Gemcitabine, Oxaliplatin and Capecitabine in Patients With Advanced Cholangiocarcinoma
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Purpose
In Denmark approximately 200 new cases of cholangiocarcinoma are diagnosed every year. No standard treatment exists for patients with advanced cholangiocarcinoma, and improved systemic treatments are needed.
Duplets of gemcitabine, oxaliplatin and capecitabine have been evaluated in various cancers and several different regimens are well tolerated and active, especially in upper gastrointestinal cancers, exocrine pancreatic cancer and non-small cell lung cancer.
The triplet combination of these agents has not been studied, but a triplet combination of gemcitabine, oxaliplatin and 5-FU infusion has been evaluated in a phase I study.
Bi-weekly combination of gemcitabine and oxaliplatin has proven active and tolerable and warrants further study. In addition, fixed dose rate infusion of gemcitabine has shown interesting as the ability of mononuclear cells to accumulate gemcitabine triphosphate during therapy seems to be saturable.
We propose a phase I-II study of a bi-weekly schedule of gemcitabine, oxaliplatin and capecitabine. This regimen could be feasible in an out-patients setting.
The phase I part is a standard dose escalation study for patients with solid tumors. In the phase II part the recommended dose is studied in patients with advanced cholangiocarcinoma.
| Condition | Intervention | Phase |
|---|---|---|
|
Cholangiocarcinoma |
Drug: Gemcitabine Drug: Oxaliplatin Drug: Capecitabine |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase I-II Study of bi-Weekly Fixed Dose Rate Gemcitabine, Oxaliplatin and Capecitabine in Patients With Advanced Cholangiocarcinoma |
- Response
- Safety
- Time to progression
- SUrvival
| Estimated Enrollment: | 39 |
| Study Start Date: | June 2004 |
| Study Completion Date: | February 2008 |
Design
Open, non-randomized phase I/II study.
Purpose:
Phase I part To find MTD and RFTD for the combination of gemcitabine, oxaliplatin and capecitabine.
Dose Escalating Schedule Dose level Dose Gemcitabine 10 mg/m2/min 600-1000 mg/m2 day 1 and 14 Capecitabine p.o. x 2 daily. 1000-1250 mg/m2 day 1-7 and 14-21 Oxaliplatin 60-80 mg/m2day 1 and 14 Drugs: G C O Level 1 600 1000 60 Level 2 800 1000 60 Level 3 1000 1000 60 Level 4 1000 1250 60 Level 5 1000 1250 80 Level 6 1200 1250 80 Start level: Level 1, 3 patients per level
Phase II part The primary endpoint is the objective response rate The secondary endpoint is toxicity, response duration and time to progression.
Treatment:
Gemcitabine Gemcitabine is given intravenously on day 1 and 14 with a fixed dose rate of 10 mg/m2/min.
Oxaliplatin Oxaliplatin is given intravenously on day 1 and 14 as a 2 hours infusion.
Capecitabine Capecitabine is given orally and administered in tablets of 150 mg and 500 mg. The dose is administered twice daily with 12 hours interval, in the morning and evening during or latest 30 minutes after a meal.
Eligibility| Ages Eligible for Study: | 18 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Histologically proven intra- or extrahepatic cholangiocarcinoma, papilla of the Vater or gallbladder carcinoma.
- PS 0-2
- Age 18-75
- Life expectancy > 12 weeks
- Normal bone marrow function (neutrophiles > 1,5 x 109/l and platelets > 100 x 109/l)
- Bilirubin < 1,5 x UNL
- Transaminases < 3 x UNL
- Normal renal function, Cr-EDTA clearance > 50 ml/min
- No chemotherapy, radiotherapy or immunotherapy 4 weeks prior to inclusion
- No known DPD-deficiency
- No neuropathy
- No uncontrolled, severe concurrent medical disease
- Signed informed consent
Exclusion Criteria:
- Chemotherapy, radiotherapy or immunotherapy 4 weeks prior to inclusion
- Experimental therapy < 8 weeks prior to inclusion
- Uncontrolled, severe concurrent medical disease
- Prior malignancy during the last 5 years, except for non-melanoma skin cancer and carcinoma in situ cervix uteri.
- Allergy to gemcitabine, oxaliplatin or capecitabine
- Pregnancy or lactation
Contacts and Locations| Denmark | |
| Rigshospitalet | |
| Copenhagen, Denmark, 2100 | |
| Vejle Sygehus | |
| Vejle, Denmark, 7100 | |
| Principal Investigator: | Ulrik Lassen, MD., PH.D. | Rigshospitalet, Dept. of Oncology |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00350961 History of Changes |
| Other Study ID Numbers: | GEMOXEL cholangiocarcinoma |
| Study First Received: | July 10, 2006 |
| Last Updated: | August 25, 2008 |
| Health Authority: | Denmark: Danish Medicines Agency |
Keywords provided by Rigshospitalet, Denmark:
|
Cholangiocarcinoma Fixed dose rate Gemcitabine Oxaliplatin Capecitabine |
Additional relevant MeSH terms:
|
Cholangiocarcinoma Adenocarcinoma Carcinoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Gemcitabine Capecitabine Fluorouracil Oxaliplatin Antimetabolites, Antineoplastic Antimetabolites |
Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Antineoplastic Agents Therapeutic Uses Antiviral Agents Anti-Infective Agents Enzyme Inhibitors Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Radiation-Sensitizing Agents |
ClinicalTrials.gov processed this record on May 19, 2013