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首页> 外文期刊>Annals of surgical oncology >Adoptive immunotherapy with tumor-infiltrating lymphocytes and subcutaneous recombinant interleukin-2 plus interferon alfa-2a for melanoma patients with nonresectable distant disease: a phase I/II pilot trial. Melanoma Istituto Scientifico Tumori Gro
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Adoptive immunotherapy with tumor-infiltrating lymphocytes and subcutaneous recombinant interleukin-2 plus interferon alfa-2a for melanoma patients with nonresectable distant disease: a phase I/II pilot trial. Melanoma Istituto Scientifico Tumori Gro

机译:I / II期先导试验:采用肿瘤浸润淋巴细胞和皮下重组白介素2加上干扰素Alfa-2a的过继免疫疗法,用于无法切除的远处疾病的黑色素瘤患者。黑色素瘤科学研究所

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摘要

BACKGROUND: On the basis of our previous experience, we designed this study to determine the activity and toxicity of outpatient treatment with autologous tumor-infiltrating lymphocytes (TIL) together with intermediate-dose recombinant interleukin-2 (rIL-2) and low-dose recombinant interferon alfa-2a (rIFN-alpha2a), for patients with metastatic melanoma. METHODS: Between April 1992 and October 1994, we processed 38 melanoma samples derived from 36 patients with metastases. Proliferative cultures of expanded lymphocytes (TIL) were infused only once into patients with metastatic melanoma. rIL-2 was administered subcutaneously for 1 month, starting on the day of TIL infusion, at an escalating dose of 6-18 x 10(6) IU/m2/day for the first week and at the maximum-tolerated dose for the subsequent 3 weeks and then, after a 15-day interval, for 1 week/month for 3 months. rIFN-alpha2a was administered subcutaneously at 3 X 10(6) IU three times each week until progression. RESULTS: Of 38 melanoma samples, 19 (50%) resulted in proliferative cultures and were infused. The median number of expanded lymphocytes was 18 x 10(9) (range, 1-43 x 10(9)), and the median period of culture was 52 days (range, 45-60). rIL-2 was administered at doses ranging between 6 and 18 x 10(6) IU/m2/day. Toxicity was mild or moderate, and no life-threatening side effects were encountered. Two of 19 treated patients experienced complete responses of their metastatic sites (soft tissue), 10 had stable disease, and 7 showed progressive disease. The response rate was 11% (95% confidence interval, 2-35%). CONCLUSIONS: Outpatient treatment with TIL plus rIL-2 and rIFN-alpha2a is feasible, although, within the context of the small sample size, the activity of the combination was no different from the reported activity of any of the components used alone.
机译:背景:根据我们以往的经验,我们设计了这项研究,以确定自体肿瘤浸润淋巴细胞(TIL)与中等剂量重组白介素2(rIL-2)和小剂量门诊治疗的活性和毒性。重组干扰素α-2a(rIFN-alpha2a),用于转移性黑色素瘤患者。方法:从1992年4月到1994年10月,我们处理了38例来自36例转移灶患者的黑色素瘤样品。转移性黑色素瘤患者仅需输注一次增殖淋巴细胞(TIL)的增殖培养物。从TIL输注之日起,皮下注射rIL-2,持续1个月,第1周以6-18 x 10(6)IU / m2 / day的递增剂量给药,随后的最大耐受剂量3周,然后在间隔15天后,每月1周,共3个月。每周3次以3 X 10(6)IU皮下注射rIFN-alpha2a,直至进展。结果:在38个黑色素瘤样本中,有19个(50%)导致了增殖培养并被注入。扩增淋巴细胞的中位数为18 x 10(9)(范围为1-43 x 10(9)),培养的中位数为52天(范围为45-60)。 rIL-2的剂量介于6到18 x 10(6)IU / m2 /天之间。毒性是轻度或中度的,没有遇到危及生命的副作用。 19例接受治疗的患者中有2例对其转移部位(软组织)完全反应,其中10例疾病稳定,7例疾病进展。回应率为11%(95%置信区间,2-35%)。结论:尽管在小样本量的情况下,联合用药的活性与单独使用的任何成分的报道活性无差异,但用TIL加rIL-2和rIFN-α2a进行门诊治疗是可行的。

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