HuaMC-1: MRD Test in Common Risk Stage II Colorectal Cancer

Sponsor
First Affiliated Hospital Xi'an Jiaotong University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05795010
Collaborator
Second Affiliated Hospital of Xi'an Jiaotong University (Other)
60
1
6
9.9

Study Details

Study Description

Brief Summary

Patients with colorectal cancer who were confirmed as stage II general risk type in the postoperative pathological report began to be enrolled. Observe the sensitivity of the detection of micro-MRD before operation and the postoperative positive rate of this type of patients.

Condition or Disease Intervention/Treatment Phase
  • Other: MRD test

Detailed Description

This observation part is about the patients with general risk stage II colorectal cancer who have received R0 resection after screening by nanofiltration criteria. Twenty milliliters of venous blood samples were reserved before surgery, and tumor tissue samples were reserved within 30 minutes in vitro during surgery. After the pathological diagnosis of the patients after surgery, they began to be enrolled. To observe the sensitivity of MRD detection in preoperative diagnosis of patients with general risk stage II colorectal cancer, and to study its positive rate one month and three months after operation.

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Case-Only
Time Perspective:
Other
Official Title:
Observation of MRD Detection for Preoperative Sensitivity and Postoperative Positive Rate in Common Risk Stage II Colorectal Cancer
Anticipated Study Start Date :
Mar 30, 2023
Anticipated Primary Completion Date :
Apr 10, 2023
Anticipated Study Completion Date :
Sep 30, 2023

Outcome Measures

Primary Outcome Measures

  1. Positive rate of preoperative MRD test [six months]

    To observe the positive rate of preoperative MRD detection for stage II colorectal cancer

Secondary Outcome Measures

  1. Positive rate of MRD test 1 month and 3 months after operation [nine months]

    Observe the positive rate of MRD detection at 1 month and 3 months after operation for stage II colorectal cancer

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18-75;

  • Pathologically confirmed rectal adenocarcinoma;

  • Pathological differentiation is highly or moderately differentiated;

  • The pathological stage was pT3N0, that is, invasion of the proper muscular layer of the intestinal wall without lymph node metastasis;

  • No new adjuvant treatment before operation

  • There was no vascular infiltration and nerve infiltration in postoperative pathology;

  • No preoperative intestinal obstruction or tumor site perforation;

  • No postoperative pathological margin was positive or unknown;

  • The distance between the pathological cutting edge and the tumor was more than 1 cm;

  • Invasion of mesentery of intestinal wall ≤ 2mm;

  • More than 12 lymph nodes were submitted for examination;

  • Nonlocal recurrence and distant metastasis;

  • No multiple primary carcinoma of colon and rectum;

  • Physical condition score PS ≤ 2 points;

  • Patients and their families can understand and are willing to participate in this study and provide written informed consent.

Exclusion Criteria:
  • Multiple intestinal carcinomatosis

  • Previous history of malignant tumor,

  • There are concurrent malignant tumors in the whole body except for colorectal cancer

  • Colorectal cancer with preoperative anti-tumor treatment

  • Pregnant or lactating women

  • There are serious complications during or after operation, affecting the prognosis

  • Hepatitis B or Hepatitis C antibody positive

  • HIV antibody positive

  • Other diseases considered by the research doctor to affect the prognosis and survival

  • Other conditions that the research doctor believes are not consistent with this study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 First Affiliated Hospital of Xian Jiaotong University Xi'an Shaanxi China 710061

Sponsors and Collaborators

  • First Affiliated Hospital Xi'an Jiaotong University
  • Second Affiliated Hospital of Xi'an Jiaotong University

Investigators

  • Study Chair: Yongchun Song, MD, First Affiliated Hospital of Xian Jiaotong University

Study Documents (Full-Text)

More Information

Publications

Responsible Party:
First Affiliated Hospital Xi'an Jiaotong University
ClinicalTrials.gov Identifier:
NCT05795010
Other Study ID Numbers:
  • XJTU1AF2023LSK-174
First Posted:
Apr 3, 2023
Last Update Posted:
Apr 3, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
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 Apr 3, 2023