Tucker David, Rule Simon
a Department of Haematology , Derriford Hospital , Plymouth , UK.
b Plymouth Hospitals NHS Trust , Plymouth , UK.
Expert Rev Anticancer Ther. 2017 Jun;17(6):491-506. doi: 10.1080/14737140.2017.1328280. Epub 2017 May 17.
Mantle cell lymphoma (MCL) usually takes an aggressive clinical course and carries a poor prognosis. Recently, progress has been made in the treatment of MCL including the development of a number of novel agents which target intracellular pathways and the extracellular microenvironment. These agents have transformed the landscape of available therapeutic options. Areas covered: The current literature on the novel agents which currently hold a licence for the treatment of MCL in the context of front-line therapy and in the relapsed/refractory setting is summarized. In addition, targeted therapies showing promise at an earlier stage of development will also be discussed. A literature search was performed using the terms 'mantle cell lymphoma', 'bortezomib', 'temsirolimus', 'lenalidomide', 'ibrutinib', 'novel agents', 'targeted molecular therapies' and derivations thereof. Expert commentary: In addition to improvements in immunochemotherapy, a succession of new molecular targets and corresponding drugs has revolutionised MCL therapy. The discovery of a novel agent which disrupts external signalling pathways through inhibition of Bruton's tyrosine kinase has been a particularly exciting breakthrough. The best way to sequence and combine these agents with existing regimens and how to overcome the problem of drug resistance represent new challenges in this rapidly developing field.
套细胞淋巴瘤(MCL)通常呈侵袭性临床病程,预后较差。最近,MCL的治疗取得了进展,包括开发了许多靶向细胞内信号通路和细胞外微环境的新型药物。这些药物改变了可用治疗选择的格局。涵盖领域:总结了目前在一线治疗和复发/难治性情况下已获许可用于治疗MCL的新型药物的现有文献。此外,还将讨论在早期开发阶段显示出前景的靶向治疗。使用“套细胞淋巴瘤”、“硼替佐米”、“替西罗莫司”、“来那度胺”、“伊布替尼”、“新型药物”、“靶向分子疗法”及其衍生词进行了文献检索。专家评论:除了免疫化疗的改进外,一系列新的分子靶点和相应药物彻底改变了MCL治疗。通过抑制布鲁顿酪氨酸激酶破坏外部信号通路的新型药物的发现是一个特别令人兴奋的突破。如何将这些药物与现有方案进行排序和联合,以及如何克服耐药性问题,是这个快速发展领域的新挑战。