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Table 2 Therapeutic intervention and follow-up in patients with somatotropinoma

From: Sporadic and genetic forms of paediatric somatotropinoma: a retrospective analysis of seven cases and a review of the literature

Patient

Genetic mutation

IGF1 (μg/L) and MRI at diagnosis

First-type therapy

Second-type therapy

Third-type therapy

Fourth-type therapy

Control of disease

Last IGF1 (μg/L) and MRI

F-U (Years)

1

MAS

406 (+3SD) Hyperplasia 565 (+4SD)

Octreotide LAR 30 mg (monthly- 18 months)

+ Cabergoline 1 mg/week

Pegvisomant 20 mg/day

 

C

333 (-1SD) NA

7

2

MENI

Invasive Macroadenoma (36 × 27 × 28 mm) 1259 (+4SD)

Trans-sphenoidal surgery

Octreotide LAR 30 mg monthly (6 months - growth of adenoma with visual disturbance; 3 surgeries)

+ Cabergoline with visual (1 mg/week)

Proton therapy

NC

689 (+2.5SD) 14 × 10 mm (-68%)

3

3

AIP

Invasive Macroadenoma (21 × 26 mm) 997 (+4SD)

Lanreotide LAR 90 mg monthly (6 months)

Octreotide LAR 30 mg monthly + cabergoline (1 mg/week)

Transphenoidal surgery

 

NC

1184 (+4SD) 10 × 12 × 9 mm (-50%)

4

4

AIP

Invasive Macroadenoma (16 × 21 × 11 mm) 934 (+4SD)

Lanreotide LAR 60 mg monthly (6 months)

Transphenoidal surgery

  

C

451 (0SD) No visible adenoma

6

5

Negative genetic analysis (Carney, MEN1, AIP)

Non invasive macroadenoma (19 × 14 × 20 mm)

Lanreotide LAR 60 mg monthly

   

C

282 (+1SD) No visible adenoma

4

6

Negative genetic analysis (MEN1, AIP)

777 (+3SD) Invasive macroadenoma (26 × 26 × 32 mm)

Octreotide LAR 30 mg monthly (6 months) added to the previous Dopamine agonist treatment (Cabergoline 1,5 mg/week)

   

NC

717(+3SD) 34 × 21 × 23 mm (+6%)

2

7

Negative genetic analysis (Carney, MEN1, AIP)

574 (+4SD) Microadenoma (7,6 × 9 × 7,5 mm)

Trans-sphenoidal surgery

   

C

504 (+1,5 SD) No visible adenoma

4