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NCT04849481Recruiting

The Research Plan of Taiwan Precision Medicine

The Research Plan of Taiwan Precision Medicine: Lung Cancer

Source: ClinicalTrials.gov · Last updated 8 Apr 2026

Brief summary (registry, in English)

Non-small-cell lung cancer (NSCLC) is one of the top three most common cancers in Taiwan. Targetable driver mutations in NSCLC are more prevalent in Asian population compared to those in Western population, which offers chances to apply suitable targeted therapies worldwide. For patients who failed to the treatment of tyrosine kinase inhibitors (TKIs), the genetic mutations from next-generation sequencing (NGS) reports can serve as the reference of treatment selection. Moreover, the expression of PD-1/PD-L1 serves as a helpful indicator for the response of immune checkpoint inhibitors (ICIs). On the other hand, patients with wild-type EGFR/ALK mutations and PD-L1-negative NSCLC who received chemotherapy had relative poorer survival than those received suitable targeted therapies and ICIs. To further elucidate the underlying molecular genomic aberrations, as well as the clinical demographics and therapeutic outcomes in above subpopulations, it is necessary to have a national, multi-centers and population-focused research project to collect data completely. Tumor tissue will be collected from advanced NSCLC patients with wild-type EGFR/ALK or with EGFR/ALK mutation after resistant to TKIs for next-generation sequencing analysis in a platform of data storage and sharing. The purpose of the precision medicine project is to establish tumor molecular profiling of specific NSCLC populations in Taiwan, to facilitate patients to have corresponding potential targeted therapeutics and suitable clinical trials, and to extend the median overall survival.

Status (registry)
Recruiting
Study type
Observational
Enrollment
550 (estimated)
First submitted
15 Apr 2021
Start date
23 Jun 2021
Primary completion date
31 Dec 2030
Lead sponsor
National Health Research Institutes, Taiwan
Diseases
Lung cancer
NCT number
NCT04849481

What you commit to

  • Study type: Observational
  • Planned participants: 550
  • From 23 Jun 2021 to the primary completion date, 31 Dec 2030
  • 13 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Ages 20 and above.
  • Pathological reports showed adenocarcinoma, squamous cell carcinoma, large cell carcinoma, adenosquamous carcinoma, and sacromatoid carcinoma.
  • For patients with squamous cell carcinoma, only never smokers and light smokers (less than 10 cigarettes per day) are indicated.
  • For patients with advanced EGFR (-) and ALK (-) adenocarcinoma or other histological types regardless of EGFR/ALK status, treatment-naïve or failure to ≤ two lines of systemic treatment is allowed.
  • For patients with advanced EGFR (+) or ALK (+) adenocarcinoma, failure to ≤ two lines of systemic treatment, including tyrosine kinase inhibitor is allowed.
  • For patients with advanced EGFR exon 20 insertion/mutation (excluding T790M mutation) adenocarcinoma, failure to ≤ four lines of systemic treatment, including tyrosine kinase inhibitor is allowed.
  • Reacquisition of tumor tissue after the failure of previous systemic treatment
  • Willingness to provide the residual biopsy/operative slides.
  • Life expectancy more than 3 months.
  • Patients fully understand the protocol with the willingness to have regular follow-up.
  • For patients with advanced EGFR exon 20 insertion/mutation (excluding T790M mutation) adenocarcinoma: if the patient had died before 2022/07/31, the waiver of Informed Consent Form(s) is allowed under the permission of Independent Ethics Committee/Institutional Review Board (IEC/IRB). Exclusion Criteria
    • 1.Inability to cooperate by providing a complete medical history. 2.No available tumor tissues for genetic testing. 3.Undesirable compliance.

Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chang Gung Medical Foundation
Coordinator of this site? Confirm its status
Chiayi CityTaiwanRecruiting
Dalin Tzu Chi Hospital
Coordinator of this site? Confirm its status
DalinTaiwanRecruiting
Kaohsiung Medical University Chung-Ho Memorial Hospital
Coordinator of this site? Confirm its status
Kaohsiung CityTaiwanRecruiting
Chang Gung Medical Foundation
Coordinator of this site? Confirm its status
Kaohsiung CityTaiwanRecruiting
China Medical University Hospital
Coordinator of this site? Confirm its status
TaichungTaiwanRecruiting
Chung Shan Medical University Hospital
Coordinator of this site? Confirm its status
TaichungTaiwanRecruiting
Taichung Veterans General Hospital
Coordinator of this site? Confirm its status
TaichungTaiwanRecruiting
National Cheng Kung University Hospital
Coordinator of this site? Confirm its status
TainanTaiwanRecruiting
Taipei Veterans General Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanRecruiting
Taipei Medical University-Shuang Ho Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanRecruiting
Tri-Service General Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanRecruiting
National Taiwan University Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanRecruiting
Taoyuan General Hospital
Coordinator of this site? Confirm its status
TaoyuanTaiwanRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.