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The transplant iron score as a predictor of stem cell transplant survival

Jonathan A Storey1,7 email, Rebecca F Connor1,7 email, Zachary T Lewis2 email, David Hurd1,7 email, Gregory Pomper2 email, Yi K Keung1,7 email, Manisha Grover3 email, James Lovato4,6 email, Suzy V Torti5,7 email, Frank M Torti1,6,7 email and István Molnár1,7 email

Department of Internal Medicine, Section on Hematology and Oncology, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Department of Medicine, New York University Downtown Hospital, New York, NY, USA

Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Department of Biochemistry, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Department of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Comprehensive Cancer Center of Wake Forest University, Wake Forest University School of Medicine, Winston-Salem, NC, USA

author email corresponding author email

Journal of Hematology & Oncology 2009, 2:44doi:10.1186/1756-8722-2-44

Published: 24 October 2009

Abstract

Recent studies have suggested that the presence of iron overload prior to stem cell transplantation is associated with decreased survival. Within these studies, the criteria used to define iron overload have varied considerably. Given the lack of consensus regarding the definition of iron overload in the transplant setting, we sought to methodically examine iron status among transplant patients. We studied 78 consecutive patients at risk for transfusion-related iron overload (diagnoses included AML, ALL, MDS, and aplastic anemia) who received either autologous or allogeneic stem cell transplant. Multiple measures of iron status were collected prior to transplantation and examined for their association with survival. Using this data, three potentially prognostic iron measures were identified and incorporated into a rational and unified scoring system. The resulting Transplant Iron Score assigns a point for each of the following variables: (1) greater than 25 red cell units transfused prior to transplantation; (2) serum ferritin > 1000 ng/ml; and (3) a semi-quantitative bone marrow iron stain of 6+. In our cohort, the score (range 0 to 3) was more closely associated with survival than any available single iron parameter. In multivariate analysis, we observed an independent effect of iron overload on transplant survival (p = 0.01) primarily attributable to an increase in early treatment-related deaths (p = 0.02) and lethal infections. In subgroup analysis, the predictive power of the iron score was most pronounced among allogeneic transplant patients, where a high score (≥ 2) was associated with a 50% absolute decrease in survival at one year. In summary, our results lend further credence to the notion that iron overload prior to transplant is detrimental and suggest iron overload may predispose to a higher rate of lethal infections.


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