Retrospective analysis of hematopoietic cell transplantation for blastic plasmacytoid dendritic cell neoplasm: conditioning intensity matters

被引:9
作者
Bruch, Peter-Martin [1 ,2 ]
Dietrich, Sascha [1 ,2 ,3 ]
Finel, Herve [3 ]
Boumendil, Ariane [3 ]
Greinix, Hildegard [4 ]
Heinicke, Thomas [5 ]
Bethge, Wolfgang [6 ]
Beelen, Dietrich [7 ]
Schmid, Christoph [8 ]
Martin, Hans [9 ]
Castagna, Luca [10 ]
Scheid, Christof [11 ]
Schaefer-Eckart, Kerstin [12 ]
Bittenbring, Joerg [13 ]
Finke, Juergen [14 ]
Sengeloev, Henrik [15 ]
Heiblig, Mael [16 ]
Cornelissen, Jan [17 ]
Chevallier, Patrice [18 ]
Mohty, Mohamad [19 ]
Robinson, Stephen [20 ]
Montoto, Silvia [21 ]
Dreger, Peter [2 ]
机构
[1] Dusseldorf Univ Hosp, Dept Hematol Oncol & Clin Immunol, Dusseldorf, Germany
[2] Heidelberg Univ, Dept Med 5, Heidelberg, Germany
[3] European Soc Blood & Marrow Transplantat EBMT, Paris, France
[4] Med Univ Graz, Div Hematol, Graz, Austria
[5] Univ Hosp Magdeburg, Magdeburg, Germany
[6] Univ Hosp Tubingen, Tubingen, Germany
[7] Univ Hosp Essen, Essen, Germany
[8] Univ Hosp Augsburg, Augsburg, Germany
[9] Univ Hosp Frankfurt, Frankfurt, Germany
[10] Osped Villa Sofia Cervello, BMT Unit, Palermo, Italy
[11] Univ Cologne, Cologne, Germany
[12] Paracelsus Med Privat Univ, Klinikum Nurnberg, Nurnberg, Germany
[13] Univ Hosp Saarland, Homburg, Germany
[14] Univ Hosp Freiburg, Freiburg, Germany
[15] Rigshosp, Copenhagen, Denmark
[16] Hop St Antoine, Paris, France
[17] Erasmus MC Canc Inst, Rotterdam, Netherlands
[18] CHU, Nantes, France
[19] Sorbonne Univ, St Antoine Hosp, INSERM, UMRs 938, Paris, France
[20] Univ Hosp Bristol, Bristol, Avon, England
[21] St Bartholomews Hosp, London, England
关键词
D O I
10.1038/s41375-022-01782-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Blastic plasmacytoid dendritic cell neoplasia (BPDCN) is a rare myeloid malignancy with a generally poor prognosis. Although preliminary evidence suggests that hematopoietic cell transplantation (HCT) could improve outcome in patients with BPDCN, the individual contributions of conditioning and graft-versus-tumor (GVT) effects to HCT success are undefined. We present a retrospective study of 162 adult patients who underwent a first HCT (allogeneic 146, autologous 16) between 2009 and 2017, and were registered with the EBMT. Median age was 57 (range 20-73) years, and disease status at HCT was first complete remission (CR1) in 78%. Among patients receiving allogeneic HCT (alloHCT), myeloablative conditioning (MAC), reduced intensity conditioning (RIC) and in-vivo T-cell depletion (TCD) were used in 54%, 46%, and 59% respectively. Total body irradiation (TBI) was the conditioning backbone in 61% of MAC and 26% of RIC transplants. One-year overall survival (OS) and progression-free survival (PFS) rates were comparable after alloHCT and autologous HCT (autoHCT). Among alloHCT recipients, MAC with TBI significantly improved OS and PFS, independently of CR1, age, Karnofsky index and TCD. Accordingly, MAC (ideally based on TBI) should be preferred for alloHCT recipients with BPDCN. In patients who are not elegible for MAC alloHCT, autoHCT could be considered.
引用
收藏
页码:465 / 472
页数:8
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