# Cost-effectiveness of personalized medical treatment in acromegaly: a post hoc analysis of the ACROFAST study

**Authors:** Montserrat Marques-Pamies, Laura Ricou, Joan Gil, Miguel Sampedro-Núñez, Betina Biagetti, Olga Giménez-Palop, Marta Hernández, Silvia Martínez, Cristina Carrato, Rocío Villar-Taibo, Marta Araujo-Castro, Concepción Blanco, Inmaculada Simón-Muela, Andreu Simó-Servat, Gemma Xifra, Federico Vázquez, Isabel Pavón, José Antonio Rosado, Rogelio García-Centeno, Roxana Zavala, Felicia Alexandra Hanzu, Mireia Mora, Anna Aulinas, Nuria Vilarrasa, Alberto Torres, Soledad Librizzi, María Calatayud, Paz de Miguel Novoa, Cristina Alvarez-Escola, Antonio Picó, Isabel Salinas, Carmen Fajardo-Montañana, Rosa Cámara, Ignacio Bernabéu, Mireia Jordà, Susan M Webb, Mónica Marazuela, Elena Valassi, Manel Puig-Domingo

PMC · DOI: 10.1210/jendso/bvag030 · Journal of the Endocrine Society · 2026-03-06

## TL;DR

Personalized treatment for acromegaly using biomarkers is more effective and cost-effective than standard treatment.

## Contribution

Demonstrates that personalized treatment based on biomarkers reduces costs and improves disease control in acromegaly.

## Key findings

- Personalized treatment increased disease control probability by 2.53 times compared to standard treatment.
- IGF1 normalization occurred in 78% of personalized treatment patients versus 53% with standard treatment.
- Average cost per patient for disease control was 22% lower with personalized treatment.

## Abstract

Medical treatment of acromegaly is currently performed through a trial-and-error approach using first-generation somatostatin receptor ligands (fgSRLs) as first-line drugs, with an efficacy of 50%. Some biomarkers can predict patient response, potentially benefiting nonresponders by using personalized treatment approaches. The ACROFAST study revealed that the probability of disease control was 2.53 times higher (CI 1.30-4.80) with personalized treatment, and insulin-like growth factor 1 (IGF1) normalization occurred in 78% vs 53% of patients, compared with standard treatment (P < .05).

To evaluate the cost-effectiveness of personalized medicine based on predictive biomarkers, from the results of the ACROFAST study.

Post hoc analysis from the ACROFAST study comparing cost-effectiveness of a protocol of medical treatment based on predictive biomarkers to fgSRLs (n = 32) vs standard treatment (n = 36) for 12 months. Costs analyzed were visits, examinations, study of biomarkers (121€/patient), and pharmacological treatment according to the prices established by the Spanish National Health Care System. Medium-term costs were evaluated, considering a projection of up to 2 years in uncontrolled cases, assuming positive and negative scenarios with additional monitoring costs and a 25% likelihood of disease progression per follow-up visit.

The personalized protocol reduced the average cost per patient required to achieve disease control by 22% (15 127€ vs 19 420€). These results represent an annual saving of 15 263€ per patient achieving hormonal control compared to the standard treatment.

Personalized medicine, using a relatively straightforward biomarker-based protocol, enables a greater proportion of patients to attain hormonal control and proves to be a cost-effective strategy for managing acromegaly.

## Linked entities

- **Proteins:** IGF1 (insulin like growth factor 1)
- **Diseases:** acromegaly (MONDO:0019933)

## Full-text entities

- **Genes:** GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}
- **Diseases:** endocrine and other chronic disorders (MESH:D004700), cardiovascular complications (MESH:D002318), Acromegaly (MESH:D000172), Rare Diseases (MESH:D035583), tumor (MESH:D009369), diabetes (MESH:D003920), pituitary adenoma (MESH:D010911), metabolic dysregulation (MESH:D021081)
- **Chemicals:** PEGV (MESH:C406545), fgSRL (-), OCT (MESH:D015282)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12964116/full.md

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Source: https://tomesphere.com/paper/PMC12964116