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Clinical Trials/NCT04149444
NCT04149444
Withdrawn
Phase 2

A Phase 2 Study of Trifluridine/Tipiracil in Triple Negative Metastatic Breast Cancer

AHS Cancer Control Alberta1 site in 1 countryFebruary 2020

Overview

Phase
Phase 2
Intervention
Trifluridine/Tipiracil
Conditions
Metastatic Triple Negative Breast Cancer
Sponsor
AHS Cancer Control Alberta
Locations
1
Primary Endpoint
Overall Response Rate (ORR)
Status
Withdrawn
Last Updated
5 years ago

Overview

Brief Summary

This is an open-label, single arm, multi-stage, phase II trial of Trifluridine/tipiracil as a palliative treatment for patients with metastatic triple negative breast cancer who have failed both a taxane and anthracycline or have contraindications to these agents.

Detailed Description

This is an open-label, single arm, multi-stage, phase II trial of Trifluridine/tipiracil (TAS-102) as a palliative treatment for patients with metastatic triple negative breast cancer who have failed both a taxane and anthracycline or have contraindications to these agents. The trial will begin with a safety run-in of 10 patients treated as follows: Cycle 1: Trifluridine/tipiracil administered at 30 mg/m2 orally bid, 5 days per week, with 2 days of rest, for 2 weeks, followed by 14 day rest. Intra-patient dose escalation to 35 mg/m2 orally bid, 5 days per week, with 2 days of rest, for 2 weeks, followed by 14 day rest for subsequent cycles in the absence of dose limiting toxicities. As long as at least 80% of patients tolerate dose escalation, the trial will proceed to the next stage. Patients enrolled in stages I and II will start Trifluridine/tipiracil at 35 mg/m2 orally bid, 5 days per week, with 2 days of rest, for 2 weeks, followed by 14 day rest.

Registry
clinicaltrials.gov
Start Date
February 2020
End Date
June 9, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years
  • Life expectancy of ≥ 3 months
  • Histologically or cytologically confirmed locally recurrent or metastatic breast cancer that is Estrogen receptor negative, Progesterone receptor negative, and HER2 normal on local testing
  • Up to three prior chemotherapy regimens for advanced and/or metastatic disease
  • Prior therapy with an anthracycline and a taxane in the adjuvant or metastatic setting or documented unsuitability
  • Patients who developed advanced or metastatic disease within 6 months of completing adjuvant therapy are eligible with no prior therapy for advanced disease.
  • Resolution of all chemotherapy- or radiation-related toxicities to ≤ grade 1 (except for stable sensory neuropathy ≤ grade 2 and alopecia) prior to commencement of study participation
  • Eastern Cooperative Oncology Group performance status of 0 to 2
  • Adequate renal function: creatinine clearance ≥ 40 mL/min Cockcroft and Gault formula
  • Adequate bone marrow function: absolute neutrophil count (ANC) ≥ 1.5 x 10\^9/L, hemoglobin ≥ 10.0 g/dL (a hemoglobin \<10.0 g/dL is acceptable if it is corrected by growth factor or transfusion), and platelet count ≥ 100 x 10\^9/L

Exclusion Criteria

  • Radiation therapy encompassing more than 30% of marrow
  • Spinal cord compression not definitively treated with surgery and/or radiation, or previously diagnosed and treated spinal cord compression without evidence that disease has been clinically stable for at least 2 weeks prior to randomization.
  • Leptomeningeal disease
  • Patients who are receiving any other investigational agents
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to Trifluridine/tipiracil .
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • Pregnant women are excluded from this study because Trifluridine/tipiracil is an agent with the potential for teratogenic or abortifacient effects.

Arms & Interventions

ARM 1

Dose escalation cohort - First 10 patients enrolled on study. Trifluridine/Tipiracil 30mg/m2 - to start, if no significant dose limiting side effects the dose will be increased to 35mg/m2 for the duration of the trial. After first 10 patients enrolled on study - Trifluridine/Tipiracil 35mg/m2 Each cycle is 28 days. Two doses per day during days 1-5 with a two day rest for days 6 and 7. Then two doses per day for days 8-12, followed by a rest period for days 13-28 with the next cycle starting the day after day 28.

Intervention: Trifluridine/Tipiracil

Outcomes

Primary Outcomes

Overall Response Rate (ORR)

Time Frame: 8 weeks

The Primary Endpoint ORR is calculated by taking the number of patients who at 8 weeks following initiation of Trifluridine/tipiracil have either a CR or a PR on first scan and dividing it over the total number of evaluable patients. Patients with stable disease are not included in this calculation.

Secondary Outcomes

  • Progression Free Survival (PFS)(From date of randomization until the date of first documented progression or date of death from any cause, whichever comes first, assessed up to 45 months.)
  • Disease Control Rate (DCR)(From date of randomization until the date of first documented progression or date of death from any cause, whichever comes first, assessed up to 45 months.)
  • Overall Survival(From date of randomization until the date of first documented progression or date of death from any cause, whichever comes first, assessed up to 45 months.)
  • Safety and Tolerability: All adverse events experienced by all patients(From date of randomization until the date of first documented progression or date of death from any cause, whichever comes first, assessed up to 45 months.)
  • Quality of Life - Using EQ5D - A standardized questionnaire measuring quality of life(From date of randomization until the date of first documented progression or date of death from any cause, whichever comes first, assessed up to 32 months.)

Study Sites (1)

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