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:Novel Treatment Options for Multiple Myeloma.
Novel Treatment Options for Multiple Myeloma.
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。
多发性骨髓瘤(MM)是美国第二常见的血液系统恶性肿瘤,其特征是缓解与复发的反复循环,且每线治疗后对治疗的耐药性不断增加。尽管 MM 几乎无法治愈,但近期的治疗突破已从根本上重塑了其治疗格局。本综述探讨了不断演变的诊疗范式,涵盖从新诊断 MM 到复发/难治性疾病。在一线治疗中,治疗策略已从传统上强调自体干细胞移植资格转向基于患者是否适合四联疗法的更广泛分类。在复发/难治性治疗中,新型免疫疗法,包括CAR-T 细胞疗法和双特异性抗体,已彻底改变了治疗方式,为既往选择有限的患者带来了新希望。精准医学在 MM 治疗中发挥着日益重要的作用,venetoclax 在 t(11;14) 易位患者中显示出显著疗效,推动了该亚组的靶向治疗。在未来,研究性 CAR-T 产品和 cereblon E3 连接酶调节剂,如 mezigdomide 和 iberdomide,可能比当前疗法提供更快、更持久的缓解。
此外,belantamab mafodotin,一种于 2022 年从美国市场撤出的抗体药物偶联物,在近期随机试验取得积极结果后即将重新获批。虽然这些疗法具有显著潜力,但在管理毒性、确保治疗可及性和优化序贯策略方面仍存在挑战。随着治疗手段的扩展,制定兼顾疗效与生活质量的个体化 MM 治疗计划变得更加必要。
Multiple myeloma (MM), the second most common hematologic malignancy in the United States, is characterized by repeated cycles of remission and relapse, with increasing resistance to treatment after each line of therapy. Despite the virtually incurable nature of MM, recent therapeutic breakthroughs have fundamentally reshaped its treatment landscape. This review explores evolving care paradigms, spanning from newly diagnosed MM to relapsed or refractory disease. In the frontline setting, treatment strategies have shifted beyond their traditional emphasis on autologous stem-cell transplant eligibility to a broader categorization of patients on the basis of their suitability for quadruplet therapy.
In the relapsed/refractory setting, novel immunotherapies, including chimeric antigen receptor T-cell (CAR-T) therapies and bispecific antibodies, have revolutionized treatment, offering new hope for patients with previously limited options.
Precision medicine is playing a growing role in MM treatment, with venetoclax showing significant efficacy in patients with t(11;14) translocation, advancing targeted therapy for this subgroup. On the horizon, investigational CAR-T products and cereblon E3 ligase modulators, such as mezigdomide and iberdomide, may provide faster, more durable responses compared with current therapies.
In addition, belantamab mafodotin, an antibody-drug conjugate withdrawn from the US market in 2022, is on the verge of reapproval after positive results from recent randomized trials. While these therapies offer significant potential, challenges remain in managing toxicity, ensuring treatment accessibility, and optimizing sequencing strategies. As the therapeutic arsenal expands, the need for personalized MM treatment plans that balance efficacy with quality of life becomes even more essential.
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