Secondary MGUS after autologous hematopoietic progenitor cell transplantation in plasma cell myeloma: a matter of undetermined significance

Plasma cell myeloma, characterized by clonally aberrant plasma cells that produce abnormal monoclonal Igs, is the most common indication for autologous hematopoietic progenitor cell transplantation (AHPCT) in North America. We observed appearance of new monoclonal gammopathies different from the ori...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2012-09, Vol.47 (9), p.1212-1216
Hauptverfasser: Manson, G V, Campagnaro, E, Balog, A, Kaplan, D, Sommers, S R, Fu, P, Rajkumar, S V, Lazarus, H M
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container_end_page 1216
container_issue 9
container_start_page 1212
container_title Bone marrow transplantation (Basingstoke)
container_volume 47
creator Manson, G V
Campagnaro, E
Balog, A
Kaplan, D
Sommers, S R
Fu, P
Rajkumar, S V
Lazarus, H M
description Plasma cell myeloma, characterized by clonally aberrant plasma cells that produce abnormal monoclonal Igs, is the most common indication for autologous hematopoietic progenitor cell transplantation (AHPCT) in North America. We observed appearance of new monoclonal gammopathies different from the original protein in the post-AHPCT setting and termed this condition ‘secondary MGUS’ (monoclonal gammopathy of undetermined significance). Hence, we performed a retrospective, single institution review of serum protein electrophoresis/immunofixation electrophoresis data in 92 AHPCT recipients from the period 2000–2009. In all, 22 of 92 patients (24%) undergoing AHPCT met criteria for secondary MGUS. Contrary to previous studies, often referred to as ‘abnormal protein banding,’ we did not observe this condition as a favorable prognostic indicator in affected patients when compared with the control group ( P =0.686). However, we did note that a subgroup of the study cohort who developed secondary MGUS after a prolonged latency (>10 months) had an improved median OS compared with the remainder of the study cohort (75 months vs 41 months, P =0.005). As there have been significant advancements in understanding the pathobiology and clinical significance of MGUS, we believe that secondary MGUS merits dedication of resources for investigation to determine its true clinical relevance, prognostic value and pathophysiology.
doi_str_mv 10.1038/bmt.2011.244
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subjects 692/699/249/1573
692/699/67/1990/804
692/700/565/545/576/1855
Adult
Aged
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Autografts
Benign monoclonal gammopathy
Biological and medical sciences
Bone marrow
Bone marrow transplantation
Bone marrow, stem cells transplantation. Graft versus host reaction
Care and treatment
Cell Biology
Cells (biology)
Data processing
Diagnosis
Electrophoresis
Female
Hematologic and hematopoietic diseases
Hematology
Hematopoietic Stem Cell Transplantation - adverse effects
Hematopoietic Stem Cell Transplantation - methods
Hematopoietic stem cells
Hemopoiesis
Humans
Immunodeficiencies. Immunoglobulinopathies
Immunoglobulinopathies
Immunopathology
Internal Medicine
Latency
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Male
Medical sciences
Medicine
Medicine & Public Health
Middle Aged
Monoclonal gammopathies
Monoclonal gammopathy
Monoclonal Gammopathy of Undetermined Significance - etiology
Multiple myeloma
Multiple Myeloma - blood
Multiple Myeloma - surgery
Myeloma
original-article
Patients
Plasma cells
Progenitor cells
Proteins
Public Health
Retrospective Studies
Serum proteins
Stem cell transplantation
Stem Cells
Subgroups
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation
Transplantation, Autologous
title Secondary MGUS after autologous hematopoietic progenitor cell transplantation in plasma cell myeloma: a matter of undetermined significance
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