Gene Expression Signatures Predict First-Year Response to Somapacitan Treatment in Children With Growth Hormone Deficiency

J Clin Endocrinol Metab. 2024 Apr 19;109(5):1214-1221. doi: 10.1210/clinem/dgad717.

Abstract

Context: The pretreatment blood transcriptome predicts growth response to daily growth hormone (GH) therapy with high accuracy.

Objective: Investigate response prediction using pretreatment transcriptome in children with GH deficiency (GHD) treated with once-weekly somapacitan, a novel long-acting GH.

Methods: REAL4 is a randomized, multinational, open-label, active-controlled parallel group phase 3 trial, comprising a 52-week main phase and an ongoing 3-year safety extension (NCT03811535). A total of 128/200 treatment-naïve prepubertal children with GHD consented to baseline blood transcriptome profiling. They were randomized 2:1 to subcutaneous somapacitan (0.16 mg/kg/week) or daily GH (0.034 mg/kg/day). Differential RNA-seq analysis and machine learning were used to predict therapy response.

Results: 121/128 samples passed quality control. Children treated with somapacitan (n = 76) or daily GH (n = 45) were categorized based on fastest and slowest growing quartiles at week 52. Prediction of height velocity (HV; cm/year) was excellent for both treatments (out of bag [OOB] area under curve [AUC]: 0.98-0.99; validation AUC: 0.83-0.84), as was prediction of secondary markers of growth response: HV standard deviation score (SDS) (0.99-1.0; 0.75-0.78), change from baseline height SDS (ΔHSDS) (0.98-1.0; 0.61-0.75), and change from baseline insulin-like growth factor-I SDS (ΔIGF-I SDS) (0.96-1.0; 0.85-0.88). Genes previously identified as predictive of GH therapy response were consistently better at predicting the fastest growers in both treatments in this study (OOB AUC: 0.93-0.97) than the slowest (0.67-0.85).

Conclusion: Pretreatment transcriptome predicts first-year growth response in somapacitan-treated children with GHD. A common set of genes can predict the treatment response to both once-weekly somapacitan and conventional daily GH. This approach could potentially be developed into a clinically applicable pretreatment test to improve clinical management.

Keywords: and RNA sequencing; growth hormone deficiency; long-acting growth hormone; predictive markers; pretreatment blood transcriptome; somapacitan.

Publication types

  • Randomized Controlled Trial
  • Clinical Trial, Phase III

MeSH terms

  • Body Height
  • Child
  • Dwarfism, Pituitary* / drug therapy
  • Dwarfism, Pituitary* / genetics
  • Growth Hormone / deficiency
  • Growth Hormone / therapeutic use
  • Histidine*
  • Human Growth Hormone*
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Mannitol*
  • Phenol*
  • Transcriptome

Substances

  • Growth Hormone
  • Histidine
  • Human Growth Hormone
  • Insulin-Like Growth Factor I
  • Mannitol
  • Phenol
  • somapacitan

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