Volume 85, Issue 3 pp. 160-163
Research Article
Free Access

Host immunity affects survival in myelodysplastic syndromes: Independent prognostic value of the absolute lymphocyte count

Nisha L. Jacobs

Nisha L. Jacobs

Department of Medicine, Division of Hematology, Oncology, and Transplantation, University of Minnesota, Minneapolis, Minnesota

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Shernan G. Holtan

Shernan G. Holtan

Department of Medicine, Division of Hematology, Mayo Clinic Graduate School of Medicine, Rochester, Minnesota

N.L.J. and S.G.H. contributed equally to this work.

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Luis F. Porrata

Luis F. Porrata

Department of Medicine, Division of Hematology, Mayo Clinic Graduate School of Medicine, Rochester, Minnesota

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Svetomir N. Markovic

Svetomir N. Markovic

Department of Medicine, Division of Hematology, Mayo Clinic Graduate School of Medicine, Rochester, Minnesota

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Ayalew Tefferi

Ayalew Tefferi

Department of Medicine, Division of Hematology, Mayo Clinic Graduate School of Medicine, Rochester, Minnesota

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David P. Steensma

Corresponding Author

David P. Steensma

Leukemia Group, Division of Hematologic Malignancies, Department of Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts

Dana-Farber Cancer Institute, 44 Binney Street, Suite D1B30 (Mayer 1B21), Boston, MA 02115Search for more papers by this author
First published: 22 December 2009
Citations: 30

Conflict of interest: Nothing to report.

Abstract

The prognostic significance of the peripheral blood absolute lymphocyte count (ALC) has been carefully examined in lymphoid malignancies, but the importance of the baseline ALC in chronic myeloid neoplasms is less clear. In a recent analysis of myelodysplastic syndromes (MDS) associated with deletion of chromosome 5q, we observed that an ALC < 1.2× 109 cells/L at diagnosis is independently associated with poorer survival. Clinicopathological data from 503 patients with non-del(5q) MDS evaluated at Mayo Clinic between 1996 and 2007 were reviewed to determine the prognostic impact of ALC at diagnosis in non-del(5q) MDS. Patients with MDS and an ALC at diagnosis ≥1.2× 109 (N = 248) experienced a superior overall survival (OS) compared with patients with an ALC < 1.2× 109/L (N = 255, median OS of 26.6 months versus 18.5 months, P < 0.001, respectively). ALC at diagnosis was an independent predictor for OS when compared with the International Prognostic Scoring System and the WHO-based Prognostic Scoring System. This study suggests that ALC at diagnosis is a prognostic factor for OS in MDS, and argues in favor of further studies to assess the role of host immunity in MDS clinical outcomes. Am. J. Hematol. 2010. © 2009 Wiley-Liss, Inc.

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