Status:
UNKNOWN
Trifluridine/Tipiracil (TAS-102) With or Without Thalidomide for the Treatment of Metastatic Colorectal Cancer
Lead Sponsor:
Fujian Cancer Hospital
Conditions:
Metastatic Colorectal Cancer
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
Thalidomide has both anti-angiogenesis and antiemetic effects, and its combined use with TAS-102 may reduce the gastrointestinal reactions associated with TAS-102, while enhancing antitumor efficacy a...
Detailed Description
In the past decade, the use of targeted drugs has greatly improved the overall survival of patients with mCRC. However, there are currently few effective drugs available clinically. Trifluridine/Tipir...
Eligibility Criteria
Inclusion
- Have histological or cytological documentation of adenocarcinoma of the colon or rectum (mCRC).
- For patients with disease progression after conventional treatment, TAS-102 is determined as the third-line therapy or beyond according to the routine treatment practice of the researcher.
- Aged no less than 20 years.
- Have a measurable disease, according to RECIST version 1.1 6.Eastern Cooperative Oncology Group performance status 0-2. 7.Life expectancy of at least 12 weeks. 8.For women with reproductive potential, serum tests were performed within 7 days before the start of study treatment β- Human chorionic gonadotropin (β- HCG) pregnancy test, the result is negative. Women with reproductive potential must agree to take appropriate contraceptive measures with informed consent until at least 6 months after the last use of the study drug.
- Sufficient bone marrow, liver and kidney functions and meet the following laboratory requirements:
- Platelet count ≥75 × 109 /L
- Hemoglobin level ≥90 g/L
- Absolute neutrophil count ≥1.5× 109 /L
- a) Total bilirubin ≤1.5 × upper limit of normal (ULN) b) Alanine aminotransferase and aspartate aminotransferase ≤2.5 × ULN (≤5 × ULN for patients with liver metastases) d) Serum creatinine ≤1.5 × ULN e) Glomerular filtration rate ≥30 ml/min/1.73 m2, according to the modified diet in renal disease abbreviated formula 10.Able to take oral drugs. 11.Have signed written informed consent.
- Exclusion criteria
- With arterial or venous thrombosis or embolic events such as myocardial infarction, cerebral thrombosis, intracerebral hemorrhage, deep venous thrombosis or pulmonary embolism within 6 months before the start of the study.
- Evidence or history of any bleeding diathesis, irrespective of severity. Any hemorrhage or bleeding event ≥ grade 3 (adverse events per CTCAE v5.0) within 4 weeks prior to the start of treatment.
- Peripheral neuropathy \> grade 1 (adverse events per CTCAE v5.0).
- History of uncontrolled or medicated heart disease.
- Seizure disorder requiring medication.
- Known history of human immunodeficiency virus (HIV) infection.
- Patients with an active infection.
- Other uncontrolled concurrent diseases determined by the researchers as not meeting the study conditions.
- Patients with ascites and pleural effusion with clinical symptoms requiring treatment.
- Known allergy to any of the study drug ingredients.
- Unable to swallow oral medication.
- Prior exposure to TAS-102 or thalidomide.
- Patients who have brain metastases.
Exclusion
Key Trial Info
Start Date :
October 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2023
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT05266820
Start Date
October 1 2021
End Date
December 1 2023
Last Update
March 18 2022
Active Locations (6)
Enter a location and click search to find clinical trials sorted by distance.
1
Fujian Medical University Cancer Hospital, Fujian Cancer Hospital
Fuzhou, Fujian, China
2
First Affiliated Hospital of Fujian Medical University
Fuzhou, China
3
Fujian Provincial people's Hospital
Fuzhou, China
4
Fuzhou First Hospital affiliated to Fujian Medical University
Fuzhou, China