TY - JOUR
T1 - CD34 Stem Cell Boost in Pediatric Allogeneic Stem Cell Transplant Recipients
T2 - A Case Series and Review of Literature
AU - Bowman, Sara
AU - Stanek, Joe
AU - Bajwa, Rajinder
AU - Polishchuk, Veronika
AU - Abu-Arja, Rolla
AU - Rangarajan, Hemalatha G.
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/6
Y1 - 2023/6
N2 - Patients with poor graft function (PGF) or declining donor chimerism (DC) post allogeneic hematopoietic cell transplantation (HCT) may benefit from a CD34-selected stem cell boost (SCB). We retrospectively studied outcomes of fourteen pediatric patients (PGF: 12 and declining DC: 2), with a median age of 12.8 (range 0.08–20.6) years at HCT, who received a SCB. Primary and secondary endpoints included resolution of PGF or improvement in DC (≥ 15% increase), overall survival (OS) and transplant-related mortality (TRM), respectively. The median CD34 dose infused was 7.47 × 106/kg (range 3.51 × 106–3.39 × 107/kg). Among patients with PGF who survived ≥ 3 months post-SCB (n = 8), we observed a non-significant decrease in the cumulative median number of red cell transfusions, platelet transfusions, and GCSF but not intravenous immunoglobulin doses in the 3 months before and after SCB. Overall response rate (ORR) was 50%, with 29% complete and 21% partial responses. ORR was better in recipients who received lymphodepletion (LD) pre-SCB versus none (75% versus 40%; p = 0.56). The incidence of acute and chronic graft-versus-host-disease was 7% and 14%, respectively. The 1-year OS was 50% (95% CI 23–72%) and TRM was 29% (95% CI 8–58%). SCB was effective in half of our cohort with possible benefit of LD pre-SCB.
AB - Patients with poor graft function (PGF) or declining donor chimerism (DC) post allogeneic hematopoietic cell transplantation (HCT) may benefit from a CD34-selected stem cell boost (SCB). We retrospectively studied outcomes of fourteen pediatric patients (PGF: 12 and declining DC: 2), with a median age of 12.8 (range 0.08–20.6) years at HCT, who received a SCB. Primary and secondary endpoints included resolution of PGF or improvement in DC (≥ 15% increase), overall survival (OS) and transplant-related mortality (TRM), respectively. The median CD34 dose infused was 7.47 × 106/kg (range 3.51 × 106–3.39 × 107/kg). Among patients with PGF who survived ≥ 3 months post-SCB (n = 8), we observed a non-significant decrease in the cumulative median number of red cell transfusions, platelet transfusions, and GCSF but not intravenous immunoglobulin doses in the 3 months before and after SCB. Overall response rate (ORR) was 50%, with 29% complete and 21% partial responses. ORR was better in recipients who received lymphodepletion (LD) pre-SCB versus none (75% versus 40%; p = 0.56). The incidence of acute and chronic graft-versus-host-disease was 7% and 14%, respectively. The 1-year OS was 50% (95% CI 23–72%) and TRM was 29% (95% CI 8–58%). SCB was effective in half of our cohort with possible benefit of LD pre-SCB.
KW - CD34 stem cell boost
KW - Outcomes
KW - Pediatrics
KW - Post stem cell transplant
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UR - http://www.scopus.com/inward/citedby.url?scp=85151956138&partnerID=8YFLogxK
U2 - 10.1007/s44228-023-00042-w
DO - 10.1007/s44228-023-00042-w
M3 - Article
C2 - 37027103
AN - SCOPUS:85151956138
SN - 2590-0048
VL - 5
SP - 155
EP - 164
JO - Clinical Hematology International
JF - Clinical Hematology International
IS - 2-3
ER -