Cyclosporin A as a modifier agent in the salvage treatment of acute leukemia (AL).
Fiche publication
Date publication
juin 1993
Journal
Leukemia
Auteurs
Membres identifiés du Cancéropôle Est :
Pr BASTIE Jean-Noël, Pr DELMER Alain
Tous les auteurs :
Marie JP, Bastie JN, Coloma F, Faussat Suberville AM, Delmer A, Rio B, Delmas-Marsalet B, Leroux G, Casassus P, Baumelou E
Lien Pubmed
Résumé
Sixteen adult patients with relapsed (7 patients) or refractory (9 patients) acute leukemia received mitoxantrone (10 mg/m2 per day for 3 days) and etoposide (200 mg/m2 per day for 3 days) with escalating dose of cyclosporin A (CsA) from a loading dose of 2 mg to 6.5 mg/kg per 2 h followed by 3 days continuous infusion of 5-15 mg/kg per day. The major toxicities were stomatitis and prolonged aplasia, occurring for 15 mg/kg per day of CsA. Transient conjugated hyperbilirubinemia occurred in all patients, and was CsA dose-dependent (r = 0.7). Adequate serum levels of CsA (> 1 microgram/ml) were obtained in 3/6 patients treated with 10 mg/kg per day and 4/4 patients with 15 mg/kg per day. The pharmacokinetic of mitoxantrone showed an unusual increase of carboxylic metabolites, parallel to CsA levels. We observed six responses (two complete and four partial remissions), and eight resistances. Two patients died at days 3 and 8 from sepsis. Before treatment, 7/16 patients tested for P-gp with C219 were positive (> 10% positive cells). 3/6 responders were P-gp-positive. At time of leukemic regrowth, cells expressing P-gp before therapy reverted to P-gp-negative cells.
Mots clés
Adult, Aged, Antineoplastic Combined Chemotherapy Protocols, adverse effects, Carrier Proteins, antagonists & inhibitors, Cyclosporine, administration & dosage, Etoposide, administration & dosage, Female, Humans, Leukemia, drug therapy, Male, Membrane Glycoproteins, antagonists & inhibitors, Middle Aged, Mitoxantrone, administration & dosage, P-Glycoprotein
Référence
Leukemia. 1993 Jun;7(6):821-4