To determine whether MDR1 reversal by the addition of the P-glycoprotein (P-gp) inhibitor PSC-833 to standard induction chemotherapy would improve event-free survival (EFS), 419 untreated patients with acute myeloid leukemia (AML) aged 60 years and older were randomized to receive 2 induction cycles of daunorubicin and cytarabine with or without PSC-833. Patients in complete remission were then given 1 consolidation cycle without PSC-833. Neither complete response (CR) rate (54% versus 48%; P = .22), 5-year EFS (7% versus 8%; P = .53), disease-free survival (DFS; 13% versus 17%; P = .06) nor overall survival (OS; 10% in both arms; P = .52) were significantly improved in the PSC-833 arm. An integrated P-gp score (IPS) was determined based on P-gp function and P-gp expression in AML cells obtained prior to treatment. A higher IPS was associated with a significantly lower CR rate and worse EFS and OS. There was no significant interaction between IPS and treatment arm with respect to CR rate and survival, indicating also a lack of benefit of PSC-833 in P-gp-positive patients. The role of strategies aimed at inhibitory P-gp and other drug-resistance mechanisms continues to be defined in the treatment of patients with AML.

Additional Metadata
Keywords Aged, Aged, 80 and over, Cyclosporins/adverse effects/*therapeutic use, Cytarabine/adverse effects/*therapeutic use, Daunorubicin/adverse effects/*therapeutic use, Drug Therapy, Combination, Female, Follow-Up Studies, Humans, Leukemia, Myelocytic, Acute/diagnosis/*drug therapy/*metabolism, Male, Middle Aged, P-Glycoprotein/*metabolism, Research Support, Non-U.S. Gov't, Survival Rate, Treatment Outcome
Persistent URL hdl.handle.net/1765/8251
Citation
van der Holt, B., Verhoef, G.E.G., Ferrant, A., Fey, M.F., Crump, M., Theobald, M., … Vellenga, E.. (2005). The value of the MDR1 reversal agent PSC-833 in addition to daunorubicin and cytarabine in the treatment of elderly patients with previously untreated acute myeloid leukemia (AML), in relation to MDR1 status at diagnosis. Blood. Retrieved from http://hdl.handle.net/1765/8251