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Treatment of pancreatic cancer with a combination of docetaxel, gemcitabine and granulocyte colony-stimulating factor: A phase II study of the Greek Cooperative Group for Pancreatic Cancer
Authors:G. P. Stathopoulos   D. Mavroudis   N. Tsavaris   C. Kouroussis   G. Aravantinos   S. Agelaki   S. Kakolyris   S. K. Rigatos   S. Karabekios  V. Georgoulias
Affiliation:(1) Second Department of Internal Medicine-Oncology Unit, University of Athens, "lsquo"Ippokration"rsquo" Hospital, Greece;(2) Department of Medical Oncology, University General Hospital, Heraklion, Crete, Greece;(3) Department of Pathophysiology, University of Athens "lsquo"Laikon"rsquo" General Hospital, Athens, Greece;(4) Third Department of Medical Oncology, "lsquo"Anargyri"rsquo" Anticancer Hospital, Athens, Greece
Abstract:Purpose:To evaluate the tolerance and efficacy of front-linedocetaxel plus gemcitabine treatment in patients with inoperable pancreaticcancer.Patients and methods:Fifty-four patients with locally advancedor metastatic pancreatic cancer were enrolled. Gemcitabine (1000mg/m2) was administered on days 1 and 8 and docetaxel (100mg/m2) on day 8, every three weeks; rh-G-CSF (150ìg/m2 s.c.) was given prophylactically on days9–15.Results: Seven (13%) patients achieved partial response and18 (33%) stable disease (intent-to-treat). The median duration ofresponse was 24 weeks, time to tumour progression 32 weeks, and overallsurvival 26 weeks. Performance status was improved in 33% of patients,pain in 43%, asthenia in 16%, weight gain in 28% andappetite in 27%. Grade 3–4 neutropenia occurred in 17(31%)patients and grade 3–4 thrombocytopenia in four (4%). Six(11%) patients developed febrile neutropenia and one of them died fromsepsis.Conclusions:This combination is a relatively well-toleratedout-patient regimen for patients with inoperable pancreatic cancer.
Keywords:chemotherapy  docetaxel  gemcitabine  pancreatic cancer
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