Abstract
The immunophenotype is one of the prognostic factors in children with acute lymphoblastic leukemia (ALL) (Crist et al. 1984, 1985, 1989; Sallan et al. 1980; Greaves et al. 1981; Pui et al. 1986). B-cell ALL (B-ALL) cases have the worst prognosis and patients with B-cell precursor ALL the most favorable prognosis. Precursor B-ALL can be subdivided into three groups: pro-B-ALL (CD10−, cytoplasmic μ chain− [cμ−]; common ALL (c-ALL) (CD10+/cμ−) and pre-B-ALL (CD10+ or −/cμ+). The small group of patients whose cells lack the common ALL (c-ALL) antigen characteristic of the earliest stage of B-cell differentiation (pro-B-ALL) show poorer responses by comparison with the c-ALL+ cases. In some studies the pre-B-ALL cases did worse than the cALL cases, but this is probably due to a small subset of patients with a specific chromosomal abnormality on their leukemic cells (Crist et al. 1990). Also, patients with T-cell ALL (T-ALL) have an unfavorable prognosis. Some of these findings are still controversial because in some studies the immunophenotype is related to other clinical and biological features like white blood cell (WBC) count and organomegaly. Also, when effective treatments are used, the prognostic value of immunophenotype could be diminished (Borowitz 1990; Poplack and Reaman 1988; Miller 1988).
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© 1993 Springer-Verlag Berlin · Heidelberg
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Pieters, R. et al. (1993). Cellular Drug Sensitivity of Immunophenotypic Subgroups of Childhood Acute Lymphoblastic Leukemia. 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_22
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DOI: https://doi.org/10.1007/978-3-642-84895-7_22
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