CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Management of marginal zone lymphomas.
Management of marginal zone lymphomas.
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边缘区淋巴瘤(MZL)约占B细胞非霍奇金淋巴瘤的7%,包括3种不同的亚型——即结外(EMZL)、结内和脾(SMZL)。初始评估需要根据器官相关特点进行特定的诊断和分期程序。特别是,尽管正电子发射断层扫描/计算机断层扫描最初不被推荐,但近期数据重新评估了其在MZL常规分期中的作用,尤其是在仅计划局部治疗或怀疑组织学转化时。近期研究结果改善了MZL患者的风险分层,突出了前线治疗后早期进展与更差总生存期之间的关联。相当一部分MZL病例可能与特定细菌(即胃EMZL中的幽门螺杆菌)或病毒感染(丙型肝炎病毒)相关,在疾病早期阶段,不同比例的患者可能对抗感染治疗有应答。受累部位放疗在不可接受或对抗感染治疗无应答的局限性EMZL管理中具有核心作用。尽管基于利妥昔单抗的治疗(晚期EMZL中的苯达莫司汀-利妥昔单抗或SMZL中的利妥昔单抗单药治疗)已显示出良好结果,但当前的治疗格局预计将迅速改变,因为新兴的新型药物,尤其是布鲁顿酪氨酸激酶抑制剂,已显示出有前景的疗效和安全性特征,促使其在复发 setting 中获得批准。
此外,多种新型药物(磷脂酰肌醇3-激酶抑制剂、CAR-T 细胞、双特异性抗体)正在MZL患者中进行测试,初步结果令人鼓舞。
Marginal zone lymphomas (MZLs) represent about 7% of B-cell non-Hodgkin lymphomas and include 3 different subtypes-namely, extranodal (EMZL), nodal, and splenic (SMZL). The initial assessment requires specific diagnostic and staging procedures depending on organ-related peculiarities. In particular, although positron emission tomography/computed tomography was not initially recommended, recent data have reassessed its role in the routine staging of MZL, especially when only localized treatment is planned or there is a suspicion of histologic transformation. Recent findings have improved the risk stratification of MZL patients, highlighting the association of early progression after frontline therapy with worse overall survival.
A significant fraction of MZL cases may be related to specific bacterial (ie, Helicobacter pylori in gastric EMZL) or viral infections (hepatis C virus), and in the earlier phases of disease, a variable percentage of patients may respond to anti-infective therapy. Involved-site radiotherapy has a central role in the management of localized EMZL not amenable to or not responding to anti-infective therapy.
Although rituximab-based treatments (bendamustine- rituximab in advanced EMZL or rituximab monotherapy in SMZL) have demonstrated favorable results, the current therapeutic scenario is predicted to rapidly change as emerging novel agents, especially Bruton's tyrosine kinase inhibitors, have demonstrated promising efficacy and safety profiles, leading to their approval in the relapsed setting.
Moreover, a large variety of novel agents (phosphatidylinositol 3-kinase inhibitors, chimeric antigen receptor T-cells, bispecific antibodies) are being tested in MZL patients with encouraging preliminary results.
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