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Application of peripheral blood Tregs cell detection in predicting the efficacy of chemotherapy / targeted therapy in patients with advanced colorectal cancer.

Application of peripheral blood Tregs cell detection in predicting the efficacy of chemotherapy / targeted therapy in patients with advanced colorectal cancer.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036505
Enrollment
Unknown
Registered
2020-08-23
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-14

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

Conditions

colorectal cancer

Interventions

case series:Nil

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) They voluntarily participated in the study and signed a written informed consent; (2) 18-75 years old patients; (3) Histologically confirmed colorectal cancer; (4) Metastatic lesions appeared for the first time, but radical resection was impossible; (5) The status of Ras and BRAF genes in tumor tissue was clear; (6) CT or MRI confirmed that at least one measurable lesion met RECIST 1.1 standard; (7) The estimated survival time was at least 12 weeks; (8) The ECoG score of physical condition was 0-1; (9) Sufficient important organ function (Hematology, liver and kidney function, etc.);

Exclusion criteria

Exclusion criteria: (1) They had received chemotherapy for CRC in the past, except for adjuvant treatment which was over 9 months (including oxaliplatin / irinotecan) before the start of the study, and the end of adjuvant therapy > 6 months (without oxaliplatin / irinotecan); (2) Radiotherapy or surgery was performed within 30 days before treatment; (3) He had previously received monoclonal antibody therapy, VEGF pathway targeting therapy, EGFR pathway targeting therapy or other signal transduction pathway inhibitors; (4) Ovious cavity or necrosis in the tumor; (5) Poor control of infection; (6) Poor control of serous cavity effusion; (7) Have a clear history of neurological or mental illness, including epilepsy or dementia; (8) Other exclusion criteria refer to clinical study requirements.

Design outcomes

Primary

MeasureTime frame
Tregs cell value;DFS;

Countries

China

Contacts

Public ContactChuan Liu

Shanghai General Hospital

chuanliu2005@163.com+86 15921295283

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026