Onkologische Praxis Oldenburg/Delmenhorst, Oldenburg, Germany.
Onkotrakt AG, Hamburg, Germany.
Future Oncol. 2020 May;16(15):1001-1012. doi: 10.2217/fon-2020-0180. Epub 2020 Apr 14.
Present real-world data for rituximab (biosimilar and reference)-containing regimens in extrapolated indications in non-Hodgkin lymphoma (NHL)/chronic lymphocytic leukemia (CLL). Data collected from office-based oncologic practices in Germany (July 2017-June 2019). Of 1741 patients, 1241 had NHL; 500 had CLL. Of 7595 therapy cycles, 28.3% used reference rituximab; 55.2% used rituximab biosimilars; 2.0% used subcutaneous rituximab; 14.5% used rituximab, not otherwise specified. Rituximab biosimilars were used across all indications; 57.3% of cycles were administered in extrapolated indications. Over 24 months, the proportion of rituximab prescriptions that were for biosimilars increased from 12.0 to 83.0%. Our real-world data in NHL and CLL depicts increasing use of rituximab biosimilars across multiple treatment protocols, including extrapolated indications.
提供利妥昔单抗(生物类似药和参照药)在非霍奇金淋巴瘤(NHL)/慢性淋巴细胞白血病(CLL)的扩展适应证中的真实世界数据。数据来自德国的基于办公室的肿瘤学实践(2017 年 7 月至 2019 年 6 月)。1741 例患者中,1241 例患有 NHL;500 例患有 CLL。在 7595 个治疗周期中,28.3%使用参照利妥昔单抗;55.2%使用利妥昔单抗生物类似药;2.0%使用皮下利妥昔单抗;14.5%使用未特指的利妥昔单抗。利妥昔单抗生物类似药用于所有适应证;57.3%的周期在扩展适应证中使用。在 24 个月内,生物类似药的利妥昔单抗处方比例从 12.0%增加到 83.0%。我们在 NHL 和 CLL 的真实世界数据表明,利妥昔单抗生物类似药在多种治疗方案中的使用不断增加,包括扩展适应证。