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首页> 外文期刊>Investigational New Drugs >Phase II trial of R115777 (NSC #70818) in patients with advanced colorectal cancer: A Southwest Oncology Group study
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Phase II trial of R115777 (NSC #70818) in patients with advanced colorectal cancer: A Southwest Oncology Group study

机译:R115777(NSC#70818)在晚期大肠癌患者中进行的II期临床试验:西南肿瘤小组的一项研究

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Purpose: The purpose of this Phase II multi-institutional trial was to determine the efficacy and toxicity of R115777 in previously untreated patients with metastatic colorectal carcinoma. Patients and methods: Patients were required to have histologically confirmed colorectal cancer with distant metastatic disease that was not surgically curable. They could not have received prior chemotherapy for metastatic disease. R115777 was given at a dose of 300 mg p.o. twice a day for 21days every 28 days until tumor progression or toxicity or other reason for discontinuation occurred. The primary endpoint was to determine the confirmed response probability with this treatment. Results: There were 55 eligible patients accrued to the study. There were no complete responses, but one confirmed partial response for a confirmed response probability of 2% (95%CI 0–10%). Three additional patients had an unconfirmed partial response for an overall response probability of 7%. The time to treatment failure was 1.7 months and the estimated median survival was 8.1 months. One patient died of treatment related infection and there were 7 other patients with grade 4 toxicities consisting of neutropenia, leukopenia, febrile neutropenia and thrombocytopenia, depression, increased bilirubin, anemia, and pneumonitis/infiltrates. Conclusion: R115777 given as a single agent by this dose and schedule is ineffective in patients with metastatic colorectal cancer.
机译:目的:这项II期多机构试验的目的是确定R115777在先前未经治疗的转移性结直肠癌患者中的疗效和毒性。患者和方法:要求患者经组织学确认为大肠癌并伴有远距离转移性疾病,无法手术治愈。他们可能未曾因转移性疾病接受过化学疗法。 R115777的剂量为300 mgp.o。每28天每天两次,共21天,直到出现肿瘤进展或毒性或其他终止原因。主要终点是确定这种治疗的确诊反应概率。结果:有55名符合条件的患者被纳入研究。没有完整的反应,但是有一个证实的部分反应,确证的反应概率为2%(95%CI 0-10%)。另外三名患者有未证实的部分缓解,总缓解率为7%。治疗失败的时间为1.7个月,估计中位生存期为8.1个月。一名患者死于与治疗有关的感染,还有其他7名4级毒性反应,包括中性粒细胞减少,白细胞减少,高热性中性粒细胞减少和血小板减少,抑郁症,胆红素升高,贫血和肺炎/浸润。结论:R115777以此剂量和时间表作为单一药物给予对转移性结直肠癌患者无效。

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