S-1, Gemcitabine and Erlotinib for Advanced Pancreatic Cancer

NCT ID: NCT01693419

Last Updated: 2017-08-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 37 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-08-31
• Study Completion Date: 2016-12-31

Brief Summary

This study will conduct a phase II study of gemcitabine, erlotinib, and S-1 as first-line chemotherapy in patients with advanced pancreatic cancer and evaluate the EGFR expression, KRAS mutation, and BRAF mutation as predictive or prognostic markers

Detailed Description

Pancreatic ductal adenocarcinoma, also known as pancreatic cancer, is an eighth cause of cancer-related deaths in the world. The estimated worldwide incidence of pancreatic cancer was 277,000 cases and an estimated 266,000 patients died from the disease in 20081.

Pancreatic cancer is more common in elderly persons than in younger persons, and characterised by early locoregional spread and distant metastasis. As a result, less than 20% of patients are diagnosed with localized, potentially curable disease, and the median survival is no longer than 3-4 months without effective treatment2.

Single-agent chemotherapy with gemcitabine was considered as standard of care for patients with advanced pancreatic cancer, since Burris et al. demonstrated superiority of gemcitabine over 5-fluorouracil (5-FU) in respect of a survival benefit as well as an improvement in disease related symptoms in a randomized study3.

Nevertheless, the activity of gemcitabine monotherapy in pancreatic cancer was modest, and there was a clear need to improve its efficacy by combining it with other anticancer drugs.

Multiple agents such as 5-FU4, capecitabine5,6, cisplatin7,8, oxaliplatin9, pemetrexed10, irinotecan11, cetuximab12, and bevacizumab13, in combination with gemcitabine have been tested in clinical trials, however, they have failed to improve the outcome.

The only agent that, in combination with gemcitabine, has shown a small, but statistically significant improvement, with a hazard ratio (HR) of 0.82, the absolute improvement in median overall survival (OS) of 5.9 months with gemcitabine versus 6.2 months with the combination, is erlotinib, a small-molecule inhibitor of the epidermal growth factor receptor (EGFR)14. Considering the modest improvement in survival by adding erlotinib to gemcitabine, new combination therapy that have a great impact is urgently needed.

S-1 is an oral fluoropyrimidine derivative that combines tegafur (FT) with two modulators; 5-chloro-2, 4-dihydroxypyridine (CDHP) and oteracil potassium (Oxo) in a 1:0.4:1 molar concentration ratio. The phase II trials of a combination of gemcitabine and S-1 have demonstrated objective response rates of 32-48% and median survival of 8-12 months 15-17.

Therefore, we will conduct a phase II study of gemcitabine, erlotinib, and S-1 as first-line chemotherapy in patients with advanced pancreatic cancer and evaluate the EGFR expression, KRAS mutation, and BRAF mutation as predictive or prognostic markers.

Conditions

Pancreas Neoplasms

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

GES (Gemcitabine, Erlotinib, S-1)

Treatment will be delivered as a 3-week cycle.

1. Gemcitabine 1000 mg/m² IV on day 1, 8

2. Erlotinib 100 mg/day PO on day 1

3. S-1 60 mg/m²/day PO on day 1-14

Group Type: EXPERIMENTAL

GES (Gemcitabine, Erlotinib, S-1)

Intervention Type: DRUG

Treatment will be delivered as a 3-week cycle.

1. Gemcitabine 1000 mg/m² IV on day 1, 8

2. Erlotinib 100 mg/day PO on day 1

3. S-1 60 mg/m²/day PO on day 1-14

Interventions

GES (Gemcitabine, Erlotinib, S-1)

Treatment will be delivered as a 3-week cycle.

1. Gemcitabine 1000 mg/m² IV on day 1, 8

2. Erlotinib 100 mg/day PO on day 1

3. S-1 60 mg/m²/day PO on day 1-14

Intervention Type: DRUG

Other Intervention Names

Gemzar; Tarceva; TS-1

Eligibility Criteria

Inclusion Criteria

• Pathologically confirmed locally advanced unresectable, recurrent or metastatic adenocarcinoma of pancreas (Stage III-IV ; TNM staging system)
• Measurable or evaluable disease by RECIST criteria 1.1
• Minimum age of 18 years
• ECOG Performance status 0-1
• Prior adjuvant chemotherapy without gemcitabine, erlotinib or S-1 is allowed if more than 4 weeks elapsed since completion of chemotherapy.
• More than 4 weeks since completion of prior radiotherapy (measurable or evaluable lesions should be outside the radiation field)
• Adequate organ functions
• Patients must sign an informed consent indicating that they are aware of the investigational nature of the study in keeping with the policy of the hospital.

Exclusion Criteria

• Patients treated previously with gemcitabine, erlotinib, or S-1 as adjuvant chemotherapy.
• Patients with CNS metastases
• Patients with active infection, severe heart disease, uncontrollable hypertension or diabetes mellitus, myocardial infarction during the preceding 6 months, pregnancy, or breast feeding
• Any previous or concurrent malignancy other than non-melanoma skin cancer or in situ cancer of uterine cervix
• Known history of cerebral or leptomeningeal metastases or neurologic disease

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Jeil Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: collaborator

Hallym University Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dae Young Zang, DM, PhD

Role: PRINCIPAL_INVESTIGATOR

Hallym University Medical Center

Locations

Hallym University Medical Center

Anyang, , South Korea

Countries

South Korea

Other Identifiers

HMC-HO-GI-1201

Identifier Type: -

Identifier Source: org_study_id