IMRT Plus Cisplatin Versus IMRT in Patients With Stage 2 Nasopharyngeal Carcinoma
Primary Purpose
Nasopharyngeal Carcinoma
Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Intensity modulated radiotherapy
Cisplatin
Sponsored by
About this trial
This is an interventional treatment trial for Nasopharyngeal Carcinoma focused on measuring Nasopharyngeal Carcinoma, Intensity modulated radiotherapy, Cisplatin
Eligibility Criteria
Inclusion Criteria:
- The sex of the subject is not limited, the age is from 18 to 70 years old;
- Histologically proven nasopharyngeal squamous cell carcinoma, World Health Organization (WHO) II-III type;
- Union Internationale Contre le Cancer(UICC) stage 9 clinical stage II patients;
- Karnofsky score ≥ 80 points;
- No evidence of distant metastasis;
- Having an nasopharyngeal MRI before treatment ,which can measure the size of the tumor in order to analyze the effect.
Exclusion Criteria:
- The subject had previously suffered from other malignancies (except non-melanotic skin cancer or cervical carcinoma in situ);
- Previously received immunotherapy;
- Previously received chemotherapy;
- Previously received radiation therapy;
- Patients who had previously undergone surgical treatment for head and neck tumors (excluding cervical lymphadenectomy);
- Evidence of distant metastases or other malignancies at the same time.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
IMRT group
IMRT plus cisplatin group
Arm Description
Intensity modulated radiotherapy once a day, 5 times a week, continuous treatment for about 6 weeks (DT 70Gy)
Intensity modulated radiotherapy once a day, 5 times a week, continuous treatment for about 6 weeks (DT 70Gy),plus synchronous cisplatin (100mg / m2 / times) chemotherapy, once every 3 weeks, a total of 2 times
Outcomes
Primary Outcome Measures
Overall survival rate
Refers to the time from included to death due to any cause.
Secondary Outcome Measures
Full Information
NCT ID
NCT03068936
First Posted
February 15, 2017
Last Updated
February 27, 2017
Sponsor
Nanfang Hospital, Southern Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03068936
Brief Title
IMRT Plus Cisplatin Versus IMRT in Patients With Stage 2 Nasopharyngeal Carcinoma
Official Title
Intensity Modulated Radiotherapy Plus Cisplatin Versus Intensity Modulated Radiotherapy in Patients With Stage 2 Nasopharyngeal Carcinoma: A Phase 3 Multicenter, Open-label, Randomized, Non-inferior Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2017 (Anticipated)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
September 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nanfang Hospital, Southern Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Nasopharyngeal carcinoma has high incidence in the southern China, especially in Guangdong Province. In the world, the standardized morbidity has reached 30/10 million in men while in women, about 13/10 million. At present, the incidence of nasopharyngeal carcinoma in China accounted for more than 80% of the world. The cancer-related deaths is in the eighth, which is a serious threat to our people's health and life. A recent multi-center phase II study of stage II nasopharyngeal carcinoma showed that: compared with Intensity Modulation Radiotherapy (IMRT) plus cisplatin, the 3 year local control rate, regional control rate, distant metastasis-free survival rate and disease-specific survival rate of IMRT were similar, but the side effects of radiotherapy alone group were lower.
Based on the results of the phase II clinical study, the investigators designed this phase III clinical study, with the aim to compared the efficacy and toxicity of these two treatment programs. And finally to provide sufficient evidence for the treatment of stage II nasopharyngeal carcinoma.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasopharyngeal Carcinoma
Keywords
Nasopharyngeal Carcinoma, Intensity modulated radiotherapy, Cisplatin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
716 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
IMRT group
Arm Type
Experimental
Arm Description
Intensity modulated radiotherapy once a day, 5 times a week, continuous treatment for about 6 weeks (DT 70Gy)
Arm Title
IMRT plus cisplatin group
Arm Type
Other
Arm Description
Intensity modulated radiotherapy once a day, 5 times a week, continuous treatment for about 6 weeks (DT 70Gy),plus synchronous cisplatin (100mg / m2 / times) chemotherapy, once every 3 weeks, a total of 2 times
Intervention Type
Radiation
Intervention Name(s)
Intensity modulated radiotherapy
Other Intervention Name(s)
IMRT
Intervention Description
Intensity modulated radiotherapy once a day, 5 times a week, continuous treatment for about 6 weeks (DT 70Gy)
Intervention Type
Drug
Intervention Name(s)
Cisplatin
Intervention Description
Synchronous cisplatin (100mg / m2 / times) chemotherapy, once every 3 weeks, a total of 2 times
Primary Outcome Measure Information:
Title
Overall survival rate
Description
Refers to the time from included to death due to any cause.
Time Frame
up to 3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The sex of the subject is not limited, the age is from 18 to 70 years old;
Histologically proven nasopharyngeal squamous cell carcinoma, World Health Organization (WHO) II-III type;
Union Internationale Contre le Cancer(UICC) stage 9 clinical stage II patients;
Karnofsky score ≥ 80 points;
No evidence of distant metastasis;
Having an nasopharyngeal MRI before treatment ,which can measure the size of the tumor in order to analyze the effect.
Exclusion Criteria:
The subject had previously suffered from other malignancies (except non-melanotic skin cancer or cervical carcinoma in situ);
Previously received immunotherapy;
Previously received chemotherapy;
Previously received radiation therapy;
Patients who had previously undergone surgical treatment for head and neck tumors (excluding cervical lymphadenectomy);
Evidence of distant metastases or other malignancies at the same time.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dehua Wu
Phone
18602062748
Email
18602062748@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
IMRT Plus Cisplatin Versus IMRT in Patients With Stage 2 Nasopharyngeal Carcinoma
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