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[辅助免疫疗法降低IV期黑色素瘤的进展速率并诱导肿瘤特异性免疫反应]

[Decreased rate of progression and induction of tumor-specific immune response by adjuvant immunotherapy in stage IV melanoma].

作者信息

Enk A H, Wölfel T, Knop J

机构信息

Universitäts-Hautklinik Mainz.

出版信息

Hautarzt. 1999 Feb;50(2):103-8. doi: 10.1007/s001050050872.

Abstract

Stage IV melanoma is still a disease with poor prognosis. Although modern chemo- or chemoimmunotherapies give high response rates in stage IV patients, remissions are usually followed by fast relapses. In order to avoid early relapses after chemotherapy, patients with stage IV disease and either stable disease or partial or complete remission following therapy were treated with 9 million IU IFN alpha subcutaneously 5 times weekly and 6 million IU IL-2 subcutaneously twice weekly. Compared with untreated controls, the rate of progression in the treatment group was reduced from 95% to 35%. Also, time to progression was significantly prolonged. Median survival times in the control group were 25 weeks, whereas median survival time in the treatment group has not yet been reached. Furthermore, TNF-ELISPOT assays showed a significant increase in MAGE-3 reactive cytotoxic T-cells in the treatment, but not in the control group. Thus, immunotherapy in stage IV disease seems to prolong survival in melanoma patients.

摘要

IV期黑色素瘤仍然是一种预后较差的疾病。尽管现代化学疗法或化学免疫疗法在IV期患者中具有较高的缓解率,但缓解后通常会迅速复发。为了避免化疗后早期复发,对患有IV期疾病且病情稳定或治疗后部分或完全缓解的患者,给予900万国际单位的α干扰素皮下注射,每周5次,以及600万国际单位的白细胞介素-2皮下注射,每周2次。与未治疗的对照组相比,治疗组的疾病进展率从95%降至35%。而且,疾病进展时间显著延长。对照组的中位生存时间为25周,而治疗组的中位生存时间尚未达到。此外,肿瘤坏死因子酶联免疫斑点分析显示,治疗组中MAGE-3反应性细胞毒性T细胞显著增加,而对照组中没有。因此,IV期疾病的免疫疗法似乎可以延长黑色素瘤患者的生存期。

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