What is the Best Treatment for Acute Promyelocytic Leukemia?
- 1 January 1993
- journal article
- research article
- Published by Taylor & Francis in Leukemia & Lymphoma
- Vol. 11 (sup2) , 29-35
- https://doi.org/10.3109/10428199309064259
Abstract
The modern treatment of acute myelogenous leukemia (AML), consists of a polychemothera-peutic induction treatment followed by a post-remission therapy of variable intensity and duration and acute promyelocytic leukemia (APL) does not differ from this behavior. However, differently from the other AML subtypes, APL shows a high response rate to induction monochemotherapies with anthracycline drugs. This high response rate to anthra-cycline monochemotherapies is very peculiar of APL. Moreover, it has been suggested that maintanance treatment regimens incorporating the drugs Methotrexate and 6–Mercaptopurine, two drugs generally not utilized in the post-remission treatment of other AML subtypes, may be effective in prolonging the leukemia-free survival of APL. Furthermore, the results firstly obtained by a Chinese group in 1988 by using the vitamin A derivative all-trans retinoic acid (ATRA) have been successively confirmed by several other groups in the world. Therefore, at present the all-trans retinoic acid appears to be the best CR inducer in APL. However, these CRs are short lasting when maintained with ATRA alone and eventually all patients relapse. As a consequence, patients achieving CR with ATRA still require intensive post-remission chemotherapy to maintain the CR. As for bone marrow transplantation procedures, it is our opinion that they do not represent the treatment of choice of APL in first CR considering the very good results obtained with standard pharmacological approaches. In conclusion, only future randomized prospective trials will clarify which, among the several proposed therapeutic approaches, should be preferred in this very peculiar subtype of AML.Keywords
This publication has 44 references indexed in Scilit:
- The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RARCell, 1991
- Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RARα with a novel putative transcription factor, PMLCell, 1991
- Rearrangements of the RAR‐α gene in acute promyelocytic leukaemia:British Journal of Haematology, 1991
- Epidemiology of acute promyelocytic leukemia in ItalyAnnals of Oncology, 1991
- The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locusNature, 1990
- Molecular Analysis of Acute Promyelocytic Leukemia Breakpoint Cluster Region on Chromosome 17Science, 1990
- Microgranular promyelocytic leukemia: A multiparameter examinationAmerican Journal of Hematology, 1989
- Acquired alpha‐2‐antiplasmin deficiency in acute promyelocytic leukaemiaBritish Journal of Haematology, 1988
- Surface marker analysis in acute myeloid leukaemia and correlation with FAB classificationBritish Journal of Haematology, 1986
- Proposals for the Classification of the Acute Leukaemias French‐American‐British (FAB) Co‐operative GroupBritish Journal of Haematology, 1976