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Risk Factors for Small Adult Height in Childhood Cancer Survivors
Auteurs
Charlotte Demoor-Goldschmidt, Rodrigue S. Allodji, Neige Journy, Carole Rubino, Wael Salem Zrafi, Ghazi Debiche, Damien Llanas, Cristina Veres, Cécile Thomas-Teinturier, Hélène Pacquement, Giao Vu-Bezin, Brice Fresneau, Delphine Berchery, Stephanie Bolle, Ibrahima Diallo, Nadia Haddy, Florent de Vathaire
Résumé
PURPOSE
Between 10% and 20% of childhood cancer survivors (CCS) experience impaired growth, leading to small adult height (SAH). Our study aimed to quantify risk factors for SAH or growth hormone deficiency among CCS.
METHODS
The French CCS Study holds data on 7,670 cancer survivors treated before 2001. We analyzed self-administered questionnaire data from 2,965 CCS with clinical, chemo/radiotherapy data from medical records. SAH was defined as an adult height ≤ 2 standard deviation scores of control values obtained from a French population health study.
RESULTS
After exclusion of 189 CCS treated with growth hormone, 9.2% (254 of 2,776) had a SAH. Being young at the time of cancer treatment (relative risk [RR], 0.91 [95% CI, 0.88 to 0.95] by year of age), small height at diagnosis (≤ 2 standard deviation scores; RR, 6.74 [95% CI, 4.61 to 9.86]), pituitary irradiation (5-20 Gy: RR, 4.24 [95% CI, 1.98 to 9.06]; 20-40 Gy: RR, 10.16 [95% CI, 5.18 to 19.94]; and ≥ 40 Gy: RR, 19.48 [95% CI, 8.73 to 43.48]), having received busulfan (RR, 4.53 [95% CI, 2.10 to 9.77]), or > 300 mg/m
CONCLUSION
CCS are at a high risk of SAH. CCS treated with radiotherapy, busulfan, or lomustine should be closely monitored for growth, puberty onset, and potential pituitary deficiency.