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Study of TRIFLURIDINE/TIPIRACIL in Previously Treated Cholangiocarcinoma (MOCHA)

Primary Purpose

Cholangiocarcinoma, Bile Duct Cancer

Status
Terminated
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Trifluridine/Tipiracil
Sponsored by
Sunnybrook Health Sciences Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cholangiocarcinoma focused on measuring Cholangiocarcinoma, Bile Duct Cancer, FTD/TPI, TRIFLURIDINE/TIPIRACIL

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Histologically documented locally advanced or metastatic biliary tract cancer (intra or extrahepatic cholangiocarcinoma or gallbladder cancer) previously treated with first line standard chemotherapy (gemcitabine-based chemotherapy at least one cycle). Patients who develop a recurrence after adjuvant capecitabine therapy must have subsequently received at least one cycle of a gemcitabine-based therapy to be eligible. Patients who have received gemcitabine in the adjuvant setting but progressed within 6 months of their last cycle will be eligible for the study.
  2. Presence of measurable disease as assessed by CT scan of the chest, abdomen and pelvis based on RECIST 1.1.
  3. ECOG performance status of 0 or 1.
  4. Expected life expectancy of ≥ 3 months.
  5. Age 18 years and above
  6. Able to swallow and retain oral medication.
  7. Adequate hematologic function defined by the following laboratory parameter:

    1. Hemoglobin ≥ 9g/dL
    2. Absolute neutrophil count ≥1.5 x 109/L
    3. Platelet count ≥75x 109/L
  8. Adequate hepatic and renal function as defined by:

    1. AST and ALT ≤ 3.0 X ULN (≤ 5 if liver metastasis present)
    2. Total bilirubin ≤ 1.5X ULN
    3. Calculated creatinine clearance ≥50 ml/min using Cockcroft-Gault formula
  9. Patients who have treated brain metastasis (via local radiation standards or surgical resection or local techniques) and who are either off steroids or on a stable dose of steroids for at least one month (30 days), AND who are off anticonvulsants, AND have radiological documented stability of lesions for at least 3 months may be eligible.
  10. Patients must have the ability to read, understand, and sign an informed consent and must be willing to comply with study treatment and procedures.

Exclusion Criteria:

  1. Any malignancy related to HIV, history of HIV, history of known HBV surface antigen positivity (subjects with documented laboratory evidence of HBV clearance may be enrolled) or positive HCV antibody. Testing for these diseases is not mandatory unless clinically indicated
  2. Chemotherapy, radiotherapy, immunotherapy, or other anti-cancer therapy including investigational drugs within 28 days prior to enrolment.
  3. Patients with unresolved Grade 3/4 toxicities from prior therapies.
  4. Any major surgery within the last four weeks.
  5. Previous or concurrent malignancies, excluding curatively treated in situ carcinoma of the cervix or uterus or non-melanoma skin cancer or in-situ carcinoma of the prostate (Gleason score ≤ 7, with all treatment being completed 6 months prior to enrollment, unless at least 5 years have elapsed since last treatment and the patient is considered cured)
  6. Patients with locally or centrally known FGFR2 fusion (Sunnybrook, Ottawa and PMCC sites only).
  7. Female patients of childbearing potential and men able to father children who do not agree to use adequate methods of contraception from time of enrolment until 6 months after the last date of treatment administration.
  8. Women who are breastfeeding
  9. Patients with suspected or documented leptomeningeal disease.

Sites / Locations

  • Sunnybrook Health Sciences Centre

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Trifluridine/Tipiracil

Arm Description

FTD/TPI at 35 mg/m2 (based on BSA) that is administered in tablet form, orally, twice daily, within one hour of morning and evening meals, on days 1-5 and days 8-12 of a 28 day cycle.

Outcomes

Primary Outcome Measures

Median progression-free survival (PFS)
As measured on the basis of RECIST v1.1 criteria

Secondary Outcome Measures

Safety and tolerability of FTD/TPI: CTCAE version 5.0
Assessed by using CTCAE version 5.0 and tolerability
Disease Control Rate (Complete Response, Partial Response, Stable Disease) of FTD/TPI
As measured on the basis of RECIST v1.1 criteria
Duration of response of FTD/TPI
As measured on the basis of RECIST v1.1 criteria
Median overall survival of patients with cholangiocarcinoma treated with FTD/TPI.
As measured on the basis of RECIST v1.1 criteria
Quality of life: European Organisation for Research and Treatment of Cancer Quality-of-life Questionnaire Core 30
As measured by the European Organisation for Research and Treatment of Cancer Quality-of-life Questionnaire Core 30 (EORTC-QLQ C30) Functioning, symptoms, and global health status scores will be calculated, graphed, and summarized at baseline and each follow-up visit. General linear mixed model will be conducted to detect significant changing over time for functioning, symptoms and global health status scores. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. Thus a high score for a functional scale represents a high / healthy level of functioning, a high score for the global health status / QoL represents a high QoL, but a high score for a symptom scale / item represents a high level of symptomatology / problems

Full Information

First Posted
August 22, 2019
Last Updated
November 28, 2022
Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Taiho Oncology, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT04076761
Brief Title
Study of TRIFLURIDINE/TIPIRACIL in Previously Treated Cholangiocarcinoma
Acronym
MOCHA
Official Title
A Multi-Centre, Open-Label Phase 2 Study of TRIFLURIDINE/TIPIRACIL in Previously Treated Cholangiocarcinoma (The MOCHA Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Terminated
Why Stopped
Lack of Funding
Study Start Date
December 11, 2019 (Actual)
Primary Completion Date
September 30, 2022 (Actual)
Study Completion Date
September 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Taiho Oncology, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a multi-centre, open-label, single arm phase 2 study to assess the efficacy of TRIFLURIDINE/TIPIRACIL, in patients with advanced cholangiocarcinoma as measured by median progression-free survival (PFS). This study will enroll a total of 47 patients over a 12-month period, according to a two stage enrollment design. Nine patients will be enrolled during the first stage and the trial will be terminated if 4 or more out of the 9 have disease progression. If the trial goes on to the second stage, a total of 47 patients (38 in second stage) will be required. Patients will be seen prior to enrolment (within 28 days of treatment), every 4 weeks while on treatment, at the end of treatment, and 30 days post-treatment. Patients will remain on long-term follow-up and will be seen every 12 weeks (+/- 14 days) until 1 year post-treatment when they will enter into the survival follow-up period and will be contacted every 12 weeks by phone until progression or toxicity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholangiocarcinoma, Bile Duct Cancer
Keywords
Cholangiocarcinoma, Bile Duct Cancer, FTD/TPI, TRIFLURIDINE/TIPIRACIL

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Trifluridine/Tipiracil
Arm Type
Experimental
Arm Description
FTD/TPI at 35 mg/m2 (based on BSA) that is administered in tablet form, orally, twice daily, within one hour of morning and evening meals, on days 1-5 and days 8-12 of a 28 day cycle.
Intervention Type
Drug
Intervention Name(s)
Trifluridine/Tipiracil
Other Intervention Name(s)
FTD/TPI, Lonsurf
Intervention Description
FTD/TPI is an orally administered combination of a thymidine-based nucleic acid analogue, trifluridine, and a thymidine phosphorylase inhibitor, tipiracil hydrochloride. Trifluridine is the active cytotoxic component of FTD/TPI; its triphosphate form is incorporated into DNA, with such incorporation appearing to result in its anti- tumor effects. Tipiracil hydrochloride is a potent inhibitor of thymidine phosphorylase and, when combined with trifluridine to form FTD/TPI, prevents the rapid degradation of the trifluridine, allowing for the maintenance of adequate plasma levels of the active drug.
Primary Outcome Measure Information:
Title
Median progression-free survival (PFS)
Description
As measured on the basis of RECIST v1.1 criteria
Time Frame
From enrolment until the date of objective radiological disease progression according to RECIST v1.1 or death (by any cause in the absence of progression) up to 1 year
Secondary Outcome Measure Information:
Title
Safety and tolerability of FTD/TPI: CTCAE version 5.0
Description
Assessed by using CTCAE version 5.0 and tolerability
Time Frame
Day 1 of each new treatment cycle (each cycle is 28 days), and at the end of treatment visit (up to 1 year after enrolment)
Title
Disease Control Rate (Complete Response, Partial Response, Stable Disease) of FTD/TPI
Description
As measured on the basis of RECIST v1.1 criteria
Time Frame
From enrolment until the date of objective radiological disease progression according to RECIST v1.1 or death (by any cause in the absence of progression) up to 1 year
Title
Duration of response of FTD/TPI
Description
As measured on the basis of RECIST v1.1 criteria
Time Frame
From enrolment until the date of objective radiological disease progression according to RECIST v1.1 or death (by any cause in the absence of progression) up to 1 year
Title
Median overall survival of patients with cholangiocarcinoma treated with FTD/TPI.
Description
As measured on the basis of RECIST v1.1 criteria
Time Frame
From enrolment until the date of objective radiological disease progression according to RECIST v1.1 or death (by any cause in the absence of progression) up to 1 year
Title
Quality of life: European Organisation for Research and Treatment of Cancer Quality-of-life Questionnaire Core 30
Description
As measured by the European Organisation for Research and Treatment of Cancer Quality-of-life Questionnaire Core 30 (EORTC-QLQ C30) Functioning, symptoms, and global health status scores will be calculated, graphed, and summarized at baseline and each follow-up visit. General linear mixed model will be conducted to detect significant changing over time for functioning, symptoms and global health status scores. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. Thus a high score for a functional scale represents a high / healthy level of functioning, a high score for the global health status / QoL represents a high QoL, but a high score for a symptom scale / item represents a high level of symptomatology / problems
Time Frame
Baseline, and Day 1 of each new treatment cycle (each cycle is 28 days), and at the end of treatment visit (up to 1 year after enrolment)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically documented locally advanced or metastatic biliary tract cancer (intra or extrahepatic cholangiocarcinoma or gallbladder cancer) previously treated with first line standard chemotherapy (gemcitabine-based chemotherapy at least one cycle). Patients who develop a recurrence after adjuvant capecitabine therapy must have subsequently received at least one cycle of a gemcitabine-based therapy to be eligible. Patients who have received gemcitabine in the adjuvant setting but progressed within 6 months of their last cycle will be eligible for the study. Presence of measurable disease as assessed by CT scan of the chest, abdomen and pelvis based on RECIST 1.1. ECOG performance status of 0 or 1. Expected life expectancy of ≥ 3 months. Age 18 years and above Able to swallow and retain oral medication. Adequate hematologic function defined by the following laboratory parameter: Hemoglobin ≥ 9g/dL Absolute neutrophil count ≥1.5 x 109/L Platelet count ≥75x 109/L Adequate hepatic and renal function as defined by: AST and ALT ≤ 3.0 X ULN (≤ 5 if liver metastasis present) Total bilirubin ≤ 1.5X ULN Calculated creatinine clearance ≥50 ml/min using Cockcroft-Gault formula Patients who have treated brain metastasis (via local radiation standards or surgical resection or local techniques) and who are either off steroids or on a stable dose of steroids for at least one month (30 days), AND who are off anticonvulsants, AND have radiological documented stability of lesions for at least 3 months may be eligible. Patients must have the ability to read, understand, and sign an informed consent and must be willing to comply with study treatment and procedures. Exclusion Criteria: Any malignancy related to HIV, history of HIV, history of known HBV surface antigen positivity (subjects with documented laboratory evidence of HBV clearance may be enrolled) or positive HCV antibody. Testing for these diseases is not mandatory unless clinically indicated Chemotherapy, radiotherapy, immunotherapy, or other anti-cancer therapy including investigational drugs within 28 days prior to enrolment. Patients with unresolved Grade 3/4 toxicities from prior therapies. Any major surgery within the last four weeks. Previous or concurrent malignancies, excluding curatively treated in situ carcinoma of the cervix or uterus or non-melanoma skin cancer or in-situ carcinoma of the prostate (Gleason score ≤ 7, with all treatment being completed 6 months prior to enrollment, unless at least 5 years have elapsed since last treatment and the patient is considered cured) Patients with locally or centrally known FGFR2 fusion (Sunnybrook, Ottawa and PMCC sites only). Female patients of childbearing potential and men able to father children who do not agree to use adequate methods of contraception from time of enrolment until 6 months after the last date of treatment administration. Women who are breastfeeding Patients with suspected or documented leptomeningeal disease.
Facility Information:
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada

12. IPD Sharing Statement

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Study of TRIFLURIDINE/TIPIRACIL in Previously Treated Cholangiocarcinoma

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