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:Treatment Strategy for Multiple Myeloma to Improve Immunological Environment and Maintain MRD Negativity.
Treatment Strategy for Multiple Myeloma to Improve Immunological Environment and Maintain MRD Negativity.
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改善免疫环境和清除微小残留病(MRD)是多发性骨髓瘤(MM)患者获得长期生存的两大主要治疗目标。免疫调节药物(IMiD)、单克隆抗体药物(MoAb)以及自体干细胞移植(ASCT)所用的自体移植物,均可改善免疫微环境。ASCT、MoAb和蛋白酶体抑制剂(PI)可能有助于实现MRD阴性。免疫环境改善可能有助于维持MRD阴性,但目前尚无专门针对持续MRD阴性的治疗方案。若MRD持续阳性,是否继续或更换当前治疗仍存在争议。在这种情况下,可能需要对残留骨髓瘤细胞进行遗传学、免疫表型和临床特征分析,以选择有效治疗。本综述依据当前可用疗法,包括IMiD、PI、MoAb和ASCT,以及CAR-T 细胞等预期免疫疗法,讨论如何通过改善免疫环境和维持MRD阴性制定MM“治愈”策略。
Improving the immunological environment and eradicating minimal residual disease (MRD) are the two main treatment goals for long-term survival in patients with multiple myeloma (MM). Immunomodulatory drugs (IMiDs), monoclonal antibody drugs (MoAbs), and autologous grafts for autologous stem cell transplantation (ASCT) can improve the immunological microenvironment.
ASCT, MoAbs, and proteasome inhibitors (PIs) may be important for the achievement of MRD negativity. An improved immunological environment may be useful for maintaining MRD negativity, although the specific treatment for persistent MRD negativity is unknown.
However, whether the ongoing treatment should be continued or changed if the MRD status remains positive is controversial. In this case, genetic, immunophenotypic, and clinical analysis of residual myeloma cells may be necessary to select the effective treatment for the residual myeloma cells.
The purpose of this review is to discuss the MM treatment strategy to "cure MM" based on currently available therapies, including IMiDs, PIs, MoAbs, and ASCT, and expected immunotherapies, such as chimeric antigen receptor T cell (CAR-T) therapy, via improvement of the immunological environment and maintenance of MRD negativity.
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