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Blood, 1 July 2006, Vol. 108, No. 1, pp. 63-73.
Prepublished online as a Blood First Edition Paper on March 7, 2006; DOI 10.1182/blood-2005-11-4354.
Previous Article | Next Article 
Submitted November 3, 2005
Accepted February 21, 2006
Pretreatment cytogenetics add to other prognostic factors predicting complete remission and long-term outcome in patients 60 years of age or older with acute myeloid leukemia: results from cancer and leukemia group B 8461
Sherif S Farag*, Kellie J Archer, Krzysztof Mrozek, Amy S Ruppert, Andrew J Carroll, James W Vardiman, Mark J Pettenati, Maria R Baer, Mazin B Qumsiyeh, Prasad R Koduru, Yi Ning, Robert J Mayer, Richard M Stone, Richard A Larson, and Clara D Bloomfield
The Ohio State University, Columbus, OH, USA
Virginia Commonwealth University, Richmond, VA, USA; The CALGB Statistical Center, Durham, NC, USA
The Ohio State University, Columbus, OH, USA; The CALGB Statistical Center, Durham, NC, USA
University of Alabama at Birmingham, Birmingham, AL, USA
University of Chicago, Chicago, IL, USA
Wake Forest University, Winston-Salem, NC, USA
Roswell Park Cancer Institute, Buffalo, NY, USA
Duke University, Durham, NY, USA
North Shore University, Manhasset, NY, USA
University of Maryland, Baltimore, MD, USA
Dana Farber Cancer Institute, Boston, MA, USA
* Corresponding author; email: sherif.farag{at}osumc.edu.
We investigated the relative prognostic significance of cytogenetics in 635 adult acute myeloid leukemia (AML) patients 60 years treated on front-line protocols. Classification trees and tree-structured survival analysis (TSSA) were used to identify important cytogenetic groups, and their prognostic significance was then assessed in multivariable analysis (MVA). Overall, 48.5% achieved complete remission (CR); 6.6% survived at 5 years. Complex karyotypes with 3 abnormalities (complex 3) and a group including "rare aberrations" predicted lower CR rates (25% and 30%) versus other patients (56%). Compared with complex 3, the odds of CR were significantly higher for non-complex karyotypes without "rare aberrations" on MVA. Cytogenetically, complex 5 predicted inferior disease-free survival on TSSA, remaining significant on MVA together with white cell count (WBC), gender, and age. For survival, complex 5, "rare aberrations", and core-binding factor (CBF) abnormalities were prognostic (P< 0.0001), with 5-year survivals of 0%, 0%, and 19.4%, respectively, and 7.5% for remaining patients. Together with WBC, marrow blasts, gender, and age, the cytogenetic groups remained significant on MVA. In conclusion, pretreatment cytogenetics adds to other prognostic factors in older AML patients. Patients with complex 5 appear to benefit minimally from current treatment and are better suited for investigational therapy or supportive care.

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