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Blood, 15 December 2000, Vol. 96, No. 13, pp. 4075-4083
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
Karyotypic analysis predicts outcome of preremission and
postremission therapy in adult acute myeloid leukemia: a
Southwest Oncology Group/Eastern Cooperative Oncology Group study
Marilyn L. Slovak,
Kenneth
J. Kopecky,
Peter A. Cassileth,
David H. Harrington,
Karl S. Theil,
Anwar Mohamed,
Elizabeth Paietta,
Cheryl L. Willman,
David R. Head,
Jacob M. Rowe,
Stephen J. Forman, and
Frederick R. Appelbaum for the Southwest Oncology
Group and the Eastern Cooperative Oncology Group
From the City of Hope National Medical Center, Duarte,
CA.
The associations of cytogenetics with complete remission (CR)
rates, overall survival (OS), and outcomes after CR were studied in 609 previously untreated AML patients younger than 56 years old in a
clinical trial comparing 3 intensive postremission therapies: intensive
chemotherapy, autologous transplantation (ABMT), or allogeneic bone
marrow transplantation (alloBMT) from matched related donors. Patients
were categorized into favorable, intermediate, unfavorable, and unknown
cytogenetic risk groups based on pretreatment karyotypes. CR rates
varied significantly (P < .0001) among the 4 groups:
favorable, 84% (95% confidence interval [CI], 77%-90%); intermediate, 76% (CI, 71%-81%); unfavorable, 55% (CI, 48%-63%); and unknown, 54% (CI, 33%-74%). There was similar significant heterogeneity of OS (P < .0001), with the estimated
relative risk of death from any cause being 1.50 (CI, 1.10-2.05), 3.33 (CI, 2.43-4.55), and 2.66 (CI, 1.59-4.45) for the intermediate,
unfavorable, and unknown risk groups, respectively, compared with the
favorable group. In multivariate analyses, the effects of cytogenetic
risk status on CR rate and OS could not be explained by other patient or disease characteristics. Among postremission patients, survival from
CR varied significantly among favorable, intermediate, and unfavorable
groups (P = .0003), with significant evidence of
interaction (P = .017) between the effects of treatment
and cytogenetic risk status on survival. Patients with favorable
cytogenetics did significantly better following ABMT and alloBMT
than with chemotherapy alone, whereas patients with unfavorable
cytogenetics did better with alloBMT. Cytogenetic risk status is a
significant factor in predicting response of AML patients to
therapy; however, to tighten treatment correlates within
genetically defined AML subsets, a significantly larger leukemia
cytogenetic database is warranted.

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