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
About this trial
This is an interventional treatment trial for Nasopharyngeal Carcinoma
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
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
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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