Clinical Treatments in Specialized Disease of Laryngeal Carcinoma (LC) and Hypopharyngeal Carcinoma (HPC)

Sponsor
Eye & ENT Hospital of Fudan University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04908696
Collaborator
Changhai Hospital (Other), Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine (Other), Fudan University (Other), Shanghai Changzheng Hospital (Other), RenJi Hospital (Other), Shanghai 6th People's Hospital (Other), Xinhua Hospital, Shanghai Jiao Tong University School of Medicine (Other)
1,000
1
36
27.8

Study Details

Study Description

Brief Summary

For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery, open partial laryngectomy, radiotherapy, and transoral robotic surgery were performed according to NCCN guidelines (2020).

For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy performed according to NCCN guidelines (2020).

This study plan to analyze the clinical ouctomes of different treatment for the same T stage disease. The overall survival rate, disease specific survival, disease free survival, local control, regional control, and laryngeal function preservation rate were analyzed in this study.

Detailed Description

For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications.

For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy

  • radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications.

This study seek to analyze and compare the clinical ouctomes of different treatments for the same T stage disease of LC and HPC.

The main end events involving overall survival rate, disease specific survival rate, and laryngeal function preservation rate were analyzed in this study. Beside, the events of disease free survival rate, local control rate, and regional control rate were assessed.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1000 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Department of Otorhinolaryngology, Eye & ENT Hospital
Actual Study Start Date :
Dec 1, 2020
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
TLM treatment for LC and PHC patients with early stage

TLM group: Laryngeal carcinoma (LC) (supraglottic type and glottic type) and hypopharyngeal carcinoma (HPC) (pyriform sinus and posterior pharyngeal wall) patients with T1 and T2 stages can be treated with transoral laser microsurgery (CO2 laser resection) for proper indications (NCCN 2020).

Procedure: routines
For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • OPL treatment for LC and PHC patients with T1, T2, and T3 stages

    OPL group: Open partial laryngectomy with laryngeal function preservation is performed for patients with laryngeal carcinoma (LC) (supraglottic type, glottic type, and subglottic type) and hypopharyngeal carcinoma (PHC) (pyriform sinus, postcricoid, and posterior pharyngeal wall) with proper indications (NCCN 2020).

    Procedure: routines
    For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
    Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • R treatment for LC and PHC patients with early stage

    R group: radiotherapy is treated for laryngeal carcinoma (LC) and hypopharyngeal carcinoma (PHC) patients with early stage with proper indications (NCCN 2020).

    Procedure: routines
    For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
    Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • TORS treatment for LC and PHC patients with early stage

    TORS group: transoral robotic surgery is performed for proper laryngeal carcinoma (LC) and hypopharyngeal carcinoma (PHC) patients with early stage with proper indications.

    Procedure: routines
    For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
    Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • SPA treatment for LC and PHC patients with advanced stage

    SPA group: surgical treatment (S) ± postoperative adjuvant (PA) therapy is performed for laryngeal carcinoma (LC) and hypopharyngeal carcinoma (PHC) patients with advanced stage with proper indications (NCCN 2020).

    Procedure: routines
    For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
    Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • CCR treatment for LC and PHC patients with advanced stage

    CCR group: concurrent chemoradiotherapy (CCR) is performed for laryngeal carcinoma (LC) and hypopharyngeal carcinoma (PHC) patients with advanced stage with proper indications (NCCN 2020).

    Procedure: routines
    For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
    Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • ARC treatment for LC and PHC patients with advanced stage

    ARC group: neoadjuvant therapy (A) + radiotherapy/chemoradiotherapy (RC) is performed for laryngeal carcinoma (LC) and hypopharyngeal carcinoma (PHC) patients with advanced stage with proper indications (NCCN 2020).

    Procedure: routines
    For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
    Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • ASRC treatment for LC and PHC patients with advanced stage

    ASRC group: neoadjuvant therapy (A) + surgery (S) + radiotherapy (R) or chemoradiotherapy (C) is performed for laryngeal carcinoma (LC) and hypopharyngeal carcinoma (PHC) patients with advanced stage with proper indications (NCCN 2020).

    Procedure: routines
    For early stage laryngeal carcinoma and hypohparyngeal carcinoma (T1 and T2), transoral laser microsurgery (CO2 laser resection), open partial laryngectomy (vertical partial laryngectomy, cricohyoidoepiglottopexy, cricohyoidopexy, horizontal partial laryngectomy), partial hypopharyngectomy, radiotherapy, and transoral robotic surgery were performed for patients with proper indications (NCCN 2020). For advanced stage laryngeal carcinoma and hypohparyngeal carcinoma (T3 and T4), surgical treatment ± postoperative adjuvant therapy, concurrent chemoradiotherapy, neoadjuvant therapy + radiotherapy/chemoradiotherapy, or neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy were performed for patients with proper indications (NCCN 2020).
    Other Names:
  • Open partial laryngectomy with laryngeal function preservation
  • Radiotherapy
  • Transoral robotic surgery
  • Surgical treatment ± postoperative adjuvant therapy
  • Concurrent chemoradiotherapy
  • Neoadjuvant therapy + radiotherapy/chemoradiotherapy
  • Neoadjuvant therapy + surgery + radiotherapy or chemoradiotherapy
  • Outcome Measures

    Primary Outcome Measures

    1. 3 - years overall survival [Three years]

      the time between the treatment and the date of death from any causes

    2. 3 - years disease specific survival [Three years]

      the time between the treatment and the date of death from laryngeal carcinoma or hypohparyngeal carcinoma

    3. 3 - years laryngeal function preservation [Three years]

      the time between the treatment and the date of laryngeal function preservation failure

    Secondary Outcome Measures

    1. 3 - years disease free survival [Three years]

      the time between the treatment and the first evidence of disease recurrence, metastasis or death

    2. 3- local control [Three years]

      the time between the treatment and the first evidence of local recurrence

    3. 3- regional control [Three years]

      the time between the treatment and the first evidence of regional recurrence

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Laryngeal cancer: glottic type, supraglottic type, and subglottic type; hypopharyngeal cancer: pyriform sinus type, postcri-coid type, and posterior pharyngeal wall type.

    • T1, T2, T3, and T4 stage.

    • Age 18 - 90.

    • Male or female.

    • Good compliance.

    • No other severe related diseases that may impact the treatment (such as other tumors, severe heart, lung and central nervous system diseases, etc.).

    • Negative pregnancy test (for female patients with fertility).

    • Male patients with fertility and female patients with fertility and pregnancy risk must agree to use contraceptive methods throughout the study period, and continued until at least 6 months after the last dose of cisplatin. Female patients do not have fertility. Female patients with postmenopausal status.

    Exclusion Criteria:
    • Patients who have previously been diagnosed with immunodeficiency or known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related diseases.

    • Patients with a known history of active tuberculosis (TB).

    • Pregnant women or lactating women.

    • The doctors believes that it is inappropriate for patients to participate in the trial: having, for example, severe acute or chronic medical conditions (including immune colitis, inflammatory bowel disease, non-infectious pneumonia, pulmonary fibrosis) or mental illness (including recent time [within the past year] or active suicidal ideation or behavior).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Lei Tao Shanghai Shanghai China 200031

    Sponsors and Collaborators

    • Eye & ENT Hospital of Fudan University
    • Changhai Hospital
    • Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
    • Fudan University
    • Shanghai Changzheng Hospital
    • RenJi Hospital
    • Shanghai 6th People's Hospital
    • Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

    Investigators

    • Study Chair: Lei Tao, Dr., Department of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, China

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    LeiTao, Director, Eye & ENT Hospital of Fudan University
    ClinicalTrials.gov Identifier:
    NCT04908696
    Other Study ID Numbers:
    • LC & HPC T121
    First Posted:
    Jun 1, 2021
    Last Update Posted:
    Jun 1, 2021
    Last Verified:
    May 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by LeiTao, Director, Eye & ENT Hospital of Fudan University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 1, 2021