Hormone Therapy

Adult Growth Hormone Deficiency, Replacement Therapy, and Outcomes in Long-Term Childhood Cancer Survivors.

TL;DR

Untreated adult growth hormone deficiency potentially contributes to multidimensional adverse outcomes in childhood cancer survivors, and socioeconomic disadvantage independently limits access to growth hormone therapy.

Key Findings

Among childhood cancer survivors with severe adult growth hormone deficiency, only 9.0% were on growth hormone therapy.

  • 354 survivors were identified with severe aGHD out of 3902 five-year survivors of childhood cancer aged 18 years and older.
  • Only 9.0% of the 354 survivors with severe aGHD were on GHT.
  • The study was cross-sectional and used multivariable logistic regression adjusting for potential confounders.
  • IGF1 was used as a marker of GH action to assess aGHD.

Socioeconomic disadvantages were independently associated with less use of growth hormone therapy among survivors with severe aGHD.

  • Annual household income <$40,000 vs ≥$80,000 was associated with significantly lower odds of GHT use (OR 0.27; 95% CI, 0.08-0.84).
  • Health insurance coverage, income, and area deprivation index were among the socioeconomic factors assessed.
  • Associations were assessed cross-sectionally by multivariable logistic regression adjusting for potential confounders.
  • The authors note that lack of evidence and socioeconomic factors may both contribute to underutilization of GHT.

Low IGF1 levels (z score ≤ -2) were associated with significantly higher prevalence of neurocognitive impairments compared to normal IGF1 levels (z score >0).

  • Verbal reasoning impairment was significantly more prevalent in the low IGF1 group (OR 2.79; 95% CI, 1.95-3.98).
  • The low IGF1 group was defined as z score ≤ -2 and the normal IGF1 group as z score >0.
  • Multiple neurocognitive impairment outcomes were assessed, with verbal reasoning being one specific example reported.
  • Associations were assessed using multivariable logistic regression adjusting for potential confounders.

Low IGF1 levels were associated with significantly higher prevalence of diminished health-related quality of life outcomes.

  • Physical functioning was significantly worse in the low IGF1 group compared to the normal IGF1 group (OR 1.97; 95% CI, 1.35-2.86).
  • The comparison was between survivors with IGF1 z score ≤ -2 versus z score >0.
  • Health-related quality of life was among the multidimensional adverse outcomes assessed.

Low IGF1 levels were associated with significantly higher prevalence of abnormal metabolic outcomes including glucose metabolism and fat percentage.

  • Abnormal glucose metabolism was significantly more prevalent in the low IGF1 group (OR 1.82; 95% CI, 1.21-2.71).
  • Abnormal fat percentage was significantly more prevalent in the low IGF1 group (OR 3.16; 95% CI, 1.98-5.26).
  • Both metabolic outcomes were assessed cross-sectionally by multivariable logistic regression.
  • The comparison was between survivors with IGF1 z score ≤ -2 versus z score >0.

The study included 3902 five-year survivors of childhood cancer aged 18 years and older assessed cross-sectionally for aGHD and its consequences.

  • Total sample was 3902 five-year survivors of childhood cancer aged 18 years and older.
  • Outcomes assessed included adverse physical, neurocognitive, and psychosocial outcomes.
  • Associations between IGF1 levels and prevalences of adverse outcomes were assessed cross-sectionally by multivariable logistic regression.
  • IGF1 was used as a marker of GH action to assess the effect of untreated aGHD.

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Citation

Yoshida T, Baedke J, Wang H, Chen Y, Yu C, Wilson C, et al.. (2025). Adult Growth Hormone Deficiency, Replacement Therapy, and Outcomes in Long-Term Childhood Cancer Survivors.. The Journal of clinical endocrinology and metabolism. https://doi.org/10.1210/clinem/dgaf156