jRCTs041220085CompletedNot Applicable
Phase2 study of intrapatient dose-escalation of biweekly trifluridine/tipiracil + bevacizumab for patients with metastatic colorectal cancer refractory to standard therapies (E-BiTS study)
Not provided0 sites36 target enrollmentStarted: November 9, 2022Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 36
- Primary Endpoint
- -
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Single Arm Study
- Intervention Model
- Single Assignment
- Primary Purpose
- Treatment Purpose
- Masking
- Open(masking Not Used)
Eligibility Criteria
- Ages
- 20age old over to No limit (—)
- Sex
- All
Inclusion Criteria
- •Patients has been diagnosed with unresectable advanced or recurrent colorectal adenocarcinoma by histopathological diagnosis.
- •The age of patients on registration date is 20 years or older.
- •ECOG PS 0 or
- •Patients have measurable lesions.
- •Patients have a history of refractory or intolerant to the following chemotherapy.
- •(1) All three drugs, fluorinated pyrimidine anticancer drug, oxaliplatin, and irinotecan
- •(2) Angiogenesis inhibitor (bevacizumab, ramucirumab, or aflibercept)
- •(3) Anti-EGFR antibody drug (cetuximab or panitumumab) in RAS wild type
- •(4) BRAF inhibitor (encorafenib) in BRAF mutant
- •(5) Immune checkpoint inhibitors (pembrolizumabor nivolumab) in MSI-H
- •Patients who have not been treated with FTD/TPI.
- •Patients who can take orally
- •Patients are expected to live for 3 months or longer
- •Patients whose latest test values within 14 days before registration meet all of the following.
- •(1) Number of neutrophils >= 1500/mm3
- •(2) Platelet count >= 75000/mm3
- •(3) Total bilirubin <= 1.5 mg / dL
- •(4) AST <= 100 U/L
- •(5) ALT <= 100 U/L
- •(6) Serum creatinine <= 1.5 mg/dL and Ccr >= 60mL/min
- •(7) Urine protein (test paper method) 1+ or less, or UPC (Urine Protein Creatinine) ratio <= 2.0
- •Patients have given written consent to participate in the study.
Exclusion Criteria
- •Patients with double cancers requiring chemotherapy (excluding hormone therapy)
- •Patients have infectious diseases which need systemic treatment.
- •Patients have difficulty in being enrolled in this study due to clinically problematic mental illness
- •Patients with the following complications
- •(1) Renal failure
- •(2) Cirrhosis / liver failure
- •(3) Chronic lung disease requiring oxygen administration
- •(4) Concomitant with unstable angina (angina whose onset or seizures have worsened within the last 3 weeks) or a history of myocardial infarction within 6 months
- •(5) Other complications that the doctor in charge considers to be serious
- •Patients receiving continuous systemic administration of steroids or immunosuppressants
- •Patients with unstable thromboembolism.
- •Pregnant women, lactating women, women who may be pregnant now, or patients who are not willing to use contraception
- •Patients judged by the investigator to be inappropriate
Outcomes
Primary Outcomes
-
Disease control rate
Secondary Outcomes
- PFS
- OS
- RDI
- RR
- AE
Investigators
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