The current role of chemotherapy in pancreatic carcinoma is limited, and progress in the treatment of this disease represents a significant challenge to medical oncology. The most promising drug under study is gemcitabine, a relatively new antimetabolite that represents an attractive candidate for combination chemotherapy because of its excellent side-effect profile and the absence of overlapping toxicities with other chemotherapeutic agents. Combined administration of gemcitabine and anthracyclines could result in the induction of DNA breaks that are not easily repaired by the cell’s machinery, thus enhancing the apoptotic signals triggered by these lesions. Forty-four patients with locally advanced and/or metastatic pancreatic adenocarcinoma were enrolled in this multicenter study. Patients received Epirubicin 20 mg m72 for 3 weeks followed by 1 week of rest (1 cycle) and gemcitabine 1000 mg m72 after Epirubicin on the same day. All were assessable for toxicity and response, 11 patients responded to treatment with one complete response and 10 partial responses, for an overall response rate of 25%. Median survival was 10.9 months (range, 2 – 26 months). Therapy was well tolerated, with a low incidence of haematologic grade 42 toxicity. A total of 12 of 27 (44.4%) eligible patients attained a clinical benefit response. Our findings suggest that the gemcitabine-epirubicin schedule is active and well tolerated in patients with advanced pancreatic cancer.

Weekly gemcitabine plus Epirubicin as effective chemotherapy for advanced pancreatic cancer: a multicenter phase II study / B. Neri; G. Cini; L. Doni; C. Fulignati; M. Turrini; D. Pantalone; E. Mini; C. De Luca Cardillo; L.M. Fioretto; A.S. Ribecco; R. Moretti; M. Scatizzi; G. Zocchi; A. Quattrone. - In: BRITISH JOURNAL OF CANCER. - ISSN 0007-0920. - STAMPA. - 87:(2002), pp. 497-501. [10.1038/sj.bjc.6600482]

Weekly gemcitabine plus Epirubicin as effective chemotherapy for advanced pancreatic cancer: a multicenter phase II study

NERI, BRUNO
Writing – Original Draft Preparation
;
CINI, GRAZIA
Validation
;
DONI, LORIANA
Investigation
;
PANTALONE, DESIRE'
Investigation
;
MINI, ENRICO
Visualization
;
DE LUCA CARDILLO, CARLA
Visualization
;
QUATTRONE, ALESSANDRO
Supervision
2002

Abstract

The current role of chemotherapy in pancreatic carcinoma is limited, and progress in the treatment of this disease represents a significant challenge to medical oncology. The most promising drug under study is gemcitabine, a relatively new antimetabolite that represents an attractive candidate for combination chemotherapy because of its excellent side-effect profile and the absence of overlapping toxicities with other chemotherapeutic agents. Combined administration of gemcitabine and anthracyclines could result in the induction of DNA breaks that are not easily repaired by the cell’s machinery, thus enhancing the apoptotic signals triggered by these lesions. Forty-four patients with locally advanced and/or metastatic pancreatic adenocarcinoma were enrolled in this multicenter study. Patients received Epirubicin 20 mg m72 for 3 weeks followed by 1 week of rest (1 cycle) and gemcitabine 1000 mg m72 after Epirubicin on the same day. All were assessable for toxicity and response, 11 patients responded to treatment with one complete response and 10 partial responses, for an overall response rate of 25%. Median survival was 10.9 months (range, 2 – 26 months). Therapy was well tolerated, with a low incidence of haematologic grade 42 toxicity. A total of 12 of 27 (44.4%) eligible patients attained a clinical benefit response. Our findings suggest that the gemcitabine-epirubicin schedule is active and well tolerated in patients with advanced pancreatic cancer.
2002
87
497
501
Goal 3: Good health and well-being
B. Neri; G. Cini; L. Doni; C. Fulignati; M. Turrini; D. Pantalone; E. Mini; C. De Luca Cardillo; L.M. Fioretto; A.S. Ribecco; R. Moretti; M. Scatizzi;...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/344576
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