Legha S S
Cancer. 1986 Apr 15;57(8 Suppl):1675-7. doi: 10.1002/1097-0142(19860415)57:8+<1675::aid-cncr2820571307>3.0.co;2-i.
Malignant melanoma is one of the several human tumors against which interferons have demonstrated significant antitumor activity. Such activity was first observed in early clinical trials with natural human leukocyte interferon; 4 of 75 patients in different institutions achieved partial response to treatment and 5 patients showed minor regression of disease. Subsequently, in a number of trials conducted with recombinant leukocyte interferons, antitumor activity against melanoma was observed consistently. Recombinant interferons have also revealed remarkable activity against malignant melanoma in the human tumor stem-cell assay, with 18 of 60 samples (30%) showing marked inhibition in tumor growth. Recombinant interferons from two different sources were tested in Phase I and Phase II trials against malignant melanoma. In one Phase I trial with interferon alfa-2b, 4 of 23 patients responded to treatment. In another Phase I study using recombinant interferon alfa-2a, 3 of 20 patients achieved objective responses. More recently, a number of Phase II trials were initiated and the detailed results of two Phase II studies have been published. In the first trial using recombinant leukocyte interferon at a dosage times a week, objective regression of tumor was observed in 7 of 31 patients, for a response rate of 22%. Because of severe toxicity associated with this dosage, a second Phase II trial was conducted using a dosage of 12 X 10(6) U/m2 three times a week, and 6 of 30 patients experienced objective regression of disease, for a response rate of 20%. Based on the results of these early trials with recombinant leukocyte interferon, a number of clinical trials using different species of interferon at different doses and treatment schedules were initiated. The preliminary results of these trials are reported here.
恶性黑色素瘤是几种人类肿瘤之一,干扰素已被证明对其具有显著的抗肿瘤活性。这种活性最早在天然人白细胞干扰素的早期临床试验中被观察到;不同机构的75名患者中有4名对治疗产生部分反应,5名患者的疾病出现轻微消退。随后,在一些使用重组白细胞干扰素进行的试验中,始终观察到对黑色素瘤的抗肿瘤活性。重组干扰素在人类肿瘤干细胞试验中也显示出对恶性黑色素瘤具有显著活性,60个样本中有18个(30%)显示肿瘤生长受到明显抑制。来自两种不同来源的重组干扰素在针对恶性黑色素瘤的I期和II期试验中进行了测试。在一项使用干扰素α-2b的I期试验中,23名患者中有4名对治疗有反应。在另一项使用重组干扰素α-2a的I期研究中,20名患者中有3名获得了客观反应。最近,启动了多项II期试验,两项II期研究的详细结果已经发表。在第一项使用重组白细胞干扰素、每周给药一次的试验中,31名患者中有7名观察到肿瘤客观消退,缓解率为22%。由于该剂量存在严重毒性,进行了第二项II期试验,使用剂量为12×10⁶U/m²、每周三次,30名患者中有6名出现疾病客观消退,缓解率为20%。基于这些早期重组白细胞干扰素试验的结果,启动了多项使用不同种类干扰素、不同剂量和治疗方案的临床试验。这里报告了这些试验的初步结果。