Donor-Derived T-Cell Redirection With Epcoritamab Achieving Complete Response After Early Post-Allo-HSCT Relapse of
Yoshikazu Ikoma1,2, Yuto Kaneda1, Ryoma Shimazu1,3
1Department of Hematology and Infectious Disease Gifu University Hospital Gifu Japan.
Epcoritamab shows potential as a salvage therapy for relapsed diffuse large B-cell lymphoma (DLBCL) after allogeneic stem cell transplant. Re-administration post-engraftment achieved a complete response with good safety.
Area of Science:
- Hematology
- Oncology
- Immunotherapy
Background:
- Relapsed diffuse large B-cell lymphoma (DLBCL) poses treatment challenges.
- Epcoritamab is a bispecific CD3xCD20 antibody with potential in DLBCL.
- Efficacy and safety of epcoritamab after allogeneic hematopoietic stem cell transplantation (allo-HSCT) are not well-established.
Purpose of the Study:
- To evaluate the efficacy and safety of epcoritamab in a patient with relapsed DLBCL.
- To explore the potential of epcoritamab as a salvage therapy post-allo-HSCT.
Main Methods:
- Case report of a 64-year-old male patient with relapsed DLBCL.
- Administration of epcoritamab prior to and after allo-HSCT.
- Monitoring for treatment response, graft-versus-host disease (GVHD), and cytokine release syndrome (CRS).
Main Results:
- Epcoritamab showed limited efficacy (stable disease) before allo-HSCT.
- Following allo-HSCT and donor T-cell engraftment, re-administration of epcoritamab resulted in a complete response.
- No severe GVHD or CRS was observed during post-transplant epcoritamab treatment.
Conclusions:
- Epcoritamab, when used post-transplant after donor T-cell engraftment, may enhance antitumor activity.
- This approach suggests a potential role for epcoritamab as a salvage therapy for relapsed DLBCL post-allo-HSCT.
- Donor T-cell redirection with epcoritamab appears safe and effective in this setting.
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