Fosså S D, Gunderson R, Moe B
Department of Medical Oncology, Norwegian Radium Hospital, Oslo.
Cancer. 1990 Jun 1;65(11):2451-4. doi: 10.1002/1097-0142(19900601)65:11<2451::aid-cncr2820651108>3.0.co;2-3.
Five responses (lung metastases, three; lymph node metastases, two) were observed in 23 patients with metastatic renal cell carcinoma who received recombinant interferon-alpha-2A (IFN) 18 X 10(6) U in three intramuscular doses each week combined with oral prednisone (10 to 20 mg daily). The response duration was 4+, 4+, 9, 11+, and 15+ months. In general, the combination treatment of interferon and prednisone lead to a significant reduction of the subjective side effects (flu-like symptoms) as compared to a previous experience in patients treated with interferon only. Reduction of the interferon dose or discontinuation of IFN treatment was necessary in only two of 23 patients receiving IFN plus prednisone. Prednisone, however, had little effect on the hepatic toxicity often associated with high-dose IFN treatment. The subjective tolerability of a high dose of IFN is significantly increased if oral prednisone (10-20 mg) is given concomitantly in patients with metastatic renal cell carcinoma without reducing the response rate. Randomized trials will be necessary to confirm the efficacy of the IFN and prednisone combination. In addition, higher doses of IFN combined with prednisone should be evaluated in this malignancy.
在23例转移性肾细胞癌患者中观察到5例有反应(肺转移3例;淋巴结转移2例),这些患者接受重组干扰素α-2A(IFN)18×10⁶U,每周分三次肌肉注射,并联合口服泼尼松(每日10至20mg)。反应持续时间分别为4+、4+、9、11+和15+个月。总体而言,与之前仅接受干扰素治疗的患者经验相比,干扰素与泼尼松的联合治疗导致主观副作用(类流感症状)显著减少。在接受IFN加泼尼松治疗的23例患者中,仅2例需要减少干扰素剂量或停止IFN治疗。然而,泼尼松对常与高剂量IFN治疗相关的肝毒性影响不大。在转移性肾细胞癌患者中,同时给予口服泼尼松(10 - 20mg)可显著提高高剂量IFN的主观耐受性,且不降低反应率。需要进行随机试验以证实IFN与泼尼松联合治疗的疗效。此外,应评估更高剂量的IFN与泼尼松联合用于这种恶性肿瘤的情况。