Budd G T, Osgood B, Barna B, Boyett J M, Finke J, Medendorp S V, Murthy S, Novak C, Sergi J, Tubbs R
Cleveland Clinic, Ohio 44195.
Cancer Res. 1989 Nov 15;49(22):6432-6.
Because recombinant interleukin 2 (rIL-2) and recombinant alpha-interferon (rIFN-alpha) exhibit synergistic antitumor activity in C3HMT1820 T-cell lymphoma and B16 melanoma tumor systems, we have performed a Phase I study of this combination in 55 patients with advanced malignancies for whom no standard therapy exists. Successive groups of greater than or equal to 4 patients have been entered into 12 dose levels (1A-3D), with dose levels 1-3 referring to doses of rIL-2 of 0.1, 0.5, and 2.0 x 10(6) units/m2, respectively, and dose levels A-D referring to doses of recombinant human alpha 2a-interferon (rHuIFN-alpha 2a) of 0, 0.1, 1.0, and 10.0 x 10(6) units/m2. Both agents were given on Mondays, Wednesdays, and Fridays, with rIL-2 being given as i.v. bolus injections and rHuIFN-alpha 2a being given intramuscularly. Myelosuppression was dose-limiting and was related primarily to the dose of rHuIFN-alpha 2a. The maximum-tolerated dose level was reached at a dose of rIL-2 of 2.0 x 10(6) units/m2 and of rHuIFN-alpha 2a of 10.0 x 10(6) units/m2 (dose level 3D). At this dose level, 3/6 patients developed grade 3 neutropenia (absolute granulocyte count less than 1 x 10(9)/liter). Myelosuppression was transient, with no documented infections being associated with neutropenia. Hypotension was mild; a single patient was treated with a vasopressor, but all other cases of hypotension responded to fluid administration. No significant pulmonary toxicity was produced. Fever, chills, and malaise were universal but not dose-limiting. Three partial responses and one minor response were observed in patients with malignant melanoma, renal cell carcinoma, and breast cancer. Immunological studies suggested that natural killer activity was related to both the dose of rIL-2 and the dose of rHuIFN-alpha 2a, with natural killer activity being positively related to the dose of rIL-2 and maximal at the lowest dose of rHuIFN-alpha 2a of 0.1 x 10(6) units/m2.
由于重组白细胞介素2(rIL-2)和重组α干扰素(rIFN-α)在C3HMT1820 T细胞淋巴瘤和B16黑色素瘤肿瘤系统中表现出协同抗肿瘤活性,我们对55例不存在标准治疗方案的晚期恶性肿瘤患者进行了该联合用药的I期研究。每组连续纳入至少4例患者,共设置了12个剂量水平(1A - 3D),其中1 - 3剂量水平分别指rIL-2的剂量为0.1、0.5和2.0×10⁶单位/m²,A - D剂量水平分别指重组人α2a干扰素(rHuIFN-α2a)的剂量为0、0.1、1.0和10.0×10⁶单位/m²。两种药物均在周一、周三和周五给药,rIL-2采用静脉推注,rHuIFN-α2a采用肌肉注射。骨髓抑制是剂量限制性毒性,主要与rHuIFN-α2a的剂量有关。rIL-2剂量为2.0×10⁶单位/m²、rHuIFN-α2a剂量为10.0×10⁶单位/m²(剂量水平3D)时达到最大耐受剂量水平。在此剂量水平下,6例患者中有3例出现3级中性粒细胞减少(绝对粒细胞计数低于1×10⁹/L)。骨髓抑制是短暂的,没有记录到与中性粒细胞减少相关的感染。低血压症状较轻;仅1例患者接受了血管升压药治疗,其他所有低血压病例通过补液治疗有效。未产生明显的肺部毒性。发热、寒战和不适较为普遍,但并非剂量限制性毒性。在恶性黑色素瘤、肾细胞癌和乳腺癌患者中观察到3例部分缓解和1例轻微缓解。免疫学研究表明,自然杀伤活性与rIL-2的剂量和rHuIFN-α2a的剂量均相关,自然杀伤活性与rIL-2的剂量呈正相关,在rHuIFN-α2a最低剂量0.1×10⁶单位/m²时达到最大值。