Survival Benefit of Elective Neck Dissection in T1,2N0M0 Oral Squamous Cell Carcinoma

Sponsor
Sun Yat-sen University (Other)
Overall Status
Unknown status
CT.gov ID
NCT01334320
Collaborator
First Affiliated Hospital, Sun Yat-Sen University (Other), Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University (Other)
448
4
2
128
112
0.9

Study Details

Study Description

Brief Summary

Controversy over surgical treatment of clinically negative neck in early stage oral squamous cell carcinoma revolves around the uncertainty of its impact on patient prognosis. The efficacy of elective neck dissection on prognosis in T1, 2 N0M0 patients continues to be the subject of clinical debate. Currently the clinically negative patients are treated by one of the two main policies: one is elective neck dissection; the other is "watchful waiting". The objective of this multi-institutional prospective randomized controlled study is to evaluate the survival benefit of elective neck dissection on the prognosis of T1, 2 N0M0 patients with carcinoma of oral cavity. The enrolled patients with T1, 2 N0M0 oral cancer will be randomized into two groups: elective neck dissection versus watch and wait. The survival rate and the recurrence rate between two groups will be compared. The result of the study will give surgeons evidence-based instructions for the management of clinically negative neck in patients with cancer of oral cavity.

Condition or Disease Intervention/Treatment Phase
  • Procedure: elective neck dissection
N/A

Detailed Description

There are controversies on the benefits of elective neck dissection (END) for clinically negative neck in early stage oral squamous cell carcinoma. The aim of this study is to determine the need for a randomized controlled trial in order to evaluate the survival benefit of elective neck dissection on the prognosis of T1, 2 N0M0 patients with carcinoma of oral cavity. We initiate this multi-institutional study, expecting 448 primary oral cancer patients to be enrolled. And we are going to randomly divide these patients into two groups: END and "watch and wait". The END group will undergo one stage surgery of END and primary tumor excision, and the "watch and wait"group will be treated with primary tumor excision transorally as initial treatment, with rigorous postoperation consultation. All patients will be followed up with at least 5 years after initial treatment, and the survival rate and the recurrence rate between groups will be compared.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
448 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Survival Benefit of Elective Neck Dissection for Patients With T1,2N0M0 Oral Squamous Cell Carcinoma-A Prospective Multicenter Randomized Controlled Study
Study Start Date :
Apr 1, 2011
Anticipated Primary Completion Date :
Dec 1, 2015
Anticipated Study Completion Date :
Dec 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: elective neck dissection

patient underwent elective neck dissection as initial treatment, along with the excision of the primary tumor

Procedure: elective neck dissection
patient underwent elective neck dissection as initial treatment, along with the excision of the primary tumor
Other Names:
  • superior omohyoid neck dissection, SOHND
  • No Intervention: wait and see

    patient underwent primary tumor excision transorally as initial treatment, and without a cervical intervention

    Outcome Measures

    Primary Outcome Measures

    1. Whether elective neck dissection (END) has equal or higher survival rate to the wait and watch policy [5 years]

      The 5-year's survival and the disease free survival of the two group of patients are being measured and compared with one and other, so the survival benefit of the two policy is evaluated.

    Secondary Outcome Measures

    1. Does END have the equal or lower recurrence rate to the wait and watch policy [5 years]

      The recurrence includes recurrence of the primary tumor and the neck, and it's measured by clinical examination, MRI examination and ultrasonic inspection.

    2. quality of life [5 years]

      The quality of life of patients after surgery is measured by UW-QOL.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Age:20 to 70 years old, both male and female

    2. Histologically proven T1 or T2 N0 M0 (clinical) squamous cell carcinoma of the oral tongue, buccal mucosa, gingiva, floor of mouth, and hard palate

    3. The maximum diameter of the primary tumor is less than 4cm

    4. Clinical nodal staging has been confirmed negative via both clinical examination and imaging (MRI or lateral and central neck ultrasound)

    5. With at least 1-year's expected survival time

    6. Willing to join the protocol and is able to give written informed consent

    Exclusion Criteria:
    1. Patient with severe cardiac insufficiency, hepatic insufficiency, renal insufficiency, of systemic infection diseases

    2. The patient is pregnant or lactating

    3. Patients with a history of surgical treatment, radiotherapy, chemotherapy, biotherapy and targeted therapy, et al, before participating in the study

    4. Patient is currently participating in another investigational drug study

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital of Stomatology, Sun Yat-sen University Guangzhou Guangdong China 510055
    2 Cancer Center, Sun Yat-Sen University Cancer Center Guangzhou Guangdong China 510060
    3 The First Affiliated Hospital, Sun Yat-Sen University Guangzhou Guangdong China 510080
    4 Sun Yat-sen Memorial Hospital Guangzhou Guangdong China 510120

    Sponsors and Collaborators

    • Sun Yat-sen University
    • First Affiliated Hospital, Sun Yat-Sen University
    • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

    Investigators

    • Principal Investigator: Guiqing Liao, MD, DDS, Sun Yat-sen University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Gui-Qing Liao, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University
    ClinicalTrials.gov Identifier:
    NCT01334320
    Other Study ID Numbers:
    • 2010018
    First Posted:
    Apr 13, 2011
    Last Update Posted:
    Apr 10, 2015
    Last Verified:
    Apr 1, 2015
    Keywords provided by Gui-Qing Liao, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 10, 2015