AI Article Synopsis

  • G-CSF after hematopoietic stem cell transplantation (HSCT) improves neutrophil recovery in neutropenic patients, but its safety in sickle cell disease (SCD) patients was previously unknown.
  • Clinical outcomes were studied in 62 SCD patients receiving G-CSF post-HSCT, showing effective neutrophil and platelet engraftment without any SCD-related complications.
  • Common post-treatment issues included anorexia, hypertension, and electrolyte imbalances, but overall, G-CSF was determined to be safe for SCD patients following HSCT.

Article Abstract

Granulocyte colony-stimulating factor (G-CSF) used after hematopoietic stem cell transplantation (HSCT) can enhance neutrophil recovery in patients rendered neutropenic by the preparative regimen. G-CSF is contraindicated in patients with sickle cell disease (SCD), because life-threatening complications can ensue in the presence of sickle vasculopathy. The safety profile of G-CSF after HSCT for SCD has not been described, however. We report clinical outcomes in the first 100 days post-HSCT in 62 patients supported with G-CSF until neutrophil recovery on a clinical trial of reduced- intensity conditioning HSCT for SCD. The patients received G-CSF for a median of 9 days (range, 5 to 33 days) post-transplantation from the best available stem cell source. Preparation for transplantation included a target hemoglobin S level of ≤45%. Neutrophil engraftment (absolute neutrophil count >0.5 × 10/mL) was achieved at a median of 13 days (range, 10 to 34 days), and platelet engraftment (>50 × 10/mL) was achieved at a median of 19 days (range, 12 to 71 days). The median duration of inpatient hospitalization following stem cell infusion (day 0) was 21.5 days (range, 11 to 33 days). No patient developed SCD-related complications following G-CSF use. The most common organ toxicities encountered between G-CSF initiation (on day +7) and day +100 were anorexia (n = 14), hypertension (n = 11), and electrolyte imbalance requiring correction (n = 9). Central nervous system-related events were noted in 5 patients, all of whom had preexisting cerebral vasculopathy/moyamoya disease, attributed to reversible posterior leukoencephalopathy syndrome in the presence of calcineurin inhibitor therapy and hypertension. We conclude that G-CSF does not adversely impact SCD HSCT recipients and can be safely used post-transplantation to enhance neutrophil recovery.

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http://dx.doi.org/10.1016/j.jtct.2021.12.016DOI Listing

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