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套细胞淋巴瘤新型疗法的排序

英文原题:Sequencing of Novel Therapies for Mantle Cell Lymphoma.

查看英文原题

Sequencing of Novel Therapies for Mantle Cell Lymphoma.

PubMed 2021/11/23(内容时间) Curr Treat Options Oncol Q1 · IF 5.8(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

目前尚无套细胞淋巴瘤(MCL)新型疗法的标准序贯治疗方案。对于初始治疗,我们倾向于年轻、体能良好的患者接受强化诱导化疗,随后行自体干细胞移植并给予利妥昔单抗维持治疗。对于不适合强化化疗的患者,可考虑苯达莫司汀联合利妥昔单抗,或来那度胺联合利妥昔单抗。二线治疗时,我们优先选择布鲁顿酪氨酸激酶(BTK)抑制剂。一旦患者在这些药物治疗期间复发,对符合条件者将进行CAR-T 细胞治疗,通常采用皮质类固醇、来那度胺或维奈克拉作为桥接治疗。对不适合CAR-T 或临床试验的患者,采用维奈克拉、来那度胺或蛋白酶体抑制剂方案;不过,在这一阶段疗效预计有限,后续每一治疗线的应答持续时间可能缩短。对于自体移植和CAR-T 治疗后仍进展的经严格筛选患者,异基因干细胞移植仍是一种选择。目前正在开展将新型药物联合用于较早治疗线的临床试验,具有独特作用机制的新化合物也在研发中。正在进行的新药临床试验结果,将在未来几年进一步改变MCL患者治疗格局。

展开英文摘要原文

There is no standard approach to sequencing novel therapies in mantle cell lymphoma (MCL). For initial treatment, intensive induction chemotherapy followed by autologous stem cell transplant and rituximab maintenance remains our preferred approach in young, fit patients.

We consider bendamustine plus rituximab or lenalidomide plus rituximab in patients who are ineligible for intensive chemotherapy-based approaches. Bruton's tyrosine kinase inhibitors are our preferred class of agents to use in the second-line setting. When patients inevitably relapse on one of these agents, we proceed with chimeric antigen receptor T-cell (CAR T) therapy in eligible patients, often with the use of bridging therapy with corticosteroids, lenalidomide, or venetoclax.

We treat patients who are ineligible for CAR T or clinic trial with venetoclax, lenalidomide, or proteosome inhibitor-based regimens, although efficacy is expected to be limited in this setting with a shortened duration of response to each subsequent line of therapy. Allogeneic stem cell transplant remains an option for carefully selected patients who progress after autologous stem cell transplant and CAR T.

Clinical trials involving combinations of novel agents in early lines of therapy are ongoing, and new compounds with unique mechanisms of action are in development. The results of ongoing clinical trials with novel agents will further change the treatment landscape for patients with MCL in the coming years.

论文信息

作者
Romancik JT、Cohen JB
第一作者单位
Department of Hematology and Medical Oncology, Winship Cancer Institute At Emory University, Atlanta, GA, USA.United States
通讯作者单位
Department of Hematology and Medical Oncology, Winship Cancer Institute At Emory University, Atlanta, GA, USA. jonathon.cohen@emory.edu.United States
文献类型
非美国政府资助研究 · 综述
期刊
Current treatment options in oncology2021 Nov 23
原文标识
PubMed 34812968 · DOI 10.1007/s11864-021-00907-3