Independent Market Access and Reimbursement Risk Assessment.

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Pembrolizumab for treating relapsed or refractory classical Hodgkin lymphoma in people 3 years and over

As of May 2024, MARA’s assessment finds Pembrolizumab’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 clinical effectiveness: how much additional benefit the drug demonstrated over the care patients already receive — the first question every payer asks. 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

Pembrolizumab shows moderate benefit over current care, with a 64% overall response rate in the KEYNOTE-087 trial and promising survival data. However, the overall survival data is not mature, and the evidence relies on indirect comparisons, which introduces uncertainty.

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

The cost-effectiveness estimates for pembrolizumab are below £20,000 per QALY gained, which is considered acceptable by NICE. The committee noted that the most plausible ICERs were within acceptable thresholds for Healthcare resources.

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

The evidence indicates moderate improvements in HRQoL, with patient experts noting the importance of coping with the disease. However, the utility values are derived from limited data and may not fully capture the long-term impact on quality of life.

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

Pembrolizumab has a very good safety profile, with mostly mild to moderate adverse events reported. Serious adverse events are rare, indicating a favorable tolerability compared to existing therapies.

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

The evidence does not include direct comparisons with standard care, relying instead on indirect comparisons. While these suggest pembrolizumab may improve survival, the lack of direct evidence limits the robustness of the findings.

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

The trial population is broadly representative of the intended patient population, with relevant subgroup analyses. However, there are some concerns regarding the severity of disease in the real-world data compared to trial participants.

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

Pembrolizumab can be integrated into existing care pathways with minor adjustments. It serves as a bridge to stem cell transplant, fitting well into the treatment sequence for patients who cannot undergo ASCT.

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

The resource implications are manageable, with the potential for cost savings due to the effectiveness of pembrolizumab as a treatment option. The economic model indicates a reasonable budget impact.

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

The evidence base includes data from both clinical trials and real-world settings, although there are some methodological concerns and reliance on indirect comparisons that introduce uncertainty.

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

There is significant uncertainty surrounding the indirect comparisons and the economic model structure. The committee noted that while the ICER is acceptable, the high uncertainty in treatment effect estimates could impact decision-making.

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
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