Health Science Reports · 2022 · 11 citations · 9 references
MedicineHematologyPharmacologyClinical PharmacologyPediatric Clinical PharmacologyPediatric HematologyInfant PharmacotherapySickle Cell DiseaseHydroxyurea TherapyPharmacological TherapySickle Cell Anemia
Background: Sickle cell disease (SCD) is one of the most prevalent hemoglobinopathies that affects around 275,000 neonates annually. Until 2017, hydroxyurea was the only available drug for SCD treatment. Later on, L-glutamine and crizanlizumab have shown promising results in SCD therapy. Objectives: There were limited pharmacological options for the disease when in November, 2019, voxelotor was approved for the treatment of SCD patients after showing promising results in the clinical HOPE trial. Despite its favorable results, some life-threatening side effects were also observed. Uncertainty regarding the use of available pharmaceutical therapies for SCD is the major hurdle for the survival of patients. Discussion & Conclusion: An immediate attention needs to be drawn towards the drawbacks of limited pharmacological options for SCD. Article calls out to conduct more extensive trials in this advanced era of medicine where ambiguity regarding the use of SCD drugs still prevails.
9
Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease
Kenneth I. Ataga, Abdullah Kutlar, Julie Kanter et al. · New England Journal of Medicine · 2016 · 876 citations · Full text
A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease
Elliott Vichinsky, Carolyn Hoppe, Kenneth I. Ataga et al. · New England Journal of Medicine · 2019 · 609 citations · Full text
A Phase 3 Trial of <scp>l</scp> -Glutamine in Sickle Cell Disease
Yutaka Niihara, Scott T. Miller, Julie Kanter et al. · New England Journal of Medicine · 2018 · 546 citations · Full text
Jo Howard, Kenneth I. Ataga, Robert C. Brown et al. · The Lancet Haematology · 2021 · 101 citations