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Elective Level Ib Irradiation in Nasopharyngeal Carcinoma Patients Based on the International Guidelines

Primary Purpose

Nasopharyngeal Carcinoma

Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
level Ib-covering IMRT
level Ib-sparing IMRT
Sponsored by
Fujian Cancer Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nasopharyngeal Carcinoma

Eligibility Criteria

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

Inclusion Criteria:

  1. newly diagnosed, non-metastatic nasopharyngeal carcinoma histologically confirmed by biopsy;
  2. the following conditions: ① involvement of level II LNs with extracapsular extension(ECE); ② level II LNs involvement with maximum nodal axial diameter (MAD) greater than 2 cm;
  3. Eastern Cooperative Oncology Group (ECOG) score of 0 or 1.

Exclusion Criteria:

  1. level Ib involvement with positive pathological results;
  2. submandibular glands (SMGs) involvement;
  3. involvement of structures that drain to level Ib as the first echelon site (the oral cavity, anterior half of nasal cavity involvement);
  4. previous malignancy or other concomitant malignant disease.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    level Ib-covering IMRT

    level Ib-sparing IMRT

    Arm Description

    Patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II.

    Patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II

    Outcomes

    Primary Outcome Measures

    Regional relapse-free survival
    The regional relapse-free survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to the date of nodal relapse or death from any cause, whichever occurred first. Their differences will be compared between treatment arms using the log-rank test.
    level Ib recurrence rate
    The level Ib recurrent rate will be calculated by the ratio of mumbers of patients relapsed in level Ib and the numbers of cases in the whole group.

    Secondary Outcome Measures

    Local relapse-free survival
    The local relapse-free survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to documented local relapse or death from any cause. Their differences will be compared between treatment arms using the log-rank test.
    Distant metastasis-free survival
    The distant metastasis-free survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to documented distant metastasis or death from any cause. Their differences will be compared between treatment arms using the log-rank test.
    Overall survival
    The overall survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to death from any cause. Their differences will be compared between treatment arms using the log-rank test.
    Patient's quality-of-life: dry mouth
    European Organization for Research and Treatment of Cancer Quality-of-Life Head and Neck 35 items (QLQ-H&N35) version 1.0 questionnaires will be used to assess quality-of-life. All items pointing to this domain are averaged and then transformed to a scale of 0-100 according to the EORTC scoring manual. Higher scores on the symptom scales indicate more severe symptoms.
    Patient's quality-of-life: sticky saliva
    European Organization for Research and Treatment of Cancer Quality-of-Life Head and Neck 35 items (QLQ-H&N35) version 1.0 questionnaires will be used to assess quality-of-life. All items pointing to this domain are averaged and then transformed to a scale of 0-100 according to the EORTC scoring manual. Higher scores on the symptom scales indicate more severe symptoms.

    Full Information

    First Posted
    August 26, 2022
    Last Updated
    September 16, 2022
    Sponsor
    Fujian Cancer Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05519956
    Brief Title
    Elective Level Ib Irradiation in Nasopharyngeal Carcinoma Patients Based on the International Guidelines
    Official Title
    Elective Level Ib Irradiation in Nasopharyngeal Carcinoma Patients Based on the International Guidelines: an Open-label, Non-inferiority, Multicentre, Randomised Phase 3 Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 16, 2022 (Anticipated)
    Primary Completion Date
    September 1, 2025 (Anticipated)
    Study Completion Date
    September 30, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Fujian Cancer Hospital

    4. Oversight

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

    5. Study Description

    Brief Summary
    Currently, nasopharyngeal carcinoma (NPC) patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II will be recommended to receive level Ib-covering IMRT according to the International Guidelines. Our previous study, which retrospectively analyzed a cohort of 390 patients, indicated that it should be safe and feasible for patients who only had at least one of the above two radiological features. Thus, the investigators conduct this non-inferior phase 3, randomized trial to further determine the feasibility of sparing level Ib in patients who had level II involvement with ECE, and/or had a MAD of greater than 2cm in level II.
    Detailed Description
    Currently, nasopharyngeal carcinoma (NPC) patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II will be recommended to receive level Ib-covering IMRT according to the International Guidelines. Our previous study, which retrospectively analyzed a cohort of 390 patients, indicated that it should be safe and feasible for patients who only had at least one of the above two radiological features. Thus, the investigators conduct this non-inferior phase 3, randomized trial to further determine the feasibility of sparing level Ib in patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II.

    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
    398 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    level Ib-covering IMRT
    Arm Type
    Active Comparator
    Arm Description
    Patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II.
    Arm Title
    level Ib-sparing IMRT
    Arm Type
    Experimental
    Arm Description
    Patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II
    Intervention Type
    Radiation
    Intervention Name(s)
    level Ib-covering IMRT
    Intervention Description
    Patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II.
    Intervention Type
    Radiation
    Intervention Name(s)
    level Ib-sparing IMRT
    Intervention Description
    Patients who had level II involvement with extracapsular extension (ECE), and/or had a maximum nodal axial diameter (MAD) of greater than 2cm in level II.
    Primary Outcome Measure Information:
    Title
    Regional relapse-free survival
    Description
    The regional relapse-free survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to the date of nodal relapse or death from any cause, whichever occurred first. Their differences will be compared between treatment arms using the log-rank test.
    Time Frame
    3 year
    Title
    level Ib recurrence rate
    Description
    The level Ib recurrent rate will be calculated by the ratio of mumbers of patients relapsed in level Ib and the numbers of cases in the whole group.
    Time Frame
    3 year
    Secondary Outcome Measure Information:
    Title
    Local relapse-free survival
    Description
    The local relapse-free survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to documented local relapse or death from any cause. Their differences will be compared between treatment arms using the log-rank test.
    Time Frame
    3 year
    Title
    Distant metastasis-free survival
    Description
    The distant metastasis-free survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to documented distant metastasis or death from any cause. Their differences will be compared between treatment arms using the log-rank test.
    Time Frame
    3 year
    Title
    Overall survival
    Description
    The overall survival rate will be estimated using Kaplan-Meier method for each arm from the date of randomization to death from any cause. Their differences will be compared between treatment arms using the log-rank test.
    Time Frame
    3 year
    Title
    Patient's quality-of-life: dry mouth
    Description
    European Organization for Research and Treatment of Cancer Quality-of-Life Head and Neck 35 items (QLQ-H&N35) version 1.0 questionnaires will be used to assess quality-of-life. All items pointing to this domain are averaged and then transformed to a scale of 0-100 according to the EORTC scoring manual. Higher scores on the symptom scales indicate more severe symptoms.
    Time Frame
    3 year
    Title
    Patient's quality-of-life: sticky saliva
    Description
    European Organization for Research and Treatment of Cancer Quality-of-Life Head and Neck 35 items (QLQ-H&N35) version 1.0 questionnaires will be used to assess quality-of-life. All items pointing to this domain are averaged and then transformed to a scale of 0-100 according to the EORTC scoring manual. Higher scores on the symptom scales indicate more severe symptoms.
    Time Frame
    3 year

    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: newly diagnosed, non-metastatic nasopharyngeal carcinoma histologically confirmed by biopsy; the following conditions: ① involvement of level II LNs with extracapsular extension(ECE); ② level II LNs involvement with maximum nodal axial diameter (MAD) greater than 2 cm; Eastern Cooperative Oncology Group (ECOG) score of 0 or 1. Exclusion Criteria: level Ib involvement with positive pathological results; submandibular glands (SMGs) involvement; involvement of structures that drain to level Ib as the first echelon site (the oral cavity, anterior half of nasal cavity involvement); previous malignancy or other concomitant malignant disease.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Shaojun Lin, DR
    Phone
    13860603879
    Email
    linshaojun@yeah.net
    First Name & Middle Initial & Last Name or Official Title & Degree
    Qiaojuan Guo, DR
    Phone
    15080013157
    Email
    guoqiaojuan@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Shaojun Lin, DR
    Organizational Affiliation
    Fujian Cancer Hospital
    Official's Role
    Study Chair

    12. IPD Sharing Statement

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    Elective Level Ib Irradiation in Nasopharyngeal Carcinoma Patients Based on the International Guidelines

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