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A prospective investigation of the ColoProg in stage II colorectal cancer patients on the prognostic value and the predict value in postoperative adjuvant therapy efficiency

A prospective investigation of the ColoProg in stage II colorectal cancer patients on the prognostic value and the predict value in postoperative adjuvant therapy efficiency

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052603
Enrollment
Unknown
Registered
2021-11-02
Start date
2022-02-01
Completion date
Unknown
Last updated
2023-04-12

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:NA

Sponsors

Cancer Hospital Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Clinical stage II (cT3-4N0M0) colorectal adenocarcinoma and mucinous adenocarcinoma; 2. Aged 18 to 70 years; 3. The selection must be the first diagnosis of colorectal cancer and no previous history of other malignant tumors; 4. Have not received neoadjuvant therapy; 5. Able to provide MMR or MSI diagnostic report; 6. The NCCN guidelines on clinical high-risk factors (T stage, histological differentiation, vascular invasion, nerve invasion, intestinal obstruction, tumor site perforation, positive surgical margins, and safe margins) can be obtained from pathology reports and medical records. , the number of lymph nodes sent for examination); 7. Can provide the following paraffin pathological specimens: 1) The pathological specimen number matches the clinical patient information; 2) 2 paraffin sections with a thickness of 50 µm and 4 paraffin sections with a thickness of 5 µm; 3) The content of tumor tissue in the section is not less than 50%, and the proportion of necrotic tissue is less than 10%; 4) Paraffin tissue is not stained. 8. Patients voluntarily participated in this study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. After pathological diagnosis, the pathological stage of the tumor is not stage II (pT3-4N0M0); 2. Colorectal cancer cases whose pathological types are not adenocarcinoma and mucinous adenocarcinoma; 3. The test result of microsatellite instability is MSI-H or dMMR; 4. Pregnant or lactating women; 5. Any other factors that the researcher believes may affect the results of the study or lead to the termination of the study.

Design outcomes

Primary

MeasureTime frame
DNA Ploidy;Tumor stroma;

Countries

China

Contacts

Public ContactWang Xishan

Cancer Hospital Chinese Academy of Medical Sciences

wxshan1208@126.com+86 17601099616

Outcome results

None listed

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