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Clinical Cancer Research Vol. 11, 8644-8652, December 15, 2005
© 2005 American Association for Cancer Research


Imaging, Diagnosis, Prognosis

High Serum Concentration of YKL-40 Is Associated with Short Survival in Patients with Acute Myeloid Leukemia

Olav J. Bergmann1,3,5, Julia S. Johansen2, Tobias W. Klausen1, Anne K. Mylin1, Jørgen S. Kristensen5, Eigil Kjeldsen4 and Hans E. Johnsen1,6

Authors' Affiliations: 1 Research Laboratory, Departments of Hematology and 2 Rheumatology, Herlev University Hospital, Copenhagen, 3 Department of Hematology and Infectious Diseases, Ribe County Hospital, Esbjerg, 4 Cancer Cytogenetic Laboratory, 5 Department of Hematology, Aarhus University Hospital, and 6 Department of Hematology, Aalborg Hospital, Aarhus University, Aarhus, Denmark

Requests for reprints: Olav J. Bergmann, Department of Hematology and Infectious Diseases, Ribe County Hospital, Finsensgade 35, DK-6700 Esbjerg, Denmark. Phone: 45-7918-2160; Fax: 45-7918-2229; E-mail: ojb{at}ribeamt.dk.

Purpose: YKL-40 is secreted by cancer cells, macrophages, and neutrophils. It may be a growth or differentiation factor, play a role in angiogenesis, or protect against apoptosis. High serum YKL-40 is associated with poor prognosis in solid carcinomas. The aim was to examine serum YKL-40 in patients with acute myeloid leukemia (AML).

Experimental Design: YKL-40 was measured by ELISA in serum from 77 patients recently diagnosed with AML before and during the first month of chemotherapy.

Results: Forty (52%) of the AML patients had elevated serum YKL-40 (compared with age-matched healthy subjects) and their survival was shorter than in patients with normal serum YKL-40 (median, 128 days; interquartile range, 18-629 days versus 386 days; interquartile range, 180-901; P = 0.018 Mann-Whitney test). Univariate analysis of serum YKL-40 (logarithmically transformed and treated as a continuous covariate) showed significant association with survival within the first month after start of chemotherapy [hazard ratio (HR), 1.7; 95% confidence interval (CI), 1.2-2.4; P = 0.002], first 12 months (HR, 1.6; 95% CI, 1.2-2.0; P = 0.0002), and overall survival (HR, 1.3; 95% CI, 1.1-1.6; P = 0.003). Multivariate Cox analysis showed that serum YKL-40 was an independent prognostic variable for survival (first month: HR, 1.7; P = 0.011; 12 months: HR, 1.6; P = 0.0002; overall survival: HR, 1.4; P = 0.002). High serum YKL-40 at start of chemotherapy was a risk factor for pneumonia within the first month, and serum YKL-40 increased (P = 0.002) at time of pneumonia and was unchanged in patients without infections.

Conclusions: Serum YKL-40 is a prognostic biomarker of survival in AML patients. Its role in AML and infections needs to be determined.




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