# Novel therapies in myeloid neoplasms show limited benefit and increased costs over 15 years of follow-up in Southern Finland

**Authors:** Theerin Lanamtieng, Anna Mervaala-Muroke, Laura Toivanen, Kimmo Porkka, Oscar Brück

PMC · DOI: 10.1007/s00277-026-06863-y · Annals of Hematology · 2026-02-06

## TL;DR

New treatments for myeloid cancers in Finland over 15 years did not improve survival much but increased healthcare costs.

## Contribution

Long-term observational study reveals limited survival benefit and rising costs of novel therapies in myeloid neoplasms.

## Key findings

- Overall survival remained unchanged despite novel therapies in AML, MDS, and MF.
- Progression-free survival improved in AML patients, mainly due to better treatment stratification.
- Hospitalization and drug costs increased significantly with novel treatments in AML and MF.

## Abstract

Over the past two decades, targeted therapies have been adopted in the treatment of myeloid neoplasms. However, their impact on overall survival (OS) and healthcare spending remains uncertain. We performed a comprehensive retrospective observational study on patients with acute myeloid leukemia (AML, n = 684), myelodysplastic syndrome (MDS, n = 899) and myelofibrosis (MF, n = 276) diagnosed between 2009 and 2023 in a large hospital district in Southern Finland. During this 15-year period, the median age increased across all cohorts. OS remained unchanged after adjusting for age, comorbidity index and risk score in AML (HR 0.77, 95% CI 0.59–1.02), MDS (HR 1.03, 95% CI 0.81–1.31), and MF (HR 0.70, 95% CI 0.45–1.08). However, progression-free survival (PFS) improved among AML patients. For subgroup analyses, OS and PFS improved in AML receiving high-dose chemotherapy, mostly due to better stratification to fit and unfit treatment regimens. In MDS and MF cohorts, no OS benefit was observed in any subgroup. Hospitalization and drug expenses were the primary components in all cohorts and increased notably in AML and MF patients due to novel treatments. Advances in clinical care and adoption of novel agents show limited benefit but have gradually increased their financial burden. Future research should prioritize less toxic, outpatient-based treatments to enhance outcome and cost-effectiveness.

The online version contains supplementary material available at 10.1007/s00277-026-06863-y.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667), myelodysplastic syndrome (MONDO:0018881), myelofibrosis (MONDO:0044903)

## Full-text entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, MFSD11 (major facilitator superfamily domain containing 11) [NCBI Gene 79157] {aka ET}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322] {aka CD135, FLK-2, FLK2, STK1}
- **Diseases:** ELN (MESH:D004675), HDC (MESH:D000084202), acute promyelocytic leukemia (MESH:D015473), CCI (MESH:C566784), MF (MESH:D055728), death (MESH:D003643), AML (MESH:D015470), HUS (MESH:D003428), MDS (MESH:D009190), hematological and solid tumors (MESH:D019337), OS (MESH:D011475), DIPSS (MESH:D000082122), Cancer (MESH:D009369), essential thrombocythemia (MESH:D013920), PV (MESH:D011087)
- **Chemicals:** RUX (MESH:C540383), decitabine (MESH:D000077209), iron (MESH:D007501), venetoclax (MESH:C579720), HDC (-), Gemtuzumab Ozogamicin (MESH:D000079982), azacitidine (MESH:D001374)
- **Species:** Homo sapiens (human, species) [taxon 9606], Avihepevirus magniiecur (species) [taxon 1678144]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12881082/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12881082/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12881082/full.md

---
Source: https://tomesphere.com/paper/PMC12881082