Survival outcomes in blastic plasmacytoid dendritic cell neoplasm by first-line treatment and stem cell transplant.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
28 07 2020
Historique:
received: 13 03 2020
accepted: 18 06 2020
entrez: 30 7 2020
pubmed: 30 7 2020
medline: 15 5 2021
Statut: ppublish

Résumé

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematologic malignancy with dismal clinical outcomes. Conventional chemotherapies such cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) and hyperfractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone alternating with high-dose cytarabine and methotrexate (CVAD) have been commonly used for the BPDCN treatment until a recent study showed promising outcomes in patients treated with SL-401 (Tagraxofusp). In this single-institution retrospective study, we identified a total of 49 consecutive BPDCN patients. Among 42 patients who received treatment, hyper-CVAD regimen was associated with higher complete response rate compared with CHOP-based regimens or SL-401 (91% vs 50% vs 50%), although the difference did not achieve statistical significance. Furthermore, there was no significant overall survival (OS) difference between patients treated with SL-401 vs other chemotherapies as their first-line treatment (hazard ratio = 1.597; 95% CI, 0.460-5.548; P = .431). Of note, patients who received allogeneic stem cell transplant (allo-SCT) had significantly longer OS (hazard ratio = 0.160; 95% CI, 0.0453-0.56; P = .041). Extent of disease (skin vs bone marrow vs both) or younger age (<60 years old) did not have significant prognostic impact on OS. Collectively, our study confirmed the survival benefit of allo-SCT and suggests that conventional and intensive chemotherapies such as CHOP and hyper-CVAD as well as SL-401 would be comparable first-line choice for the BPDCN patients.

Identifiants

pubmed: 32722779
pii: S2473-9529(20)31568-8
doi: 10.1182/bloodadvances.2020001875
pmc: PMC7391135
doi:

Substances chimiques

Cytarabine 04079A1RDZ

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3435-3442

Subventions

Organisme : NCI NIH HHS
ID : K08 CA237627
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA076292
Pays : United States

Informations de copyright

© 2020 by The American Society of Hematology.

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Auteurs

Seongseok Yun (S)

Department of Malignant Hematology and.

Onyee Chan (O)

Department of Malignant Hematology and.

Daniel Kerr (D)

Department of Malignant Hematology and.

Nicole D Vincelette (ND)

Department of Malignant Hematology and.

Afshan Idrees (A)

Department of Hematopathology and Laboratory Medicine, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.

Qianxing Mo (Q)

Department of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.

Kendra Sweet (K)

Department of Malignant Hematology and.

Jeffrey E Lancet (JE)

Department of Malignant Hematology and.

Mohamed A Kharfan-Dabaja (MA)

Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL; and.

Ling Zhang (L)

Department of Hematopathology and Laboratory Medicine, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.

Lubomir Sokol (L)

Department of Malignant Hematology and.

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Classifications MeSH