Clonal evolution of blasts in an elderly patient with CD56(+) relapsed acute promyelocytic leukemia.

Autor: Itoh S; Division of Hematology, Third Department of Internal Medicine, Iwate Medical University School of Medicine, Morioka, Japan. shigei@iwate.med.ac.jp, Sugawara T, Enomoto S, Ono Y, Numaoka H, Utsugisawa T, Murai K, Ishida Y, Kuriya S
Jazyk: angličtina
Zdroj: American journal of hematology [Am J Hematol] 2002 Jan; Vol. 69 (1), pp. 59-63.
DOI: 10.1002/ajh.10005
Abstrakt: We describe an elderly patient with acute promyelocytic leukemia (APL), whose leukemic cells expressed CD56 antigen at relapse but not at diagnosis. Chromosome analysis revealed that blasts with t(8;15;17)(q24.1;q22;q11.2) increased from 4 of 20 cells (20%) at first relapse to 10 of 14 cells (71.4%) at second relapse. In addition, the positivity for CD56 expression on blasts judged by flow cytometric analysis using CD45 blast gating was also increased from 14.2% at first relapse to 75% at second relapse. Although conventional chemotherapy was performed for the initial disease and the first relapse, relapse developed again. Therefore, three courses of intensive postremission chemotherapy including concurrent administration of recombinant human granulocyte colony-stimulating factor (rhG-CSF) with cytarabine were performed after achievement of complete remission (CR) by the treatment with all-trans-retinoic acid (ATRA). Although PML-RARalpha mRNA was not detectable by reverse transcription polymerase chain reaction (RT-PCR), a third relapse occurred. This case demonstrated clonal evolution from a CD56(-) to a CD56(+) blast population and provided further support for the suggestion that CD56 expression might be an unfavorable prognostic factor in t(15;17) APL.
(Copyright 2002 Wiley-Liss, Inc.)
Databáze: MEDLINE
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