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High-dose regimen of interleukin-2 and interferon-alpha in combination with lymphokine-activated killer cells in patients with metastatic renal cell cancer

机译:大剂量白介素2和干扰素-α联合淋巴因子激活的杀伤细胞治疗转移性肾细胞癌患者

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摘要

textabstractSeventy-two patients with metastatic renal cell cancer were treated with the combination of high-dose interleukin-2 (IL2), interferon-alpha (IFNa), and lymphokine-activated killer cells (LAK). Seventeen patients were entered in a feasibility part of the study (protocol 1) and 55 in an efficacy part (protocol 2). Protocol 2 differed from protocol 1 in the addition of IFNa to the first 5 days of IL2 infusion. Each patient was planned to receive two induction cycles. IL2, 18 MIU/m2/day, was administered continuously i.v. on days 1-5, and IFNa, 5 MIU/m2/day (protocol 2), was administered i.m. on days 1-5, followed by three daily lymphaphereses on days 7-9. On day 12, treatment was resumed with IL2 and IFNa on days 12-15 and LAK reinfusions on days 12-14. In protocol 1, three complete (CR) and one partial (PR) responses were achieved (response rate 24%). The median duration of response and the median survival were 18.1 and 13.9 months, respectively. The 3-year survival was 35%. Of the 51 evaluable patients in protocol 2, 6 achieved a CR and 13 a PR (response rate 37%). The median duration of response was 11.1 months. The median survival was 16.9 months. The 3-year survival was 35%. There were three treatment-related deaths. Other severe toxicities included hypotension, cardiotoxicity, pulmonary edema, renal toxicity, and infectious complications. In the two induction cycles, only 54 and 42% of the planned doses could be administered. We conclude that the use of high-dose regimens of IL2 and IFNa is not warranted, unless we can define more accurately which patients may experience long-term survival as a result of treatment.
机译:七十二例转移性肾细胞癌患者接受了大剂量白介素2(IL2),干扰素-α(IFNa)和淋巴因子激活的杀伤细胞(LAK)的联合治疗。在该研究的可行性部分(协议1)输入了17位患者,在功效部分(协议2)输入了55位患者。方案2与方案1的不同之处在于,在IL2输注的前5天中添加了IFNa。每个患者计划接受两个诱导周期。 IL2,18 MIU / m2 /天,连续静脉内给药。在第1-5天,IFNa以5MIU / m 2 /天(方案2)的方式在当日给药。在1-5天进行第3天,然后在7-9天进行每天3次淋巴转移。在第12天,在第12-15天恢复用IL2和IFNa治疗,在第12-14天恢复LAK输注。在方案1中,实现了三个完全(CR)和一个部分(PR)响应(响应率为24%)。中位缓解时间和中位生存期分别为18.1和13.9个月。 3年生存率为35%。在方案2中的51名可评估患者中,有6例获得CR,13例PR(反应率37%)。中位缓解时间为11.1个月。中位生存期为16.9个月。 3年生存率为35%。有三例与治疗有关的死亡。其他严重毒性包括低血压,心脏毒性,肺水肿,肾毒性和感染性并发症。在两个诱导周期中,只能施用计划剂量的54%和42%。我们得出的结论是,除非需要更准确地定义哪些患者可以通过治疗获得长期生存,否则不建议使用大剂量的IL2和IFNa。

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