Prospective Registration of Head and Neck Cancer

Sponsor
Samsung Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT02546895
Collaborator
(none)
2,000
1
99
20.2

Study Details

Study Description

Brief Summary

Head and neck cancers account for the sixth leading cause of cancers worldwide. The annual incidence of Head and neck cancers is more than 650,000 the patients each year. Head and neck cancers are associated with smoking, alcohol consumption, human papilloma virus (type 16 and 18) and previous exposure to radiation.

So far, most of clinical and research data about head and neck cancers, such as the etiology, pathogenesis, prognosis factors and associated factors, treatment outcomes, are from Western countries. However, due to various environmental factors, for example race, genetics, geographical factors, general hygiene and health care system differences, the possibility of differences of disease characteristics between Western and Asian people should be considered.

For several decades, there have been many studies about treatment modalities (surgery, chemotherapy, and radiation therapy), complications and side effects for head and neck cancers in the West. Many institutions tried to improve the survival rate and resolve the toxicity of chemotherapy and radiation treatment for head and neck cancer patients. However there has been little information about the characteristics of head and neck cancers, effectiveness of treatment (survival rate, recurrence, and complication rate), and prognosis, particularly in Korean as well as in Asian patients.

Therefore it is necessary to evaluate and analyze the features of head and neck cancers such as etiology, pathogenesis, risk factors, prognostic factors, treatment outcomes in a site specific cohort (South Korea) separately. It could be helpful to improve the treatment outcomes of head and neck cancers overall, to design race or site specific treatments for head and neck cancers, and to develop management strategy common in Asia as well as the West.

The purpose of this study is

  1. To establish the prospective tumor registry about patient's information, treatment-related morbidities, treatment outcomes and quality of life, in addition to the prospective collection of patient samples (blood and tumor tissues).

  2. To establish the predictive model for treatment outcomes and treatment-related morbidities.

  3. To develop the biomarkers as predictive and/or prognostic factors.

Condition or Disease Intervention/Treatment Phase
  • Other: chart review

Detailed Description

Review of medical records Medical records of enrolled patients will be reviewed to evaluate clinical characteristics, treatment-related adverse events, time to progression and overall survival.

Behavioral : Questionnaires 3 times : Prior to the 1 week before treatment(radiotherapy or chemotherapy) begins or been hospitalized for surgery the same day, 1 week after the end of treatment(expected average of 8 weeks), and again 3 months after treatment Other Names : Surveys

Study Design

Study Type:
Observational
Anticipated Enrollment :
2000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prospective Registration of Head and Neck Cancer Patients for Clinical Data and Tissue Collection
Study Start Date :
Sep 1, 2015
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Outcome Measures

Primary Outcome Measures

  1. Progression-free survival [3 years]

    Revised RECIST guideline

Secondary Outcome Measures

  1. Identification of biomarkers of clinical significance (prognostic) [5 years]

    Biomarkers associated with treatment outcomes (HPV, Epidermal growth factor receptor, p53, p16, etc)

  2. Number of participants with treatment-related morbidity [5 years]

    CTCAE protocol

  3. Number of participants with treatment response [5 years]

    Number of participants with treatment response

  4. Overall survival [5 years]

    Revised RECIST guideline

  5. Scores of distress questionnaire [1 week before treatment(radiotherapy or chemotherapy) begins or been hospitalized for surgery the same day, 1 week after the end of treatment(expected average of 8 weeks), and again 3 months after treatment]

    QLQ HN43

  6. Scores of support survey [1 week before treatment(radiotherapy or chemotherapy) begins or been hospitalized for surgery the same day, 1 week after the end of treatment(expected average of 8 weeks), and again 3 months after treatment]

    QLQ HN43

  7. Quality of life score [1 week before treatment(radiotherapy or chemotherapy) begins or been hospitalized for surgery the same day, 1 week after the end of treatment(expected average of 8 weeks), and again 3 months after treatment]

    QLQ HN43

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults over 19 years-old

  • Patients diagnosed as head and neck cancer histopathologically according to American Joint Committee on Cancer, Cancer staging manual, 7th edition at Samsung Medical

Center:
  • Comprise a part of head and neck

  • Oral cavity

  • Pharynx

  • Larynx

  • Hypopharynx

  • Nasal cavity

  • Paranasal sinus

  • Nasopharynx

  • Salivary gland

  • Skin in the head and neck

  • In case patients are diagnosed at other hospitals, it can be possible to register the tissue of cancer cell with Samsung medical center and confirm the diagnosis by pathologists of Samsung medical center.

  • Histopathological type:

  • Squamous cell carcinoma

  • Malignant melanoma

  • Sarcoma and other carcinomas are included.

  • Metastasis of Unknown Origin (MUO) at head and neck is included.

  • Patients who receive a proper treatment as scheduled.

  • Informed consents: patients who understand the purpose of study and are capable of giving a written consent.

Exclusion criteria:
  • Patients who do not meet the requirements of inclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsung Medical Center Seoul Korea, Republic of 135-710

Sponsors and Collaborators

  • Samsung Medical Center

Investigators

  • Principal Investigator: Han-Sin Jeong, M.D.Ph.D., Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Principal Investigator: Se-Hoon Lee, M.D.Ph.D., Department of Hemato-Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Principal Investigator: Dongryul Oh, M.D.Ph.D., Department of Radiation Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Study Chair: Chung-Hwan Baek, M.D.Ph.D., Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Study Chair: Young-Ik Son, M.D.Ph.D., Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Study Chair: Man Ki Chung, M.D.Ph.D., Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Study Chair: Young Chan Ahn, M.D.Ph.D., Department of Radiation Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Study Chair: Myung-Ju Ahn, M.D.Ph.D., Department of Hemato-Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center
  • Study Chair: Keunchil Park, M.D.Ph.D., Department of Hemato-Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Han-Sin Jeong, Professor, Samsung Medical Center
ClinicalTrials.gov Identifier:
NCT02546895
Other Study ID Numbers:
  • 2015-06-132
First Posted:
Sep 11, 2015
Last Update Posted:
May 9, 2022
Last Verified:
May 1, 2022
Keywords provided by Han-Sin Jeong, Professor, Samsung Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 9, 2022