Pancreatic Adenocarcinoma Advanced or Metastatic Clinical Trial
Official title:
A Prospective Study to Evaluate the Combination of Metformin With Paclitaxel in the Treatment of Patients With Advanced Pancreatic Cancer After Gemcitabine Failure.
| NCT number | NCT01971034 |
| Other study ID # | NP 96/2010 |
| Secondary ID | |
| Status | Completed |
| Phase | Phase 2 |
| First received | September 6, 2013 |
| Last updated | May 14, 2014 |
| Start date | June 2011 |
| Verified date | May 2014 |
| Source | Instituto do Cancer do Estado de São Paulo |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Brazil: Ethics Committee |
| Study type | Interventional |
In Brazil pancreatic adenocarcinoma represents 2% of tumors, and 4% mortality being an uncommon disease, however very aggressive.Only 20% of cases are indicated for curative surgery, of which only 20% are alive within 5 years. For locally, advanced or metastatic disease, since 1997, single chemotherapy with gemcitabine is the standard treatment for first line, with survival around 6 months approximately.There is no standard treatment regimen for second-line, however Paclitaxel demonstrated effect on second-line phase II study. Metformin is an oral hypoglycemic drug used for treatment of diabetes mellitus. There is a growing number of preclinical studies which show antitumor effect against pancreatic adenocarcinoma, probably due to the effect of anti-insulin growth factor (IGF-1). This study will add metformin to standard treatment for second line of locally advanced or metastatic pancreatic adenocarcinoma in ICESP previously treated with gemcitabine. The objective is to evaluate whether metformin improves the efficacy of the standard treatment with paclitaxel by clinical and radiological evaluation.
| Status | Completed |
| Enrollment | 41 |
| Est. completion date | |
| Est. primary completion date | June 2012 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Pancreatic advanced or metastatic adenocarcinoma histologically confirmed. - Previously treatment with gemcitabine as adjuvant or metastatic disease. - Clinical or radiological evidence of disease progression, determined by physician. Is not mandatory RECIST (Response Evaluation Criteria in Solid Tumors) evaluation to determine the progression of disease before the study inclusion. - Patient with intolerance to gemcitabine, even without disease progression, are also eligible. - Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2 - At least 10 weeks of life expectation. - Adequate organ function defined as: - Serum AST (aspartate aminotransferase) and ALT (alanine aminotransferase)= 2.5 × ULN (upper normal limit) - Total Bilirubin = 2,0 x ULN - Absolute neutrophil count = 1,500/ mm3 - Platelets =100.000/ mm3 - Hemoglobin = 8,0 g/dl - Serum Creatinine = 1,5 ULN and clearance of creatinine estimated (Cockcroft- Gault) = 50 ml/min - Signed written informed consent. Exclusion Criteria: - Major surgical procedure within 4 weeks of the beginning of the treatment. - History of serious clinical or psychiatric disease. - Symptomatic hypoglycemia at the screening visit. - Target lesion radiotherapy within 4 weeks of the beginning of the treatment. - Treatment with any anti-cancer investigational drug. - Treatment with any IGF-I or IGFR-I - Treatment with metformin within 12 months prior to commencing study treatment - For female patients, current pregnancy and/or lactation |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Brazil | ICESP | Sao Paulo | SP |
| Lead Sponsor | Collaborator |
|---|---|
| Instituto do Cancer do Estado de São Paulo |
Brazil,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Radiologic control of disease | The radiologic image will be analyzed by RECIST 1.0 criteria. | Every 8 weeks from the date of first dose of treatment until disease progression. | No |
| Secondary | Time to progression. | Thorax and abdominal computerized tomography and Ca 19.9 tumor marker dosage every 8 weeks until disease progression. | Every 8 weeks from the date of first dose of treatment until disease progression. | No |
| Secondary | To estimate the biochemical response through the measurement of serum CA19.9 levels. | From the date of first dose of treatment until disease progression. | No | |
| Secondary | To evaluate the clinical benefits | Will be evaluate: ECOG Treatment with opioids Pain Weight |
Every 4 weeks during the treatment period until disease progression. | No |