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:An update on novel multiple myeloma targets.
An update on novel multiple myeloma targets.
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在不久的将来,多发性骨髓瘤将有许多治疗策略可用,挑战在于为每种方法找准定位以实现治愈,同时维持这些患者良好的生活质量。
引言:尽管治疗进展显著改善了结局,多发性骨髓瘤(MM)仍是难治的血液系统疾病,原因在于其生物学异质性和临床复杂性。 综述范围:对所有用于新诊断 MM 的药物类别均难治或耐药的患者,正成为每位血液科医师面临的现实问题。靶向 BCMA 等新分子的下一代免疫疗法(如偶联单克隆抗体、双特异性单克隆抗体和 CAR-T 细胞)在疾病晚期 MM 中已显示出显著疗效。在相同治疗背景下,selinexor 和 melflufen 等小分子也证明有效。目前仍在等待个体化疗法的评估结果;这些疗法针对导致疾病进展的特定基因突变或信号通路。 专家观点:近期将有多种 MM 治疗策略可供选择,挑战在于合理安排各种疗法,以期治愈患者,同时维持良好生活质量。
INTRODUCTION: Despite therapeutic progress, leading to a significant improvement of outcome, multiple myeloma (MM) remains a difficult to treat hematologic disease due to its biological heterogeneity and clinical complexity. AREAS COVERED: Treatment of patients refractory and resistant to all classes of agents used in newly diagnosed MM is becoming a relevant problem for every hematologist.
New generation immunotherapies, such as conjugated mAb, bispecific mAbs and CAR-T cells, targeting novel molecules as BCMA, have showed relevant results in very advanced MM. In the same setting, small molecules, such as selinexor and melflufen, also proved to be effective.
We are currently waiting for the results of under evaluation personalized therapy, directed against specific gene mutations or signaling pathways, responsible for disease progression. EXPERT OPINION: In the near future, many therapeutic strategies will become available for MM and the challenge will be to position each approach in order to cure, maintaining a good quality of life in these patients.
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