TY - JOUR
T1 - Factors associated with disease control failure in acromegaly patients treated with pegvisomant: an ACROSTUDY analysis
AU - Giampietro, Antonella
AU - Chiloiro, Sabrina
AU - Urbani, Claudio
AU - Pivonello, Rosario
AU - Carlsson, Martin Ove
AU - Dassie, Francesca
AU - Prencipe, Nunzia
AU - Ragonese, Marta
AU - Gomez, Roy
AU - Granato, Simona
AU - Cannavò, Salvatore
AU - Grottoli, Silvia
AU - Maffei, Pietro
AU - Colao, Annamaria
AU - Bogazzi, Fausto
AU - Bianchi, Antonio
PY - 2024
Y1 - 2024
N2 - Purpose: The aim of this study was to examine the probability of achieving acromegaly disease control according to several patient-, disease-and treatment-related factors longitudinally. Methods: We analyzed data from ACROSTUDY, an open-label, noninterventional, post-marketing safety surveillance study conducted in 15 countries. A total of 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, taking 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% CI. Results: Univariate analysis showed that age <40 years, normal or overweight, baseline IGF-1 <300 µg/L or ranged between 300 and 500 µg/L, and all pegvisomant dose <20 mg/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 µg/L had the lowest risk of un-controlled acromegaly (ES = 0.29, 95% CI: 0.23–0.36). The probability of acromegaly uncontrol was also lower for values 300–500 µg/L (ES = 0.37, 95% CI: 0.32–0.43), while it was higher for baseline IGF-1 values ≥700 µg/L (ES = 0.58, 95% CI: 0.53–0.64). Conclusion: 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.
AB - Purpose: The aim of this study was to examine the probability of achieving acromegaly disease control according to several patient-, disease-and treatment-related factors longitudinally. Methods: We analyzed data from ACROSTUDY, an open-label, noninterventional, post-marketing safety surveillance study conducted in 15 countries. A total of 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, taking 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% CI. Results: Univariate analysis showed that age <40 years, normal or overweight, baseline IGF-1 <300 µg/L or ranged between 300 and 500 µg/L, and all pegvisomant dose <20 mg/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 µg/L had the lowest risk of un-controlled acromegaly (ES = 0.29, 95% CI: 0.23–0.36). The probability of acromegaly uncontrol was also lower for values 300–500 µg/L (ES = 0.37, 95% CI: 0.32–0.43), while it was higher for baseline IGF-1 values ≥700 µg/L (ES = 0.58, 95% CI: 0.53–0.64). Conclusion: 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.
KW - acromegaly
KW - longitudinal studies
KW - pegvisomant
KW - real-world analysis
KW - acromegaly
KW - longitudinal studies
KW - pegvisomant
KW - real-world analysis
UR - https://publicatt.unicatt.it/handle/10807/315916
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85184418365&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85184418365&origin=inward
U2 - 10.1530/ec-23-0247
DO - 10.1530/ec-23-0247
M3 - Article
SN - 2049-3614
VL - 13
SP - 1
EP - 9
JO - Endocrine Connections
JF - Endocrine Connections
IS - 3
ER -