to treatment. CONCLUSIONS: TIL-ACT with a reduced IL2 decrescendo regimen results in long-lasting complete responses in patients with treatment-refractory melanoma. Larger randomized trials are needed to elucidate whether clinical efficacy is comparable with TIL-ACT followed by HD bolus IL2. Clin Cancer Res; 22(15); 3734-45. ©2016 AACR.
目的:基于自体肿瘤浸润淋巴细胞(TIL)的过继细胞转移疗法(ACT)在欧洲以外进行的多项 I 期和 II 期试验中取得了令人瞩目的临床结果。尽管是短暂的,但与经典联合 TIL 应用的高剂量(HD)IL2 相关的毒性非常严重。为了进一步研究是否可以使用较低剂量的 IL2 获得类似的结果,我们进行了一项 I/II 期试验,即在经典淋巴耗竭化疗后进行 TIL 转移,然后采用减弱的 IL2 方案。
实验设计:25 名患有进展性治疗耐药性转移性黑色素瘤、临床状况良好、年龄<70 岁且至少有一处可切除转移灶的患者符合条件。TIL 输注前进行标准淋巴耗竭化疗,然后采用静脉内、连续递减方案给予减弱剂量的 IL2(ClinicalTrials.gov 标识符:NCT00937625)。
结果:观察到经典 IL2 相关毒性,但患者可在普通肿瘤病房中进行管理,无需转入重症监护病房干预。RECIST 1.0 评估显示 3 例完全缓解和 7 例部分缓解(ORR 42%)。中位总生存期为 21.8 个月。肿瘤消退与输注的肿瘤反应性 T 细胞的绝对数量增加相关。此外,外周血中抗黑色素瘤 T 细胞反应的诱导和持续与治疗的临床反应强烈相关。
结论:采用减少的 IL2 递减方案的 TIL-ACT 可导致治疗耐药性黑色素瘤患者产生持久的完全缓解。需要更大规模的随机试验来阐明与 HD 静脉推注 IL2 后进行 TIL-ACT 相比,临床疗效是否相当。临床癌症研究;22(15);3734-45. ©2016 AACR.
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