ACUTE LEUKEMIAS WITH THE T(4,11)(Q21,Q23)

被引：58

作者：

PUI, CH

机构：

[1] Departments of Hematology-Oncology and Pathology and Laboratory Medicine, St. Jude Children's Research Hospital, Memphis, TN

[2] Department of Pediatrics, University of Tennessee, Memphis

[3] College of Medicine, Memphis, TN

来源：

LEUKEMIA & LYMPHOMA | 1992年 / 7卷 / 03期

关键词：

ALL; AML SECONDARY LEUKEMIAS; TRANSLOCATIONS; PROGNOSTIC FACTORS;

D O I：

10.3109/10428199209053620

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

The t(4;11)(q21;q23) has been associated with marked lineage heterogeneity. Most of the reported cases were classified as acute lymphoblastic leukemia (ALL). The t(4;11) is one of the commonest specific chromosomal translocations in ALL, occurring in 2% of childhood and 5% of adult cases. In childhood ALL, this translocation is associated with female sex, age less than 1 year, hyperleukocytosis, CD10-/CD19+ B-precursor cell immunophenotype, and myeloid-associated antigen (CD15) expression. There also appears to be an age-related difference in treatment outcome. Adults had the worst prognosis, and children aged 1 to 9 years appeared to have a better outcome than infants or adolescents. Reported cases of acute myeloid leukemia (AML) or secondary leukemia with the t(4;11) have not been well characterized. It is intriguing that virtually all of the reported cases with secondary leukemia had received epipodophyllotoxins or doxorubicin, agents that affect topoisomerase II and are associated with secondary AML characterized by 11q23 abnormalities. Identification of the involved gene(s) in the t(4;11) will provide a molecular approach permitting more accurate classification of these cases.

引用

页码：173 / 179

页数：7

共 129 条

[31] 11) in ALL: a new morphologic aspect, Cancer Genet. Cytogenet., 23, pp. 145-149, (1986)
[32] Bertheas Frappaz M.F., Fraisse D.J., Ehrsam A., Le Petit J.C., Vasselon C., Brizard C.P., Freycon F., Persistence of t(4
[33] 11) in cytologically normal bone marrow treated ex vivo with Astaz-Z, Cancer Genet. Cytogenet., 20, pp. 163-165, (1986)
[34] Mirro J., Kitchingman G., Williams D., Lauzon G.J., Lin C.-C., Callihan T., Zipf T.F., Clinical and laboratory characteristics of acute leukemia with the 4
[35] 11 translocation, Blood., 67, pp. 689-697, (1986)
[36] Stark B., Umiel T., Mammon E., Galili N., Dzaledetti M., Cohen I.J., Steinberg Vogel M.R., Zaizov R., Leukemia of early infancy. Early B-cell lineage associated with t(4
[37] 11), Cancer, 58, pp. 1265-1271, (1986)
[38] Testa J.R., Misawa S., Pollak A., Leavitt R., Unusual cytogenetic findings in two patients with t(4
[39] 11) acute leukemia, Inst. J. Cancer., 38, pp. 847-886, (1986)
[40] Fisher T.C., Patil S.R., Edwards R., Gingrich R.D., Burns C.P., Cytogenetic analysis of adult acute lymphoblastic leukemia including a Ph + case surviving more than 5 years, Cancer Genet. Cytogenet, 23, pp. 245-251, (1986)

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