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复发/难治性套细胞淋巴瘤的治疗选择。

Therapeutic options for relapsed/refractory mantle cell lymphoma.

机构信息

Haematology and Cancer Centre, Oxford University Hospitals National Health Service (NHS) Foundation Trust, Oxford, United Kingdom.

Department of Haematology, Sir Charles Gairdner Hospital, Perth, WA, Australia.

出版信息

Blood. 2022 Feb 3;139(5):666-677. doi: 10.1182/blood.2021013326.

Abstract

Mantle cell lymphoma (MCL) is an uncommon subtype of non-Hodgkin lymphoma in which immunochemotherapy, with or without high-dose therapy, and autologous stem cell transplantation remain standard frontline therapies. Despite their clear efficacy, patients inevitably relapse and require subsequent therapy. In this review, we discuss the key therapeutic approaches in the management of relapsed MCL, covering in depth the data supporting the use of covalent Bruton tyrosine kinase (BTK) inhibitors at first or subsequent relapse. We describe the outcomes of patients progressing through BTK inhibitors and discuss the mechanisms of covalent BTKi resistance and treatment options after covalent treatment with BTKi. Options in this setting may depend on treatment availability, patient's and physician's preference, and the patient's age and comorbidity status. We discuss the rapid recent development of anti-CD19 chimeric antigen receptor T-cell therapy, as well as the utility of allogenic stem cell transplantation and novel therapies, such as noncovalent, reversible BTK inhibitors; ROR1 antibody drug conjugates; and bispecific antibodies.

摘要

套细胞淋巴瘤(MCL)是非霍奇金淋巴瘤的一种罕见亚型,免疫化疗联合或不联合大剂量化疗和自体干细胞移植仍然是标准的一线治疗方法。尽管这些方法具有明显的疗效,但患者不可避免地会复发,需要后续治疗。在这篇综述中,我们讨论了复发性 MCL 管理中的关键治疗方法,深入探讨了支持在首次或后续复发时使用共价布鲁顿酪氨酸激酶(BTK)抑制剂的数据。我们描述了经 BTK 抑制剂治疗后进展的患者的结局,并讨论了共价 BTKi 耐药的机制和 BTKi 共价治疗后的治疗选择。在这种情况下的选择可能取决于治疗的可及性、患者和医生的偏好以及患者的年龄和合并症状况。我们讨论了抗 CD19 嵌合抗原受体 T 细胞治疗的快速发展,以及同种异体干细胞移植和新型疗法的效用,如非共价、可逆 BTK 抑制剂、ROR1 抗体药物偶联物和双特异性抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c90/9710495/17da9f3a2562/grabsf1.jpg

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