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临床试验/NCT03129412
NCT03129412招募中2 期

The Clinical Curative Efficacy and Side Effect of Oligo-metastases Nasopharyngeal Carcinoma Patients Received Radical Radiation for Primary Tumors and Treatments for Metastatic Lesions

Zhejiang Cancer Hospital1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2017年4月14日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
64
试验地点
1
主要终点
Overall survival

研究概览

简要总结

Oligo-metastases NPC patients received radiation for primary tumors and treatments for metastatic lesions.

详细描述

The patients enrolled will received 4-6 cycles chemotherapy at first.Then, radical radiotherapy for nasopharyngeal tumors and local treatments for oligometastatic lesions will assigned to those patients. The efficacy and side-effect will be evaluated and analyzed.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically conformed initial non-keratinizing squamous carcinoma in nasopharynx.
  • Clinical stages,T1-4N0-3M1,IVc(AJCC 2010).
  • The metastatic lesions ≤5 and metastatic organs ≤2
  • Karnofsky scores >70
  • Normal hemodynamic indices before the recruitment (including white blood cell count>4.0×109/L, neutrophil count>1.5×109/L, platelet count >100×109/L, hemoglobin≥90g/l, normal liver/kidney function).
  • Informed consent signed.

排除标准

  • Histologically conformed initial keratinizing carcinoma or others.
  • The metastatic lesions >5 or metastatic organs >
  • Any severe complications contraindicated chemotherapy or radiotherapy.
  • History of malignant tumors.
  • Pregnant or nursing women.
  • History of radiotherapy or chemotherpy in head and neck regions.
  • Patients refused the informed consent.

结局指标

主要结局

Overall survival

时间窗: From date of diagnosis until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months

Events of death caused by any reasons

次要结局

  • Progress free survival(From date of diagnosis until the date of first documented progression, assessed up to 36 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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