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Concurrent Chemoradiotherapy(CRT) in Locally Advanced(LA) SCCHN vs Cetuximab With Radiotherapy (RT) After Neoadjuvant Chemotherapy

Primary Purpose

Carcinoma, Squamous Cell of Head and Neck

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Cetuximab
radiation
Docetaxel
Cisplatin
Sponsored by
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carcinoma, Squamous Cell of Head and Neck

Eligibility Criteria

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

Inclusion Criteria:

  1. Histologically or cytologically confirmed first diagnosis of locally advanced squamous cell carcinoma of the head and neck
  2. Imaging (MRI, CT, bone scan) stage Ⅲ、Ⅳa (T1-2N2M0、T3N0-2M0、T4N0-2M0) (2010AJCC staging criteria)
  3. 18 years of age or older
  4. Presence of at least 1 measurable lesion according to RECIST version1.1
  5. DON'T accept surgery, chemotherapy or irradiation before trial entry
  6. Eastern Cooperative Oncology Group(ECOG) 0 or 1
  7. Expected survival period over 6months
  8. Before RT randomization, bone marrow and liver and kidney function in patients with meet the following criteria:

    • Hemoglobin(HB) ≥ 100g/L, neutrophil ≥ 2.0 × 109/L and platelet ≥ 100 × 109/L
    • Total bilirubin ≤ 1.5 times the upper limit of normal, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 1.5 times the upper limit of normal;
    • More than 1.5 times the upper limit of normal serum creatinine or creatinine clearance rate ≥ 60 ml/min, urea N ≤ 200mg/L;
    • The blood glucose level: good blood glucose control, fasting glucose, 3.9-7.2mmol/L postprandial blood glucose less than 10.0mmol/L, HbA1c < 7%;
  9. Signed written informed consent before any trail-related activities are carried out.

Exclusion Criteria:

  1. Patients accepted chemotherapy、radiotherapy or surgery;
  2. Distant metastasis before trail entry
  3. Female subjects who are pregnant or breast feeding;
  4. oral mucositis or oral mucositis has repeatedly made (1 times / month or more)before Chemotherapy or radiotherapy ;
  5. With teeth periodontitis;
  6. Any investigational medication within 30 days before trial entry;
  7. Elderly patients with dry stomatitis;
  8. Any unstable system diseases: including active infection, uncontrolled hypertension, unstable angina pectoris, within the last 3 months of the onset of angina, congestive heart failure, the group in June before the myocardial infarction, need serious mental disorder drug treatment, liver, kidney or metabolic diseases; mental / spiritual diseases such as Alzheimer's disease;
  9. Total bilirubin > 1.5 times the upper limit of normal, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) > 2.5 times the upper limit of normal;
  10. On gastrointestinal physiology is not perfect, or absorb the obstacle syndrome, or unable to tolerate oral medication, or active peptic ulcer;
  11. Past or current history of neoplasm oher than squamous cell carcinoma of the head and neck;
  12. Judgment according to the researchers, there are serious harm to patient safety or affect the patients completed the study with the disease, and patient compliance with the difference;
  13. known human immunodeficiency virus (HIV) infection;
  14. With immunodeficiency disease, or suffer from other acquired, congenital immunodeficiency disease, or a history of organ transplantation;
  15. Any disease, metabolic disorders, or physical examination or laboratory suspicion or treatment of complications in patients at high risk of drug.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    RT concurrent with cetuximab

    RT concurrent with TP

    Arm Description

    Selected 60 patients with locally advanced squamous cell carcinoma of the head and neck. They will be randomized to concurrent chemoradiotherapy versus concomitant cetuximab with radiotherapy after neoadjuvant chemotherapy.To observe the curative effect of the treatment of the cetuximab

    Selected 60 patients with locally advanced squamous cell carcinoma of the head and neck. They will be randomized to concurrent chemoradiotherapy versus concomitant cetuximab with radiotherapy after neoadjuvant chemotherapy. To observe the curative effect of concurrent radiotherapy and chemotherapy

    Outcomes

    Primary Outcome Measures

    Progression-free survival
    incidence of oral mucositis

    Secondary Outcome Measures

    Overall survival
    Overall response rate after induction chemotherapy

    Full Information

    First Posted
    April 18, 2016
    Last Updated
    April 24, 2016
    Sponsor
    Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02753140
    Brief Title
    Concurrent Chemoradiotherapy(CRT) in Locally Advanced(LA) SCCHN vs Cetuximab With Radiotherapy (RT) After Neoadjuvant Chemotherapy
    Official Title
    Concurrent Chemoradiotherapy in Locally Advanced Squamous Cell Carcinoma of the Head and Neck Versus Concomitant Cetuximab With Radiotherapy After Neoadjuvant Chemotherapy: a Randomized, Opened, Multicenter Phase II Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 2016 (undefined)
    Primary Completion Date
    March 2018 (Anticipated)
    Study Completion Date
    September 2018 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Daping Hospital and the Research Institute of Surgery of the Third Military Medical University

    4. Oversight

    5. Study Description

    Brief Summary
    Verify the effect and the incidence of oral mucositis of concurrent chemoradiotherapy in locally advanced squamous cell carcinoma of the head and neck versus concomitant cetuximab with radiotherapy after neoadjuvant chemotherapy. The predictive effect of Apurinic/apyrimidinic endonuclease 1(APE1)/ Ref-1 protein and Apurinic/apyrimidinic endonuclease 1(APE1)/Ref-1 antibody on oral mucositis.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Carcinoma, Squamous Cell of Head and Neck

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    RT concurrent with cetuximab
    Arm Type
    Experimental
    Arm Description
    Selected 60 patients with locally advanced squamous cell carcinoma of the head and neck. They will be randomized to concurrent chemoradiotherapy versus concomitant cetuximab with radiotherapy after neoadjuvant chemotherapy.To observe the curative effect of the treatment of the cetuximab
    Arm Title
    RT concurrent with TP
    Arm Type
    Experimental
    Arm Description
    Selected 60 patients with locally advanced squamous cell carcinoma of the head and neck. They will be randomized to concurrent chemoradiotherapy versus concomitant cetuximab with radiotherapy after neoadjuvant chemotherapy. To observe the curative effect of concurrent radiotherapy and chemotherapy
    Intervention Type
    Drug
    Intervention Name(s)
    Cetuximab
    Intervention Type
    Radiation
    Intervention Name(s)
    radiation
    Intervention Type
    Drug
    Intervention Name(s)
    Docetaxel
    Intervention Type
    Drug
    Intervention Name(s)
    Cisplatin
    Primary Outcome Measure Information:
    Title
    Progression-free survival
    Time Frame
    13 months
    Title
    incidence of oral mucositis
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Overall survival
    Time Frame
    5 years
    Title
    Overall response rate after induction chemotherapy
    Time Frame
    1 month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Histologically or cytologically confirmed first diagnosis of locally advanced squamous cell carcinoma of the head and neck Imaging (MRI, CT, bone scan) stage Ⅲ、Ⅳa (T1-2N2M0、T3N0-2M0、T4N0-2M0) (2010AJCC staging criteria) 18 years of age or older Presence of at least 1 measurable lesion according to RECIST version1.1 DON'T accept surgery, chemotherapy or irradiation before trial entry Eastern Cooperative Oncology Group(ECOG) 0 or 1 Expected survival period over 6months Before RT randomization, bone marrow and liver and kidney function in patients with meet the following criteria: Hemoglobin(HB) ≥ 100g/L, neutrophil ≥ 2.0 × 109/L and platelet ≥ 100 × 109/L Total bilirubin ≤ 1.5 times the upper limit of normal, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 1.5 times the upper limit of normal; More than 1.5 times the upper limit of normal serum creatinine or creatinine clearance rate ≥ 60 ml/min, urea N ≤ 200mg/L; The blood glucose level: good blood glucose control, fasting glucose, 3.9-7.2mmol/L postprandial blood glucose less than 10.0mmol/L, HbA1c < 7%; Signed written informed consent before any trail-related activities are carried out. Exclusion Criteria: Patients accepted chemotherapy、radiotherapy or surgery; Distant metastasis before trail entry Female subjects who are pregnant or breast feeding; oral mucositis or oral mucositis has repeatedly made (1 times / month or more)before Chemotherapy or radiotherapy ; With teeth periodontitis; Any investigational medication within 30 days before trial entry; Elderly patients with dry stomatitis; Any unstable system diseases: including active infection, uncontrolled hypertension, unstable angina pectoris, within the last 3 months of the onset of angina, congestive heart failure, the group in June before the myocardial infarction, need serious mental disorder drug treatment, liver, kidney or metabolic diseases; mental / spiritual diseases such as Alzheimer's disease; Total bilirubin > 1.5 times the upper limit of normal, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) > 2.5 times the upper limit of normal; On gastrointestinal physiology is not perfect, or absorb the obstacle syndrome, or unable to tolerate oral medication, or active peptic ulcer; Past or current history of neoplasm oher than squamous cell carcinoma of the head and neck; Judgment according to the researchers, there are serious harm to patient safety or affect the patients completed the study with the disease, and patient compliance with the difference; known human immunodeficiency virus (HIV) infection; With immunodeficiency disease, or suffer from other acquired, congenital immunodeficiency disease, or a history of organ transplantation; Any disease, metabolic disorders, or physical examination or laboratory suspicion or treatment of complications in patients at high risk of drug.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Zhenzhou Yang, Doctor
    Phone
    +86-13883270881
    Email
    yangzz1970@163.com

    12. IPD Sharing Statement

    Learn more about this trial

    Concurrent Chemoradiotherapy(CRT) in Locally Advanced(LA) SCCHN vs Cetuximab With Radiotherapy (RT) After Neoadjuvant Chemotherapy

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