Reduced intensity-conditioned allogeneic stem cell transplantation for multiple myeloma relapsing or progressing after autologous transplantation: a study by the European Group for Blood and Marrow Transplantation

被引:0
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作者
H W Auner
R Szydlo
A van Biezen
S Iacobelli
G Gahrton
N Milpied
L Volin
J Janssen
S Nguyen Quoc
M Michallet
H Schoemans
J el Cheikh
E Petersen
F Guilhot
S Schönland
L Ahlberg
C Morris
L Garderet
T de Witte
N Kröger
机构
[1] Centre for Haematology,Department of Medicine
[2] Hammersmith Hospital Campus,Department of Medical Statistics
[3] Imperial College London,Department of Medicine
[4] Leiden University Medical Center,Department of Medicine
[5] Centro di Biostatistica e Bioinformatica,Department of Haematology
[6] Università Tor Vergata,Department of Haematology
[7] Karolinska Institutet,Department of Haematology
[8] CHU Bordeaux,Department of Haematology
[9] Hopital Haut-Leveque,Department of Bone Marrow Transplantation
[10] Helsinki University Central Hospital,Department of Haematology
[11] VU University Medical Center,Department of Tumor Immunology
[12] Groupe Hospitalier Pitié-Salpetriere,undefined
[13] BMT Unit Pavillon E,undefined
[14] Hopital E Herriot,undefined
[15] University Hospital Gasthuisberg,undefined
[16] Unité de transplantation et thérapie cellulaire,undefined
[17] Institut Paoli Calmettes,undefined
[18] University Medical Center,undefined
[19] Hopital La Miletrie,undefined
[20] Medizinische Klinik und Poliklinik V,undefined
[21] University of Heidelberg,undefined
[22] University Hospital,undefined
[23] Queens University,undefined
[24] Hopital Saint Antoine,undefined
[25] Radboud University Medical Center,undefined
[26] University Hospital Eppendorf,undefined
来源
关键词
myeloma; allogeneic; stem cell transplantation; reduced-intensity;
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摘要
Outcomes and prognostic factors of reduced intensity-conditioned allo-SCT (RIC allo-SCT) for multiple myeloma (MM) relapsing or progressing after prior autologous (auto)-SCT are not well defined. We performed an analysis of 413 MM patients who received a related or unrelated RIC allo-SCT for the treatment of relapse/progression after prior auto-SCT. Median age at RIC allo-SCT was 54.1 years, and 44.6% of patients had undergone two or more prior auto-SCTs. Median OS and PFS from the time of RIC allo-SCT for the entire population were 24.7 and 9.6 months, respectively. Cumulative non-relapse mortality (NRM) at 1 year was 21.5%. In multivariate analysis, CMV seronegativity of both patient and donor was associated with significantly better PFS, OS and NRM. Patient–donor gender mismatch was associated with better PFS, fewer than two prior auto-SCT was associated with better OS, and shorter time from the first auto-SCT to the RIC allo-SCT was associated with lower NRM. The results of this study identify patient and donor CMV seronegativity as the key prognostic factor for outcome after RIC allo-SCT for MM relapsing or progressing after prior auto-SCT.
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页码:1395 / 1400
页数:5
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