PMID- 31613969 OWN - NLM STAT- MEDLINE DCOM- 20201109 LR - 20201109 IS - 1945-7197 (Electronic) IS - 0021-972X (Linking) VI - 105 IP - 3 DP - 2020 Mar 1 TI - Effects of Pegvisomant and Pasireotide LAR on Vertebral Fractures in Acromegaly Resistant to First-generation SRLs. LID - dgz054 [pii] LID - 10.1210/clinem/dgz054 [doi] AB - PURPOSE: Osteopathy is an emerging complication of acromegaly. In somatostatin receptor ligands (SRL)-resistant patients, pegvisomant (PegV) and pasireotide LAR (Pasi) are used for acromegaly treatment, but their effect on skeletal health is still not defined. METHODS: In a longitudinal retrospective international study, we evaluated incidence of radiological vertebral fractures (VFs) in 55 patients with acromegaly resistant to first-generation SRL. RESULTS: At study entry, prevalent VFs occurred in 23 patients (41.8%). Biochemical acromegaly control was reached in 66.7% of patients on PegV and in 66.7% of patients on Pasi. During the follow-up, incident VFs (iVFs) were detected in 16 patients (29.1%). Occurrence of iVFs was associated with prevalent VFs (P = .002), persistence of active acromegaly (P = .01) and higher value of insulin-like growth factor 1 (IGF-1) during follow-up (P = .03). Among patients with active disease at last visit, iVFs occurred less frequently in patients on treatment with Pasi (25%) compared to PegV (77.8% P = .04), independently of the IGF-1 values (P = .90). In patients who reached biochemical control, 22.7% on PegV and 12.5% on Pasi had iVFs (P = .40). Among both treatment groups, the presence of pre-existent VFs was the main determinant for iVFs. CONCLUSION: Our data show for the first time that patients with biochemically active disease treated with Pasi had lower risk of iVFs versus those treated with PegV. It also confirms that the presence of pre-existent VFs was the main determinant for iVFs. Additional studies on larger populations and with longer follow-up are needed to confirm our data and disclose the mechanisms underlying our findings. CI - (c) Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. FAU - Chiloiro, Sabrina AU - Chiloiro S AD - Pituitary Unit, Divisione di Endocrinologia, Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Rome, Italy. FAU - Giampietro, Antonella AU - Giampietro A AD - Pituitary Unit, Divisione di Endocrinologia, Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Rome, Italy. FAU - Frara, Stefano AU - Frara S AD - Vita-Salute San Raffaele University, Milano, Italy. FAU - Bima, Chiara AU - Bima C AD - Pituitary Unit, Divisione di Endocrinologia, Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Rome, Italy. FAU - Donfrancesco, Federico AU - Donfrancesco F AD - Pituitary Unit, Divisione di Endocrinologia, Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Rome, Italy. FAU - Fleseriu, Cara Maya AU - Fleseriu CM AD - University of Pittsburgh, Pittsburgh, PA, US. AD - Oregon Health and Science University, Portland, OR, US. FAU - Pontecorvi, Alfredo AU - Pontecorvi A AD - Pituitary Unit, Divisione di Endocrinologia, Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Rome, Italy. FAU - Giustina, Andrea AU - Giustina A AD - Vita-Salute San Raffaele University, Milano, Italy. FAU - Fleseriu, Maria AU - Fleseriu M AD - Oregon Health and Science University, Portland, OR, US. FAU - De Marinis, Laura AU - De Marinis L AD - Pituitary Unit, Divisione di Endocrinologia, Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Rome, Italy. FAU - Bianchi, Antonio AU - Bianchi A AD - Pituitary Unit, Divisione di Endocrinologia, Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Rome, Italy. LA - eng PT - Journal Article PL - United States TA - J Clin Endocrinol Metab JT - The Journal of clinical endocrinology and metabolism JID - 0375362 RN - 0 (Hormones) RN - 0 (Receptors, Somatostatin) RN - 12629-01-5 (Human Growth Hormone) RN - 51110-01-1 (Somatostatin) RN - 98H1T17066 (pasireotide) RN - N824AOU5XV (pegvisomant) SB - IM MH - Acromegaly/*drug therapy/pathology MH - Adult MH - Case-Control Studies MH - *Drug Resistance MH - Female MH - Follow-Up Studies MH - Hormones/*pharmacology MH - Human Growth Hormone/*analogs & derivatives/pharmacology MH - Humans MH - International Agencies MH - Longitudinal Studies MH - Male MH - Middle Aged MH - Prognosis MH - Receptors, Somatostatin/*agonists MH - Retrospective Studies MH - Somatostatin/*analogs & derivatives/pharmacology MH - Spinal Fractures/*prevention & control EDAT- 2019/10/16 06:00 MHDA- 2020/11/11 06:00 CRDT- 2019/10/16 06:00 PHST- 2019/06/25 00:00 [received] PHST- 2019/09/25 00:00 [accepted] PHST- 2019/10/16 06:00 [pubmed] PHST- 2020/11/11 06:00 [medline] PHST- 2019/10/16 06:00 [entrez] AID - 5588033 [pii] AID - 10.1210/clinem/dgz054 [doi] PST - ppublish SO - J Clin Endocrinol Metab. 2020 Mar 1;105(3):dgz054. doi: 10.1210/clinem/dgz054.