Abstract
The clinical and biologic significance of chromosomal aberrations has rendered cytogenetic investigations an indispensable tool in the diagnosis of acute lymphoblastic leukemia (ALL) (Seeker-Walker 1990; Pui et al. 1990b). Among the chromosomal changes in adult ALL, the Ph translocation and the translocation t(4;11) are consistently found, and have been shown to identify patients with an extremely unfavorable prognosis. Moreover, the presence of any karyotypic alteration in adult ALL seems to imply a poor treatment outcome than in patients without chromosomal changes (Bloomfield et al. 1986, 1989). Therefore, not only the assessment of the frequency of well-known chromosomal rearrangements but also the identification of other karyotypic abnormalities is required, and the biologic and clinical importance of the cytogenetic findings must be evaluated in relation to clinical, morphologic, and immunologic parameters. In this report on chromosomal aberrations in adult ALL, some of these aspects will be touched upon within a discussion of specific chromosomal aberrations, including the possible significance of certain secondary aberrations in Ph- positive ALL.
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Rieder, H. et al. (1993). Chromosomal Abnormalities in Adult Acute Lymphoblastic Leukemia: Results of the German ALL/AUL Study Group. In: Ludwig, WD., Thiel, E. (eds) Recent Advances in Cell Biology of Acute Leukemia. Recent Results in Cancer Research, vol 131. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84895-7_13
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DOI: https://doi.org/10.1007/978-3-642-84895-7_13
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