# Economic evaluation of cyclin-dependent kinases 4 and 6 inhibitors in advanced hormonal receptor-positive and human epidermal growth factor receptor 2 negative breast cancer: a nationwide budget impact analysis

**Authors:** Shereen Elazzazy, Nour Hisham Al-Ziftawi, Laila Shafei, Mohamed Izham Mohamed Ibrahim, Salha Bojassoum, Anas Hamad

PMC · DOI: 10.1080/20523211.2026.2626640 · Journal of Pharmaceutical Policy and Practice · 2026-02-19

## TL;DR

This study evaluates the affordability of CDK4/6 inhibitors for breast cancer treatment in Qatar over five years, finding that abemaciclib can save costs when its market share increases.

## Contribution

The study provides a nationwide budget impact analysis of CDK4/6 inhibitors in Qatar, offering insights into their affordability and cost-effectiveness.

## Key findings

- Increasing abemaciclib's market share to 60% saves QAR 14 million over five years.
- Equal market share of ribociclib and abemaciclib up to 80% remains within budget thresholds.
- Sensitivity analyses confirm the robustness of cost savings and affordability.

## Abstract

Several trials demonstrated improvements in clinical outcomes associated with cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors in breast cancer patients. The challenge remains regarding their high costs. Ribociclib and Abemaciclib are cost-effective in Qatar. Yet, their affordability was not studied. This budget impact analysis (BIA) is to assess the affordability of adopting CDK4/6 inhibitors in Qatar over five years duration (2024-2028).

We ran a BIA to evaluate two scenarios: (1) Increasing abemaciclib's market share from 20% to 60%, replacing both palbociclib and ribociclib. (2) Assuming equal market share for both ribociclib and abemaciclib up to 80%, reducing palbociclib's share. The analysis considered treatment costs, patient population, and disease prevalence. All data were retrieved from the National Center for Cancer Care and Research, and costs were presented in Qatari Riyals (QAR). Sensitivity analyses were run to ensure the robustness of the conclusion. All results were compared to Qatar's budget threshold, which is QAR 453,822.

Based on a total of 173 patients using CDK4/6 inhibitors, increasing abemaciclib's market share to 60% yielded cumulative savings of QAR 14 million over five years, which is around QAR 14,613 per patient per year. However, equally increasing ribociclib's and abemaciclib's market share to 80% resulted in a modest budget increase, remaining within acceptable thresholds. Sensitivity analyses confirmed the robustness of these findings, showing that cost reductions and higher uptake rates further enhanced savings.

Abemaciclib is a budget-saving option for HR+/HER2- breast cancer in Qatar, should it replace the market share by up to 60% over five years. In addition, ribociclib and abemaciclib are affordable treatment options if they equally contributes to up to 80% of the market share for the eligible advanced breast cancer patients. The results supported the concept of allocating CDK4/6 inhibitors as they were found to be affordable to the Qatari healthcare system.

## Linked entities

- **Proteins:** Cdk4 (Cyclin-dependent kinase 4)
- **Chemicals:** Ribociclib (PubChem CID 44631912), Abemaciclib (PubChem CID 46220502), Palbociclib (PubChem CID 5330286)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}
- **Diseases:** breast cancer (MESH:D001943), neutropenia (MESH:D009503), death (MESH:D003643), gastrointestinal adverse events (MESH:D002318), gastrointestinal toxicity (MESH:D005767), Cancer (MESH:D009369)
- **Chemicals:** RIBO (MESH:C000589651), CDK4/6 inhibitors (-), letrozole (MESH:D000077289), ABMA (MESH:C000590451), PLBO (MESH:C500026)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12922424/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12922424/full.md

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Source: https://tomesphere.com/paper/PMC12922424