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Leukemia
January 2000, Volume 14, Issue 1, Pages 163 - 168
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Title

Geographic heterogeneity of cellular characteristics of acute myeloid leukemia: a comparative study of Australian and Japanese adult cases

K Nakase1, K Bradstock2, M Sartor2, D Gottlieb2, K Byth2, K Kita1, H Shiku1, N Kamada3 & the Japanese Cooperative Group of Leukemia/Lymphoma

1The Second Department of Internal Medicine, Mie University School of Medicine, Tsu, Japan

2The Department of Haematology, Westmead Hospital, Westmead, New South Wales, Australia

3The Department of Hematology, Research Institute of Nuclear Medicine and Biology, Hiroshima University, Hiroshima, Japan

Correspondence to: K Nakase, Department of Internal Medicine, Saiseikai Matsusaka Hospital, 1-15-6 Asahimachi, Matsusaka, Mie 515-8557, Japan; Fax: 011 81 598 51 6557


Abstract

We assessed a large number of adults (368 from Australia and 494 from Japan) with de novo acute myeloid leukemia (AML) to define the biological differences between the two populations. In this study, AML was classified using the French–American–British (FAB) criteria into seven groups (M1–M7). M2 was more common in Japan than in Australia, whereas M4 occurred more frequently in Australia than in Japan. Other FAB subtypes were evenly distributed. Cytogenetically, Japanese M2 displayed a higher frequency of t(8;21) than Australian (33.1% vs 15.3%, P < 0.05). The t(15;17), inv/del(16), 11q23 aberrations and 5/7/8 abnormalities were seen at similar frequencies. Immunophenotypically, Japanese M4/M5 more frequently displayed CD13 and CD14 than Australian, whereas the stem cell markers, CD34 and HLA-DR were observed at a relatively higher rate in Australian M3 than in Japanese M3. The B cell antigen, CD19 was more frequently seen in Japanese M2 than in Australian M2, but found more often in Australian M5 than in Japanese M5. In both populations, a close relationship was observed between the expression of CD19 and t(8;21). These findings suggest different biological characteristics of AML between the two populations, the main differences being generated by a higher frequency of t(8;21) chromosomal abnormality in Japanese AML. Leukemia(2000) 14, 163–168.

Keywords
acute myeloid leukemia; M2; t(8;21); CD19


Received 16 December 1998; Accepted 17 August 1999


© Macmillan Publishers Ltd 2000