TY - JOUR
T1 - The paradoxical GH response at OGTT does not predict Pasireotide efficacy but matters for glucose metabolism
AU - Occhi, G.
AU - Voltan, G.
AU - Chiloiro, Sabrina
AU - Bianchi, Antonio
AU - Maffei, P.
AU - Dassie, F.
AU - Mantovani, G.
AU - Del Sindaco, G.
AU - Ferone, D.
AU - Gatto, F.
AU - Losa, M.
AU - Cannavò, S.
AU - Scaroni, C.
AU - Ceccato, F.
AU - null, null
PY - 2025
Y1 - 2025
N2 - Purpose: A paradoxical increase in GH after oral glucose load (GH-Par) characterizes about one-third of acromegaly patients and is associated with a better response to first-generation somatostatin receptor ligands (fg-SRLs). Pasireotide is typically considered as a second-/third-line treatment. Here, we investigated the predictive role of GH-Par in pasireotide response and adverse event development. Methods: we collected a multicenter Italian retrospective cohort of 59 patients treated with pasireotide for at least 3 months, all having GH profile from OGTT. IGF-1 normalization or at least 30% reduction at the last follow-up visit defined a responder patient. Results: Considering the entire cohort, median IGF-1 levels before pasireotide (available in 57 patients) were 1.38 times the upper limit of normal (ULN) in patients with large (median size 18 mm) and invasive (82%) adenomas after failure of fg-SRL treatment. After a 40-month median treatment, pasireotide effectively reduced IGF-1 ULN levels in 41 patients, 37 of whom achieving normalization, and 4 with a ≥ 30% reduction. Thirteen patients were classified as GH-Par. The median pasireotide duration, dosage, and efficacy (9/12 responder in the GH-Par group and 32/45 in the GH-NPar) were similar between groups. However, the occurrence of new-onset or worsening glucose metabolism alterations (GMAs) after pasireotide was more frequent in GH-NPar (from 37 to 80%; p < 0.001) compared to GH-Par patients (from 69 to 76%), likely due to the higher prevalence of pre-existing GMAs in the GH-Par group before starting pasireotide (p = 0.038). Conclusions: The GH-Par does not predict the response to pasireotide in acromegaly but can predict a worse metabolic profile.
AB - Purpose: A paradoxical increase in GH after oral glucose load (GH-Par) characterizes about one-third of acromegaly patients and is associated with a better response to first-generation somatostatin receptor ligands (fg-SRLs). Pasireotide is typically considered as a second-/third-line treatment. Here, we investigated the predictive role of GH-Par in pasireotide response and adverse event development. Methods: we collected a multicenter Italian retrospective cohort of 59 patients treated with pasireotide for at least 3 months, all having GH profile from OGTT. IGF-1 normalization or at least 30% reduction at the last follow-up visit defined a responder patient. Results: Considering the entire cohort, median IGF-1 levels before pasireotide (available in 57 patients) were 1.38 times the upper limit of normal (ULN) in patients with large (median size 18 mm) and invasive (82%) adenomas after failure of fg-SRL treatment. After a 40-month median treatment, pasireotide effectively reduced IGF-1 ULN levels in 41 patients, 37 of whom achieving normalization, and 4 with a ≥ 30% reduction. Thirteen patients were classified as GH-Par. The median pasireotide duration, dosage, and efficacy (9/12 responder in the GH-Par group and 32/45 in the GH-NPar) were similar between groups. However, the occurrence of new-onset or worsening glucose metabolism alterations (GMAs) after pasireotide was more frequent in GH-NPar (from 37 to 80%; p < 0.001) compared to GH-Par patients (from 69 to 76%), likely due to the higher prevalence of pre-existing GMAs in the GH-Par group before starting pasireotide (p = 0.038). Conclusions: The GH-Par does not predict the response to pasireotide in acromegaly but can predict a worse metabolic profile.
KW - Acromegaly
KW - GH profile
KW - Glucose metabolism alterations
KW - Oral glucose tolerance test
KW - Pasireotide
KW - Acromegaly
KW - GH profile
KW - Glucose metabolism alterations
KW - Oral glucose tolerance test
KW - Pasireotide
UR - https://publicatt.unicatt.it/handle/10807/316006
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85217540730&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85217540730&origin=inward
U2 - 10.1007/s40618-025-02534-3
DO - 10.1007/s40618-025-02534-3
M3 - Article
SN - 1720-8386
VL - 48
SP - 1173
EP - 1183
JO - Journal of Endocrinological Investigation
JF - Journal of Endocrinological Investigation
IS - 5
ER -