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Immunological Markers Screening for Colorectal Cancer

Therapeutic Effect and Prognosis Predication Related Immunocyte Subgroup and Immunologic Factors Screeing for Colorectal Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02222753
Enrollment
5000
Registered
2014-08-21
Start date
2014-01-31
Completion date
Unknown
Last updated
2014-08-21

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

Conditions

Colorectal Cancer

Brief summary

Colorectal cancer incidence is increasing at an alarming rate in China. Recent reports concluded aberrant immunological function was associated with colorectal cancer outcome, however, the influence of immunocyte subgroup and immunologic factors on cancer outcome in colorectal cancer survivors is largely unknown.The investigators will explore the impact of immunocyte subgroup and immunologic factors on colorectal cancer disease-specific, disease-free and overall survival. The investigators will recruit approximately 5,000 patients as a prospective study cohort. During follow up, the investigators will explore the association of these factors with outcome of patients. The investigators believe that this project will improve the understanding of the impact of immunocyte subgroup and immunologic factors on colorectal cancer outcome.

Interventions

None listed

Sponsors

Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Air Force Military Medical University, China
CollaboratorOTHER
Second Military Medical University
CollaboratorOTHER
China-Japan Friendship Hospital
CollaboratorOTHER
Chinese Academy of Medical Sciences
CollaboratorOTHER
Peking University Cancer Hospital & Institute
CollaboratorOTHER
Chinese PLA General Hospital
CollaboratorOTHER
State Key Laboratory of Cancer Biology
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

Patient must have a histologically proven adenocarcinoma of colon or rectum cancer. * Patients must have a performance status of 0,1, or 2 by the Southwest Oncology Group criteria. * Patients must have recovered from any effects of surgery. * Evaluable disease must be present outside radiation field. At least 3 weeks must have elapsed after discontinuation of radiation therapy. * Patients must provide a signed consent to participate in the study. * Patients must complete all questionnaires.

Exclusion criteria

Patients with a proven history of peptic ulcer disease or gastroesophageal reflux. * History of other malignancy, except for cancers that have been treated with a curative intent and patient is without evidence of active disease. * Unresolved bacterial infection requiring treatment with antibiotics. * Pregnant or lactating women may not participate in the study. * Patients known to have HIV-1 virus infection because of the undetermined effect of this chemotherapy regimen in patients with HIV-1 and the potential for serious interaction with anti-HIV medications. * Gilbert's disease. * Other serious concurrent infection * Clinically significant cardiac disease not well controlled with medication (e.g. congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmias) or myocardial infarction within the last 12 months.

Design outcomes

Primary

MeasureTime frameDescription
Disease-specific survival5 yearsDisease-specific survival is defined as the time elapsed from surgery to death due to CRC. Concretely, the cause of death obtained in the follow up was classified according to ICD-10 conventions. Disease-specific deaths included those with an underlying cause attributed to ICD-10 codes C18.0-C20.0 or C26.0.

Secondary

MeasureTime frameDescription
Overall survival5 yearsOverall survival is defined as the time elapsed from surgery to the date of death from any cause.

Other

MeasureTime frameDescription
Disease-free survival5 yearsDisease-free survival is defined as the time elapsed from surgery to the first occurrence of any of the following events: recurrence of colorectal cancer; colorectal cancer distant metastasis; development of second non-colorectal malignancy excluding basal cell carcinomas of the skin and carcinoma in situ of the cervix; or death from any cause without documentation of a cancer-related event.

Countries

China

Contacts

Primary ContactLong Cui, M.D.
longcuidr@126.com

Outcome results

None listed

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