About this trial
This observational study evaluates growth and endocrine outcomes in pediatric oncology patients who underwent prepubertal HSCT compared to those who did not. The study focuses on final height, pubertal growth spurt, and sex hormone production, with data collected retrospectively and prospectively through standard clinical follow-up.
Eligibility criteria
Qualifiers
HSCT performed for pediatric oncology between January 2005 and December 2020;
Pubertal development not yet initiated at the time of HSCT (testicular volume < 4 ml bilaterally, uterine volume < 2.5 ml).
Diagnosis of pediatric oncology between January 2005 and December 2020;
No HSCT performed before the onset of pubertal development (testicular volume < 4 ml bilaterally, uterine volume < 2.5 ml) during the same period.
Disqualifiers
Delayed puberty (testicular volume < 4 ml at age > 14 years or Tanner stage 2 breast development at age > 13 years) requiring exogenous hormone therapy with testosterone or estradiol;
For pediatric oncology patients not undergoing prepubertal HSCT, having received HSCT during pubertal development.
Trial design
Treatments tested in this trial
- Not listed