Hamad Anas, AbdulAziz Omar, Abu Tabar Osama, Al Balushi Sara, Alblooshi Sana, Alfar Mohamad, Dawoud Eren, Khan Fahmeeda, Nabeel Abdulrahman, Sayam Wael, ElSheashaey Ahmad
Pharmacy Department National Center for Cancer Care & Research, Hamad Medical Corporation, Doha, Qatar.
College of Pharmacy, QU Health Sector, Qatar University, Doha, Qatar.
J Health Econ Outcomes Res. 2025 Jul 18;12(2):21-26. doi: 10.36469/001c.140955. eCollection 2025.
Cancer remains a leading global health challenge, with high mortality rates and increasing financial burdens on healthcare systems. In the Gulf Cooperation Council countries, generic oncology medications offer a cost-effective alternative to patented treatments. However, disparities in regulatory frameworks and concerns about quality and supply reliability hinder their widespread adoption. Addressing these challenges is crucial to ensuring optimal access to oncology treatments. This study employed multicriteria decision analysis to evaluate key factors influencing the selection of off-patent oncology drugs. A structured survey was conducted among 10 formulary management experts from the United Arab Emirates, Qatar, Kuwait, Bahrain, and Oman. Participants engaged in a 3-hour workshop to assess and prioritize critical decision-making criteria through guided discussions, case studies, and weighting surveys. The analysis identified manufacturing quality (30.8%), cost (20%), and use in reference countries (14.6%) as the most critical factors in selecting generic oncology mediations. Supply reliability (13%), regulatory aspects (8%), and pharmacovigilance services and extra services (6.8% each) also played supporting roles. The structured evaluation framework developed through this study provides insights into the factors shaping formulary decisions in the Gulf Cooperation Council region and highlights areas requiring regulatory and logistical improvements. This expert consensus underscores the need for a balanced approach that ensures quality, affordability, and accessibility in adopting oncology generics. Strengthening regulatory frameworks, improving pharmacovigilance, and enhancing stakeholder education are essential steps to optimizing the integration of oncology drugs into regional healthcare systems. These findings provide a foundation for policy recommendations aimed at improving generic drug adoption and patient outcomes in oncology care.
癌症仍然是一项重大的全球健康挑战,死亡率高,给医疗系统带来日益沉重的经济负担。在海湾合作委员会国家,非专利肿瘤药物为专利治疗提供了一种具有成本效益的替代方案。然而,监管框架的差异以及对质量和供应可靠性的担忧阻碍了它们的广泛采用。应对这些挑战对于确保肿瘤治疗的最佳可及性至关重要。本研究采用多标准决策分析来评估影响非专利肿瘤药物选择的关键因素。对来自阿拉伯联合酋长国、卡塔尔、科威特、巴林和阿曼的10名处方集管理专家进行了结构化调查。参与者参加了一个为期3小时的研讨会,通过引导讨论、案例研究和权重调查来评估关键决策标准并确定其优先级。分析确定生产质量(30.8%)、成本(20%)和在参考国家的使用情况(14.6%)是选择非专利肿瘤药物的最关键因素。供应可靠性(13%)、监管方面(8%)以及药物警戒服务和额外服务(各6.8%)也起到了辅助作用。通过本研究开发的结构化评估框架深入了解了塑造海湾合作委员会地区处方集决策的因素,并突出了需要监管和后勤改进的领域。这一共识强调了采取平衡方法的必要性,以确保在采用肿瘤仿制药时的质量、可承受性和可及性。加强监管框架、改善药物警戒以及加强利益相关者教育是优化肿瘤药物融入区域医疗系统的关键步骤。这些发现为旨在改善肿瘤护理中仿制药采用和患者治疗效果的政策建议奠定了基础。