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Phase 2 N=39 Treatment

A Trial of Gemcitabine, Infusional 5-Fluorouracil and Cisplatin for Advanced Pancreatic and Biliary Cancers

Pancreatic Cancer · Biliary Cancer

Enrolled (actual)
39
Serious AEs
25.6%
Results posted
Feb 2016
Primary outcome: Primary: The Percentage of Untreated and Previously Treated Patients That Had a Partial Response to Treatment — 40; 7.1 percentage of patients

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Gemcitabine (Drug); 5-FU (Drug); Cisplatin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Michigan Rogel Cancer Center
Primary completion
Dec 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
The Percentage of Untreated and Previously Treated Patients That Had a Partial Response to Treatment
40; 7.1
SECONDARY
Median Overall Survival of Previously Treated and Previously Untreated Patients
10.3; 4.9

Summary

Multi-agent chemotherapy has value for patients with advanced pancreatic-biliary cancers leading to responses in a substantial minority and increasing survival. The use of the FOLFIRINOX regimen is limited by its' intensity and toxicity. Previous protocol and clinical experience within the University of Michigan Pancreatic Program leads to an expectation of tolerance and efficacy of the proposed regimen. Advantages of the proposed regimen relative to FOLFIRINOX include: 1. Substitution of gemcitabine for irinotecan. Single agent activity of gemcitabine is at least as good as irinotecan (probably better, especially when delivered by FDR [fixed-dose rate] infusion) and gemcitabine is much better tolerated with less diarrhea, nausea/emesis, myelosuppression and alopecia. 2. Deletion of leucovorin infusion and 5FU bolus injection will lessen myelosuppression, mucositis and diarrhea. 3. Substitution of cisplatin for oxaliplatin will reduce cost of therapy and avoid cold aggravated dysesthesia. Presuming evidence of efficacy and confirmation of tolerance with the proposed regimen, the investigators believe this treatment may be more widely applicable to pancreatic-biliary cancer patients, including those with advanced disease as well as being considered for use in locally advanced and neo- and adjuvant settings.

Eligibility Criteria

Inclusion Criteria

  • Patients must have histologic or cytologic diagnosis of pancreatic adenocarcinoma or biliary tract cancer (intrahepatic or extrahepatic cholangiocarcinoma or gallbladder carcinoma).
  • Patients must have clinical/radiologic evidence of metastatic disease.
  • Previous systemic therapy for metastatic disease limited to one cytotoxic chemotherapy regimen not containing cisplatin. Previous therapy for metastatic disease might have included gemcitabine or infusional 5-FU but not both agents.
  • ECOG (Eastern Cooperative Oncology Group) performance status 1,500/mm3, platelet count >100,000/mm3) and renal function (serum creatinine grade 2 are ineligible.
  • Previous systemic therapy for metastatic disease limited to one cytotoxic chemotherapy regimen not containing cisplatin.
  • Previous therapy for metastatic disease might have included gemcitabine or infusional 5-FU but not both agents.
  • Serious concomitant medical disorders incompatible with study participation including active infection requiring systemic therapy.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01661114). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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