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Clinical Sequencing Project for Metastatic Cancer Patients for Personalized Cancer Clinic.

Clinical Sequencing Project for Metastatic Cancer Patients for Personalized Cancer Clinic.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02593591
Enrollment
40
Registered
2015-11-02
Start date
2015-11-06
Completion date
2018-07-31
Last updated
2019-12-30

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

Conditions

Colorectal Cancer

Brief summary

The next generation of personalized medical treatment according to the type of personal genetic information are evolving rapidly. The genome analysis needs systematic infra and database based on personal genetic information. Therefore, a big data of genome-clinical information is important. To determine the feasibility of the use of tumor's molecular profiling and targeted therapies in the treatment of advanced cancer and to determine the clinical outcome(Response rate,PFS, duration of response and overall survival )of patients with advanced cancer, the investigators are going to take a tumor tissue of patients and process molecular profiling and receive molecular profile directed treatments.

Interventions

None listed

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Subject is at least 19 years of age. 2. Subject has a histologically or cytologically confirmed diagnosis of Colorectal cancer. 3. Prior treatment with anti-PDL1 antibody or immune check point inhibitor or ramucirumab therapy in the First-line or maintenance setting is allowed 4. They must have refractory or progressive disease for which there is no further curative therapy available. 5. Be willing to provide fresh tissue for biomarker analysis, and, based on the adequacy of the tissue sample quality for assessment of biomarker status. 6. Must have a life expectancy of 3 months or more 7. Written and voluntary informed consent understood, signed and dated.

Exclusion criteria

1\. Patients who do not have enough tissue for acquisition

Design outcomes

Primary

MeasureTime frame
Response rate1 year

Secondary

MeasureTime frame
Progression Free Survival1 year
Duration of response1 year
overall survival1 year

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026