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临床试验/EUCTR2004-001103-35-DK
EUCTR2004-001103-35-DK进行中(未招募)不适用

Exemestane in Advanced or Recurrent Endometrial Carcinoma.A multicentre non-randomized Phase II study

ordic Society for Gynecologic Oncology0 个研究点目标入组 70 人开始时间: 2007年1月26日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • Advanced endometrial cancer (stage III-IV), not considered for treatment modalities apart from hormonal treatment
  • Relapse after primary treatment with interval > 1 month
  • Measurable tumour by X-ray examination and/or CT and/or MRI outside irradiated area.
  • Histological verified endometrial cancer. Only patients with tumors of endometrioid type will be accepted.
  • Post-menopausal women
  • Expected survival > 6 month
  • Age must be at least 18 years
  • Performance status must be 0-2 (WHO/ECOG, appendix I)
  • Informed consent given according to ICH/EU GCP guidelines and local or national laws
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Congestive heart failure grade III-IV
  • Severe hepatic or renal impairment not allowing for adequate use of the proposed regimens. ASAT or ALAT > 4 times of the upper limit of the normal values. S-Creatinine >150 mmol/l
  • Other malignancies within the last 5 years apart from cancer in situ cervicis uteri or basal cell carcinoma of the skin.
  • History of tromboembolic signs.
  • Any treatment that interact with the study drug like carbamazepine or cyclosporine.
  • Other primary hormonal therapy.
  • Tumors consisting of or with elements of serous papillary (UPSC) or clear cell type.
  • Inclusion in other trials.
  • Any cancer treatment or use of any investigation agent within one month of the study entry.
  • Circumstances at the time of the entry that would not permit completion of the study or follow-up.
  • Patients with symptomatic brain metastases.
  • Pregnancy, lactation or child bearing potential patients without adequate contraception
  • Dementia or significantly altered status that would prohibit the understanding and giving of informed consent.

研究者

发起方
ordic Society for Gynecologic Oncology

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