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


Journal

Leukemia
ISSN: 1476-5551
Titre abrégé: Leukemia
Pays: England
ID NLM: 8704895

Informations de publication

Date de publication:
02 2023
Historique:
received: 28 08 2022
accepted: 25 11 2022
revised: 23 11 2022
pubmed: 23 12 2022
medline: 8 2 2023
entrez: 22 12 2022
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 36550212
doi: 10.1038/s41375-022-01782-z
pii: 10.1038/s41375-022-01782-z
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

465-472

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

Références

Herling M, Teitell MA, Shen RR, Medeiros LJ, Jones D. TCL1 expression in plasmacytoid dendritic cells (DC2s) and the related CD4+ CD56+ blastic tumors of skin. Blood. 2003;101:5007–9.
doi: 10.1182/blood-2002-10-3297
Laribi K, Baugier de Materre A, Sobh M, Cerroni L, Valentini CG, Aoki T, et al. Blastic plasmacytoid dendritic cell neoplasms: results of an international survey on 398 adult patients. Blood Adv. 2020;4:4838–48.
doi: 10.1182/bloodadvances.2020002474
Garnache-Ottou F, Vidal C, Biichle S, Renosi F, Poret E, Pagadoy M, et al. How should we diagnose and treat blastic plasmacytoid dendritic cell neoplasm patients? Blood Adv. 2019;3:4238–51.
doi: 10.1182/bloodadvances.2019000647
Martin-Martin L, Almeida J, Pomares H, Gonzalez-Barca E, Bravo P, Gimenez T, et al. Blastic plasmacytoid dendritic cell neoplasm frequently shows occult central nervous system involvement at diagnosis and benefits from intrathecal therapy. Oncotarget. 2016;7:10174–81.
doi: 10.18632/oncotarget.7101
Taylor J, Haddadin M, Upadhyay VA, Grussie E, Mehta-Shah N, Brunner AM, et al. Multicenter analysis of outcomes in blastic plasmacytoid dendritic cell neoplasm offers a pretargeted therapy benchmark. Blood 2019;134:678–87.
doi: 10.1182/blood.2019001144
Reimer P, Rudiger T, Kraemer D, Kunzmann V, Weissinger F, Zettl A, et al. What is CD4+CD56+ malignancy and how should it be treated? Bone Marrow Transplant. 2003;32:637–46.
doi: 10.1038/sj.bmt.1704215
Dietrich S, Andrulis M, Hegenbart U, Schmitt T, Bellos F, Martens UM, et al. Blastic plasmacytoid dendritic cell neoplasia (BPDC) in elderly patients: results of a treatment algorithm employing allogeneic stem cell transplantation with moderately reduced conditioning intensity. Biol Blood Marrow Transplant. 2011;17:1250–4.
doi: 10.1016/j.bbmt.2010.12.706
Roos-Weil D, Dietrich S, Boumendil A, Polge E, Bron D, Carreras E, et al. Stem cell transplantation can provide durable disease control in blastic plasmacytoid dendritic cell neoplasm: a retrospective study from the European Group for Blood and Marrow Transplantation. Blood. 2013;121:440–6.
doi: 10.1182/blood-2012-08-448613
Aoki T, Suzuki R, Kuwatsuka Y, Kako S, Fujimoto K, Taguchi J, et al. Long-term survival following autologous and allogeneic stem cell transplantation for blastic plasmacytoid dendritic cell neoplasm. Blood. 2015;125:3559–62.
doi: 10.1182/blood-2015-01-621268
Kharfan-Dabaja MA, Reljic T, Murthy HS, Ayala E, Kumar A. Allogeneic hematopoietic cell transplantation is an effective treatment for blastic plasmacytoid dendritic cell neoplasm in first complete remission: systematic review and meta-analysis. Clin Lymphoma Myeloma Leuk. 2018;18:703–9.e1
doi: 10.1016/j.clml.2018.07.295
Kharfan-Dabaja MA, Al Malki MM, Deotare U, Raj RV, El-Jurdi N, Majhail N, et al. Haematopoietic cell transplantation for blastic plasmacytoid dendritic cell neoplasm: a North American multicentre collaborative study. Br J Haematol. 2017;179:781–9.
doi: 10.1111/bjh.14954
Yun S, Chan O, Kerr D, Vincelette ND, Idrees A, Mo Q, et al. Survival outcomes in blastic plasmacytoid dendritic cell neoplasm by first-line treatment and stem cell transplant. Blood Adv. 2020;4:3435–42.
doi: 10.1182/bloodadvances.2020001875
Bacigalupo A, Ballen K, Rizzo D, Giralt S, Lazarus H, Ho V, et al. Defining the intensity of conditioning regimens: working definitions. Biol Blood Marrow Transplant. 2009;15:1628–33.
doi: 10.1016/j.bbmt.2009.07.004
Pemmaraju N, Konopleva M. Approval of tagraxofusp-erzs for blastic plasmacytoid dendritic cell neoplasm. Blood Adv. 2020;4:4020–7.
doi: 10.1182/bloodadvances.2019000173
Leclerc M, Peffault de Latour R, Michallet M, Blaise D, Chevallier P, Rohrlich PS, et al. Can a reduced-intensity conditioning regimen cure blastic plasmacytoid dendritic cell neoplasm? Blood. 2017;129:1227–30.
doi: 10.1182/blood-2016-09-726653
Kaloyannidis P, Zomas A, Paterakis G, Vadikoliou C, Mallouri D, Sakkas L, et al. GVL effect in plasmacytoid DC leukemia/lymphoma. Bone marrow Transplant. 2010;45:961–2.
doi: 10.1038/bmt.2009.270
Ben Amor R, Hicheri Y, Pautas C, Jouault H, Kuentz M, Cordonnier C, et al. Successful non-myeloablative allogeneic HLA-identical stem cell transplantation for CD4/CD56 positive acute leukemia. Transplantation. 2007;84:1066–7.
doi: 10.1097/01.tp.0000286098.28481.7d
D’Souza A, Fretham C, Lee SJ, Arora M, Brunner J, Chhabra S, et al. Current use of and trends in hematopoietic cell transplantation in the United States. Biol Blood Marrow Transplant. 2020;26:e177–e82.
doi: 10.1016/j.bbmt.2020.04.013
Pemmaraju N, Lane AA, Sweet KL, Stein AS, Vasu S, Blum W, et al. Tagraxofusp in blastic plasmacytoid dendritic-cell neoplasm. N Engl J Med. 2019;380:1628–37.
doi: 10.1056/NEJMoa1815105
Montero J, Stephansky J, Cai T, Griffin GK, Cabal-Hierro L, Togami K, et al. Blastic plasmacytoid dendritic cell neoplasm is dependent on BCL2 and sensitive to venetoclax. Cancer Discov. 2017;7:156–64.
doi: 10.1158/2159-8290.CD-16-0999
Hourigan CS, Dillon LW, Gui G, Logan BR, Fei M, Ghannam J, et al. Impact of conditioning intensity of allogeneic transplantation for acute myeloid leukemia with genomic evidence of residual disease. J Clin Oncol. 2020;38:1273–83.
doi: 10.1200/JCO.19.03011
Wang W, Khoury JD, Miranda RN, Jorgensen JL, Xu J, Loghavi S, et al. Immunophenotypic characterization of reactive and neoplastic plasmacytoid dendritic cells permits establishment of a 10-color flow cytometric panel for initial workup and residual disease evaluation of blastic plasmacytoid dendritic cell neoplasm. Haematologica. 2021;106:1047–55.
doi: 10.3324/haematol.2020.247569

Auteurs

Peter-Martin Bruch (PM)

Department of Hematology, Oncology, and Clinical Immunology, Düsseldorf University Hospital, Düsseldorf, Germany.
Department Medicine V, University of Heidelberg, Heidelberg, Germany.

Sascha Dietrich (S)

Department of Hematology, Oncology, and Clinical Immunology, Düsseldorf University Hospital, Düsseldorf, Germany. haem-onk.direktion@med.uni-duesseldorf.de.
Department Medicine V, University of Heidelberg, Heidelberg, Germany. haem-onk.direktion@med.uni-duesseldorf.de.
European Society for Blood and Marrow Transplantation (EBMT), Paris, France. haem-onk.direktion@med.uni-duesseldorf.de.

Herve Finel (H)

European Society for Blood and Marrow Transplantation (EBMT), Paris, France.

Ariane Boumendil (A)

European Society for Blood and Marrow Transplantation (EBMT), Paris, France.

Hildegard Greinix (H)

Medical University of Graz, Division of Hematology, Graz, Austria.

Thomas Heinicke (T)

University Hospital Magdeburg, Magdeburg, Germany.

Wolfgang Bethge (W)

University Hospital Tübingen, Tübingen, Germany.

Dietrich Beelen (D)

University Hospital Essen, Essen, Germany.

Christoph Schmid (C)

University Hospital Augsburg, Augsburg, Germany.

Hans Martin (H)

University Hospital Frankfurt, Frankfurt am Main, Germany.

Luca Castagna (L)

Ospedale Villa Sofia Cervello, BMT unit, Palermo, Italy.

Christof Scheid (C)

University of Cologne, Cologne, Germany.

Kerstin Schäfer-Eckart (K)

Klinikum Nürnberg, Paracelsus Medizinische Privatuniversität, Nürnberg, Germany.

Jörg Bittenbring (J)

University Hospital Saarland, Homburg, Germany.

Jürgen Finke (J)

University Hospital Freiburg, Freiburg, Germany.

Henrik Sengeloev (H)

Rigshospitalet, Copenhagen, Denmark.

Mael Heiblig (M)

Hôpital Saint Antoine, Paris, France.

Jan Cornelissen (J)

Erasmus MC Cancer Institute, Rotterdam, Netherlands.

Patrice Chevallier (P)

CHU, Nantes, France.

Mohamad Mohty (M)

Sorbonne University, Saint-Antoine Hospital, INSERM UMRs 938, Paris, France.

Stephen Robinson (S)

University Hospital of Bristol, Bristol, UK.

Silvia Montoto (S)

St Bartholomew's Hospital, London, UK.

Peter Dreger (P)

Department Medicine V, University of Heidelberg, Heidelberg, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH