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临床试验/NL-OMON54837
NL-OMON54837招募中3 期

Randomised Phase Ill Trial of molecular profile-based versus standard recommendations for adjuvant radiotherapy for women with early stage endometrial cancer: PORTEC-4a - PORTEC-4a

eids Universitair Medisch Centrum0 个研究点目标入组 450 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
450

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
18 至 64(—)

入选标准

  • Adult patients with histologically confirmed endometrioid type endometrial
  • carcinoma, FIGO 2009 stage I, with one of the following combinations of stage,
  • grade, age, and LVSI:
  • 1. Stage IA, grade 3 (any age, with or without LVSI)
  • 2. Stage IB, grade 1 or 2 and age >60 years
  • 3. Stage IB, grade 1-2 with documented LVSI
  • 4. Stage IB, grade 3 without LVSI
  • 5. Stage II (microscopic), grade 1
  • Surgery consisted of Total Abdominal or Laparoscopic Hysterectomy and Bilateral
  • Salpingo-Oophorectomy (TH-BSO) with or without pelvic lymphadenectomy, lymph
  • node sampling or sentinel node procedure (not recommended, but permitted)
  • WHO-performance status 0-2
  • Written informed consent

排除标准

  • The following criteria exclude the patient from enrolment in this trial:
  • 1. Any other stage and type of endometrial. carcinoma
  • 2. Non-endometrioid endometrial carcinoma, such as serous or clear cell
  • carcinoma (at least 10% in mixed types), or undifferentiated or neuroendocrine
  • 3. Uterine sarcoma (including carcinosarcoma)
  • 4. Previous malignancy (except for non-melanomatous skin cancer) < 5 yrs
  • 5. Previous pelvic radiotherapy
  • 6. Verwacht interval between the operation and start of radiotherapy exceeding

研究者

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