Ph 2 Study of TAS-102 / Bevacizumab Maintenance Therapy Post Induction Chemotherapy in Metastatic Colorectal Cancer
Status: | Terminated |
---|---|
Conditions: | Colorectal Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 8/9/2018 |
Start Date: | February 2016 |
End Date: | November 2017 |
An Open-Label, Multi-center, Phase 2 Study of Switch Maintenance With TAS-102 Plus Bevacizumab Following Oxaliplatin or Irinotecan-Based Fluoropyrimidine-Containing Induction Chemotherapy in Patients With Metastatic Colorectal Cancer
Phase II study of TAS-102 plus bevacizumab switch maintenance therapy in patients with mCRC
Study Drug:
TAS-102 (trifluridine and tipiracil hydrocholoride) and bevacizumab
Dosing Details:
Starting dose of TAS-102 is 35 mg/m2 administered orally twice daily, after meals, for 5 days
a week with 2 days rest for 14 days, followed by 14 days rest (1 treatment cycle).
Bevacizumab 5 mg/kg intravenously every 14 days. The treatment cycle repeats every 28 days.
Patients may take TAS-102 plus bevacizumab until they exhibit progression of disease,
withdraw consent, or experience unacceptable toxicity.This is a single arm study. All
patients receive the same study treatment.
TAS-102 (trifluridine and tipiracil hydrocholoride) and bevacizumab
Dosing Details:
Starting dose of TAS-102 is 35 mg/m2 administered orally twice daily, after meals, for 5 days
a week with 2 days rest for 14 days, followed by 14 days rest (1 treatment cycle).
Bevacizumab 5 mg/kg intravenously every 14 days. The treatment cycle repeats every 28 days.
Patients may take TAS-102 plus bevacizumab until they exhibit progression of disease,
withdraw consent, or experience unacceptable toxicity.This is a single arm study. All
patients receive the same study treatment.
Inclusion criteria:
- Written informed consent
- Histologically proven, unresectable, evaluable metastatic colorectal cancer
- 16 to 20 weeks of first-line therapy with oxaliplatin, and/or irinotecan-based
flourorpyrimidine-containing chemotherapy plus Bevacizumab
- Patients must have stable disease (or better) during the initial induction
chemotherapy with first-line chemotherapy.
- No progressive disease at the time of initiation of maintenance therapy
- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1
- Adequate organ and marrow function
- Women of child-bearing potential and men must agree to avoid pregnancy
- Patient must start maintenance therapy at least 14 days after the last administered
induction chemotherapy but no later than 30 days.
Exclusion Criteria
- Patients whose tumors have progressed on first-line treatment
- Patients with active concurrent malignancy, other than superficial, non-invasive
squamous cell carcinoma of the skin or uterine cervix, within the past three years.
- Women who are pregnant or lactating
- Unstable heart disease
- Uncontrolled active infection requiring antibiotics within one week prior to first
dose.
- Patients with active CNS malignancy.
- Persistent protein in the urine
- Patients with bowel obstruction or uncontrolled vomiting.
- Patients with serious psychiatric or medical conditions that could interfere with
treatment.
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