Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) International Registry
1 other identifier
observational
200
14 countries
20
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2022
Longer than P75 for all trials
20 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 21, 2022
CompletedFirst Posted
Study publicly available on registry
June 24, 2022
CompletedStudy Start
First participant enrolled
July 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2032
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 1, 2032
February 17, 2026
February 1, 2026
10 years
June 21, 2022
February 12, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Overall survival
Time from diagnosis to death
5 years
Secondary Outcomes (3)
Complete remission rate
5 years
Mean duration of the first remission
5 years
Event-free survival
5 years
Eligibility Criteria
All patients with BPDCN diagnosed since 01.01.2010
You may qualify if:
- Diagnosis of BPDCN
- Signed informed consent form for prospective patients
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (20)
Sylvester Comprehensive Cancer Center, University of Miami
Miami, Florida, 33136, United States
Moffitt Cancer Center
Tampa, Florida, 33612, United States
Seattle Children's Cancer and Blood Disorders Center
Seattle, Washington, 98145, United States
Hematology Center named after prof. R. Yeolyan
Yerevan, 0014, Armenia
University of Calgary
Calgary, Alberta, T2N 1N4, Canada
Children's Hospital of Eastern Ontario, University of Ottawa
Ottawa, Ontario, K1H 8L1, Canada
Cyprus Society of Haematology
Nicosia, 2019, Cyprus
Oncology Center, Mansoura University Faculty of Medicine
Al Mansurah, 7650030, Egypt
M. Iashvili Children's Central Hospital
Tbilisi, 0159, Georgia
Department of Medical Oncology, Dr. B.R.A Institute Rotary Cancer Hospital, All India Institute of Medical Sciences
New Delhi, 110029, India
Pediatric Hematology Oncology, Children's Welfare Teaching Hospital, Medical City, College of Medicine, University of Baghdad
Baghdad, 61023, Iraq
University of Perugia - Azienda Ospedaliera Perugia
Perugia, 06129, Italy
Department of Biomedicine and Prevention, University of Rome Tor Vergata
Roma, 00133, Italy
Department of hematology, Kuwait Cancer Control Center
Kuwait City, 42262, Kuwait
Fundeni Clinical Institute, Department of Acute Leukemia
Bucharest, 022328, Romania
China Medical University Children's Hospital
Taichung, 40447, Taiwan
Turkish Pediatric Cancer Registry
Ankara, 06690, Turkey (Türkiye)
Istanbul University, Oncology Institute
Istanbul, 34093, Turkey (Türkiye)
University of Health Sciences, Umraniye Research and Education Hospital, Pediatric Hematology and Oncology Department, Pediatric Bone Marrow Transplantation Unit
Istanbul, 34766, Turkey (Türkiye)
Broomfield Hospital, Haematology Mid and South Essex University Hospitals Group
Chelmsford, Essex, CM1 7ET, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Astghik Voskanyan, MD
Immune Oncology Research Institute, Yerevan, Armenia
- STUDY DIRECTOR
Gevorg Tamamyan, MD, PhD, DSc
Immune Oncology Research Institute, Yerevan, Armenia
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- OTHER
- Target Duration
- 5 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 21, 2022
First Posted
June 24, 2022
Study Start
July 1, 2022
Primary Completion (Estimated)
July 1, 2032
Study Completion (Estimated)
July 1, 2032
Last Updated
February 17, 2026
Record last verified: 2026-02