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Record W4417008854 · doi:10.1182/blood-2025-2971

Splenomegaly patterns and clinical impact in African children with sickle cell anemia on hydroxyurea treatment

2025· article· en· W4417008854 on OpenAlexaff
Léon Tshilolo, George Tomlinson, Luke R. Smart, Teresa Latham, Peter Olupot‐Olupot, Brígida Santos, Banu Aygün, Susan E. Stuber, Adam Lane, Thomas N. Williams, Russell E. Ware

Bibliographic record

VenueBlood · 2025
Typearticle
Languageen
FieldMedicine
TopicHemoglobinopathies and Related Disorders
Canadian institutionsPublic Health Ontario
Fundersnot available
KeywordsSickle cell anemiaSplenectomyAnemiaMalariaSplenic infarctionClinical trialFetal hemoglobinHemoglobinopathyComplication

Abstract

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Abstract Introduction. Splenomegaly is a challenging complication for children with sickle cell anemia (SCA) in sub-Saharan Africa, with little experience gained from high-income countries where splenic infarction and involution occur early in life. The etiology, persistence, and consequences of splenomegaly are poorly understood, especially regarding the effects of hydroxyurea treatment. Realizing Effectiveness Across Continents with Hydroxyurea (REACH, NCT01966731 and NCT06171217) is an ongoing Phase 1/2 trial of open-label hydroxyurea with dose optimization to maximum tolerated dose (MTD) for children with SCA in four African countries. With over 5,000 participant-years of treatment exposure, we address the characteristics and consequences of splenomegaly in this clinical setting. Methods. Children aged 1-10 years with SCA were enrolled at 4 clinical sites in Angola, Democratic Republic of Congo, Kenya, and Uganda. After a 3-month screening phase, hydroxyurea was prescribed at fixed dose for 6 months, escalated to MTD by Month 24, and subsequently optimized with mild myelosuppression. Spleen size below the costal margin was recorded at each scheduled and unscheduled visit. Cross-sectional analysis compared age, sex, clinical site, growth parameters, alpha thalassemia (1-gene or 2-gene deletion), and G6PD deficiency across four baseline spleen categories: non-palpable, moderate (1-4 cm), large (≥ 5 cm), or splenectomy with correlations. Longitudinal analysis categorized the frequency of palpable splenomegaly over repeated assessments as never (splenectomy), rare (<5%), intermittent (5-50%), or persistent (>50%). Mean laboratory values and current optimized daily doses were calculated in these categories, plus rates per 100 patient-years (pt-yr) for dose-limiting toxicities (DLT), transfusions, malaria infections, and deaths. Rate ratios (RR) and 95% confidence intervals were calculated for persistent vs. non-persistent splenomegaly. Results: A total of 606 children started hydroxyurea. At enrollment, 10/606 (1.7%) had splenectomy, 49/606 (8.1%) had moderate splenomegaly, and 50/606 (8.3%) had large splenomegaly. Compared to no palpable spleen, any splenomegaly at baseline was associated with a lower hemoglobin (6.9±1.3 vs 7.3±1.0 g/dL, p<0.001) and lower platelet count (287±117 vs 432±168 x 109/L, p<0.001). Children with alpha thalassemia had a greater prevalence of baseline splenomegaly (20.0% vs 12.4%, p=0.0019), but G6PD deficiency had no effect. Excluding 10 children with splenectomy at enrollment, palpable splenomegaly was recorded at least once during treatment in 346/596 (58.1%) children, usually in the first 2 years. Children with 2-gene deletion alpha thalassemia also had a higher risk of developing splenomegaly (~70% vs. ~50%, p=0.004). Over 8.5±2.4 years of follow-up and a median of 54 assessments per child, palpable splenomegaly was rare in 384/596 (64.4%), intermittent in 148/596 (24.8%), and persistent in 64/596 (10.7%). The average optimized hydroxyurea doses for these 3 categories were 28.6±5.3 mg/kg/day, 27.1±6.1 mg/kg/day, and 23.1±6.4 mg/kg/day, p<0.001. Lab consequences of persistent splenomegaly, compared to rare or intermittent splenomegaly, included a lower hemoglobin (6.9±1.4 vs 8.2±1.3 g/dL, p<0.001), lower MCV (90±12 vs 97± 14 fL, p<0.001), and lower platelet count (201±83 vs 383±171 x 109/L, p<0.001), but a slighter higher absolute neutrophil count (4.3±2.1 vs 3.9±1.8 x 109/L, p=0.122). Additional consequences of persistent splenomegaly included a high rate of DLT (67.0/100 pt-yr; RR=3.72 [2.62-5.37]; p<0.001), particularly for anemia and thrombocytopenia. Transfusions (31.0/100 pt-yr; RR=4.54 [3.08-6.78]; p<0.001) and all-cause death (2.3/100 pt-yr, RR=2.38 [1.15-4.55]; p=0.028) were also more common. Malaria was highest in children with intermittent splenomegaly (31.6/100 pt-yr; RR=1.58 [1.27-1.96]; p<0.001). Conclusions. Splenomegaly is common among children with SCA living in sub-Saharan Africa and complicates their clinical care despite sustained hydroxyurea at MTD. Persistent splenomegaly is especially problematic and associated with lower baseline lab values, lower hydroxyurea doses, more DLT, and greater clinical morbidity including more transfusions and more deaths. The importance of alpha thalassemia and recurrent malaria in the development of splenomegaly remains poorly understood. New recommendations for wider malaria chemoprophylaxis may help reduce splenomegaly in children with SCA.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.006
Threshold uncertainty score0.012

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.269
Teacher spread0.262 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
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