Induction Chemotherapy in Patients With Locoregionally Advanced Nasopharyngeal Carcinoma

NCT01245959 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 476

Last updated 2014-02-13

No results posted yet for this study

Summary

The purpose of this study is to compare induction chemotherapy (docetaxel+cisplatin+fluorouracil) plus concurrent chemoradiotherapy with concurrent chemoradiotherapy in patients with locoregionally advanced nasopharyngeal carcinoma (NPC), in order to confirm the value of induction chemotherapy in NPC patients.

Conditions

  • Nasopharyngeal Carcinoma

Interventions

DRUG

Docetaxel, cisplatin and fluorouracil

Patients receive docetaxel (60mg/m2 on day 1), cisplatin (60mg/m2 on day 1) and fluorouracil (600mg/m2 on Days 1 to 5) every three weeks for three cycles before the radiotherapy.

RADIATION

Concurrent chemoradiotherapy

Patients receive radical radiotherapy and cisplatin (100mg/m2) every three weeks for three cycles during radiotherapy.

Sponsors & Collaborators

  • Fudan University

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Huazhong University of Science and Technology

    collaborator OTHER
  • Peking University Cancer Hospital & Institute

    collaborator OTHER
  • Zhejiang Cancer Hospital

    collaborator OTHER
  • Central South University

    collaborator OTHER
  • Jiangsu Cancer Institute & Hospital

    collaborator OTHER
  • First People's Hospital of Foshan

    collaborator OTHER
  • The Third Affiliated Hospital of Harbin Medical University

    collaborator OTHER
  • Cancer Hospital of Guangxi Medical University

    collaborator OTHER
  • Jiangxi Provincial Cancer Hospital

    collaborator OTHER
  • Guangzhou Medical University

    collaborator OTHER
  • Sun Yat-sen University

    lead OTHER

Principal Investigators

  • Jun Ma, M.D. · Sun Yat-sen University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
59 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2016-04-30
Completion
2018-04-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01245959 on ClinicalTrials.gov