Glufosfamide administered using a 1-hour infusion given as first-line treatment for advanced pancreatic cancer. A phase II trial of the EORTC-new drug development group.

Détails

ID Serval
serval:BIB_29582
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Glufosfamide administered using a 1-hour infusion given as first-line treatment for advanced pancreatic cancer. A phase II trial of the EORTC-new drug development group.
Périodique
European Journal of Cancer
Auteur⸱e⸱s
Briasoulis E., Pavlidis N., Terret C., Bauer J., Fiedler W., Schöffski P., Raoul J.L., Hess D., Selvais R., Lacombe D., Bachmann P., Fumoleau P.
ISSN
0959-8049 (Print)
ISSN-L
0959-8049
Statut éditorial
Publié
Date de publication
2003
Volume
39
Numéro
16
Pages
2334-2340
Langue
anglais
Notes
Publication types: Clinical Trial ; Clinical Trial, Phase II ; Journal Article ; Multicenter Study ; Randomized Controlled Trial Publication Status: ppublish
Résumé
The activity of glufosfamide (beta-D-glucopyranosyl-N,N'-di-(2-chloroethyl)-phosphoric acid diamide) against pancreatic cancer was investigated in a multicentre, phase II clinical study. Chemotherapy-nai;ve patients with advanced or metastatic disease were treated with glufosfamide (5 g/m(2)) using a 1-h intravenous (i.v.) infusion every 3 weeks. Patients were randomised between active-hydration and normal fluids to evaluate the nephroprotective effect of forced diuresis. Patients experiencing >0.4 mg/dl (>35 micromol/l) increase in serum creatinine compared with their baseline value were taken off treatment for safety reasons. The evaluation of response was according to the Response evaluation criteria in solid tumours (RECIST). Blood sampling was performed for pharmacokinetic analyses. 35 patients from 13 institutions were registered over a 13-month period. A total of 114 treatment cycles (median 3, range 1-8) were administered to 34 patients; 18 patients were allocated to the hydration arm. Overall haematological toxicity was mild. Metabolic acidosis occurred in 2 patients treated in the active-hydration arm, grade 3 hypokalaemia was recorded in 5 patients and grade 3 hypophosphataemia in 4 patients. One patient had a grade 4 increase in serum creatinine level, concomitantly to disease progression. Active-hydration did not show a nephroprotective effect and the plasma pharmacokinetics (Pk) of glufosfamide was not significantly influenced by hydration. Two confirmed partial remissions (PR) were reported (response rate 5.9%, 95% Confidence Interval (CI) 0.7-19.7%) and 11 cases obtained disease stabilisation (32.4%). An extra mural review panel confirmed all of the responses. Median overall survival was 5.3 months (95% CI 3.9-7.1) and time to progression (TTP) was 1.4 months (95% CI 1.3-2.7). In conclusion, glufosfamide administered using a 1-h infusion every 3 weeks has a modest activity in advanced pancreatic adenocarcinoma. Haematological toxicity is particularly mild, but regular monitoring of renal function is recommended.
Mots-clé
Adenocarcinoma/drug therapy, Adult, Aged, Antineoplastic Agents/administration & dosage, Antineoplastic Agents/adverse effects, Disease Progression, Disease-Free Survival, Female, Humans, Infusions, Intravenous, Male, Middle Aged, Pancreatic Neoplasms/drug therapy, Phosphoramide Mustards/administration & dosage, Phosphoramide Mustards/adverse effects, Prospective Studies, Treatment Outcome
Pubmed
Web of science
Création de la notice
19/11/2007 13:27
Dernière modification de la notice
20/08/2019 14:09
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