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首页> 外文期刊>British Journal of Cancer >Irinotecan plus raltitrexed as first-line treatment in advanced colorectal cancer: a phase II study
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Irinotecan plus raltitrexed as first-line treatment in advanced colorectal cancer: a phase II study

机译:伊立替康联合雷替曲星作为晚期大肠癌的一线治疗药物:II期研究

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To evaluate the efficacy and toxicity of irinotecan (CPT-11) in combination with raltitrexed as first-line treatment of advanced colorectal cancer (CRC). A total of 91 previously untreated patients with advanced CRC and measurable disease were enrolled in this phase II study. The median age was 62 years (range 31–77); male/female 54/37; ECOG performance status was 0 in 50 patients (55%), one in 39 (43%) and two in two (2%). Treatment consisted of CPT-11 350?mg?m?2 in a 30-min intravenous infusion on day 1, followed after 30?min by a 15-min infusion of raltitrexed 3?mg?m?2. Measurements of efficacy included the following: response rate, time to disease progression and overall survival. Of the 83 evaluable patients valuable to objective response, there were five complete responses (6%) and 23 partial responses (28%), for an overall response rate of 34% (95% CI: 25.9–46.5%). In all, 36 patients (43%) had stable disease, whereas 19 (23%) had a progression. The median time to progression was 11.1 months and the median overall survival was 15.6 months. A total of 487 cycles of chemotherapy were delivered with a median of five per patient. Grade 3–4 WHO toxicities were as follows: diarrhoea in 13 patients (15%), nausea/vomiting in four (4%), transaminase increase in six (7%), stomatitis in two (2%), febrile neutropenia in three (3%), anaemia in five (6%) and asthenia in three (3%). The combination CPT-11–raltitrexed is an effective, well-tolerated and convenient regimen as front-line treatment of advanced CRC.
机译:为了评估伊立替康(CPT-11)与雷替曲塞联合作为晚期大肠癌(CRC)的一线治疗的疗效和毒性。 II期研究共纳入91名先前未接受治疗的晚期CRC和可测量疾病的患者。中位年龄为62岁(范围31-77);男/女54/37; ECOG表现状态为50例患者中为0(55%),39例中为1(43%),2例中为2(2%)。在第1天的30分钟静脉输注中,先用CPT-11 350?mg?m?2进行治疗,然后在30?分钟后,再用拉替曲曲3mg?m?m?2进行15分钟的输注。功效的测量包括以下内容:响应率,疾病进展时间和总生存期。在83例对客观缓解有价值的可评估患者中,有5例完全缓解(6%)和23例部分缓解(28%),总缓解率为34%(95%CI:25.9-46.5%) )。共有36例患者(43%)病情稳定,而19例(23%)患者病情稳定。中位进展时间为11.1个月,中位总生存时间为15.6个月。总共进行了487个化疗周期,每位患者中位数为5个。 WHO的3-4级毒性如下:腹泻13例(15%),恶心/呕吐4例(4%),转氨酶增加6例(7%),口腔炎2例(2%),发热性中性粒细胞减少症的比例为3(3%),贫血的比例为5(6%),乏力的比例为3(3%)。 CPT-11-雷替曲沙联合治疗是一种有效,耐受性强且方便的方案,可作为晚期CRC的一线治疗。

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