Independent Market Access and Reimbursement Risk Assessment.

Built by former payers, HTA reviewers, and Industry Experts. 

Olaparib for treating hormone-relapsed metastatic prostate cancer with BRCA1 or BRCA2 mutations that has progressed after a newer hormonal treatment

As of May 2023, MARA’s assessment finds Olaparib’s reimbursement risk concentrated in comparator selection, with cost effectiveness a strength; the current MARA Rating and full rationale are available in the report.

The assessment also weighs patient population and subgroups: how closely the trial population matches the patients who would receive the drug in practice; payers often restrict funding to the groups where the evidence is strongest. The strength recorded in cost effectiveness carries weight because that domain asks whether the price asked stands in a defensible relationship to the benefit delivered — the core of most European reimbursement decisions.

Oncology

This rating sits within MARA’s Oncology coverage, alongside 153 other independently assessed treatments in the same area.

What payers will ask

Is the clinical benefit the kind payers reward? — Clinical effectiveness

Clinical trial evidence shows that olaparib provides a significant improvement in overall survival and progression-free survival compared to retreatment with abiraterone or enzalutamide, which are not considered effective. However, the lack of direct comparisons with cabazitaxel and other relevant treatments introduces some uncertainty.

Does the economic case hold at the expected price? — Cost effectiveness

The cost-effectiveness estimates for olaparib are within acceptable thresholds for Healthcare resources, particularly when considering its life-extending properties. The committee concluded that the ICERs were acceptable, especially given the end-of-life criteria.

Is there quality-of-life evidence payers weigh? — Quality of life

The evidence suggests that olaparib may improve quality of life compared to standard treatments, although specific HRQoL data is limited. The committee noted that the treatment could help maintain or improve quality of life for patients with hormone-relapsed metastatic prostate cancer.

Does the safety profile hold up for payers? — Safety and Adverse Effects

Olaparib has a favorable safety profile with manageable adverse effects compared to traditional chemotherapy options. The committee noted that adverse effects are generally mild to moderate, with serious events being rare.

Was the drug compared against what payers expect? — Comparator Selection

While the company selected cabazitaxel as a comparator for the prior taxane group, there is limited direct evidence comparing olaparib with other relevant treatments like docetaxel. The committee acknowledged that the indirect comparisons introduce uncertainty.

Is the population defined the way payers need it? — Patient Population and Subgroups

The trial population is generally representative of the intended patient population, with analyses conducted for relevant subgroups. However, there are concerns regarding the generalizability of some trial results to the Healthcare.

Does the drug fit how care is delivered and paid for? — Care Pathway Integration

Olaparib can be integrated into existing treatment pathways with minor adjustments. The committee noted that it fits well within the current treatment landscape for hormone-relapsed metastatic prostate cancer.

Are the wider system costs understood? — Resource Use and Cost Implications

The budget impact of olaparib is manageable, and the treatment is expected to be resource-efficient, particularly given its potential to delay the need for more costly interventions like chemotherapy.

Would the evidence survive payer scrutiny? — Evidence Quality and Robustness

The evidence base is supported by a robust Phase 3 trial (PROfound), although there are some methodological concerns and uncertainties regarding indirect comparisons.

How exposed is the case to uncertainty? — Uncertainty, Sensitivity, and Broader Impacts

While there are uncertainties related to the indirect comparisons and the generalizability of trial results, the overall context supports the use of olaparib, particularly given the unmet need in this patient population.

Be alerted when this rating changes:

Sample two-page MARA Rating report for the fictional drug Samplinib: the rating with its decision record, and the ten graded payer questions with the reasoning behind each
Every MARA rating is delivered as a two-page reasoned report (sample, fictional product) — see it in full
Full Legal Disclaimer and Usage Terms

The MARA Rating® is an independent opinion of a drug’s market access pharma risk profile and is provided for informational purposes only—not as investment, medical, legal or any other type of advice. See our full disclaimer here.