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Prospective Registration of Head and Neck Cancer

Prospective Registration of Head and Neck Cancer Patients for Clinical Data and Tissue Collection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02546895
Enrollment
2000
Registered
2015-09-11
Start date
2015-09-01
Completion date
2024-12-31
Last updated
2026-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and Neck Cancer

Keywords

head and neck cancer patients, clinical data, tissue collection, prospective registration, patients

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.

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

Interventions

OTHERchart review

The patient charts will be reviewed to determine pretreatment characteristics, treatment-related adverse events, time to progression and overall survival. Behavioral: Questionnaires Completion of 3 questionnaires 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. It may take about 30 minutes to complete the questionnaires each time.

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Progression-free survival3 yearsRevised RECIST guideline

Secondary

MeasureTime frameDescription
Identification of biomarkers of clinical significance (prognostic)5 yearsBiomarkers associated with treatment outcomes (HPV, Epidermal growth factor receptor, p53, p16, etc)
Number of participants with treatment-related morbidity5 yearsCTCAE protocol
Number of participants with treatment response5 yearsNumber of participants with treatment response
Overall survival5 yearsRevised RECIST guideline
Scores of distress questionnaire1 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 treatmentQLQ HN43
Scores of support survey1 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 treatmentQLQ HN43
Quality of life score1 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 treatmentQLQ HN43

Countries

South Korea

Contacts

PRINCIPAL_INVESTIGATORHan-Sin Jeong, M.D.Ph.D.

Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center

PRINCIPAL_INVESTIGATORSe-Hoon Lee, M.D.Ph.D.

Department of Hemato-Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center

PRINCIPAL_INVESTIGATORDongryul Oh, M.D.Ph.D.

Department of Radiation Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center

STUDY_CHAIRChung-Hwan Baek, M.D.Ph.D.

Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center

STUDY_CHAIRYoung-Ik Son, M.D.Ph.D.

Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center

STUDY_CHAIRMan Ki Chung, M.D.Ph.D.

Department of Otorhinolaryngology-Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center

STUDY_CHAIRYoung Chan Ahn, M.D.Ph.D.

Department of Radiation Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center

STUDY_CHAIRMyung-Ju Ahn, M.D.Ph.D.

Department of Hemato-Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center

STUDY_CHAIRKeunchil Park, M.D.Ph.D.

Department of Hemato-Oncology, Sungkyunkwan University School of Medicine, Samsung Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 24, 2026