We studied 24 patients affected by Acute Promyelocytic Leukemia (APL) treated according to the original Jean Bernard’s protocol (an induction phase with high doses of DNR, followed by a manteinance phase with MTX and 6-MP, and periodic reinduction cycles with DNR and MethylGAG). We obtained 21 CR (87.5%), while 3 patients died during the induction treatment. The 5-year mortality rate of all the patients was 46.1%; 12 patients are still alive and 9 (37.5%) relapsed at different times from the first remission. From the accurate analysis of these cases we concluded that the microgranular variant of the disease and the impossibility to perform a correct maintenance therapy are negative prognostic indexes and, ultimately, a possible indication to BMT in adult patients affected by APL
Acute promyelocytic leukaemia (APL): chemotherapy or bone marrow transplantation?
C Porta;
1989-01-01
Abstract
We studied 24 patients affected by Acute Promyelocytic Leukemia (APL) treated according to the original Jean Bernard’s protocol (an induction phase with high doses of DNR, followed by a manteinance phase with MTX and 6-MP, and periodic reinduction cycles with DNR and MethylGAG). We obtained 21 CR (87.5%), while 3 patients died during the induction treatment. The 5-year mortality rate of all the patients was 46.1%; 12 patients are still alive and 9 (37.5%) relapsed at different times from the first remission. From the accurate analysis of these cases we concluded that the microgranular variant of the disease and the impossibility to perform a correct maintenance therapy are negative prognostic indexes and, ultimately, a possible indication to BMT in adult patients affected by APL| File | Dimensione | Formato | |
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1. Bone Marrow Transplant 1989.pdf
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