Phase 2 Study of GEMOX-T in Previously Untreated Patients With Advanced Pancreatic Cancer

Soonchunhyang University Hospital1 site in 1 country33 target enrollmentJanuary 2011

Overview

Brief Summary

Erlotinib is an orally available, reversible tyrosine kinase inhibitor of epidermal growth factor receptor (EGFR). Association of chemoresistance with the activity of certain tyrosine kinases (e.g. ErbB-1 and Src) has been described for pancreatic cancer and makes a strong case for combining gemcitabine with tyrosine kinase inhibitors. In a phase III trial, the addition of erlotinib to gemcitabine improved survival compared with gemcitabine alone in advanced pancreatic cancer (MJ Moor et al). Also, gemcitabine in combination with oxaliplatin is superior to gemcitabine alone in terms of progression free survival and response rate in one phase III trial (Louvet et al). Taken together, combining erlotinib with gemcitabine and oxaliplatin may further improve the overall survival and clinical benefit of advanced pancreatic cancer.

Detailed Description

Open, uncontrolled, multicenter, phase II study This study will enroll previous chemo-naïve patients with locally advanced unresectable or metastatic pancreatic cancer. Study regimen: * Erlotinib 100 mg po qd daily AND * Gemcitabine 1000 mg/m² with 150mL of normal saline intravenously infusion over 100min on Day 1 * Oxaliplatin 100 mg/m2 with 500mL of 5DW intravenously a 2-hour infusion on D2 Every 2 weeks Each two weeks is a cycle. If at end of 12 cycles response continues, will administer Gemcitabine and erlotinib until progression.

Registry

clinicaltrials.gov

Start Date

January 2011

End Date

March 2014

Last Updated

12 years ago

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

Soonchunhyang University Hospital

Responsible Party

Principal Investigator

Jina Yun

Division of Oncology-Hematology Department of Internal medicine

Soonchunhyang University Hospital

Eligibility Criteria

Inclusion Criteria

•Age over 18 years
•ECOG performance status of ≤2
•Histologically confirmed adenocarcinoma of the pancreas
•The disease is Locally advanced deemed by the surgeon to be unresectable, or metastatic disease.
•Prior chemotherapy is not permitted, except for fluorouracil given concurrently as a radiosensitizer.
•Patients must have normal organ function evidenced by
•Number of absolute neutrophil counts (ANC) \> 1.5 x 109/L
•Number of thrombocytes \> 100 x 109/L
•Total bilirubin \< 1.5 x upper limit of normal (although patients with a Total bilirubin count between 1.5 and 3 x upper limit of normal in whom a decrease is anticipated, ex. Biliary stent insertion)ALAT, ASAT \< 3 x upper limit of normal (in case of liver metastasis, 5 x upper limit of normal)
•Alkaline phosphatase \< 3 x upper limit of normal (in case of liver metastasis, 5 x upper limit of normal)

Exclusion Criteria

•Tumor type other than adenocarcinoma
•Evidence of uncontrolled CNS disease (patients with controlled CNS disease for 4 weeks using the same imaging method and for whom are off steroid will be eligible)
•Uncontrolled Nausea and Vomiting
•Diagnosis of other malignancy in the last 5 years excluding non-melanoma skin cancer and in -situ cervical cancer.
•Subjects unlikely to comply with protocol, e.g. uncooperative attitude, inability to return for follow- up visits and unlikelihood of completing the study.
•Any known history of hypersensitivity to the study drugs.
•Pregnant or lactating women.
•Symptomatic peripheral sensory neuropathy (NCI CTCAE v3.0 ≥ grade 2)
•Other serious illness or medical condition, notably heart or lung failure, active uncontrolled infection
•Prior radiotherapy was administered to target lesions selected for this study, or radiotherapy to the non-target lesions has been completed within 4 weeks before being included in the study.

Arms & Interventions

Tarceva, Gemcitabine, Oxaliplatin

* Erlotinib 100 mg po qd daily AND * Gemcitabine 1000 mg/m² with 150mL of normal saline intravenously infusion over 100min on Day 1 * Oxaliplatin 100 mg/m2 with 500mL of 5DW intravenously a 2-hour infusion on D2 Every 2 weeks Each two weeks is a cycle. If at end of 12 cycles response continues, will administer Gemcitabine and erlotinib until progression.

Intervention: Erlotinib

Tarceva, Gemcitabine, Oxaliplatin

* Erlotinib 100 mg po qd daily AND * Gemcitabine 1000 mg/m² with 150mL of normal saline intravenously infusion over 100min on Day 1 * Oxaliplatin 100 mg/m2 with 500mL of 5DW intravenously a 2-hour infusion on D2 Every 2 weeks Each two weeks is a cycle. If at end of 12 cycles response continues, will administer Gemcitabine and erlotinib until progression.

Intervention: Gemcitabine

Tarceva, Gemcitabine, Oxaliplatin

* Erlotinib 100 mg po qd daily AND * Gemcitabine 1000 mg/m² with 150mL of normal saline intravenously infusion over 100min on Day 1 * Oxaliplatin 100 mg/m2 with 500mL of 5DW intravenously a 2-hour infusion on D2 Every 2 weeks Each two weeks is a cycle. If at end of 12 cycles response continues, will administer Gemcitabine and erlotinib until progression.

Intervention: Oxaliplatin

Outcomes

Primary Outcomes

Response rate

Time Frame: 24 months (01/2011 and end of study 01/2013)

Responses are assessed every 2 cycles according to RECIST; the imaging tests are performed in a week preceding the corresponding cycles, and can also be repeated at any other time if clinically indicated, for example, to confirm disease progression. At any time, patients with progressive disease are withdrawn.