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临床试验/JPRN-jRCT2080224829
JPRN-jRCT2080224829已完成3 期

A Phase III, Randomized, Multi-Center, Double-Blind, Global Study to Determine the Efficacy and Safety of Durvalumab in Combination With and Following Chemoradiotherapy Compared to Chemoradiotherapy Alone for Treatment in Women With Locally Advanced Cervical Cancer

AstraZeneca KK0 个研究点目标入组 72 人开始时间: 2019年8月9日最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
72

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
>= 18age old 至 ot applicable(—)
性别
Female

入选标准

  • 2. Aged at least 18 years
  • 3. Documented evidence of cervical adenocarcinoma or squamous carcinoma FIGO (2009) Stages IB2 to IIB node positive or FIGO (2009) IIIA-IVA any node
  • 4. No prior chemotherapy or radiotherapy for cervical cancer
  • 5. WHO/ECOG performance status of 0-1
  • 6. At least 1 lesion, not previously irradiated, that q
  • ualifies as a RECIST 1.1 Target Lesion at baseline

排除标准

  • 1. Diagnosis of small cell (neuroendocrine) histology or mucinous adenocarcinoma cervical cancer
  • 2. Intent to administer a fertility-sparing treatment regimen
  • 3. Undergone a previous hysterectomy
  • 4. Evidence of metastatic disease per RECIST 1.1 including lymph nodes 15 mm (short axis) or more above the L1 cephalad body in the inguinal region or outside the planned radiation field
  • 5. History of allogeneic organ transplantati
  • 6. Active or prior documented autoimmune or inflammatory disorders
  • 7. Uncontrolled intercurrent illness
  • 8.History of another primary malignancy and active primary immunodeficiency

研究者

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