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Precision Medicine for Colorectal Cancer Liver Metastasis Guided by Multi-omics Data Under the Umbrella Theory

Precision Medicine for Colorectal Cancer Liver Metastasis Guided by Multi-omics Data Under the Umbrella Theory

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04525807
Enrollment
200
Registered
2020-08-25
Start date
2020-09-01
Completion date
2022-09-01
Last updated
2020-08-25

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

Conditions

Colorectal Cancer Metastatic

Brief summary

In order to more accurately discover the cause of drug resistance in tumor treatment, and to provide a new basis for precise treatment. Therefore, based on the umbrella theory of precision medicine, we carried out this single-center, prospective, and observational study to include patients with liver metastases from colorectal cancer. By combining genome, transcriptome, and proteomic sequencing data, we established a basis for colorectal cancer liver Transfer the multi-omics data of the sample, describe the reason for the resistance of the first-line treatment, and search for new therapeutic targets.

Interventions

DIAGNOSTIC_TESTMulti-omics

Use multi-omics to analyze

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* ECOG score 0-2 points * Pathologically diagnosed patients with colorectal cancer * Combined with liver metastases confirmed by imaging, and the lesion is measurable (RECIST standard) * The lesion is available * First-line treatment failed; hematology, liver and kidney function tests are suitable for back-line treatment * Informed consent

Exclusion criteria

* With brain metastases * History of other malignancies * Pregnancy or breastfeeding * Have received other drug clinical studies within 30 days before the start of this study

Design outcomes

Primary

MeasureTime frameDescription
Objective response rate1 yearRefers to the proportion of patients whose tumors have shrunk to a certain amount and maintained for a certain period of time, including complete remission (CR) and partial remission (PR) cases

Secondary

MeasureTime frameDescription
progression-free survival1 yearRefers to the date from initial diagnosis to tumor progression
Overall survival3 yearsRefers to the date from initial diagnosis to last follow-up or death date

Outcome results

None listed

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