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临床试验/NCT05062005
NCT05062005招募中3 期

Induction Chemotherapy+Chemoradiotherapy vs. Chemoradiotherapy for Locally Advanced Nasopharyngeal Carcinoma

First Affiliated Hospital, Sun Yat-Sen University1 个研究点 分布在 1 个国家目标入组 447 人开始时间: 2021年9月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
447
试验地点
1
主要终点
FFS (Failure-free Survival)

研究概览

简要总结

This trial is a multi-center phase III clinical trial. The purpose of this trial is to explore whether concurrent chemoradiotherapy is not inferior to induction chemotherapy combined with concurrent chemoradiotherapy in patients with locally advanced nasopharyngeal carcinoma.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • Age 18-65 years old;
  • Pathologically confirmed non-keratinizing nasopharyngeal carcinoma;
  • Stage T3-4N0-1 (according to the UICC/AJCC 8th);
  • No distant metastasis;
  • Have not received anti-cancer treatment in the past;
  • ECOG (Eastern Cooperative Oncology Group of the United States): 0-1;
  • Adequate hematologic, hepatic and renal function.

排除标准

  • The purpose of treatment is palliative;
  • Diagnosed with other malignant tumors at the same time;
  • Malignant tumor history;
  • Pregnancy or breastfeeding, or expect to become pregnant during the clinical trial period;
  • Combined serious illness.

研究组 & 干预措施

Induction Chemotherapy+Chemoradiotherapy

Other

干预措施: Induction Chemotherapy (Drug)

Induction Chemotherapy+Chemoradiotherapy

Other

干预措施: Concurrent Chemotherapy (Drug)

Induction Chemotherapy+Chemoradiotherapy

Other

干预措施: Definitive Radiotherapy (Radiation)

Chemoradiotherapy

Other

干预措施: Concurrent Chemotherapy (Drug)

Chemoradiotherapy

Other

干预措施: Definitive Radiotherapy (Radiation)

结局指标

主要结局

FFS (Failure-free Survival)

时间窗: 3 year

Defined as the time from randomization to tumor recurrence, distant metastasis, or death due to any reason, whichever occurs first. Patients who withdraw or who are lost to follow-up will be censored at the date last known to be alive and progression free. Patients not having an event will be censored at the date last seen alive.

次要结局

  • LRFS (Locoregional Recurrence-free Survival)(3 year)
  • OS (Overall Survival)(3 year)
  • AE (Adverse events)(3 year)
  • DMFS (Distant Metastasis-free Survival)(3 year)

研究者

发起方
First Affiliated Hospital, Sun Yat-Sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Chen Yong

Professor

First Affiliated Hospital, Sun Yat-Sen University

研究点 (1)

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