CANDIDATE: CirculAting Tumor DNA in Patients DIagnosed With Lung Metastasis From Colorectal Cancer: candiDate Selection for Local AblaTive thErapy

Sponsor
Yonsei University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04704960
Collaborator
(none)
400
1
33.9
11.8

Study Details

Study Description

Brief Summary

The investigators will detect circulating tumor DNA in blood of patients with lung metastases from colorectal cancer using NGS technology and intend to use it for predicting the outcome of local treatment (surgery or radiation) and recurrence of lung metastases.

Condition or Disease Intervention/Treatment Phase
  • Other: Diagnostic Test: liquid biopsy

Detailed Description

The investigators produce customized gene target panel by selecting genes that are commonly found in colorectal cancer and metastasis from existing literature.

In patients diagnosed with lung metastases from colorectal cancer, 20mL of whole blood is collected before and after local treatment (surgery or radiation) and cell-free DNA (cfDNA) is extracted from the collected blood. Thereafter, 20 mL of whole blood is additionally collected once after 3 months (±2 months) and once after 6 months (±2 months) during follow-up and cfDNA is extracted. The investigators perform sequencing from the extracted cfDNA.

The investigators compare the mutations detected in cfDNA before and after local treatment and identify the trend of reducing mutations in cfDNA after local treatment. So The investigators discover biomarkers for the outcome of local treatment. The investigators also search for mutations for target drugs from mutation profiling of cfDNA.

Study Design

Study Type:
Observational
Anticipated Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
CirculAting Tumor DNA in Patients DIagnosed With Lung Metastasis From Colorectal Cancer: candiDate Selection for Local AblaTive thErapy
Anticipated Study Start Date :
Feb 1, 2021
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Lung metastases from colorectal cancer, local ablative therapy (surgery or radiation)

patients diagnosed with lung metastases from colorectal cancer and undergoing surgery or radiation for lumg metastasis

Other: Diagnostic Test: liquid biopsy
detection of tumor DNA alteration in cf-DNA

Outcome Measures

Primary Outcome Measures

  1. correlation between circulating tumor DNA (ctDNA) before and after local treatment (surgery or radiation) and recurrence of lung metastases from colorectal cancer [about 6 month but additional extension for patients with relapse after local treatment]

    The investigations investigate whether ctDNA changes and f/u ctDNA fraction after local treatment (surgery or radiation) can be useful as markers to predict the outcome of local treatments.

Secondary Outcome Measures

  1. mutations related to target drug [about 6 month but additional extension for patients with relapse after local treatment]

    The investigations check for target drug related mutations from mutation profiling of ctDNA.

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. adults over 19 years of age

  2. those who understand research and have written consent

  3. cases diagnosed with lung metastases from colorectal cancer

Exclusion Criteria:
  1. pregnant women, nursing women

  2. those who lack the ability to voluntarily agree

  3. participation in other clinical trials where drugs for clinical trials are administered within the past four weeks as of the date of participation in clinical trials

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Laboratory Medicine, Yonsei University College of Medicine Seoul Korea, Republic of

Sponsors and Collaborators

  • Yonsei University

Investigators

  • Principal Investigator: Seung-Tae Lee, Severance Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yonsei University
ClinicalTrials.gov Identifier:
NCT04704960
Other Study ID Numbers:
  • 4-2020-1176
First Posted:
Jan 12, 2021
Last Update Posted:
Jan 14, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 14, 2021