Aksoy H, Baltaci S, Türkölmez K, Seçkiner I, Bedük Y
Department of Urology, Ankara University, School of Medicine, Turkey.
Int Urol Nephrol. 2001;33(3):457-9. doi: 10.1023/a:1019510628249.
To evaluate the efficacy and toxicity of interferon alpha-2b (IFN-alpha2b) and levamisole treatment regimen in patients with metastatic renal cell carcinoma (RCC). Seventeen patients with metastatic RCC were treated using recombinant IFN-alpha2b at a dose of 10 MU/m2 body surface subcutaneously three times in a week, for 3 months, with levamisole 50 mg t.d.s orally on days 1-3 on alternate weeks. The mean follow-up period was 10.7 (range 2-23) months. We achieved 1 complete response (lasting for 12+ months) and 1 partial response (lasting for 15 months), for an objective response rate of 11.7%. A further 7 patients (41%) had a stabilization of disease. The overall toxicity was moderate, with mainly grade I or II side effects. Grade III toxicities reported among 3 patients including vomiting (2 patients) and anorexia (1 patient). There was no treatment related death. Although additions of levamisole to IFN-alpha do not result in any significant increase in treatment toxicity, the response rate appears to be no better than IFN-alpha monotherapy reported in the literature.
评估干扰素α-2b(IFN-α2b)联合左旋咪唑治疗方案对转移性肾细胞癌(RCC)患者的疗效和毒性。17例转移性RCC患者接受治疗,采用重组IFN-α2b,剂量为10 MU/m²体表面积,皮下注射,每周3次,共3个月,左旋咪唑50 mg,每日3次,口服,于第1 - 3天服用,每隔一周重复。平均随访期为10.7(范围2 - 23)个月。我们获得了1例完全缓解(持续12个月以上)和1例部分缓解(持续15个月),客观缓解率为11.7%。另有7例患者(41%)病情稳定。总体毒性为中度,主要为Ⅰ级或Ⅱ级副作用。3例患者报告有Ⅲ级毒性,包括呕吐(2例)和厌食(1例)。无治疗相关死亡。虽然在IFN-α基础上加用左旋咪唑并未导致治疗毒性显著增加,但缓解率似乎并不比文献报道的IFN-α单药治疗更好。