Phase II Study of Gemcitabine Plus Nab-paclitaxel Versus S1 Plus Nab-paclitaxel in Metastatic Adenocarcinoma of the Pancreas
Overview
- Phase
- Phase 2
- Intervention
- S1 or Gemcitabine
- Conditions
- Pancreatic Cancer
- Sponsor
- Wuhan Union Hospital, China
- Enrollment
- 132
- Locations
- 1
- Primary Endpoint
- PFS
- Last Updated
- 6 years ago
Overview
Brief Summary
A randomized multi-center phase II trial of nab-paclitaxel in combination with gemcitabine verus S1 with gemcitabine as first-Line treatment for locally advanced or metastatic pancreatic cancer
Detailed Description
A Phase II, open-label randomized, multicenter trial to compare nab-paclitaxel in combination with gemcitabine verus S1 with gemcitabine with respect to overall survival, objective tumor response rate and Progression Free Survival (PFS) in patients diagnosed with locally advanced or metastatic adenocarcinoma of the pancreas.
Investigators
Tao Zhang
Chief of Gastrointestinal Oncology
Wuhan Union Hospital, China
Eligibility Criteria
Inclusion Criteria
- •Histological or cytological confirmation of pancreatic adenocarcinoma
- •Distant metastatic or unresctable locally advanced diseases
- •CTScan (or MRI if scanner contraindicated) completed within 3 weeks of the start of treatment
- •At least one lesion measurable by RECIST v1.1 criteria
- •Life expectancy\> 3 months
- •No previous chemotherapy (adjuvant chemotherapy with gemcitabine authorised if administered more than 6 months prior to inclusion)
- •No previous radiotherapy (unless at least one measurable target lesion outside the irradiation zone)
- •Pain must be monitored before inclusion
- •18 years \< age \< 70
- •Performance status: 0-1
Exclusion Criteria
- •Concurrent other effective treatment (including radiotherapy)
- •Resectable patients
- •Allergy history to other drugs in the same class patients with pregnancy or lactation
- •Known severe internal medical diseases
- •Abnormal heart function or relevant history of myocardial infarction and severe arrhythmia
- •Immunocompromised patients, such as HIV positive
- •Uncontrollable mental illness
- •Other conditions the researchers considered ineligible for the study
Arms & Interventions
S/nab
Nab-paclitaxel 125 mg/m² (D1, D8, q3w) and S-1 (40 mg BID for body surface area \< 1.25 m²; 50 mg BID for body surface area of 1.25-1.5 m²; and 60 mg BID for body surface area \>1.5 m²; D1-14, q3w)
Intervention: S1 or Gemcitabine
Gem/nab
Nab-paclitaxel 125 mg/m² (D1, D8, q3w) and Gemcitabine 1000 mg/m² (D1, D8, q3w)
Intervention: S1 or Gemcitabine
Outcomes
Primary Outcomes
PFS
Time Frame: 6 month
progression-free survival
Secondary Outcomes
- OS(1 year)
- ORR(6 month)
- Safety profile :Adverse events of nab-Paclitaxel plus S-1(1 year)
- DCR(6 month)