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. 2019 May 16;14(5):e0216927. doi: 10.1371/journal.pone.0216927

Table 4. Neoplasms reported during whole study period.

Indication for rhGH treatment Sex Age at the baseline (years) Age at neoplasm diagnosis (years) Neoplasm type rhGH at the time of diagnosis Relationship with rhGH Action undertaken Outcome
Malignant
Organic GHD female 19 21 craniopharyngioma recurrence*, yes possible rhGH stopped ongoing
Organic GHD male 9 14 craniopharyngioma recurrence yes unlikely rhGH interrupted resolved
17 craniopharyngioma recurrence, yes unlikely none resolved
Organic GHD female 13 14 craniopharyngioma recurrence*, yes possible rhGH stopped resolved
15 craniopharyngioma recurrence yes unlikely none resolved
17 craniopharyngioma recurrence,§ off-treatment unlikely none resolved
Organic GHD male 7 8 craniopharyngioma recurrence*, off-treatment possible rhGH stopped resolved
Idiopathic GHD male 12 13 medulloblastoma yes unlikely rhGH stopped death
TS female 8 9 ovarian dysgerminoma stage unspecified yes not related rhGH interrupted resolved
Benign
Idiopathic GHD female 9 9 skin papilloma* yes possible none resolved
Idiopathic GHD male 6 8 skin papilloma yes unlikely none resolved
Idiopathic GHD male 3 11 skin papilloma yes not related none resolved
TS female 4 11 neurofibroma yes not related none ongoing
TS female 10 13 osteochondroma yes not related none ongoing

*Evaluated as related to rhGH treatment,

reported as SAE,

Epilepsy was reported as AE approximately 2 years after this was resolved (ongoing).

§CSF leak was reported as AE 6 days after this was resolved (resolved after 9 days).

GHD growth hormone deficiency, rhGH recombinant human growth hormone, TS Turner syndrome