Factors associated with disease control failure in acromegaly patients treated with pegvisomant: an ACROSTUDY analysis.


Journal

Endocrine connections
ISSN: 2049-3614
Titre abrégé: Endocr Connect
Pays: England
ID NLM: 101598413

Informations de publication

Date de publication:
01 Jan 2024
Historique:
received: 19 06 2023
accepted: 10 01 2024
medline: 10 1 2024
pubmed: 10 1 2024
entrez: 10 1 2024
Statut: aheadofprint

Résumé

Aim of this study was to examine the probability of achieving acromegaly disease control according to several patient-, disease- and treatment-related factors longitudinally. We analyzed data from ACROSTUDY, an open-label, non-interventional, post-marketing safety surveillance study conducted in 15 countries. 1546 patients with acromegaly and treated with pegvisomant, with available information on baseline IGF-1 level, were included. Factors influencing IGF-1 control were assessed up to 10 years of follow-up by mixed effects logistic regression models, keeping into account changing values of covariates at baseline and at yearly visits. Twenty-eight anthropometric, clinical, and treatment-related covariates were examined through univariate and multivariate analyses. We tested whether the probability of non-control was different than 0.50 (50%) by computing effect sizes (ES) and the corresponding 95% confidence intervals (CI). Univariate analysis showed that age <40 years, normal or overweight, baseline IGF-1<300 ug/L or ranged between 300 and 500ug/L, and all pegvisomant dose <20mg/day were associated with a lower probability of acromegaly uncontrol. Consistently, in multivariate analyses, the probability of uncontrolled acromegaly was influenced by baseline IGF-1 value: patients with IGF-1<300 ug/L had the lowest risk of not-controlled acromegaly (ES=0.29, 95%CI:0.23-0.36). The probability of acromegaly uncontrol was also lower for values 300-<500ug/L (ES=0.37, 95%CI:0.32-0.43), while it was higher for baseline IGF-1 values ≥700ug/L (ES=0.58, 95%CI:0.53-0.64). Baseline IGF-l levels were a good predictor factor for long-term acromegaly control. On the contrary, our data did not support a role of age, sex, BMI, and pegvisomant dose as predictors of long-term control of acromegaly.

Identifiants

pubmed: 38197875
doi: 10.1530/EC-23-0247
pii: EC-23-0247
doi:
pii:

Types de publication

Journal Article

Langues

eng

Auteurs

Antonella Giampietro (A)

A Giampietro, Pituitary Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, 00168, Italy.

Sabrina Chiloiro (S)

S Chiloiro, Pituitary Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy.

C Urbani (C)

C Urbani, Department of Medicine, Endocrinology II Unit, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.

Rosario Pivonello (R)

R Pivonello, Dipartimento Di Medicina Clinica E Chirurgia, Sezione Di Endocrinologia, Università degli Studi di Napoli Federico II, Napoli, Italy.

Martin Ove Carlsson (MO)

M Carlsson, Global Medical Affairs, Pfizer Rare Disease, Brussels, Belgium.

Francesca Dassie (F)

F Dassie, Department of Medicine - DIMED, University of Padua, Padova, Italy.

Nunzia Prencipe (N)

N Prencipe, Department of Medical Science, Division of Endocrinology, Diabetology and Metabolism, University of Turin, Torino, Italy.

Marta Ragonese (M)

M Ragonese, Department of Human Pathology, Unit of Endocrinology, University of Messina, Messina, Italy.

Roy Gomez (R)

R Gomez, Global Medical Affairs, Pfizer Rare Desease, Bruxelles, Belgium.

Simona Granato (S)

S Granato, Medical Department, Pfizer Italia, Rome, Italy.

Salvatore Cannavò (S)

S Cannavò, Department of Human Pathology, Unit of Endocrinology, University of Messina, Messina, Italy.

Silvia Grottoli (S)

S Grottoli, Department of Medical Science, Division of Endocrinology, Diabetology and Metabolism, University of Turin, Torino, Italy.

Pietro Maffei (P)

P Maffei, Department of Medicine - DIMED, University of Padua, Padova, Italy.

Annamaria Colao (A)

A Colao, Dipartimento Di Medicina Clinica E Chirurgia, Sezione Di Endocrinologia, Università degli Studi di Napoli Federico II, Napoli, Italy.

Fausto Bogazzi (F)

F Bogazzi , Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Antonio Bianchi (A)

A Bianchi, Department of Endocrinology, Pituitary Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy.

Classifications MeSH