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NCT Number: NCT05430971

Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) International Registry

Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) is a very rare hematologic malignancy. Despite recent advances, at present there is no consensus on the optimal treatment of BPDCN. The optimal therapy of disease remains to be determined, and due to the rarity of cases, there is a need for international collaboration to collect data on BPDCN clinical presentations, diagnostics, treatment regimens and outcomes. Therefore, the objectives of this study are: (1) to build a large database of patients with BPDCN, (2) to investigate the characteristics and outcome of the disease with different treatment regimens, (3) to evaluate prognostic factors, and (4) to generate data-based prospective treatment recommendations.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Hematology Center named after prof. R. Yeolyan, Yerevan, Armenia

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About this study

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematologic malignancy. In 2008, it was recognized by the WHO as a distinct entity and separately listed in the group of acute myeloid leukemias and related precursor neoplasms.

The final diagnosis of BPDCN relies on a compatible immunophenotype. The triple positive CD4+CD56+CD123+ phenotype associated with negativity for lineage-specific markers is a minimum requirement for defining BPDCN. The highly specific marker BDCA2/CD303, as well as other plasmacytoid dendritic cell-associated antigens (e.g. TCL1 and CD2AP), might be of great support to exclude potential mimickers of BPDCN (acute myeloid and monocytic leukemias, precursor lymphoblastic T-cell leukemia/lymphomas and T- and NK/T cell lymphomas.

At present, there is no consensus on the optimal treatment of BPDCN. The majority of patients receive multi-agent chemotherapy with AML or ALL treatment regimens, while a few patients undergo allogeneic haematopoietic stem cell transplantation (HSCT). In recent years, different novel and innovative therapies are in development to target surface molecules in BPDCN. The patients are still in need of better treatments and the optimal therapy of disease remains to be determined.

This is a multicenter, international prospective and retrospective registry with the aim of collecting data of patients with a diagnosis of BPDCN globally.

Patients will be recruited directly by the national study groups / participating centers.

Participating centers will collect and verify informed consent of all prospective patients enrolled at their center.

The following data will be collected through questionnaires:

  • Patient characteristics
  • BPDCN characteristics
  • Treatment details
  • Outcomes
  • Cause of death
  • End of data collection

Quality control and data management will be conducted by the Immune Oncology Research Institute.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of BPDCN
  • Signed informed consent form for prospective patients

Exclusion criteria

-

Treatment and study plan

Primary outcomes

  1. Overall survival

    Time frame: 5 years

    Time from diagnosis to death

Secondary outcomes

  1. Complete remission rate

    Time frame: 5 years

    The proportion of patients with complete remission

  2. Mean duration of the first remission

    Time frame: 5 years

    Time from first remission to disease progression or death

  3. Event-free survival

    Time frame: 5 years

    Time from diagnosis to occurrence of a complication

Study contacts

Contact information is provided by the study sponsor or research team.

Astghik Voskanyan, MD

CONTACT

[email protected]

+374 10 28 38 00

Davit Melkonyan

CONTACT

[email protected]

+374 10 28 38 00

Sponsors and collaborators

Lead sponsor

Immune Oncology Research Institute

Other

Registry information

Important dates

Study start
2022
Primary completion
2032
Study completion
2032
First posted
Jun 24, 2022
Registry last updated
Jun 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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