Woods Beth, Palacios Alfredo, Sculpher Mark
Centre for Health Economics, University of York, York, UK.
Pharmacoeconomics. 2025 Apr;43(4):363-373. doi: 10.1007/s40273-024-01450-3. Epub 2024 Dec 31.
Current approaches to the pricing and funding of new pharmaceuticals often focus on a one-time decision about a product for each clinical indication. This can result in multiple options being available to health systems without a clear signal about how to prioritise between them. This runs the risk that, as available treatments, evidence, and drug prices evolve, clinical and patient choices may not be aligned with the objective of allocating resources to promote population health. We propose a framework for using cost-effectiveness analysis to support pricing and funding policies for new pharmaceuticals in multi-comparator indications, some of the key aspects of which evolve over time. The framework comprises three core considerations: (1) designing proportionate processes, (2) assessing the costs and benefits of recommending multiple treatment options, and (3) appropriate application of cost-effectiveness analysis 'decision rules' to support recommendations and price negotiations. We highlight that proportionate processes require prioritisation of topics for reassessment to be aligned with clear objectives, the need for full flexibility of decision making at the point of reassessment, and that in some contexts contractual re-specification rather than typical deliberative health technology assessment processes may be more appropriate. We discuss reasons why the recommendation of multiple treatment options rather than a single cost-effective treatment may be appropriate and urge health technology assessment bodies to explicitly address the trade-offs that may be associated with recommending multiple treatments. Finally, we discuss how value-based pricing could be achieved when multiple competitor manufacturers offer confidential discounts.
当前新药品定价和资金投入的方法通常聚焦于针对每种临床适应症对产品做出一次性决策。这可能导致卫生系统有多种选择,但却没有关于如何在这些选择之间进行优先排序的明确信号。这存在一种风险,即随着可用治疗方法、证据和药品价格的演变,临床和患者的选择可能与将资源分配以促进人群健康这一目标不一致。我们提出了一个框架,用于利用成本效益分析来支持针对具有多个对照指标的新药品的定价和资金投入政策,其中一些关键方面会随时间演变。该框架包含三个核心考量因素:(1)设计适当的流程,(2)评估推荐多种治疗方案的成本和效益,以及(3)适当地应用成本效益分析的“决策规则”以支持推荐和价格谈判。我们强调,适当的流程要求重新评估主题的优先排序要与明确的目标相一致,在重新评估时决策要有充分的灵活性,并且在某些情况下,合同重新规定而非典型的审议性卫生技术评估流程可能更为合适。我们讨论了推荐多种治疗方案而非单一的具有成本效益的治疗方案可能合适的原因,并敦促卫生技术评估机构明确解决与推荐多种治疗方案可能相关的权衡问题。最后,我们讨论了当多个竞争制造商提供保密折扣时如何实现基于价值的定价。