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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01911988
Other study ID # XHGC 001
Secondary ID
Status Active, not recruiting
Phase N/A
First received July 23, 2013
Last updated October 19, 2016
Start date June 2013

Study information

Verified date October 2016
Source Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine association between Peripheral Immune Cells(PIC) and recurrence in stage II/III colorectal cancer


Description:

The investigators hypothesize differentiation of Peripheral Immune Cells(PIC) would result in resistance of chemotherapy and tumor local of metastatic recurrence.

The primary endpoint of this study is Disease Free Survival and the secondary endpoint is 5-year Overall Survival.

5ml peripheral blood will be sorted and counted through flow cytometry at the point of before primary treatment(surgery for colon cancers, neoadjuvant therapy for rectal cancers) , before the first chemotherapy postoperatively and 1 month after last chemotherapy.

Patients will be followed up with 3 monthly assessments in the first two years and 6 monthly assessments in the rest three years. Stratification factors include age , BMI , gender , tumor location , rectal or colon cancer stage,the chemotherapy (FOLFOX, XELOX, DeGramont or Capecitabine ),laparoscopic or laprotomy, anastomosis, concomitant medications and complications.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1
Est. completion date
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Clinically /Pahohistologically diagnosed as stageII/III CRC

- ECOG 0-2

- Age 18-90

- Gender both

Exclusion Criteria:

- Distant metastases noticed before or during surgery

- History of malignant tumor disease

- History of autoimmune diseases or immunodeficiencies

- History of hematological disease

- History of hepatic cirrhosis or Splenomegaly

- History of chronic kidney disease

- History of organ transplant

- History of chronic inflammatory disease

- Use of hematological drugs within 1 year prior to surgery

- Use of immunodulatory drugs within 1 year prior to surgery

- Use of chemotherapeutic drugs within 1 year prior to surgery

- Long term Use of non-steroid anti-inflammatory drugs(>6 months)

- Unable or Unwilling to undergo all the standard treatment

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Medical Center of Colon&Rectal Cancers Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disease Free Survival The time from resection to the time of disease recurrence(local or metastatic) or death from any cause. 5 years Yes
Secondary 5 years overall survival the time from resection to the time of death from any cause 5 years or the time of death Yes
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