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Clinical Trials in China / NCT06952400
Recruiting Observational

The Registry Study of Genetic Alterations of Melanoma in Taiwan

NCT06952400 · tracked via the Priya Life Science China tracker
Sponsor
National Health Research Institutes, Taiwan
Phase
Observational
Started
2022-08-22
Last updated
2025-05-06

Condition(s) studied

Primary Melanoma of the Extremity

Study summary

Cutaneous melanoma is the most aggressive malignancy in skin cancers. Cutaneous melanoma is a rare disease in Taiwan with an incidence rate of around 1/100,000. Acral lentiginous melanoma is the most common subtype and comprises more than half of cutaneous melanoma in Asia including Taiwan but only 1% in Caucasians. In addition, mucosal melanoma accounts for more than 20% of malignancy melanoma in Taiwan but only 1% in Caucasians. Acral and mucosal melanomas have distinct epidemiological, clinical, pathological and genetic features from non-acral melanoma which is commonly seen in Western countries. Comparing with melanoma in Caucasians, Asian melanoma has higher recurrence rate after primary surgery, lower response rate to immunotherapy, and shorter progression-free survival for immunotherapy and targeted therapy leading generally poor survival outcomes regardless stage.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: 1. Age \> 18 years old 2. Pathologically confirmed melanoma. (Patients with additional malignancies requiring treatment or follow-up are allowed. Only treatment for melanoma should be recorded). 3. ECOG performance status \< 3 4. Cohort 1(early acral melanoma): melanoma, stage I/II; Cohort 2 (locally advanced acral melanoma): melanoma, stage III, resectable; and Cohort 3 (advanced): unresectable / metastatic melanoma, stage III/IV or recurrent melanoma (unresectable). Staging is based on AJCC Cancer Staging System 8th edition). The patients with advanced melanoma with available comprehensive NGS report are included in cohort 4. 5. Willingness to provide archival or newly obtained tumor tissues for this study proposal 6. Life expectancy more than 3 months - 7. Patients fully understand the protocol with the willingness to have regular follow-up Exclusion Criteria: 1. Inability to cooperate by providing a complete medical history 2. No available tumor tissues for genetic testing (archived tissue sampling more than 5 years from screening date) 3. Undesirable compliance (Mental status is not fit for further treatment or data collection.)

Primary outcome measure(s)

Trial sites (16)

FacilityCityRegionStatus
Taipei Veterans General Hospital Taipei Taiwan/Taipei Recruiting
CHANG GUNG MEMORIAL HOSPITAL, Chiayi Chiayi City Taiwan Recruiting
Kaohsiung Chang Gung Memorial Hospital Kaohsiung City Taiwan Recruiting
Kaohsiung Medical University Kaohsiung City Taiwan Recruiting
National Taiwan University Hospital ,NTUH Hsin-Chu Branch Sindian City Taiwan Recruiting
China Medical University Hospital Taichung Taiwan Recruiting
Chung Shan Medical University Hospital Taichung Taiwan Recruiting
Taichung Veterans General Hospital Taichung Taiwan Recruiting
National Cheng Kung University Hospital Tainan Taiwan Recruiting
Koo Foundation Sun Yat-Sen Cancer Center Taipei Taiwan Recruiting
MacKay Memorial Hospital Taipei Taiwan Recruiting
National Taiwan University Hospital Taipei Taiwan Recruiting
Taipei Medical University -Ministry of Health and Welfare Shuang-Ho Hospital Taipei Taiwan Recruiting
Wan Fang Hospital, Taipei Medical University Taipei Taiwan Recruiting
CHANG GUNG MEMORIAL HOSPITAL, Linkou Taoyuan Taiwan Recruiting
Taoyuan General Hospital, Ministry of Health and Welfare Taoyuan Taiwan Recruiting

More National Health Research Institutes, Taiwan trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06952400 on ClinicalTrials.gov ↗ ← All trials in China