Lopez Hanninen E, Fenner M, Kirchner H, Deckert M, Duensing S, Menzel T, Poliwoda H, Atzpodien J
Department of Hematology and Oncology, M H H Univ Medical Center, Hannover, Germany.
Cancer Biother. 1993 Winter;8(4):301-6. doi: 10.1089/cbr.1993.8.301.
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)
我们报告了34例转移性肾细胞癌患者,这些患者在先前的抗肿瘤治疗进展后,接受了皮下重组干扰素-α和静脉注射长春碱联合治疗。预处理包括化疗(n = 3)、激素治疗(n = 6)和免疫治疗(白细胞介素-2/干扰素-α,n = 25)。在本研究中,治疗疗程包括分别为600万U/m²的重组干扰素-α皮下给药,每周三次(20例患者,第2组)。治疗持续8周。此外,所有患者在第2、5和8周静脉注射长春碱,剂量为6mg/m²。在第1组治疗的14例患者中,1例部分缓解6个月(总缓解率7.14%;95%置信区间,0.18 - 33.87%),4例疾病稳定(中位持续时间,5.0个月)。在第2组治疗的20例患者中,1例完全缓解(缓解持续时间,34 + 个月);此外,2例部分缓解(中位缓解持续时间,10.5 + 个月;总缓解率,15%;95%置信区间3.21 - 37.89%),13例疾病稳定(中位持续时间5.9 + 个月)。比较第1组和第2组患者的治疗结果时,缓解率无显著差异。相比之下,与第1组患者相比,第2组治疗的进展性疾病患者明显更少(p = 0.024)。这种治疗组合总体耐受性良好,全身毒性低至中度。此外,分别比较第1组和第2组患者时,治疗相关全身毒性的频率或强度无显著差异。(摘要截断于250字)