Case Report: Safety and efficacy of blinatumomab in combination with donor lymphocyte infusion for the prophylaxis of relapse following allogeneic hematopoietic stem cell transplantation in a pediatric patient with acute lymphoblastic leukemia - Report - MDSpire

Case Report: Safety and efficacy of blinatumomab in combination with donor lymphocyte infusion for the prophylaxis of relapse following allogeneic hematopoietic stem cell transplantation in a pediatric patient with acute lymphoblastic leukemia

  • By

  • Yi-Tong Li

  • Yu Li

  • Li-Na Wang

  • Li-Bin Huang

  • June 17, 2026

  • 0 min

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Clinical Report: Evaluating Blinatumomab with DLI in Pediatric ALL

Overview

This report presents a case of a 5-year-old boy with high-risk acute lymphoblastic leukemia (ALL) who received blinatumomab combined with donor lymphocyte infusion (DLI) after allogeneic hematopoietic stem cell transplantation (HSCT). The treatment was well-tolerated, leading to sustained remission.

Background

Acute lymphoblastic leukemia (ALL) is the most prevalent malignant hematological disease in children, with high-risk cases associated with poor prognosis. Allogeneic HSCT is a critical treatment option, yet post-transplant relapse remains a significant challenge.

Data Highlights

No numerical data or trial data presented in the article.

Key Findings

  • A 5-year-old boy with high-risk ALL received blinatumomab and DLI after HSCT.
  • Post-treatment minimal residual disease (MRD) assessments showed negative results after blinatumomab.
  • The child experienced grade 1 cytokine release syndrome (CRS) during treatment but no severe adverse effects.
  • The combined regimen maintained sustained remission.
  • Larger prospective trials are needed to confirm the safety and efficacy of this treatment approach.

Clinical Implications

Continuous monitoring of MRD is essential for assessing treatment effectiveness.

Conclusion

This case report presents findings on the combination of blinatumomab with DLI for relapse prevention in pediatric ALL.

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