A Randomized Phase 2 Study of ARQ 197 Versus Gemcitabine in Treatment-Naïve Patients With Unresectable Locally Advanced or Metastatic Pancreatic Adenocarcinoma
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||A Randomized Phase 2 Study of ARQ 197 Versus Gemcitabine in Treatment-Naïve Patients With Unresectable Locally Advanced or Metastatic Pancreatic Adenocarcinoma|
- Evaluate progression-free survival (PFS) in patients receiving ARQ 197 versus gemcitabine. [ Time Frame: 6 month ] [ Designated as safety issue: No ]
- Evaluate overall response rate (ORR) in patients receiving ARQ 197 versus gemcitabine [ Time Frame: ongoing ] [ Designated as safety issue: No ]
- Evaluate 6-month and 1-year overall survival (OS) rates in patients treated with ARQ197 versus gemcitabine [ Time Frame: 6 and 12 month ] [ Designated as safety issue: No ]
- Further characterize the safety profile of ARQ 197 [ Time Frame: ongoing ] [ Designated as safety issue: No ]
|Study Start Date:||November 2007|
|Study Completion Date:||April 2008|
|Primary Completion Date:||April 2008 (Final data collection date for primary outcome measure)|
Drug: ARQ 197
120 mg capsule administered twice daily for 240 mg total daily dose
Active Comparator: 2
1000 mg/m2 administered as an intravenous infusion over 30 minutes once weekly for 4 weeks for the first 28 days (cycle). Each subsequent cycle will consist of 1000 mg/m2 administered as an intravenous infusion over 30 minutes once weekly for 3 weeks with no drug administered in the 4th week.
Other Name: Gemzar
This is a multi-center, open-label randomized phase 2 study designed to evaluate the PFS of treatment-naïve patients with unresectable (locally advanced or metastatic) pancreatic adenocarcinoma following treatment with either ARQ 197 (ARQ arm) or gemcitabine alone (GEM arm). The study will also evaluate other efficacy and safety parameters including ORR, OS and adverse events in the two treatment arms. Patients randomly assigned to the GEM arm will receive gemcitabine alone. Patients assigned to the ARQ arm will receive oral ARQ 197 alone.
ARQ 197 is an investigational oral drug supplied as capsules in multiple strengths. For the study initial shipment the capsules were 120 mg each, 30 count. In the ARQ arm, patients will take 120 mg of ARQ 197 twice daily, once in the morning and once in the evening one hour prior to or two hours after a meal. ARQ 197 treatment will be continued until unacceptable toxicity, documented progression of disease, or another discontinuation criterion is met.
Gemcitabine is a commercially available drug for the treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. In the GEM arm, gemcitabine will be administered by intravenous infusion over 30 minutes at a dose of 1000 mg/m2. The dosing schedule of gemcitabine will be once weekly for the first cycle (4 weeks), then once weekly for 3 consecutive weeks followed by a week of rest for each subsequent cycle. Gemcitabine therapy will be continued until unacceptable toxicity, documented progression of disease, or another discontinuation criterion is met.
A treatment cycle is defined as 28 days for both treatment arms. Cycles may be repeated every 4 weeks (28 days) based on toxicity and response. The assigned treatment should continue until unacceptable toxicity, disease progression (clinical or radiological) or another discontinuation criterion is met.
Tumor evaluations: Tumor evaluations will be performed in 8-week intervals. Tumor response (complete response, partial response, stable disease, progressive disease and ORR) will be evaluated using Response Evaluation Criteria in Solid Tumors (RECIST).
Progression-free survival: The time of disease progression-free will be calculated from randomization until disease progression per RECIST or death due to any cause. Patients who are alive and progression free will be censored at the date of their last tumor evaluation.
Overall survival: Overall survival time will be calculated from the date of randomization until death due to any cause.
Safety assessments: Data on vital signs, physical examination, adverse events, serum chemistry, hematological laboratory tests, and electrocardiograms will be collected.
This study is designed to establish potential efficacy of ARQ 197 in treatment naive pancreatic cancer patients in a controlled, randomized study. The sample size of 30 Evaluable patients per treatment group is considered adequate to provide meaningful estimates of the PFS and ORR and OS rates, however, this study is not powered to show statistically significant differences between the treatment groups. Therefore, the analyses will be primarily descriptive in nature. Taking into account an anticipated drop-out/loss-to-follow-up rate of 20%, the total sample size will be 72 patients.
Primary and secondary objectives will be analyzed in the two treatment arms using appropriate patient populations and statistical methods.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00558207
|Oddzial Kliniczny Kliniki Onkologii Szpital Uniwersytecki w Krakowie|
|Krakow, Poland, 31-531|
|Oddzial Chemioterapii, Wojewodzki Szpital Specjalistyczny|
|Krakow, Poland, 31-826|
|Oddział Onkologii Klinicznej, Regionalny Szpital Specjalistyczny "Latawiec"|
|Swidnica, Poland, 58-100|
|Oddział Onkologii Klinicznej SP ZOZ Wojewódzki Szpital Zespolony im. L. Rydygiera|
|Torun, Poland, 53/59|
|Klinika Onkologii WIM Warszawa|
|Warszawa, Poland, 00-909|
|Oddział Chemioterapii Dolnośląskie Centrum Onkologii|
|Wroclaw, Poland, 53-413|
|Principal Investigator:||Cezary Szczylik, PhD||Klinika Onkologii WIM|
|Principal Investigator:||Janusz Pawlega, PhD||Oddzial Kliniczny Kliniki Onkologii|
|Principal Investigator:||Piotr Koralewski, MD||Oddzial Chemioterapii Krakow|
|Principal Investigator:||Emilia Filipczyk-Cisarz, MD||Oddzial Chemioterapii Dolnoslaskie Centrum Onkologii|
|Principal Investigator:||Ewa Kilar, MD||Regionalny Szpital Specjalistyczny Latawiec|
|Principal Investigator:||Piotr Sawrycki, MD||Oddzial Onkologii Klinicznej im L Rydygiera|