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Maintenance Chemotherapy in High-metastatic Risk Nasopharyngeal Carcinoma Patients of N3 Stage

Primary Purpose

Nasopharyngeal Carcinoma

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Gemcitabine
standard chemoradiotherapy
Sponsored by
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nasopharyngeal Carcinoma

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • AJCC/UICC 8th edition N3 nasopharyngeal carcinoma
  • Pathology: WHO II/II
  • No prior anti-tumor treatment
  • Age 18-60
  • KPS≥70
  • Adequate blood supply
  • Informed consent obtained

Exclusion Criteria:

  • Pathology: WHO I
  • Pregnant
  • Combined with other malignant tumor

Sites / Locations

  • Fudan Universtiy Shanghai Cancer CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

maintenance arm

control arm

Arm Description

Gemcitabine maintenance treatment

observe and follow-up

Outcomes

Primary Outcome Measures

Distant metastatic free survival
from enrollment to distant metastatis

Secondary Outcome Measures

Full Information

First Posted
December 27, 2017
Last Updated
July 4, 2019
Sponsor
Fudan University
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1. Study Identification

Unique Protocol Identification Number
NCT03403829
Brief Title
Maintenance Chemotherapy in High-metastatic Risk Nasopharyngeal Carcinoma Patients of N3 Stage
Official Title
A Phase III Randomized Trial of Maintenance Chemotherapy in High-metastatic Risk Nasopharyngeal Carcinoma Patients of N3 Stage
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
December 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Up to now, IMRT has largely improved the local control of locally advanced nasopharyngeal carcinoma (NPC), leaves the distant metastasis as the main treatment failure modality of patients with bulky lymph nodes (especially N3 stage). Although concurrent chemoradiotherapy (CCRT) continues to stand as the standard treatment of these patients, the role of adjuvant chemotherapy remains controversial due to its relatively severe toxicities and inferior compliance. However, our retrospective study of 2D-RT and IMRT era had proved adjuvant chemotherapy played key role in N3 NPC patients in terms of reducing distant metastasis and improving overall survival. Maintenance chemotherapy of gemicitabine single drug is promising with adequate efficacy and moderate toxicities. So we aim to conduct "A Phase III Randomized Trial of Maintenance Chemotherapy in High-metastatic Risk Nasopharyngeal Carcinoma Patients of N3 Stage" to evaluate the effectiveness and compliance of gemicitabine as maintenance chemotherapy in N3 nasopharyngeal carcinoma.
Detailed Description
We aim to conduct "A Phase III Randomized Trial of Maintenance Chemotherapy in High-metastatic Risk Nasopharyngeal Carcinoma Patients of N3 Stage" to evaluate the effectiveness and compliance of gemicitabine as maintenance chemotherapy in N3 nasopharyngeal carcinoma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasopharyngeal Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
360 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
maintenance arm
Arm Type
Experimental
Arm Description
Gemcitabine maintenance treatment
Arm Title
control arm
Arm Type
Sham Comparator
Arm Description
observe and follow-up
Intervention Type
Drug
Intervention Name(s)
Gemcitabine
Other Intervention Name(s)
standard chemoradiotherapy
Intervention Description
Gemcitabine maintenance chemotherapy
Intervention Type
Radiation
Intervention Name(s)
standard chemoradiotherapy
Intervention Description
standard chemoradiotherapy
Primary Outcome Measure Information:
Title
Distant metastatic free survival
Description
from enrollment to distant metastatis
Time Frame
5 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: AJCC/UICC 8th edition N3 nasopharyngeal carcinoma Pathology: WHO II/II No prior anti-tumor treatment Age 18-60 KPS≥70 Adequate blood supply Informed consent obtained Exclusion Criteria: Pathology: WHO I Pregnant Combined with other malignant tumor
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chaosu Hu
Phone
862164175590
Email
hucsu62@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chaosu Hu, M.D
Organizational Affiliation
Fudan University Shanghai cancer centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fudan Universtiy Shanghai Cancer Centre
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chaosu Hu
Phone
+8674175590
Ext
1400
Email
hucsu62@163.com

12. IPD Sharing Statement

Learn more about this trial

Maintenance Chemotherapy in High-metastatic Risk Nasopharyngeal Carcinoma Patients of N3 Stage

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