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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:比较临床评价紫杉醇 - 紫杉醇与紫杉醇联合化疗复发和铂 - 难治性卵巢癌的疗效和耐受性

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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:紫杉醇(T)和通用药物的疗效和耐受性的临床评估 - 紫杉醇 - Lance(P) - 在两组患者中进行了两组患者(9)或铂 - 难治性卵巢癌(17)。 在第I组中,19-71岁的患者(平均年龄 - 47 YRS)接受了6-7次课程,而在第II次,患者患有肿瘤进展的44-72岁(平均年龄 - 52 YRS) - 15.0 各种化学治疗方案的课程。 在标准前提下,T和P被注射135mg / sq,静脉内,滴注,在3小时内,通常与铂药物或用半环同时。 在最终分析中,总响应没有临床显着差异 - 44-30%和44-48%,报告了副作用发病率的任何显着差异。

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