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利妥昔单抗:20 年临床应用后的 13 个开放性问题。

Rituximab: 13 open questions after 20years of clinical use.

机构信息

Oncology Institute of Southern Switzerland, Ospedale San Giovanni, 6500 Bellinzona, Switzerland.

Oncology Institute of Southern Switzerland, Ospedale San Giovanni, 6500 Bellinzona, Switzerland.

出版信息

Cancer Treat Rev. 2017 Feb;53:38-46. doi: 10.1016/j.ctrv.2016.11.015. Epub 2016 Dec 22.

Abstract

Rituximab improved the prognosis of all B-cell derived lymphoproliferative diseases, but despite 20years of intensive use, it remains a drug with a number of still obscure characteristics and unanswered questions. These include the mechanism of action and of resistance, the optimal schedule, the interaction with chemotherapy, as well as predictive factors for response rate and duration. Despite being very well tolerated, the question of its long term side effects and the risks of the administration near to a pregnancy have only recently been addressed. Also the indications are still not all clear: rituximab induces remissions as a single agent and improves the effect of chemotherapy, but its use as maintenance or as a substitute for watch and wait is still debated. Also, it is still unclear if its efficacy derives at least partly by reducing the risk of histological transformation in indolent NHL and reducing the risk of CNS relapse in aggressive NHL. Finally, despite of 20years of research, it is still unclear if rituximab can be efficiently substituted by biosimilars or new anti-CD20 antibodies. In this review we address all these questions and analyze the literature addressing these aspects.

摘要

利妥昔单抗改善了所有 B 细胞来源的淋巴增殖性疾病的预后,但尽管已经使用了 20 年,它仍然是一种具有许多仍不明确的特征和未解决问题的药物。这些问题包括作用机制和耐药机制、最佳方案、与化疗的相互作用,以及反应率和持续时间的预测因素。尽管利妥昔单抗具有很好的耐受性,但关于其长期副作用和在接近妊娠时使用的风险问题,直到最近才得到解决。此外,适应证也并非完全明确:利妥昔单抗作为单一药物诱导缓解,并提高化疗效果,但作为维持治疗或替代观察和等待的方法仍存在争议。此外,其疗效是否至少部分归因于降低惰性 NHL 组织学转化的风险和降低侵袭性 NHL 中枢神经系统复发的风险,目前仍不清楚。最后,尽管已经进行了 20 年的研究,但利妥昔单抗是否可以被生物类似物或新型抗 CD20 抗体有效地替代,目前仍不清楚。在这篇综述中,我们将讨论所有这些问题,并分析涉及这些方面的文献。

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