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:2026 Update on the Management of Diffuse Large B-Cell Lymphoma.
2026 Update on the Management of Diffuse Large B-Cell Lymphoma.
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弥漫性大B细胞淋巴瘤(DLBCL)是西半球最常见的非霍奇金淋巴瘤(NHL),由生物学特征和临床预后各异的异质性淋巴瘤组成。R-CHP仍是一线治疗基础;适合强化治疗的患者一线方案为泊洛妥珠单抗-R-CHP(pola-R-CHP)或R-CHOP,老年、体弱或不适合强化治疗者可接受R-mini-CHOP或姑息治疗。针对高危疾病的一线试验正通过在R-CHOP中加入新药、采用CAR-T 及双特异性抗体改善结局;老年或不适合强化治疗人群的试验则在减少或省略化疗。依据细胞起源(COO)进行风险适配,并使用中期PET成像或循环肿瘤DNA(ctDNA)指导治疗升级或降级的策略仍在研究中。二线根治性治疗包括CAR-T 或自体干细胞移植,具体取决于一线治疗后疾病进展的时间。复发/难治阶段治疗选择迅速扩展,包括双特异性抗体联合化疗、双特异性抗体联合抗体药物偶联物,以及维布妥昔单抗联合来那度胺和利妥昔单抗。多项新型试验正推动治疗减少对化疗的依赖,涉及靶向药物与抗体联合、新型双特异性抗体及其组合、免疫调节药物和细胞疗法。本综述总结近期数据,并讨论改善DLBCL管理的持续探索。
Diffuse large B-cell lymphoma (DLBCL) is the most common type of NHL in the Western Hemisphere. It comprises a heterogenous group of lymphomas, with different biology and clinical prognoses. R-CHP remains the backbone of therapy, and frontline therapeutic options in fit patients are pola-R-CHP and R-CHOP, whereas elderly or frail/unfit patients may be treated with R-mini-CHOP or palliation. Frontline trials aim to improve outcomes for patients with high-risk disease utilizing R-CHOP + novel agents, CAR-T, and bispecific antibodies. Trials in the elderly/unfit population are minimizing and omitting chemotherapy. Risk-adapted approaches targeting cell of origin (COO) and utilizing interim PET imaging or ctDNA to guide therapy escalation or deescalation remain under investigation.
Second line therapy curative-intent approaches include CAR-T or autologous stem cell transplantation, depending upon timing of disease progression after first-line therapy. In the relapsed/refractory setting, there has been a rapid growth in the therapeutic armamentarium, including bispecific antibody combinations with chemotherapy, bispecific antibodies with antibody-drug conjugates, and brentuximab vedotin + lenalidomide + rituximab.
Multiple novel trials are further advancing the field away from chemotherapy including targeted therapy-antibody combinations, new bispecific antibodies and bispecific antibody combinations, immunomodulatory agents, and cellular therapy. In this review, we summarize recent data and discuss ongoing efforts to improve the management of DLBCL.
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