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临床试验/JPRN-C000000448
JPRN-C000000448已完成2 期

A phase II study of Irinotecan (CPT-11) for Leiomyosarcoma of Uterus - A phase II study of Irinotecan (CPT-11) for Leiomyosarcoma of Uterus

Japanese Gynecologic Oncology Group0 个研究点目标入组 35 人开始时间: 2006年7月13日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
35

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 75years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1) Patients with previous CPT-11 chemotherapy. 2) Patients with any history of serious drug reactions or hypersensitivity to CPT-11 3) Patients with massive pleural, cardiac effusion, and/or ascites 4) Patients with symptomatic brain metastasis 5) Patients with active infections 6) Patients with diarrhea (watery stool) five times or more in a day 7) Patients with unstable angina, history of cardiac infarction within 6 months, or arrhythmia that requires medical treatment 8) Patients with intestinal paralysis or illeus 9) Patients with interstitial pneumonia or pulmonary fibrosis 10) Patients with active concomitant malignancy. * Patients with history of any other malignancy within 5 years are ineligible. * Patients with carcinoma in situ or intramucosal malignancy that was curable with local therapy are eligible. 11) Patients with uncontrolled diabetes mellitus 12) Patients who are under the treatment with Atzanavir 13) Patients during pregnancy or breast-feeding, or unwilling to the use of contraception 14) Patients who are inappropriate to enter this study with any safety reasons, judged by the treating physician

研究者

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