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Pharmacogenomics Study of CPT-11 as the First-line Chemotherapy for mCRC (PSIFL)

H

Huazhong University of Science and Technology

Status

Unknown

Conditions

Colorectal Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT01282658
TJCC-001

Details and patient eligibility

About

Irinotecan (CPT-11) is now widely used as the first-line chemotherapy for mCRC. There were 4 key enzymes for CPT-11 metabolizing, CYP3A4, UDP-glucuronosyltransferase, carboxylesterase(CES), and ATP-binding cassette (ABC) transporters. Genetic variations of those enzymes may cause the heterogeneity in safety and efficacy of CPT-11. The aim of this study is to figure out the correlation between the genetic polymorphism and the drug response.

Full description

collect blood samples,determining genetic contribution to the safety and efficacy of CPT-11.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Histologically confirmed colorectal cancer
  2. ≥ 18 years old
  3. Measurable disease, defined as to RECIST criteria
  4. Unresectable metastatic disease OR First recurrence/metastasis after adjuvant therapy and not suitable for operation
  5. FOLFIRI±cetuximab/bevacizumab as the first-line therapy
  6. Without expected course of radiotherapy during the first-line chemotherapy
  7. No previous CPT-11 chemotherapy
  8. ECOG performance status (PS) 0-2
  9. Not pregnant or nursing and Negative pregnancy test
  10. Voluntarily signed the informed consent
  11. Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
  12. AST and ALT ≤ 2.5 times ULN (≤ 5 times ULN if f liver metastases present)
  13. Creatinine clearance > 50 mL/min OR serum creatinine ≤ 1.5 times ULN

Exclusion criteria

  1. Brain metastases with obvious symptoms
  2. Severe bone marrow failure and can not be corrected
  3. Chronic diarrhea history
  4. Bowel obstruction without control
  5. Mental illness without control
  6. Clinically significant (i.e., active) cardiovascular disease, including any of the following: Cerebrovascular accidents/ Myocardial infarction/ Unstable angina/ New York Heart Association class II-IV congestive heart failure/ Serious cardiac arrhythmia requiring medication/ Uncontrolled hypertension
  7. Other co-existing malignancy or malignancy diagnosed within the past 5 years, except for basal cell or squamous cell carcinoma, or carcinoma in situ of the cervix
  8. Pelvic radiotherapy for the past 1 year
  9. Known allergy to any of the components of the study medications
  10. Serious, nonhealing wound or ulcer

Trial design

200 participants in 1 patient group

Colorectal cancer

Trial contacts and locations

1

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Central trial contact

Yuan X Lin, PHD; huang liu, MD

Data sourced from clinicaltrials.gov

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