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Clinical Trials/NCT05077839
NCT05077839
Recruiting
Phase 2

Trifluridine/Tipiracil Combined With Oxaliplatin and Bevacizumab Versus XELOX Plus Bevacizumab in the First-line Treatment of Advanced Colorectal Cancer (TOBACO): a Randomized, Controlled, Phase II Study

Tianjin Medical University Cancer Institute and Hospital1 site in 1 country184 target enrollmentSeptember 1, 2021

Overview

Phase
Phase 2
Intervention
Trifluridine/Tipiracil
Conditions
First-line Treatment
Sponsor
Tianjin Medical University Cancer Institute and Hospital
Enrollment
184
Locations
1
Primary Endpoint
ORR
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

This is a two-group, parallel, randomized, standard-control phase II study comparing the safety and efficacy of trifluridine/tipiracil combined with oxaliplatin and bevacizumab versus XELOX plus bevacizumab in the first-line treatment of advanced colorectal cancer. This study was conducted in the Department of Gastrointestinal Medical Oncology, Tianjin Medical University Cancer Institute and Hospital.

Patients with advanced colorectal cancer will be randomly assigned (1:1) to trifluridine/tipiracil combined with oxaliplatin and bevacizumab (experimental group) or XELOX plus bevacizumab (control group) after signing informed consent. In this study, 184 patients will be enrolled, 92 patients will receive trifluridine/tipiracil combined with oxaliplatin and bevacizumab and 92 patients will receive standard therapy.

In the experimental group, the treatment regimen is trifluridine/tipiracil 35mg/m2 orally taken on d1-5 and d8-12, oxaliplatin 85mg/m2 and bevacizumab 5mg/kg intravenously infused on d1 and d15 every 4 weeks, up to 6 cycles. Then patients will be given trifluridine/tipiracil and bevacizumab maintenance treatment. Patients enrolled in this group could acquire trifluridine/tipiracil free of charge.

The control group was XELOX plus bevacizumab regimen, bevacizumab 7.5mg/kg, d1 oxaliplatin 130mg/m2, d1, capecitabine 1000mg/m2, orally, bid (half an hour after breakfast and dinner), d1-14, every 3 weeks, up to 8 cycles. Then patients will be given capecitabine and bevacizumab maintenance treatment.

Patients received regular and periodic reviews, with imaging evaluations every 8 weeks. Safety will be evaluated by AE and laboratory tests. All patients were followed up every 3 months until death according to the plan.

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
August 31, 2025
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Signed the informed consent.
  • Colonic adenocarcinoma confirmed histologically or histopathologically.
  • No previous chemotherapy for advanced colorectal cancer, or patients who had received adjuvant chemotherapy after radical resection and relapsed 12 months after the completion of adjuvant chemotherapy.
  • ECOG physical status score is 0 or
  • There are measurable metastatic lesions according to RECIST version 1.
  • Appropriate organ function according to the following laboratory test values obtained within 7 days prior to use on Day 1 of Cycle 1:
  • Hemoglobin value ≥9.0g/dL.
  • Absolute neutrophil count ≥1,500/mm3 (≥1.5\*109/L).
  • Platelet count ≥100,000/mm3 (≥100\*109/L).
  • Total serum bilirubin ≤1.5\* upper normal limit (ULN).

Exclusion Criteria

  • Has a serious illness or medical condition, including but not limited to the following:
  • There are other active malignant tumors at the same time, excluding those that have not occurred for more than 5 years or carcinoma in situ that can be cured by adequate treatment.
  • Known presence of brain metastases or leptomeningeal metastases.
  • Systemic active infection (i.e., infection causes body temperature ≥38℃).
  • Clinically significant intestinal obstruction, pulmonary fibrosis, renal failure, liver failure, or symptomatic cerebrovascular disease.
  • Uncontrolled diabetes.
  • Severe/unstable angina, New York Heart Association (NYHA) grade III or IV symptomatic congestive heart failure.
  • Gastrointestinal bleeding of clinical significance.
  • Known presence of human immunodeficiency virus (HIV) or acquired routine immunodeficiency syndrome (AIDS) -associated disease, or active hepatitis B or C.
  • There are psychiatric disorders that may increase the risk associated with participating in the study or taking the study drugs, or may interfere with the interpretation of the study results.

Arms & Interventions

experimental group

In the experimental group, the treatment regimen is trifluridine/tipiracil 35mg/m2 orally taken on d1-5 and d8-12, oxaliplatin 85mg/m2 and bevacizumab 5mg/kg intravenously infused on d1 and d15 every 4 weeks, up to 6 cycles. Then patients will be given trifluridine/tipiracil and bevacizumab maintenance treatment.

Intervention: Trifluridine/Tipiracil

Outcomes

Primary Outcomes

ORR

Time Frame: 48 months

the rate of patients with PR and CR

Secondary Outcomes

  • PFS(48 months)
  • OS(48 months)

Study Sites (1)

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