Evidence map›Paper›PMID 41869026›Full record

ArticleFrontiers in endocrinology2026

Disease burden, treatment experiences and preferences in patients with acromegaly: a qualitative study.

Jennifer Quinn, Andrea De Palma, Rebecca McKeown, Rocco Adiutori, Charlotte E Kosmas, Isabelle Petit

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In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Jennifer QuinnGlobal Value & Access, Debiopharm International SA, Lausanne, Switzerland.
Andrea De PalmaErasmus School of Health Policy & Management, Erasmus Rotterdam University, Rotterdam, Netherlands.
Rebecca McKeownICON plc, Insights, Evidence and Value, Reading, United Kingdom.
Rocco AdiutoriMapi Research Trust, Lyon, France.
Charlotte E KosmasICON plc, Insights, Evidence and Value, Reading, United Kingdom.
Isabelle PetitGlobal Value & Access, Debiopharm International SA, Lausanne, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Acromegaly is a rare disease with limited treatment options. Understanding treatment burden and patient preferences is important for evaluating new treatments and optimizing adherence. Methods: Patients with acromegaly (≥18 years) from the United States (US) participated in qualitative semi-structured interviews to explore: 1) the impact of acromegaly on quality of life, 2) patients' experiences with current treatment, 3) preferences for new treatments. Results: Fifteen US patients with acromegaly participated, reporting a range of symptoms; physical changes/swelling, fatigue/tiredness and excessive sweating. Frequently reported impacts included limited socializing (n = 6), anxiety (n = 4), embarrassment due to sweating/odor (n = 4) and clothing adaptations due to swelling (n = 4). Frequently reported impacts associated with monthly injectable treatment included unpleasantness of injections/blood tests (n = 6), clinic waiting time (n = 5), travelling to the clinic (n = 3), and treatment frequency (n = 3). Over half of patients preferred daily oral treatment options (n = 8, 53.3%). When asked about preference around hypothetical treatment frequency, 60.0% (n=9) preferred a hypothetical 3-monthly injection compared to a monthly injection if it was as efficacious as the monthly injection or recommended by their doctor. Conclusion: Patients experience a wide range of symptoms and impacts, with a high burden of treatment associated with monthly injections. Patients demonstrated preferences for less frequent treatments, with a preference for reducing their current monthly injections to three or six monthly. When considering new treatments, the efficacy and safety profile were of most importance to patients with acromegaly.

Indexed as

AcromegalyCost of IllnessPatient PreferenceQuality of LifeAdultAgedFemaleHumansMaleMiddle AgedQualitative ResearchSymptom Burdenacromegalydisease burdensomatostatinstreatment burdentreatment experiencetreatment preference

Identifiers

PMID41869026
PMCPMC12999441

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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.