TY - JOUR
T1 - Granulocyte Colony-Stimulating Factor Is Safe and Well Tolerated following Allogeneic Transplantation in Patients with Sickle Cell Disease
AU - Shah, Niketa C.
AU - Bhoopatiraju, Sweta
AU - Abraham, Allistair
AU - Anderson, Eric
AU - Andreansky, Martin
AU - Bhatia, Monica
AU - Chaudhury, Sonali
AU - Cuvelier, Geoff D.E.
AU - Godder, Kamar
AU - Grimley, Michael
AU - Hale, Gregory
AU - Kamani, Naynesh
AU - Jacobsohn, David
AU - Ngwube, Alexander
AU - Gilman, Andrew L.
AU - Skiles, Jodi
AU - Yu, Lolie C.
AU - Shenoy, Shalini
N1 - Funding Information:
Financial disclosure: Authors would like to thank The Children's Discovery Institute, Washington University, and St. Louis Children's Hospital (St. Louis, MO) for their support for the trial. Conflict of interest statement: G.D.E.C. reports consulting role for Miltenyi Biotech, S.C. reports advisory role for Bristol Myers Squibb. S.S. reports cosnulting role for Takeda, Janssen, Bristol Myers Squibb, Graphite and Data Safety Mornitoring Committe role for NHLBI and Aruvant. The other authors have no conflicts of interest to report. Authorship statement: S.S. designed the trial; S.S. and N.S. created the concept for this report; S.B. N.S. and S.S. collected the data; and N.S. and S.S. wrote the manuscript. All authors contributed with study participation, data reporting, critical review, and manuscript preparation. Financial disclosure: See Acknowledgments on page 174.e4.
Publisher Copyright:
© 2021 The American Society for Transplantation and Cellular Therapy
PY - 2022/3
Y1 - 2022/3
N2 - 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 × 103/mL) was achieved at a median of 13 days (range, 10 to 34 days), and platelet engraftment (>50 × 103/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.
AB - 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 × 103/mL) was achieved at a median of 13 days (range, 10 to 34 days), and platelet engraftment (>50 × 103/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.
KW - Granulocyte colony-stimulating factor
KW - Sickle cell disease
KW - Stem cell transplantation
UR - http://www.scopus.com/inward/record.url?scp=85124167481&partnerID=8YFLogxK
U2 - 10.1016/j.jtct.2021.12.016
DO - 10.1016/j.jtct.2021.12.016
M3 - Article
C2 - 34958973
AN - SCOPUS:85124167481
SN - 2666-6367
VL - 28
SP - 174.e1-174.e5
JO - Transplantation and Cellular Therapy
JF - Transplantation and Cellular Therapy
IS - 3
ER -