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临床试验/NCT03243825
NCT03243825已完成不适用

Comparative Study of Neoadjuvant Chemo/Brachytherapy and Chemotherapy Alone Before Radical Hysterectomy in Stage Ib2-IIa2 Cervical Cancer

Chinese Academy of Medical Sciences1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2012年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
120
试验地点
1
主要终点
proportion of post-operative chemo-radiotherapy

研究概览

简要总结

For stage Ib2-IIa2 cervical cancer patients, neoadjuvant therapy followed by radical hysterectomy and pelvic lymphadenectomy is one of the managements. Post-operative concurrent chemo-radiotherapy is necessary if the patients have high-risk factors, including positive surgical margin, parametrium and pelvic nodes. Our previous retrospective study showed that combination of neoadjuvant chemotherapy and brachytherapy reduced the proportion of post-operative concurrent chemo-radiotherapy compared to neoadjuvant chemotherapy alone.

详细描述

In the present study, the patients with stage Ib2-IIa2 cervical cancer will receive either neoadjuvant chemo/brachytherapy or neoadjuvant chemotherapy before radical hysterectomy and pelvic+/- para-aortic lymph node dissection. According to the surgical findings, post-operative chemo-radiotherapy will be performed.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
25 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Histology confirmed cervical cancer
  • Clinical stage Ib2 or IIa2 (FIGO 2009)

排除标准

  • Patients who not suitable for surgery
  • Personal history of pelvic radiotherapy

研究组 & 干预措施

chemo/brachytherapy

Experimental

Patients in this arm will receive neoadjuvant chemotherapy (paclitaxel/cisplatinum) and brachytherapy before radical hysterectomy.

干预措施: combination group (Radiation)

chemotherapy

Active Comparator

Patients in this arm will receive neoadjuvant chemotherapy (paclitaxel/cisplatinum) before radical hysterectomy.

干预措施: chemotherapy group (Drug)

结局指标

主要结局

proportion of post-operative chemo-radiotherapy

时间窗: 2 months

次要结局

  • 3-year disease-free survival(3 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ning Li

Doctor

Chinese Academy of Medical Sciences

研究点 (1)

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