Evidence map›Paper›PMID 38197875›Full record

ArticleEndocrine connections2024

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

Antonella Giampietro, Sabrina Chiloiro, Claudio Urbani, Rosario Pivonello, Martin Ove Carlsson, Francesca Dassie, Nunzia Prencipe, Marta Ragonese, Roy Gomez, Simona Granato and 6 more

Open access · goldAbstract read
In one paragraph

Article in Endocrine connections, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Can acromegaly be controlled in all cases?Journal of neuroendocrinology · 2026
    Review
  3. Current treatment landscape of acromegaly.The Journal of clinical endocrinology and metabolism · 2026
    Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 9 institutions in 2 countries.

Antonella GiampietroPituitary Unit, Department of Endocrinology, Fondazione A Gemelli, IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0001-5756-2045
Sabrina ChiloiroPituitary Unit, Department of Endocrinology, Fondazione A Gemelli, IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
Claudio UrbaniEndocrinology II Unit, Department of Medicine, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Rosario PivonelloDipartimento Di Medicina Clinica E Chirurgia, Sezione Di Endocrinologia, Università Federico II di Napoli, Naples, Italy.
Martin Ove CarlssonGlobal Medical Affairs, Pfizer Rare Disease, Brussels, Belgium.
Francesca DassieDepartment of Medicine - DIMED, University of Padua, Padua, Italy.
Nunzia PrencipeDivision of Endocrinology, Diabetology and Metabolism, Department of Medical Science, University of Turin, Turin, Italy.
Marta RagoneseUnit of Endocrinology, Department of Human Pathology, University of Messina, Messina, Italy.
Roy GomezGlobal Medical Affairs, Pfizer Rare Disease, Brussels, Belgium.
Simona GranatoMedical Department, Pfizer Italia, Rome, Italy.
Salvatore CannavòUnit of Endocrinology, Department of Human Pathology, University of Messina, Messina, Italy.
Silvia GrottoliDivision of Endocrinology, Diabetology and Metabolism, Department of Medical Science, University of Turin, Turin, Italy.
Pietro MaffeiDepartment of Medicine - DIMED, University of Padua, Padua, Italy.
Annamaria ColaoDipartimento Di Medicina Clinica E Chirurgia, Sezione Di Endocrinologia, Università Federico II di Napoli, Naples, Italy.
Fausto BogazziDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Antonio BianchiPituitary Unit, Department of Endocrinology, Fondazione A Gemelli, IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
Università Cattolica del Sacro Cuore · ITPfizer (Belgium) · BEUniversity of Messina · ITUniversity of Naples Federico II · ITUniversity of Padua · ITUniversity of Turin · ITAzienda Ospedaliera Universitaria Pisana · ITPfizer (Italy) · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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. Significance statement: Among factors that could influence and predict the efficacy of pegvisomant therapy in controlling acromegaly, a central role of baseline IGF-1 values on the probability of achieving a biochemical control of acromegaly during the treatment with pegvisomant was identified, in a real-life setting.

Indexed as

acromegalylongitudinal studiespegvisomantreal-world analysis

Identifiers

PMID38197875
PMCPMC10895310
OpenAlexW4390704372

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.