Unresectable Pancreatic Cancer
Conditions
Keywords
Pancreatic Cancer, Unresectable, Maintenance Treatment
Brief summary
Background: Monotherapy with S-1, oral fluoropyrimidine, shows non-inferiority to gemcitabine in overall survival (OS) with good tolerability for advanced pancreatic cancer in Asian patients. It is also shown that nimotuzumab plus gemcitabine could improve OS and progression free survival (PFS) in patients with unresectable pancreatic cancer. However, it is still unknown whether nimotuzumab plus S1 would improve more to OS and PFS than single S-1. Maintenance treatment, as a new treatment pattern, has also been tried in these patients after first line treatment to improve the OS. Thus, this study is designed to compare nimotuzumab plus S1 to placebo plus S1 as maintenance treatment in patients with locally advanced or metastatic pancreatic cancer who has benefited from the first-line treatment of gemcitabine combined with nimotuzumab and S1 (complete response+partial response+stable disease). Patients and methods: 60 patients will be enrolled,and randomized in a 1:1 ratio to group nimotuzumab plus S1 and group placebo plus S1. nimotuzumab/placebo: 400 mg/w, intravenous infusion, Infusion time ≥ 60 min, d1, once every two weeks. S1: oral, 40 mg (Body surface area\<1.5 m2) or 60 mg (Body surface area\>1.5 m2), d1-d14, every three weeks for a cycle. Treatment interventions will be stopped under the conditions of disease progression or intolerable toxic reaction or participants ask to quit. The primary endpoint is the time to disease progression since randomization (TTP), secondary points include OS, 3 years overall survival rate (OSR) and safety.
Interventions
DRUGNimotuzumab plus S1
Nimotuzumab Injection: 400 mg/w, Intravenous infusion, Infusion time ≥ 60 min, d1, once every two weeks;S1: 40 mg (Body surface area\<1.5 m2) or 60 mg (Body surface area\>1.5 m2) ,oral,d1-d14, every three weeks for a cycle
DRUGPlacebo plus S1
Placebo: 400 mg/w, Intravenous infusion, Infusion time ≥ 60 min, d1, once every two weeks;S1: 40 mg (Body surface area\<1.5 m2) or 60 mg (Body surface area\>1.5 m2) ,oral,d1-d14, every three weeks for a cycle
Sponsors
Chinese PLA General Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* 18-75 years; * Karnofsky Performance Status≥ 60; * histologically proven locally advanced or metastatic pancreatic cancer,and unsuitable for radiotherapy or surgery resection; * benefited from the first line treatment of gemcitabine plus nimotuzumab and S1 (complete response+partial response+stable disease); * at least 4 weeks from the end of the first-line treatment; * with at least 1 measurable and evaluable lesion; * anticipated over survival≥12 weeks; * AST/ALT≤2.5 ULN (≤5 ULN for patients with hepatic metastases); total bilirubin≤2 ULN （≤3 ULN for patients with hepatic metastases); neutrophil count≥1.5×109/L; platelet counts≥100×109/L; hemoglobin level≥90 g/L; creatinine clearance rate≥ 60 mL/min * written informed consent
Exclusion criteria
* previously received the following treatments: anticancer chemotherapy/molecularly targeted therapy as palliative treatment, or targeted chemotherapy and no progression, another interventional clinical trail within 4 weeks; * underwent major surgery within 4 weeks; * with brain or leptomeningeal metastases; * history of malignancy other than pancreatic cancer; * presented symptomatic abdominal fluid and needed treatment; * with other serious diseases such as diabetes,active infection; * known for allergy to anti epidermal growth factor receptor antibody
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| TTP | 3 years |
Secondary
| Measure | Time frame |
|---|---|
| Adverse Events | 3 years |
| OS | 3 years |
| OSR | 1-3 years |
Countries
China
Contacts
Primary ContactYi Hu, PhD
Outcome results
None listed