# Tagraxofusp maintenance post-hematopoietic stem cell transplantation provides long-term survival and manageable safety for a patient with blastic plasmacytoid dendritic cell neoplasm

**Authors:** Qaiser Bashir, Marina Konopleva, Glorette Abueg, Jeremy Ramdial, Chitra Hosing, Samer A. Srour, Amin Alousi, Uday R. Popat, Yago Nieto, Gheath Alatrash, Richard E. Champlin, Elizabeth J. Shpall, Muzaffar Qazilbash, Naveen Pemmaraju

PMC · DOI: 10.1016/j.lrr.2025.100518 · 2025-06-12

## TL;DR

A 68-year-old woman with a rare blood cancer achieved long-term remission using tagraxofusp after a stem cell transplant.

## Contribution

This is the first case study showing long-term tagraxofusp maintenance post-transplant for blastic plasmacytoid dendritic cell neoplasm.

## Key findings

- The patient remained in complete remission for over 17 months with no high-grade toxicity.
- Tagraxofusp maintenance therapy was feasible and effective post-hematopoietic stem cell transplantation.
- Minimal residual disease was undetectable during and after the treatment period.

## Abstract

Presented here is the case of a 68-year-old woman with blastic plasmacytoid dendritic cell neoplasm (BPDCN) treated with tagraxofusp (TAG) maintenance therapy post-allogeneic hematopoietic stem cell transplantation (allo-HCT). Prior to allo-HCT, the patient was treated with hydroxyurea and mini-CVD (cyclophosphamide, vincristine, and dexamethasone alternating with methotrexate (Methotrexate) and cytarabine) + venetoclax + TAG for 5 cycles, which induced morphologic complete remission with minimal residual disease. After allo-HCT, the patient had persistent cytogenic abnormalities 45,XX,der(7)add(7)(p13)del(7)(q11.2q22)add(7)(q32),add(12)(p13),-15,del(16)(q23),-17,+22,+2mar[1]/46,XX[19], and was then treated with TAG maintenance therapy at 9 mg/kg on a 28-day cycle for 16 cycles. At mid-treatment (cycle 6 of 16 cycles of TAG) and prior to TAG discontinuation (due to travel burden), the patient was negative for minimal residual disease and was in complete remission. There was no high-grade toxicity or capillary leak syndrome. The patient remains in complete remission as of present day (>17 months CR). This is the first case study illustrating the feasibility of long-term TAG maintenance post-allo-HCT to control BPDCN.

## Linked entities

- **Chemicals:** hydroxyurea (PubChem CID 3657), cyclophosphamide (PubChem CID 2907), vincristine (PubChem CID 5978), dexamethasone (PubChem CID 5743), methotrexate (PubChem CID 4112), cytarabine (PubChem CID 6253), venetoclax (PubChem CID 49846579)
- **Diseases:** blastic plasmacytoid dendritic cell neoplasm (MONDO:0019467), capillary leak syndrome (MONDO:0001956)

## Full-text entities

- **Diseases:** toxicity (MESH:D064420), cytogenic abnormalities (MESH:D000014), BPDCN (MESH:D018307), capillary leak syndrome (MESH:D019559)
- **Chemicals:** hydroxyurea (MESH:D006918), cyclophosphamide, vincristine, and dexamethasone (-), venetoclax (MESH:C579720), cytarabine (MESH:D003561), Methotrexate (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12213941