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Durable Engraftment and Excellent Overall Survival After CD34-Selected Peripheral Blood Stem Cell Boost in Pediatric
Ellen Fraint1, Sana Farooki2, Elizabeth Klein3
1Department of Pediatrics, Stem Cell Transplantation and Cellular Therapies Service, MSK Kids, Memorial Sloan Kettering Cancer Service, New York, New York; Division of Pediatric Hematology, Oncology, and Cellular Therapy, Children's Hospital at Montefiore and Albert Einstein College of Medicine, Bronx New York.
Insights
CD34-selected stem cell boost (CD34+SCB) offers a safe and effective treatment for poor graft function (PGF) after pediatric allogeneic stem cell transplantation (alloSCT), leading to durable recovery and improved survival.
Area of Science:
- Pediatric Hematology Oncology
- Stem Cell Transplantation
- Immunology
Background:
- Poor graft function (PGF) is a critical complication following allogeneic stem cell transplantation (alloSCT), with historically poor outcomes and limited treatment options.
- Few studies have reported outcomes for CD34-selected stem cell boost (CD34+SCB) in pediatric alloSCT recipients experiencing PGF.
Purpose of the Study:
- To evaluate the safety and efficacy of CD34+SCB for treating PGF in pediatric alloSCT recipients.
- To assess hematopoietic recovery, overall survival, and graft-versus-host disease (GVHD) development after CD34+SCB for PGF.
Main Methods:
- Retrospective analysis of 14 pediatric patients who received CD34+SCB for PGF between 2008-2020.
- PGF defined by transfusion/growth factor support needs and donor chimerism ≥85%.
- Peripheral blood stem cells from the original donor were used for CD34+SCB.
Main Results:
- A 79% probability of complete recovery (CR) by 60 days post-boost.
- Overall survival rates of 78% at both 2 and 5 years.
- One fatal case of GVHD, with no other CD34+SCB-related toxicities observed.
Conclusions:
- CD34+SCB is a safe and effective strategy for PGF in pediatric alloSCT patients, including those with infections.
- The treatment facilitates durable trilineage hematopoietic recovery and improves long-term survival.
- This approach provides a viable option for managing PGF when standardized treatments are lacking.
Abstract:
Poor graft function (PGF) is a life-threatening complication after allogeneic stem cell transplantation (alloSCT). Historically, outcomes of patients with PGF have been very poor, and there are no standardized approaches to treatment. Furthermore, few outcomes after CD34-selected stem cell boost (CD34+SCB) for PGF in pediatric alloSCT recipients have been reported. Here we report on a single center experience with CD34+SCB for PGF after alloSCT in patients treated on the Pediatric Transplant and Cellular Therapy Service at MSK Kids, Memorial Sloan Kettering Cancer Center. A retrospective analysis of patients transplanted for malignant and nonmalignant disorders who received a CD34+SCB between 2008 to 2020 for treatment of PGF defined as the need for granulocyte colony-stimulating factor (G-CSF) and/or packed red blood cell or platelet transfusion support with bone marrow donor chimerism ≥85%. Peripheral blood stem cells from the original donor were the source for CD34+SCB. Durable complete recovery (durable CR) was defined as recovery of peripheral blood counts without recurrent need for G-CSF or transfusion support. The main outcomes of interest were recovery of hematopoiesis and overall survival. Development of graft versus host disease (GVHD) was an additional outcome of interest. Fourteen patients with PGF received a boost. Six patients had no known infection, while 8 patients had PGF associated with an infection. The probability of CR at 60 days was 79% (95% confidence interval [CI], 57%-100%). The overall survival at both 2 and 5 years was 78% (95% CI, 56%-100%). One patient developed GVHD, which was fatal. No other CD34+SCB-related toxicities were observed. While including patients with PGF as recently defined by the American Society for Transplantation and Cellular Therapy, as well as PGF in patients with concomitant infections, we demonstrate that CD34+SCB is safe and can provide for durable trilineage hematopoietic recovery and long-term survival in pediatric patients after alloSCT.
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