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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
Nanfang Hospital, Southern Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nasopharyngeal Carcinoma focused on measuring Nasopharyngeal Carcinoma, Intensity modulated radiotherapy, Cisplatin

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    February 15, 2017
    Last Updated
    February 27, 2017
    Sponsor
    Nanfang Hospital, Southern Medical University
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    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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