deKernion J B, Sarna G, Figlin R, Lindner A, Smith R B
J Urol. 1983 Dec;130(6):1063-6. doi: 10.1016/s0022-5347(17)51686-9.
An extended phase II trial of human leukocyte (alpha) interferon was done in 48 patients with measurable metastatic renal cell carcinoma, 43 of whom were evaluable. Of these patients 1 (2.5 per cent) had a complete response that was maintained after 19 months, 6 (14 per cent) had a partial response and an additional 23 per cent had either a minimal response or stabilization of previously growing metastases for greater than 3 months. Toxicity caused termination of treatment in only 1 patient and generally was tolerable. Major toxicity consisted of fever (80 per cent), fatigue (80 per cent) and hematologic toxicity (42 per cent), which was severe in only 2 patients. Characteristics of patients responding to therapy were good performance status, previous nephrectomy and metastases limited to the lungs. The results achieved with human leukocyte interferon were superior to those achieved by immunotherapy or chemotherapy at this and other institutions, and further trials are warranted.
对48例可测量的转移性肾细胞癌患者进行了人白细胞(α)干扰素的扩展II期试验,其中43例可评估。这些患者中,1例(2.5%)完全缓解,缓解持续19个月;6例(14%)部分缓解,另有23%有微小反应或先前进展的转移灶稳定超过3个月。毒性仅导致1例患者终止治疗,总体上可耐受。主要毒性包括发热(80%)、疲劳(80%)和血液学毒性(42%),仅2例患者毒性严重。对治疗有反应的患者特征为体能状态良好、既往接受过肾切除术且转移灶局限于肺部。在本机构和其他机构,人白细胞干扰素取得的结果优于免疫疗法或化疗,因此有必要进行进一步试验。