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Comparative clinical appraisal of the effectiveness and tolerability of paclitaxel-LANCE and taxol in combination chemotherapy for recurrences and platinum-refractory ovarian carcinoma

机译:紫杉醇-LANCE和紫杉醇联合化疗联合化疗治疗铂和难治性卵巢癌的有效性和耐受性的比较临床评价

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摘要

A clinical appraisal of efficacy and tolerability of taxol (T) and a generic drug--paclitaxel--LANCE (P)--was carried out in two groups of patients with recurrences (9) or platinum-refractory ovarian carcinoma (17). In group I, patients aged 19-71 (mean age--47 yrs) had received 6-7 courses, while, in group II, patients aged 44-72 (mean age--52 yrs) who suffered tumor progression--15.0 courses of various chemotherapeutic regimens. Following standard premedication, T and P were injected 135 mg/sq., intravenously, dropwise, during 3 hrs, as a rule, either concurrently with platinum drugs or with hemzar. In the final analysis, there was no clinically significant difference in overall response--44-30% and 44-48%, respectively, nor any significant difference in side-effect incidence was reported.
机译:对两组复发(9)或铂难治性卵巢癌(17)的患者进行了紫杉醇(T)和通用药物-紫杉醇-LANCE(P)的疗效和耐受性的临床评估。在第一组中,年龄19-71(平均年龄--47岁)的患者接受了6-7疗程,而在第二组中,44-72(平均年龄--52岁)的患者经历了-15.0的肿瘤进展各种化疗方案的课程。在标准的用药前,通常在3个小时内静脉滴注T和P 135 mg / sq,通常与铂类药物或hemzar并用。在最终分析中,总体反应无临床显着性差异,分别为44-30%和44-48%,也未报告副作用发生率有任何显着差异。

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