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Barriers to the Use of Trastuzumab for HER2+ Breast Cancer and the Potential Impact of Biosimilars: A Physician Survey in the United States and Emerging Markets

机译:使用曲妥珠单抗治疗HER2 +乳腺癌的障碍和生物仿制药的潜在影响:美国和新兴市场的医师调查

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摘要

Trastuzumab in combination with chemotherapy has become a standard of care for patients with HER2+ breast cancer. The cost of therapy, however, can limit patient access to trastuzumab in areas with limited financial resources for treatment reimbursement. This study examined access to trastuzumab and identified potential barriers to its use in the United States, Mexico, Turkey, Russia and Brazil via physician survey. The study also investigated if the availability of a biosimilar to trastuzumab would improve access to and use of HER2 monoclonal antibody therapy. Across all countries, a subset of oncologists reported barriers to the use of trastuzumab in a neoadjuvant, adjuvant or metastatic setting. Common barriers to the use of trastuzumab included issues related to insurance coverage, drug availability and cost to the patient. Overall, nearly half of oncologists reported that they would increase the use of HER2 monoclonal antibody therapy across all treatment settings if a lower cost biosimilar to trastuzumab were available. We conclude that the introduction of a biosimilar to trastuzumab may alleviate cost-related barriers to treatment and could increase patient access to HER2-directed therapy in all countries examined.
机译:曲妥珠单抗联合化疗已成为HER2 +乳腺癌患者的标准治疗方法。但是,治疗费用可能会限制患者在治疗报销的财政资源有限的地区使用曲妥珠单抗。这项研究检查了曲妥珠单抗的可及性,并通过医师调查确定了在美国,墨西哥,土耳其,俄罗斯和巴西使用曲妥珠单抗的潜在障碍。该研究还调查了曲妥珠单抗生物仿制药的可用性是否会改善HER2单克隆抗体疗法的获取和使用。在所有国家/地区,一部分肿瘤学家报告说在新辅助,辅助或转移性环境中使用曲妥珠单抗存在障碍。使用曲妥珠单抗的常见障碍包括与保险范围,药物供应和患者费用有关的问题。总体而言,近一半的肿瘤学家报告说,如果可获得与曲妥珠单抗相比成本更低的生物仿制药,他们将在所有治疗环境中增加HER2单克隆抗体疗法的使用。我们得出的结论是,在所有接受研究的国家/地区,将曲妥珠单抗生物仿制药的引入可能减轻与成本相关的治疗障碍,并可能增加患者获得HER2导向治疗的机会。

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