白细胞介素-2在IV期黑色素瘤治疗中的作用:EORTC黑色素瘤合作小组项目。

U Keilholz, A M Eggermont
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引用次数: 0

摘要

目的:回顾欧洲癌症研究和治疗组织(EORTC)项目中关于IV期黑色素瘤患者使用白细胞介素(IL)-2的现有信息。患者和方法:收集了27项试验中631例患者的数据库,采用基于高剂量il -2的方案,为随机试验提供假设和有效的分层因素。随后,126名患者被纳入一项评估干扰素α (ifn - α)和IL-2的试验,有或没有顺铂,325名患者被纳入一项正在进行的EORTC试验(18951),以评估达卡巴嗪、顺铂和ifn - α,有或没有IL-2。结果:数据库显示,接受ifn - α和IL-2联合化疗或不联合化疗的患者的长期生存率为23%,5年生存率为13%。化疗的增加提高了反应率,但没有提高生存率。首个测试顺铂在晚期黑色素瘤化疗免疫治疗方案中的作用的随机试验显示,顺铂有缓解作用,但没有生存益处。目前的试验(EORTC 18951)正在测试IL-2对生存的影响,但仍不成熟。在转化研究项目中,我们有证据表明,在基于il -2的治疗后持续完全缓解的患者通过聚合酶链反应试验有残留疾病的证据,同时外周血中存在黑色素瘤反应性T细胞。结论:对IL-2在晚期黑色素瘤中的作用及一定程度上的机制的成熟研究结果正在出现。
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The role of interleukin-2 in the management of stage IV melanoma: the EORTC melanoma cooperative group program.

Purpose: To review the current information available from the European Organization for Research and Treatment of Cancer (EORTC) programs on the use of interleukin (IL)-2 in stage IV melanoma patients.

Patients and methods: A database from 631 patients treated within 27 trials with high-dose IL-2-based regimens was compiled to develop hypotheses and valid stratification factors for randomized trials. Subsequently, 126 patients were enrolled in a trial evaluating interferon alfa (IFN-alpha) and IL-2 with or without cisplatin, and 325 patients were enrolled in an ongoing EORTC trial (18951) to evaluate dacarbazine, cisplatin, and IFN-alpha, with or without IL-2.

Results: The database suggests long-term survival rates of 23% and a 5-year survival rate of 13% for patients receiving a combination of IFN-alpha and IL-2 with or without chemotherapy. The addition of chemotherapy improved response rate but not survival. The first randomized trial testing the role of cisplatin in a chemoimmunotherapy regimen for advanced melanoma revealed a palliative effect for cisplatin but no survival benefit. The current trial (EORTC 18951), which is testing the impact of IL-2 on survival, is still immature. In the translational research program, we have evidence that patients in continuous complete remission after IL-2-based treatment have evidence of residual disease by polymerase chain reaction assay and, at the same time, melanoma-reactive T cells are present in the peripheral blood.

Conclusion: Mature results defining the role and, to some extent, the mechanism of IL-2 in advanced melanoma are emerging.

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