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Pre-Transplant Serum Leptin Levels and Relapse of Acute Myeloid Leukemia after Allogeneic Transplantation
Authors:Mark-Alexander Schwarzbich,Hao Dai,Lambros Kordelas,Dietrich W. Beelen,Aleksandar Radujkovic,Carsten Mü  ller-Tidow,Peter Dreger,Thomas Luft
Affiliation:1.Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany; (M.-A.S.); (A.R.); (C.M.-T.); (P.D.);2.Department of Epidemiology, German Cancer Research Centre (DKFZ), 69120 Heidelberg, Germany;3.Department of Bone Marrow Transplantation, University Hospital, 45122 Essen, Germany; (L.K.); (D.W.B.)
Abstract:Weight loss and metabolic activity influence outcome after allogeneic stem cell transplantation (alloSCT). This study evaluates pre-conditioning Leptin, a peptide hormone involved in metabolism and immune homeostasis, as a prognostic factor for survival, relapse and non-relapse mortality (NRM) following alloSCT. Leptin serum levels prior to conditioning were determined in a cohort of patients transplanted for various hematologic malignancies (n = 524) and correlated retrospectively with clinical outcome. Findings related to patients with acute leukemia (AL) from this sample were validated in an independent cohort. Low pre-conditioning serum Leptin was an independent prognostic marker for increased risk of relapse (but not of NRM and overall mortality) following alloSCT for AL of intermediate and advanced stage (beyond first complete remission). Multivariate analysis revealed a hazard ratio (HR) for relapse of 0.75 per log2 increase (0.59–0.96, p = 0.020). This effect was similar in an independent validation cohort. Pre-conditioning serum Leptin was validated as a prognostic marker for early relapse by fitting the multivariate Cox model to the validation data. Pre-conditioning serum Leptin levels may serve as an independent prognostic marker for relapse following alloSCT in intermediate and advanced stage AL patients. Prospective studies are required to prove whether serum Leptin could be used for guiding nutritional intervention in patients with AL undergoing alloSCT.
Keywords:leptin   Adiponectin   allogeneic stem cell transplantation   acute myeloid leukemia   AML   acute lymphoblastic leukemia   ALL   relapse   survival   body mass index
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