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Record W4417016390 · doi:10.1182/blood-2025-2518

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) international registry: Assessment of the allo-HCT outcomes

2025· article· en· W4417016390 on OpenAlexaff
Lusine Harutyunyan, Marina Konopleva, Maria Badikyan, Alvaro J. Alencar, Arusyak Ivanyan, Carolyn Owen, Ching‐Tien Peng, Dickran Kazandjian, Funda Tekkeşin, Justin Taylor, Hasanein H. Ghali, Hasmik Maghaqyan, Karen Bedirian, Maria Paola Martelli, Enrico Attardi, Maria Teresa Voso, Mariam Abramashvili, Mazin Faisal Al‐Jadiry, Michalis Michael, Min‐Yu Su, Daniel Coriu, Maria Camelia Stancioaica, Hayk Grigoryan, Nerses Ghahramanyan, Nare Martirosyan, Nino Totogashvili, Pavel Kotouček, Rejin Kebudi, Robin Ohannessian, Ruzanna Papyan, Shushan Hovsepyan, Shefali Mehra, Salma Elashwah, Sameer Bakhshi, Samvel Bardakhchyan, Shaimaa El‐Ashwah, M. Tezer Kutluk, Deniz Tuğcu, Ahmad Alhuraiji, Naveen Pemmaraju, Rami S. Komrokji, Gevorg Tamamyan, Astghik Voskanyan

Bibliographic record

VenueBlood · 2025
Typearticle
Languageen
FieldMedicine
TopicCutaneous lymphoproliferative disorders research
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsLeukocytosisChemotherapyLeukopeniaHematopoietic stem cell transplantationBone marrowHematologyPlasmacytoid dendritic cellTransplantationInterleukin-3 receptor

Abstract

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Abstract Background: Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) is an underdiagnosed rare disease with poor outcomes and limited treatment options. The main treatment approaches for BPDCN include chemotherapy and CD123-targeted tagraxofusp, with allogeneic hematopoietic stem cell transplantation (allo-HCT) considered for eligible patients. The aim of this study is to evaluate the outcomes of allo-HCT based on the data from the BPDCN international registry. Methods: The BPDCN international registry (ClinicalTrials.gov ID: NCT05430971) was initiated on 1st July, 2022. Data on characteristics, diagnostics, treatment options and treatment responses are collected retrospectively and prospectively from 17 medical centers worldwide. We evaluated baseline characteristics, treatment response, and outcomes of BPDCN patients who underwent allo-HCT. Results: Of the total 70 patients with BPDCN, 16 underwent allo-HCT. Five of the patients were female. Fifteen of the patients were adults, one patient was 11 years old. The median age was 49 (11-80). In 13 patients (81.25%), the diagnosis was confirmed by bone marrow (BM) examination, other patients were diagnosed by skin biopsy. Splenomegaly was found in 2 patients, 7 patients had lymphadenopathy, one patient had central nervous system (CNS) involvement, and all 16 patients had skin involvement. Complete blood count (CBC) results were available for 14 patients. 7 patients had normal HGB levels (12-16 g/dL), and 7 patients had anemia. Leukopenia (WBC<4×109/L) was observed in 6 patients, 1 patient had leukocytosis (WBC 67.2×109/L), and seven patients had normal WBC (4-10×109/L). Thrombocytopenia was observed in five patients (PLT<140×109/L). Immunophenotyping results were as follows: CD123 expression was assessed in 15 patients and was positive in 14 (93%). CD4 was tested in 14 patients, with 12 (86%) showing positivity. CD56 was also assessed in 14 patients and was positive in 12 (86%). Additional markers were evaluated in smaller subsets: CD2AP was assessed in 2 patients and was positive in 1; CD303/BDCA-2 was tested in 2 patients with 1 positive result; and TCL-1 was assessed in 3 patients, showing positivity in 2. Conventional karyotypingwas performed in 8 patients. Cytogenetic abnormalities included one case with 46, XX, der(X)t(X;5) (q28; p13). Another patient demonstrated a complex karyotype involving t(1;16), der(10), t(1;17), del(6), del(12), del(15), and monosomy 17. Molecular analysis was performed in 10 patients (62.5%), and revealed TET2 mutationsin 3 patients, while DNMT3A, CBLC, and EZH2 mutations were identified in 1 and 2 patients, respectively. Initial treatment has utilized ALL-based regimens in 12 patients and included Hyper-CVAD (n=6), cytarabine/idarubicin/VP16 (n=1), ALL-IC BFM 2009 (n=3), GMALL (n=1), EPOCH (n=1). Two patients received venetoclax monotherapy, another 2 were enrolled in SL-401 (tagraxofusp) clinical trial. All patients underwent allo-HCT in first remission except one in SL-401 clinical trial who experienced relapse, the second-line treatment was Hyper-CVAD followed by allo-HCT. Four patients experienced relapse after allo-HCT. Second line therapy was used in all patients, with gemcitabine/oxaliplatin/dexamethasone regimen (n=1), venetoclax/azacytidine (n=1), venetoclax monotherapy (n=1) and SL-401 clinical trial (n=1)․ First two patients experienced stable disease (SD) with duration of 72 and 4 months respectively, the other two were alive at last contact. As of the last follow- up, 10 (63%) patients were alive with median follow-up of 27 months (range 8-146 months). The follow-up period was calculated from the date of diagnosis up to last contact or death date. Among the cohort, three patients died from causes unrelated to disease progression, two deaths were attributed to disease progression, and one patient was lost to follow-up. Conclusion: The data confirmed the efficacy of allo-HCT in patients with BPDCN. Our previously reported data highlighted the importance of allo-HCT for the tagraxofusp group, as outcomes were less favorable in those who did not undergo allo-HCT. Based on current evidence, we conclude that optimizing access to tagraxofusp followed by allo-HCT may offer the best potential to improve outcomes in BPDCN.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.120
Threshold uncertainty score0.455

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.009
GPT teacher head0.320
Teacher spread0.310 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations1
Published2025
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