BACKGROUND: Gemcitabine (Gemzar) and 5-fluorouracil (5-FU) plus folinic acid (FA) both have proven activity in the treatment of patients with advanced pancreatic cancer. The present study was initiated to investigate the efficacy of gemcitabine in combination with 5-FU-FA. PATIENTS AND METHODS: Thirty-eight patients, median age 60 years (range 34-70) with inoperable, stage IV, pancreatic cancer were enrolled into the study and treated on an outpatient basis. All except one patient received at least one cycle of treatment with gemcitabine (1000 mg/m2), followed by FA (200 mg/m2) and 5-FU (750 mg/m2) administered as a 24-hour continuous infusion on days 1, 8, 15 and 22 of a 42-day schedule. No patient had received prior chemotherapy or radiotherapy. All 38 patients were assessed for efficacy, toxicity and time to progressive disease. RESULTS: Two patients (5%), achieved a partial response and thirty-four patients (89%) achieved stable disease. There were two early deaths (< or = 4 weeks). The median time to progression was 7.1 months (range 0.4-18.1+; 95% confidence interval (95% CI): 5.3-7.9 months). Three patients had a progression-free interval of greater than 12 months and 12 of 38 patients (32%) survived longer than 12 months. The median overall survival was 9.3 months (range 0.5-26.5; 95% CI: 7.3-13.0 months). The incidence of grade 3 and 4 toxicities was low. CONCLUSIONS: The combination of gemcitabine and 5-FU-FA is active and well tolerated and seems to offer an improvement in progression-free interval over both gemcitabine monotherapy and 5-FU-FA therapy.
BACKGROUND:Gemcitabine (Gemzar) and 5-fluorouracil (5-FU) plus folinic acid (FA) both have proven activity in the treatment of patients with advanced pancreatic cancer. The present study was initiated to investigate the efficacy of gemcitabine in combination with 5-FU-FA. PATIENTS AND METHODS: Thirty-eight patients, median age 60 years (range 34-70) with inoperable, stage IV, pancreatic cancer were enrolled into the study and treated on an outpatient basis. All except one patient received at least one cycle of treatment with gemcitabine (1000 mg/m2), followed by FA (200 mg/m2) and 5-FU (750 mg/m2) administered as a 24-hour continuous infusion on days 1, 8, 15 and 22 of a 42-day schedule. No patient had received prior chemotherapy or radiotherapy. All 38 patients were assessed for efficacy, toxicity and time to progressive disease. RESULTS: Two patients (5%), achieved a partial response and thirty-four patients (89%) achieved stable disease. There were two early deaths (< or = 4 weeks). The median time to progression was 7.1 months (range 0.4-18.1+; 95% confidence interval (95% CI): 5.3-7.9 months). Three patients had a progression-free interval of greater than 12 months and 12 of 38 patients (32%) survived longer than 12 months. The median overall survival was 9.3 months (range 0.5-26.5; 95% CI: 7.3-13.0 months). The incidence of grade 3 and 4 toxicities was low. CONCLUSIONS: The combination of gemcitabine and 5-FU-FA is active and well tolerated and seems to offer an improvement in progression-free interval over both gemcitabine monotherapy and 5-FU-FA therapy.
Authors: Joan Maurel Santasusana; José Luis García López; Juan José García; Ana Isabel León Carbonero; Javier Gallego Plazas; Pedro Sánchez Rovira; Carlos Fernández Martos; M Carmen Galán Guzmán; Jesús Florián Jericó; Francisco Javier Dorta Delgado; Javier Casinello Espinosa; Marta Llanos Muñoz; Enrique Aranda Aguilar; Javier Sastre Valera; Ignacio García Ribas; Alfredo Carrato Mena Journal: Clin Transl Oncol Date: 2005-12 Impact factor: 3.405
Authors: Byeong Seok Sohn; Young Jin Yuh; Hong Suk Song; Bong-Seog Kim; Kyung Hee Lee; Joung-Soon Jang; Sung Rok Kim Journal: Oncol Lett Date: 2015-06-10 Impact factor: 2.967
Authors: Agustin A Garcia; Lawrence Leichman; Joaquina Baranda; Lalita Pandit; Heinz-Josef Lenz; Cynthia G Leichman Journal: Int J Gastrointest Cancer Date: 2003
Authors: Hanno Riess; Uwe Pelzer; Andreas Hilbig; Jens Stieler; Bernhard Opitz; Theo Scholten; Dörte Kauschat-Brüning; Peter Bramlage; Bernd Dörken; Helmut Oettle Journal: BMC Cancer Date: 2008-12-05 Impact factor: 4.430