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Phase II Study to Evaluate the Efficacy of a Chemotherapy Combination With Imatinib (GlivecĀ®) and 5-FU/Leucovorin in Patients With Advanced Carcinoma of the Gallbladder and Bile Duct

Phase 2
18 Years
Not Enrolling
Advanced or Metastatic Cholangiocellular Carcinoma and Bile Duct

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Trial Information

Phase II Study to Evaluate the Efficacy of a Chemotherapy Combination With Imatinib (GlivecĀ®) and 5-FU/Leucovorin in Patients With Advanced Carcinoma of the Gallbladder and Bile Duct

Efficacy: Tumor assessments should be performed by a CT or MRI scan, throughout the study.
All assessments should be performed within 14 days of the scheduled day according to the
visit schedules, and whenever clinically indicated otherwise. Radiological studies must use
the same techniques as used at baseline. Evaluation will be based on RECIST criteria.

Safety: Safety assessments will consist of evaluating adverse events and serious adverse
events, laboratory parameters including hematology, chemistry, vital signs, physical
examinations, and documentation of all concomitant medications and/or therapies.

Inclusion Criteria:

- Histologically/Cytologically confirmed diagnosis of advanced / metastatic carcinoma
of the gallbladder or bile duct, which is unresectable or metastatic and therefore
incurable with any conventional multimodality approach

- Performance status 0, 1 or 2 (ECOG)

- Written, voluntary informed consent

- Age > 18 years

- Adequate bone marrow function (Granulocytes > 1,5 x 109/l, Hb > 10 g/dl, Platelets >
100 x 109/l)

- Adequate hepatic and renal function ( bilirubin < 1,25 x upper normal limit or < 1,5
x upper normal limit if hyperbilirubinemia is related to underlying disease, ALAT +
ASAT < 1,5 x upper normal limit, in case of liver metastases < 5 x upper normal
limit, creatinine < 1,25 x upper normal limit)

- Female patients of childbearing potential must have negative pregnancy test within 7
days before initiation of study drug dosing. Female patients with child-bearing
potential must perform a highly effective barrier method of birth control throughout
the study with a proven efficacy of >99%. The contraception treatment should be
performed for an additional six month following discontinuation from study treatment.
Postmenopausal women must be amenorrheic for at least 12 months to be considered of
non-childbearing potential. Male patients of reproductive potential must agree to
employ an effective barrier method of birth control throughout the study and for up
to 6 months following discontinuation of study drug.

Exclusion Criteria:

- Patient has received any other investigational agents within 28 days of first day of
study drug dosing.

- Patient is < 5 years free of another primary malignancy, except: if the other primary
malignancy is not currently clinically significant nor requiring active intervention,
or if other primary malignancy is a basal cell skin cancer or a cervical carcinoma in

- Female patients who are pregnant or breast-feeding.

- Patient has a severe and/or uncontrolled medical disease.

- The concurrent use of warfarin or acetaminophen are not allowed with imatinib
mesylate and need to be replaced by other medications (e.g. by low molecular heparins
in case of warfarin).

- Radiotherapy or any major abdominal or thoracic surgery < 4 weeks before study entry
(excluding diagnostic biopsy or port implantation)

- Patient has received neoadjuvant imatinib mesylate or fluoropyrimidines prior to
study entry

- Patient with Grade III/IV cardiac problems as defined by the New York Heart
Association Criteria. (i.e., congestive heart failure, myocardial infarction within 6
months of study)

- Known incompatibility of imatinib,5-FU, or leucovorin

- Known brain metastases

- Concurrent systemic chemotherapy, immunotherapy, hormone therapy

- History of severe psychiatric illness

- Drug- or alcohol abuse

- Patient has know chronic liver disease (i.e., chronic active hepatitis, and

- Patients with dihydropyrimidine dehydrogenase deficiency (i.e. Treatment with Zostex)

- Patients that are associated with or dependent of the investigator or sponsor

- Patients with any significant history of non-compliance to medical regimens or with
inability to grant reliable informed consent.

- Patients with a creatinine clearance of < 50ml/min.

- Patients with a severe decrease of bone marrow function

- Patients with acute infections

- Patients with severe decrease of liver function

- Patients in reduced performance status (ECOG > 2)

- No active vaccinations should be performed while being on study treatment

- Anemia caused by vitamin B12 deficiency

Type of Study:


Study Design:

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Disease Control Rate (DCR)

Safety Issue:


Principal Investigator

Jan Stoehlmacher, PD Dr.

Investigator Role:

Principal Investigator

Investigator Affiliation:

University Hospital Dresden


Germany: Federal Institute for Drugs and Medical Devices

Study ID:




Start Date:

April 2007

Completion Date:

March 2010

Related Keywords:

  • Advanced or Metastatic Cholangiocellular Carcinoma and Bile Duct
  • cholangiocellular carcinoma
  • bile duct cancer
  • Carcinoma
  • Cholangiocarcinoma
  • Gallbladder Neoplasms