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Combination therapy with irinotecan and cisplatin as neoadjuvant chemotherapy in locally advanced cervical cancer

机译:伊立替康和顺铂联合治疗局部晚期宫颈癌的新辅助化疗

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摘要

To evaluate the response rate and toxicity of the combination of irinotecan (CPT-11) and cisplatin in a neoadjuvant setting, a phase II study was conducted regarding the regimen of this combination in patients with locally advanced cervical cancer. Eligibility included patients with previously untreated stage Ib2, IIb, or IIIb squamous cell carcinoma with good performance status. CPT-11 (60 mg m−2) was administered intravenously on days 1, 8 and 15, followed by cisplatin (60 mg m−2) given intravenously on day 1. Treatment was repeated every 4 weeks for a total of two or three cycles. Among 23 eligible patients (median age: 59 years), three showed complete response (13%), 15 showed partial response (65%), for an overall response rate of 78% (95% confidence interval 58–90%). Stable disease was observed in four cases (17%) and progressive disease in one (4%). The median time to failure and median survival time have not yet been reached. Of the 52 treatment cycles administered, diarrhoea and grade 3 or 4 neutropenia were observed in 10% and 75% respectively. There were no therapy-related deaths. The combination of CPT-11 with cisplatin is a promising regimen for neoadjuvant chemotherapy in locally advanced cervical cancer. The toxicities of this regimen are well tolerated. © 1999 Cancer Research Campaign
机译:为了评估伊立替康(CPT-11)和顺铂联合治疗在新辅助治疗中的反应率和毒性,对局部晚期宫颈癌患者的联合治疗方案进行了II期研究。符合条件的患者包括以前未经治疗的Ib2,IIb或IIIb鳞状细胞癌,且表现良好。在第1、8和15天静脉给予CPT-11(60 mg m-2),然后在第1天静脉给予顺铂(60 mg m-2)。每4周重复治疗,总共进行2或3次周期。在23名合格患者(中位年龄:59岁)中,三名显示出完全缓解(13%),十五名显示出部分缓解(65%),总缓解率为78%(95%置信区间58-90%)。观察到稳定的疾病4例(17%),进行性疾病1例(4%)。尚未达到中位失效时间和中位生存时间。在所给予的52个治疗周期中,分别观察到腹泻和3或4级嗜中性白血球减少症分别占10%和75%。没有与治疗有关的死亡。 CPT-11与顺铂的组合是局部晚期宫颈癌新辅助化疗的有希望的方案。该方案的毒性耐受性良好。 ©1999癌症研究运动

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