Dermato-cancérology Department, CHU Nantes, CIC 1413, CRCINA, INSERM, University of Nantes, CHU Nantes-Hôtel-Dieu, 1 Place Alexis Ricordeau, 44093, Nantes Cedex 01, France.
SEME, PHU11, Saint-Jacques Hospital, CRCINA, INSERM, University of Nantes, Nantes, France.
Cancer Immunol Immunother. 2020 Aug;69(8):1663-1672. doi: 10.1007/s00262-020-02572-1. Epub 2020 Apr 18.
Adoptive tumor-infiltrating lymphocytes (TIL) therapy and interleukin-2 (IL-2) have been investigated in melanoma.
To confirm previously observed preventive effects of TIL + IL2 in a subgroup of patients with relapsing metastatic stage III melanoma.
Open-label, randomized two-group, multicenter five-year trial in adult stage III melanoma patients with only one invaded lymph node after complete resection. Patients received TIL + IL2 or abstention. TIL + IL2 was administered within 8 weeks after lymph node resection and 4 weeks after. Disease-free survival was assessed every 2 months up to month 18, every 3 months up to month 36 and every 4 months up to 5 years. A once-a-year follow-up was scheduled beyond the five-year follow-up. Safety was assessed throughout the trial.
Overall, 49 patients accounted for the modified intent-to-treat and 47 for the PP. Slightly more male than female patients participated; mean age was 57.7 ± 11.4 years in the TIL + IL2 group and 53.5 ± 13.0 years in the abstention group. After 5 years of follow-up, 11/26 patients in the TIL + IL2 group and 13/23 in the abstention group had relapsed. There was no statistical difference between the groups (HR: 0.63 CI 95% [0.28-1.41], p = 0.258), nine patients in the TIL + IL2 and 11 in the abstention group died with no significant difference between the two groups (HR: 0.65 CI95% [0.27 - 1.59], p = 0.34). Safety was good.
We did not confirm results of a previous trial. However, ulceration of the primary melanoma may be considered predictive of the efficacy of TIL in melanoma in adjuvant setting, in a manner similar to interferon α.
过继性肿瘤浸润淋巴细胞(TIL)治疗和白细胞介素-2(IL-2)已在黑色素瘤中进行了研究。
在复发转移性 III 期黑色素瘤的亚组患者中确认先前观察到的 TIL+IL2 的预防作用。
一项开放性、随机、两组、多中心、五年期临床试验,纳入完全切除后仅有一个受累淋巴结的成人 III 期黑色素瘤患者。患者接受 TIL+IL2 或不治疗。TIL+IL2 在淋巴结切除后 8 周内和 4 周后给药。无病生存期每 2 个月评估一次,直到第 18 个月,每 3 个月评估一次,直到第 36 个月,每 4 个月评估一次,直到 5 年。在 5 年随访后,每年进行一次随访。整个试验过程中评估安全性。
总体而言,49 例患者符合修改后的意向治疗,47 例患者符合 PP。参与研究的患者中男性略多于女性;TIL+IL2 组患者的平均年龄为 57.7±11.4 岁,而对照组患者的平均年龄为 53.5±13.0 岁。5 年随访后,TIL+IL2 组 26 例患者中有 11 例复发,对照组 23 例患者中有 13 例复发。两组之间无统计学差异(HR:0.63,95%CI[0.28-1.41],p=0.258),TIL+IL2 组有 9 例患者和对照组有 11 例患者死亡,两组之间无显著差异(HR:0.65,95%CI[0.27-1.59],p=0.34)。安全性良好。
我们没有证实之前试验的结果。然而,原发性黑色素瘤的溃疡可能被认为是 TIL 在辅助治疗黑色素瘤中的疗效的预测因子,这与干扰素 α 的作用方式类似。