Trial reportTurkish journal of haematology : official journal of Turkish Society of Haematology2026
The GLOBE Trial: Efficacy and Safety of L-Glutamine Plus Hydroxyurea Versus Hydroxyurea Alone in Sickle Cell Anemia - A Double-Blind, Randomized Study
Trial report in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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5 authors.
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Abstract
Objective: Hydroxyurea (HU) reduces complications of sickle cell anemia (SCA), but the response is variable. L-glutamine, an antioxidant that improves redox balance, is implicated in a distinct pathophysiological pathway and may provide additional clinical benefit when added to HU. We evaluated HU plus L-glutamine versus HU alone in pediatric/adolescent SCA. Materials and Methods: In a 6-month, double-blind, placebo-controlled trial, 53 patients with HbSS or HbS/β Results: Over 6 months, the HU + L-glutamine group experienced significantly fewer VOCs (1.00±0.73 vs. 1.65±0.80; p=0.003) and ACS episodes (0.19 vs. 0.77; p=0.006). Hospitalizations declined by 40% (p=0.04). Hemoglobin (Hb) rose more in the combination arm (+0.78 vs. +0.32 g/dL; p=0.028), with larger reductions in reticulocytes (p=0.04) and greater fetal Hb increases (+6.2% vs. +1.6%; p<0.001). Adherence exceeded 80% in both arms and no serious adverse events occurred. Conclusion: Adding L-glutamine to HU significantly reduced VOCs, ACS, and hospitalizations while improving Hb and hemolysis markers, without added toxicity. The combination’s efficacy likely reflects synergistic effects on oxidative stress and sickle cell pathophysiology. This well-tolerated combination may improve SCA control, but larger confirmatory trials are needed.
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