Limited efficacy of interferon-alpha and vinblastine as second line biochemotherapy regimen in patients with progressive metastatic renal cell carcinoma.

E Lopez Hanninen, M Fenner, H Kirchner, M Deckert, S Duensing, T Menzel, H Poliwoda, J Atzpodien
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引用次数: 8

Abstract

We report on thirty-four patients with metastatic renal cell carcinoma who were treated with a combination of subcutaneous recombinant interferon-alpha and intravenous vinblastine upon progression after previous antineoplastic therapy. Pretreatment included chemotherapy (n = 3), hormonal therapy (n = 6) and immunotherapy (interleukin-2/interferon-alpha, n = 25). In this study, treatment courses consisted of subcutaneous doses thrice weekly of recombinant interferon-alpha at 6 million U/m2 (20 patients, group 2), respectively. Treatment was given over 8 consecutive weeks. Additionally, in all patients, vinblastine was administered intravenously at a dose of 6 mg/m2 in weeks 2, 5 and 8. Of 14 patients treated in group 1, one had a partial response for 6 months (overall response rate 7.14%; 95% confidence interval, 0.18-33.87%), and four had disease stabilization (median duration, 5.0 months). Of 20 patients treated in group 2, there was one patient who achieved a complete response (response duration, 34+ months); in addition, two patients had a partial response (median response duration, 10.5+ months; overall response rate, 15%; 95% confidence interval 3.21-37.89%), and 13 patients exhibited disease stabilization (median duration 5.9+ months). Response rates showed no significant differences when comparing treatment results in patients in group 1 vs group 2. In contrast, significantly less patients treated in group 2 had progressive disease (p = 0.024), as compared to patients in group 1. This treatment combination was overall well tolerated with low to moderate systemic toxicity. In addition, there were no significant differences in frequency or intensity of therapy-related systemic toxicities when comparing patients in group 1 and group 2, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

干扰素- α和长春碱作为进展性转移性肾细胞癌患者的二线生物化疗方案的有限疗效。
我们报告了34例转移性肾细胞癌患者,他们在先前的抗肿瘤治疗进展后接受皮下重组干扰素- α和静脉长春花碱联合治疗。预处理包括化疗(n = 3)、激素治疗(n = 6)和免疫治疗(白介素-2/干扰素- α, n = 25)。在这项研究中,疗程包括每周3次皮下剂量重组干扰素- α,剂量分别为600万U/m2(20例患者,第二组)。治疗时间为连续8周。此外,在所有患者中,长春花碱在第2、5和8周以6mg /m2的剂量静脉注射。在第1组治疗的14例患者中,1例患者在6个月的时间内部分缓解(总缓解率7.14%;95%可信区间为0.18-33.87%),4例疾病稳定(中位持续时间为5.0个月)。在2组治疗的20例患者中,有1例患者达到完全缓解(缓解持续时间,34个月以上);此外,2例患者出现部分缓解(中位缓解持续时间,10.5+个月;总体响应率,15%;95%可信区间3.21-37.89%),13例患者病情稳定(中位持续时间5.9+月)。在比较1组和2组患者的治疗结果时,有效率无显著差异。相比之下,与第1组患者相比,第2组患者的进展性疾病显著减少(p = 0.024)。总的来说,这种治疗组合耐受性良好,具有低至中度的全身毒性。此外,与第1组和第2组患者相比,治疗相关全身毒性的频率或强度没有显著差异。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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