Keilholz U, Conradt C, Legha S S, Khayat D, Scheibenbogen C, Thatcher N, Goey S H, Gore M, Dorval T, Hancock B, Punt C J, Dummer R, Avril M F, Bröcker E B, Benhammouda A, Eggermont A M, Pritsch M
Department of Medicine III (Hematology/Oncology/Transfusion Medicine), University Hospital Benjamin Franklin, Free University Berlin, Germany.
J Clin Oncol. 1998 Sep;16(9):2921-9. doi: 10.1200/JCO.1998.16.9.2921.
In patients with stage IV melanoma, durable responses have been reported with treatment regimens that involve high-dose interleukin-2 (IL-2). We analyze long-term results of 631 melanoma patients from 12 institutions who had received IL-2 alone, in combination with interferon alfa 2a or 2b (IFNalpha), or with cytotoxic drugs.
Case records that contained pretreatment parameters, response data, and updated survival information were collected. After univariate analysis, the multivariate evaluation of the impact of pretreatment parameters on response and survival was performed by logistic regression and Cox's regression, respectively.
Patients were divided into four groups according to treatment: IL-2 alone (n=117), IL-2 and chemotherapy (n=49), IL-2 and IFNalpha (n=153), and IL-2, chemotherapy, and IFNalpha (n=312). The median survival of all patients was 10.5 months and the 2- and 5-year survival rates were 19.9% and 10.4%, respectively. Independent prognostic factors for response and survival were entirely different, treatment group being the only significant factor for response, and serum lactate dehydrogenase (LDH), metastatic site, and performance predicting survival. The addition of IFNalpha to IL-2 was associated with prolonged survival, but the effect of additional chemotherapy was less obvious.
Serum LDH, metastatic site, and performance status are useful stratification factors for randomized trials in metastatic melanoma. The improved long-term survival rates observed in melanoma patients treated with IL-2/IFNalpha-containing regimens are notable in contrast to the reported 5-year survival rates of 2% to 6% achieved with chemotherapy, but because selection bias cannot be ruled out, the impact of IL-2, as well as all other components of the treatment regimens, on survival needs to be confirmed in prospective randomized trials.
在IV期黑色素瘤患者中,已报道高剂量白细胞介素-2(IL-2)治疗方案可产生持久反应。我们分析了来自12个机构的631例黑色素瘤患者接受单独IL-2、联合干扰素α2a或2b(IFNα)或细胞毒性药物治疗后的长期结果。
收集包含预处理参数、反应数据和更新生存信息的病例记录。单因素分析后,分别通过逻辑回归和Cox回归对预处理参数对反应和生存的影响进行多因素评估。
根据治疗方法将患者分为四组:单独使用IL-2(n = 117)、IL-2与化疗联合(n = 49)、IL-2与IFNα联合(n = 153)以及IL-2、化疗与IFNα联合(n = 312)。所有患者的中位生存期为10.5个月,2年和5年生存率分别为19.9%和10.4%。反应和生存的独立预后因素完全不同,治疗组是反应的唯一显著因素,而血清乳酸脱氢酶(LDH)、转移部位和体能状态可预测生存。在IL-2基础上加用IFNα与生存期延长相关,但加用化疗的效果不太明显。
血清LDH、转移部位和体能状态是转移性黑色素瘤随机试验中有用的分层因素。与报道的化疗5年生存率2%至6%相比,接受含IL-2/IFNα方案治疗的黑色素瘤患者观察到的长期生存率提高值得注意,但由于不能排除选择偏倚,IL-2以及治疗方案的所有其他组成部分对生存的影响需要在前瞻性随机试验中得到证实。