Gemcitabine and Capecitabine to Treat Patients With Advanced Pancreatic and Biliary Cancers

University of California San Francisco (UCSF)

Status and phase

Completed

Phase 1

Conditions

Biliary Cancer

Pancreatic Cancer

Treatments

Drug: gemcitabine

Drug: capecitabine

Study type

Interventional

Funder types

Other

NETWORK

Identifiers

NCT00626158

CC#074510

Details and patient eligibility

About

The purpose of this study is to find out what effects gemcitabine plus capecitabine has on patients with pancreatic or biliary cancer, and to determine the optimal dose that can be given safely of these two drugs together (called the maximum tolerated dose). Gemcitabine and capecitabine are two chemotherapy drugs used to treat pancreatic and biliary cancer. These two drugs used together are considered an acceptable standard of care for pancreatic and biliary cancers. However, in this study the dose and dosing schedule will be changed, in the hopes that the drugs will have more effect with fewer side effects than when given in the standard way.

Enrollment

45 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically-confirmed pancreatic adenocarcinoma or biliary tract carcinoma (cholangiocarcinoma or gallbladder cancer)
Disease must not be amenable to surgical resection. Patients with either locally advanced or metastatic disease are eligible
No prior systemic therapy for their diagnosis
ECOG performance score of 0-1
Evidence of either or both of the following:
1. RECIST-defined measurable disease (lesions that can be accurately measured in at least one dimension with the longest diameter ≥ 20mm using conventional techniques or ≥10 mm with spiral CT scan)
2. An elevated serum CA19-9 at baseline ( ≥ 2X ULN)
Female patients must be either surgically sterile or postmenopausal, or if of childbearing potential must have a negative pregnancy test (serum or urine) prior to enrollment and agree to use effective barrier contraception during the period of therapy. Oral, implantable, or injectable contraceptives may be affected by cytochrome P450 interactions, and are therefore not considered effective for this study. Male patients must be surgically sterile or must agree to use effective contraception during the period of therapy. The definition of effective contraception will be based on the judgment of the investigator.
Adequate bone marrow function:
1. ANC ≥ 1500/uL
2. platelet count ≥ 100,000/uL
3. hemoglobin ≥ 9.0 g/dL
Adequate hepatic function:
1. Total bilirubin ≤ 1.5 X ULN
2. AST (SGOT) ≤ 2.5 X ULN
3. ALT (SGPT) ≤ 2.5 X ULN
Adequate renal function as determined by either:
1. Calculated or measured creatinine clearance ≥ 40 mL/min (for calculated creatinine clearance, Cockroft-Gault equation will be used)
2. Serum creatinine ≤ 1.5 X ULN
Ability to swallow oral medications
Ability to understand the nature of this study protocol and give written informed consent
Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.

Exclusion criteria

Any prior systemic or investigational therapy for metastatic or locally advanced pancreatic cancer or biliary cancer. Systemic therapy administered alone or in combination with radiation in the adjuvant setting is permissible as long as it was completed > 6 months prior to the time of study enrollment.
Inability to comply with study and/or follow-up procedures.
History of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that, in the opinion of the investigator, renders the subject at high risk from treatment complications or might affect the interpretation of the results of the study.
Presence of central nervous system or brain metastases.
Pregnancy (positive pregnancy test) or lactation.
Prior malignancy except for adequately treated basal cell skin cancer, in situ cervical cancer, adequately treated Stage I or II cancer from which the patient is currently in complete remission, or any other form of cancer from which the patient has been disease-free for 5 years.
Clinically significant cardiac disease (e.g. congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmias not well controlled with medication) or myocardial infarction within the last 12 months.
Lack of physical integrity of the upper gastrointestinal tract or malabsorption syndrome.
Known, existing uncontrolled coagulopathy.
Major surgery within 4 weeks of the start of study treatment, without complete recovery.
Concurrent/pre-existing use of coumadin.