Multicenter Phase II-trial to Investigate Safety and Efficacy of an Adjuvant Therapy With Gemcitabine and Erbitux® in Patients With R0 or R1 Resected Pancreatic Cancer

Carmen Schade-Brittinger8 sites in 1 country76 target enrollmentOctober 2006

ConditionsAdenocarcinoma

InterventionsCetuximab (Erbitux®) and Gemcitabine

DrugsCetuximab (Erbitux®) and Gemcitabine

Overview

Phase: Phase 2
Intervention: Cetuximab (Erbitux®) and Gemcitabine
Conditions: Adenocarcinoma
Sponsor: Carmen Schade-Brittinger
Enrollment: 76
Locations: 8
Primary Endpoint: disease free survival
Status: Completed
Last Updated: 10 years ago

Overview Investigators Eligibility Criteria Arms & Interventions Outcomes Sites Similar Trials

Overview

Brief Summary

This is an open-label, non-randomized Phase II study to evaluate immunochemotherapy in patients with R0 OR R1-resected pancreatic cancer.

Detailed Description

Available study data indicated a possible benefit from adjuvant chemotherapy for patients with resected pancreatic cancer. The optimal therapy regimen has yet to be determined. Based on the experiences with cetuximab (Erbitux®)and gemcitabine in advanced pancreatic cancer and with gemcitabine as adjuvant therapy, the aim of this study was to evaluate the feasibility of the combined treatment of cetuximab and gemcitabine in patients with R0 or R1-resectable pancreatic cancer and to evaluate if the disease free survival can be increased by the addition of an EGFR-targeted therapy.

Registry

clinicaltrials.gov

Start Date

October 2006

End Date

January 2012

Last Updated

10 years ago

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

Carmen Schade-Brittinger

Responsible Party

Sponsor Investigator

Principal Investigator

Carmen Schade-Brittinger

Philipps University

Philipps University Marburg Medical Center

Eligibility Criteria

Inclusion Criteria

•Provided signed written informed consent.
•Men and woman age \> 18 years
•Histologically confirmed R0 OR R1 resected ductal adenocarcinoma of the pancreas
•Life expectancy \>12 weeks
•Patients with performance status of ECOG ≤ 2
•Patients without metastasis

Exclusion Criteria

•Women of child bearing potential (WOCP) who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and follow-up to 4 weeks after the study.
•Women who are pregnant or breastfeeding.
•Women with a positive pregnancy test on enrollment or prior to study drug administration.
•Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent.
•Any concurrent malignancy other than non-melanoma skin cancer, or carcinoma in situ of the cervix. (Patients with a previous malignancy but without evidence of disease for \> 5 years will be allowed to enter the trial).
•Inadequate hematologic function defined by an absolute neutrophils count (ANC) \< 1,500/mm³, a platelet count \< 100,000/mm³ and a hemoglobin \< 9 g/dL.
•Inadequate hepatic function defined by the upper limit of normal (ULN), AST and ALT levels \> 5 times the ULN.
•Serum bilirubin \> 1.5 times the ULN.
•Inadequate renal function defined by a serum creatinine \> 1.5 times the ULN.
•Prior cetuximab or other therapy that targets the EGF pathway.