Hospital Pharmacy Unit, Trento General Hospital, Autonomous Province of Trento, Trento, Italy.
School of Hospital Pharmacy, University of Sassari, Sassari, Italy.
Sci Rep. 2021 Mar 16;11(1):5956. doi: 10.1038/s41598-021-85563-1.
Comparable clinical efficacy and safety of the reference rituximab (MABTHERA) and its biosimilars has been established in randomized trials. However, safety concerns are often raised when switching from reference to biosimilar products and between different biosimilars. In this prospective observational study we aimed at evaluating the safety of switching between reference and biosimilar rituximab (TRUXIMA and RIXATHON) at Trento General Hospital (Italy). All patients (n = 83) with Non Hodgkin's Lymphoma (NHL, n = 72) and Chronic Lymphocytic Leukemia (CLL, n = 11) who received rituximab between March 2018 and March 2019 were asked to take part in the study. In 2017 and 2018 two tenders were carried out and two different biosimilars became available in the hospital, these were used sequentially. Thus, patients with or without previous treatments with the originator rituximab either received a biosimilar or were switched between different biosimilars. The incidence of adverse events in these groups of patients is described. The study population received 465 rituximab infusions and all received biosimilars. Fifty patients (60%) experienced at least one switch between different biosimilars or between rituximab originator and biosimilar, whereas 33 (40%) received one of the two biosimilars and one patient received reference rituximab. Adverse events (n = 146) were reported in 71 patients (84.5%). Treatment-related grade 3-4 events were reported in 5 patients (5.9%), whereas grade 1 rituximab related infusion events were observed in 6 patients (7.1%). No safety signal emerged in association with the use of a specific biosimilar nor with the practice of switching. Adverse events were similar, in terms of seriousness and frequency, to those described in the literature, providing further support to the clinical safety of rituximab biosimilars.
在随机试验中已经证实了参考利妥昔单抗(美罗华)及其生物类似药具有可比拟的临床疗效和安全性。然而,当从参考药物切换到生物类似药产品以及在不同的生物类似药之间切换时,常常会引发安全性方面的担忧。在这项前瞻性观察性研究中,我们旨在评估特伦托综合医院(意大利)在参考药物和生物类似药(曲妥珠单抗和里妥昔单抗)之间切换的安全性。所有接受利妥昔单抗治疗的非霍奇金淋巴瘤(NHL,n=72)和慢性淋巴细胞白血病(CLL,n=11)患者(n=83)均被要求参与该研究。2017 年和 2018 年进行了两次招标,医院中提供了两种不同的生物类似药,这些药物被依次使用。因此,有或没有先前接受过利妥昔单抗治疗的患者接受了生物类似药或在不同的生物类似药之间进行了切换。描述了这些患者群体中不良事件的发生率。研究人群接受了 465 次利妥昔单抗输注,所有患者均接受了生物类似药治疗。50 名患者(60%)经历了至少一次不同生物类似药之间或利妥昔单抗原研药和生物类似药之间的切换,而 33 名患者(40%)接受了其中一种生物类似药,1 名患者接受了参考利妥昔单抗。71 名患者(84.5%)报告了 146 次不良事件。报告了 5 名患者(5.9%)发生治疗相关的 3-4 级事件,而 6 名患者(7.1%)观察到 1 级利妥昔单抗相关输注事件。与使用特定生物类似药或切换实践相关的安全性信号未出现。不良事件在严重程度和频率方面与文献中描述的相似,为利妥昔单抗生物类似药的临床安全性提供了进一步支持。