# Real-Life Use Patterns of Androgen Receptor Pathway Inhibitors (ARPIs): A Nationwide Register-Based Study in Finland During 2012–2023

**Authors:** Terhi Kurko, Pekka Heino, Pirkko-Liisa Kellokumpu-Lehtinen, Kati Sarnola, Hanna Koskinen, Maarit Bärlund

PMC · DOI: 10.3390/cancers17193162 · Cancers · 2025-09-29

## TL;DR

This study examines how androgen receptor pathway inhibitors are used in prostate cancer patients in Finland, finding that a third use multiple drugs sequentially despite a lack of clinical evidence for this approach.

## Contribution

The study provides real-world data on sequential ARPI use and costs in Finland, highlighting a gap in clinical evidence for this practice.

## Key findings

- 32.1% of patients used at least two ARPIs sequentially.
- Sequential use cost nearly €44 million in total.
- Sequential use peaked in 2017 at 56% and dropped to 14% by 2022.

## Abstract

Androgen pathway inhibitors (ARPIs) are widely used in prostate cancer. We conducted a register data-based analysis assessing their use and especially sequential use, e.g., use of one medicine after another, in Finland by using a dataset covering the whole country during 2012–2023. We found that one-third of patients use at least two ARPIs sequentially to inhibit testosterone effect. The total cost of sequential use was nearly €44 million. However, there are no large clinical trials published demonstrating the benefits of sequential treatment. More evidence is needed to justify sequential use.

Background and Objective: Prostate cancer (PC) is the most common cancer among males in the Western World. Androgens are key growth regulators both in normal and malignant prostate growth. Several new types of androgen pathway inhibitors (ARPIs) have been developed for the treatment of PC. Despite the lack of evidence, sequential use of ARPIs has been adopted into everyday clinical practice. This study aimed to assess real-life ARPI use patterns, especially sequential use and treatment costs, in Finland. Methods: Nationwide register data on all ARPI (enzalutamide, apalutamide, darolutamide, abiraterone) purchases recorded in the National Health Insurance scheme register maintained by the Social Insurance Institution of Finland from January 2012 to December 2023 were used. The data included patient demographics and medicine purchase details, which were descriptively analysed. Results: During the study period, 8369 patients initiated ARPIs. The median age of the users was 75.1 years. Of these, 32.1% (n = 2685) used at least two ARPIs sequentially. The proportion of treatment initiations leading to sequential use increased from 36% in 2012 to 56% in 2017, then decreased to 14% in 2022. The total cost of sequential use was €43.8 million. Limitations include the unrecorded phase of PC. The study’s strength is its inclusion of all reimbursed ARPI purchases nationwide. Conclusions: Despite the lack of evidence, sequential ARPI use was initially prevalent but declined after the introduction of new guidelines. Randomised trials are needed to guide the sequential use of these medicines. Patient summary
: Androgen pathway inhibitors (ARPIs) are widely used in prostate cancer in Finland. One-third of patients use at least two ARPIs sequentially to inhibit testosterone effect. However, there are no large clinical trials published demonstrating the benefits of sequential treatment. More evidence is needed to justify sequential use.

## Linked entities

- **Chemicals:** enzalutamide (PubChem CID 15951529), apalutamide (PubChem CID 24872560), darolutamide (PubChem CID 67171867), abiraterone (PubChem CID 132971)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Diseases:** PC (MESH:D011471), cancer (MESH:D009369)
- **Chemicals:** ARPI (-), enzalutamide (MESH:C540278), darolutamide (MESH:C000607739), abiraterone (MESH:C089740), apalutamide (MESH:C572045), testosterone (MESH:D013739)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12524319/full.md

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Source: https://tomesphere.com/paper/PMC12524319