Dréno Brigitte, Nguyen Jean-Michel, Khammari Amir, Pandolfino Marie Christine, Tessier Marie Hélène, Bercegeay Sylvain, Cassidanius Alain, Lemarre Philippe, Billaudel Sylviane, Labarrière Nathalie, Jotereau Francine
Skin Cancer Unit, CHR Hôtel Dieu, Nantes, 44093 Nantes, France.
Cancer Immunol Immunother. 2002 Nov;51(10):539-46. doi: 10.1007/s00262-002-0315-1. Epub 2002 Sep 19.
The aim of this study was to demonstrate the interest of using tumor-infiltrating lymphocytes (TIL) as adjuvant therapy for stage III (regional lymph nodes) melanoma. After lymph node excision, patients without any detectable metastases were randomly assigned to receive either TIL plus interleukin-2 (IL-2) for 2 months, or IL-2 only. The primary endpoint was determination of the duration of the relapse-free interval. Eighty-eight patients determined as eligible for treatment were enrolled in the study. After a median follow-up of 46.9 months, for the study population the analysis did not show a significant extension of the relapse-free interval or overall survival. However, a significant interaction ( P<0.001) was found between the treatment and the number of invaded lymph nodes. In the group with only one invaded lymph node, the estimated relapse rate was significantly lower ( P(adjusted)=0.0285) and the overall survival was increased ( P(adjusted)=0.039) in the TIL+IL-2 arm compared with the IL-2 only arm. No differences between the two arms, either as regards the duration of disease-free survival or overall survival, were noted in the group with more than one invaded lymph node whatever the number of invaded lymph nodes. Treatment was compatible with normal daily activity. This study demonstrates for the first time that the efficiency of TIL in stage III melanoma (AJCC) is directly related to the number of invaded lymph nodes, indicating that tumor burden might be a crucial factor in the efficacy and/or in vitro expansion of T cells specific for autologous tumor antigen, a finding which could be of value in future vaccine development for the treatment of melanoma.
本研究的目的是证明使用肿瘤浸润淋巴细胞(TIL)作为III期(区域淋巴结)黑色素瘤辅助治疗的益处。在淋巴结切除术后,将无任何可检测到转移的患者随机分配,分别接受TIL加白细胞介素-2(IL-2)治疗2个月,或仅接受IL-2治疗。主要终点是确定无复发生存期的持续时间。88名被确定符合治疗条件的患者纳入了该研究。在中位随访46.9个月后,对于研究人群,分析未显示无复发生存期或总生存期有显著延长。然而,在治疗与受累淋巴结数量之间发现了显著的交互作用(P<0.001)。在只有一个受累淋巴结的组中,与仅接受IL-2治疗的组相比,TIL+IL-2组的估计复发率显著更低(P(校正)=0.0285),总生存期有所延长(P(校正)=0.039)。在受累淋巴结多于一个的组中,无论受累淋巴结数量多少,两组在无病生存期或总生存期的持续时间方面均未发现差异。治疗与正常日常活动相容。本研究首次证明,TIL对III期黑色素瘤(美国癌症联合委员会分期)的疗效与受累淋巴结数量直接相关,这表明肿瘤负荷可能是针对自体肿瘤抗原的T细胞疗效和/或体外扩增的关键因素,这一发现可能对未来黑色素瘤治疗疫苗的开发具有价值。