Abstract
30 adult patients with acute promyelocytic leukemia (APL) were seen at our institution over the past 7 years. Their white cell count at presentation ranged from 400/μl to 54,900/μl. Cytogenetic studies were successful in 28 patients, of which 26(93%) were positive for t(15;17). Molecular analysis by reverse-transcription polymerase chain reaction demonstrated the PML-RARα fusion transcript in all 30 patients. The majority of patients had breakpoints at the 3′ end with bcr1 products predominating. Complete remission rate of 92% was achieved using all-trans retinoic acid and anthracycline as induction chemotherapy in 26 patients. Of these, retinoic acid syndrome was observed in 4 cases, with 1 fatality. In conclusion, APL is a distinct entity with a highly specific molecular marker—t (15;17) translocation—that can be successfully induced into remission with all-trans retinoic acid and anthracycline in most patients.
Similar content being viewed by others
References
Degos L. Is acute promyelocytic leukemia a curable disease? Treatment strategy for a long-term survival.Leukemia 1994;8: S6-S8.
Frankel SRet al. The retinoic acid syndrome in acute promyelocytic leukemia.Ann Intern Med 1992;117: 292–296.
De Botton Set al. Incidence, clinical features, and outcome of all trans-retinoic acid syndrome in 413 cases of newly diagnosed acute promyelocytic leukemia. The European APL Group.Blood 1998;92: 2712–2718.
Estey Eet al. Treatment of newly diagnosed acute promyelocytic leukemia without cytarabine.J Clin Oncol 1997;15: 483–490.
Bennett JMet al. Proposal for the classification of the acute leukemias. French-American-British (FAB) Cooperative Group.Br J Hematol 1976;33: 451–458.
Castaigne Set al. All-trans retinoic acid as a differentiation therapy for acute promyelocytic leukemia. I. Clinical results.Blood 1990;76: 1704–1709.
Klinger HP Rapid processing of primary embryonic tissue for chromosome banding pattern analysis.Cytogenet Cell Genet 1972;11: 424–455.
ISCN.An International System for Human Cytogenetic Nomenclature. Mittelman F (ed). Published in collaboration withCytogenetics and Cell Genetics. S Karger: Basel, 1995.
Diverio Det al. Analysis of the PML/RARα fusion gene in acute promyelocytic leukemia. In: Finbarr E Cotter (ed).Molecular Diagnosis of Cancer. Humana Press: New Jersey, pp 47–54, 1996.
Diverio Det al. Improved rapid detection of the PML/RARα fusion gene in acute promyelocytic leukemia.Leukemia 1996;10: 1214–1216.
Berger Ret al. Cytogenetic studies in acute promyelocytic leukemia; a survey of secondary chromosomal abnormalities.Genes Chromosomes Cancer 1991;3: 332–337.
Schoch Cet al. Secondary chromosome aberrations in acute myeloid leukemia with t(8;21)(q22;q22), inv(16)(p13q22) or t(15;17)(q22;q21).Blood 1995;86: 43a.
Slack JLet al. Secondary cytogenetic changes in acute promyelocytic leukemia—prognostic importance in patients treated with chemotherapy alone and association with the intron 3 breakpoint of the PML gene: a Cancer and Leukemia Group B Study.J Clin Oncol 1997;15: 1786–1795.
Gallagher REet al. Association of PML/RARα fusion mRNA type with pretreatment hematologic characteristics but not treatment outcome in acute promyelocytic leukemia: an intergroup molecular study.Blood 1997;90: 1656–1663.
Lo Coco Fet al. Genetic diagnosis and molecular monitoring in the management of acute promyelocytic leukemia.Blood 1999;94: 12–22.
De Botton S, Biondi Aet al. Molecular monitoring of the myl/retinoic acid-α fusion gene in acute promyelocytic leukemia by polymerase chain reaction.Blood 1992;80: 492–497.
WC Chouet al. Clinical and biological characteristics of acute promyelocytic leukemia in Taiwan: a high relapse rate in patients with high initial and peak white blood cell counts during all-trans retinoic acid treatment.Leukemia 1997;11: 921–928.
Goddard AD, Borrow J, Freemont PS, Solomon E. Characterization of a zinc finger gene disrupted by the t(15;17) in acute promyelocytic leukemia.Science 1991;254: 1371–1374.
Fagioli Met al. Alternative splicing of PML transcripts predicts coexpression of several carboxy-terminally different protein isoforms.Oncogene 1992;7: 1083–1091.
Cross NCPet al. An optimized multiplex polymerase chain reaction (PCR) for detection of BCR-ABL fusion mRNAs in haematological disorders.Leukemia 1994;8: 186–189.
Diverio Det al. Improved rapid detection of the PML/RARα fusion gene in acute promyelocytic leukemia.Leukemia 1996;10: 1214–1216.
Biondi Aet al. Molecular monitoring of the myl/retinoic acid receptor-α fusion gene in acute promyelocytic leukemia by polymerase chain reaction.Blood 1992;80: 492–497.
Author information
Authors and Affiliations
Corresponding author
About this article
Cite this article
Lim, LC., Vellupillai, M. & Ghafar, A. Clinico-biological features of 30 patients with acute promyelocytic leukemia and response to combination induction chemotherapy with all-trans retinoic acid and anthracycline. Med Oncol 17, 301–306 (2000). https://doi.org/10.1007/BF02782195
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF02782195