Journal of Clinical Oncology, Vol 6, 56-61, Copyright © 1988 by American Society of Clinical Oncology
Correlation of karyotype and immunophenotype in childhood acute lymphoblastic leukemia
CH Pui, DL Williams, PK Roberson, SC Raimondi, FG Behm, SH Lewis, GK Rivera, DK Kalwinsky, M Abromowitch and WM Crist
Department of Hematology-Oncology, St Jude Children's Research Hospital, Memphis, TN 38101.
To correlate leukemic cell karyotype with immunophenotype, we studied 364
children with acute lymphoblastic leukemia (ALL). A prognostically
favorable cytogenetic feature, hyperdiploidy greater than 50 chromosomes,
was found in 33% of cases classified as common ALL antigen positive
(CALLA+) early pre-B (common) ALL, in contrast to 18% of pre-B cases (P =
.012), 5% of T cell cases (P less than .001), and none of the B cell cases
(P less than .001) or cases of CALLA negative (CALLA-) early pre-B ALL (P =
.002). The frequency of translocations, an adverse cytogenetic feature, was
significantly lower in CALLA+ early pre-B ALL cases (35%) than in B cell
(100%; P less than .0001), pre-B (59%; P less than .001), or CALLA- early
pre-B (62%; P = .016) cases. Thus, patterns of chromosomal change differ
widely among the major immunophenotypic groups of ALL and may account for
reported differences in responsiveness to treatment.