Clinical Hematology Oncology and HCT, Tata Medical Center, Kolkata, India.
Hemato-Oncology and Stem Cell Transplant, Apollo Hospitals, Hyderabad, India.
Cancer Rep (Hoboken). 2022 Jul;5(7):e1590. doi: 10.1002/cnr2.1590. Epub 2021 Nov 24.
Mantle cell lymphoma (MCL) is a rare type of mature B-cell lymphoid malignancy with the pathologic hallmark of translocation t(11;14) (q13, q32), which leads to an overexpression of Cyclin D1 (CCND1). The disease is also characterized by the presence of a high number of recurrent genetic alterations, which include aberrations in several cellular pathways. MCL is a heterogeneous disease with a wide range of clinical presentations and a majority presenting with aggressive disease in advanced stages.
Management of MCL is bereft with challenges due to its resistant and relapsing pattern. Despite improvements in remission durations, the disease is currently incurable with standard therapy and has a median survival of about 3-5 years. The use of small molecules like the bruton tyrosine kinase (BTK) and BCL2 inhibitors, for treating relapsed MCL has been established leading to a diminishing role for conventional chemotherapy. Combinations of small molecule inhibitors with or without chemoimmunotherapy, are showing promising results. Cellular therapy in the form of CAR-T cell therapy, has been approved recently.
Personalized cancer treatment and chemo-free regimens are showing promise and results from well-planned long-term studies are evolving. In India, there is a paucity of epidemiological, clinical, and research data in this field.
套细胞淋巴瘤(MCL)是一种罕见的成熟 B 细胞淋巴恶性肿瘤,其病理特征为易位 t(11;14)(q13,q32),导致 Cyclin D1(CCND1)过度表达。该疾病还以存在大量复发性遗传改变为特征,包括几个细胞通路的异常。MCL 是一种异质性疾病,临床表现广泛,大多数在晚期表现为侵袭性疾病。
由于其耐药和复发模式,MCL 的治疗充满挑战。尽管缓解持续时间有所改善,但目前标准疗法无法治愈该疾病,中位生存期约为 3-5 年。已证实使用小分子如布鲁顿酪氨酸激酶(BTK)和 BCL2 抑制剂治疗复发性 MCL 可减少常规化疗的作用。小分子抑制剂联合或不联合化疗免疫治疗的组合正在显示出有希望的结果。嵌合抗原受体 T 细胞疗法(CAR-T 细胞疗法)最近已获得批准。
个性化癌症治疗和无化疗方案显示出希望,来自精心设计的长期研究的结果正在不断发展。在印度,该领域的流行病学、临床和研究数据匮乏。