Biliary Tract Neoplasm
Conditions
Keywords
biliary tract neoplasm, oxaliplatin, irinotecan, S-1
Brief summary
This study will conduct a phase II study of triple combination with oxaliplatin, irinotecan, and S-1 as the first-line chemotherapy in patients with advanced biliary tract cancer.
Detailed description
It is widely accepted that the efficacy of chemotherapy for patients with inoperable, advanced, and metastatic biliary tract cancer is better than that compared to best supportive care. In general, gemcitabine based combination chemotherapies are considered as the first line treatment for patients with advanced biliary tract cancer, but these have some limitations of inconvenience of administration and unsatisfactory efficacy. S-1 monotherapy and combination with oxaliplatin have shown the objective response rate of 21-35% and 24.5%, respectively, and irinotecan combined with oxaliplatin has shown the response rate of 18-20.5% in patients with advanced metastatic biliary tract cancer. So the investigators had conducted the phase I study of three drugs (oxaliplatin, irinotecan, and S-1) with modification of dosage and schedule and will conduct a phase II study with recommended dose of triple chemotherapy from this phase I study.
Interventions
Treatment will be delivered every 2 weeks 1. Oxaliplatin 65 mg/m2 iv on day 1 2. Irinotecan 135 mg/m2 iv on day 1 3. S-1 80 mg/m2/day on day1-7
Sponsors
Jeil Pharmaceutical Co., Ltd.
Hallym University Medical Center
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Pathologically confirmed advanced, recurrent or metastatic adenocarcinoma of biliary tract system (stage IV by primary tumor, regional nodes, metastasis(TNM) staging system) * Eastern Cooperative Oncology Group (ECOG) performance status 0-2 * More than 3 months expected life span * Measurable lesion by RECIST criteria version 1.1 * Palliative chemotherapy naive * Adequate organ functions * Participants 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
* Any prior 2 years or concurrent malignancy other than non-melanoma skin cancer, in situ cancer of uterine cervix, or papillary or follicular thyroid cancer. * Participants who had received radiation therapy for target lesions 4 weeks before study enrollment * Participants who had received major surgery 4 weeks before study enrollment * Participants with active infection, severe heart disease, uncontrollable hypertension or diabetes mellitus, myocardial infarction during the preceding 12 months, pregnancy, or breast feeding * Participants with central nervous system(CNS) metastases * Participants with peripheral sensory neuropathies with impaired functional activities * Participants with gastrointestinal obstruction or bleeding inducing mal-absorption of oral chemotherapeutic agents.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| overall response rate | 1.5 year | Tumor response will be classified on the basis of the response evaluation criteria in solid tumors (RECIST) guidelines version 1.1 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| progression free survival | 1.5 year | The progression-free survival (PFS) will be measured from the start of study treatment until documented tumor progression (by RECIST) or death due to any cause |
| overall survival | 1.5 year | The overall survival (OS) will be estimated from the start of study treatment until participant's death and measured using the Kaplan-Meier method |
| toxicity profiles - the number of participants and grade of intensity of treatment related adverse events | 1.5 year | adverse events will be graded using the NCI common terminology criteria for adverse events (NCTCAE) v 4.0 |
Countries
South Korea
Outcome results
None listed