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:The changing landscape of relapsed and/or refractory multiple myeloma (MM): fundamentals and controversies.
The changing landscape of relapsed and/or refractory multiple myeloma (MM): fundamentals and controversies.
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新诊断及复发/难治性多发性骨髓瘤(RRMM)的治疗选择不断增加,拓宽了临床治疗格局,也使病情和决策复杂到目前尚无任何一种算法能够全面涵盖。患者在进入复发/难治阶段前可能经历多种临床过程,例如原发难治、完成采用新一代药物的一线治疗后早期复发,或在化疗、接受自体移植后很晚才复发,这进一步增加了临床复杂性。还应注意,主要随机临床试验(RCT)并未充分涵盖许多患者类型,因此治疗决策更加困难。对于RRMM患者,与多发性骨髓瘤本身的不良生物学特征相比,既往未使用药物的选择,以及疾病进展前既往治疗方案的数量和持续时间,对疗效的影响更大。除蛋白酶体抑制剂、免疫调节药物、抗CD38抗体和皮质类固醇外,近年来还开发了新一代药物,包括XPO抑制剂、BCL-2抑制剂、新型烷化剂,尤其是基于抗BCMA抗体偶联药物和CAR-T 细胞的免疫疗法,以治疗RRMM。本综述全面讨论RRMM的基本问题与争议,并阐述其管理和治疗的主要方面,包括临床情境的复杂性、选择适当治疗前或决定治疗时需要考虑的关键因素;与既往标准一线方案不存在交叉耐药的新药,以及相关的主要Ⅲ期临床试验;未来展望(包括重新评估已弃用治疗手段的价值);以及RRMM临床管理中的争议。
The increase in the number of therapeutic alternatives for both newly diagnosed and relapsed/refractory multiple myeloma (RRMM) patients has widened the clinical scenario, leading to a level of complexity that no algorithm has been able to cover up to date. At present, this complexity increases due to the wide variety of clinical situations found in MM patients before they reach the status of relapsed/refractory disease. These different backgrounds may include primary refractoriness, early relapse after completion of first-line therapy with latest-generation agents, or very late relapse after chemotherapy or autologous transplantation.
It is also important to bear in mind that many patient profiles are not fully represented in the main randomized clinical trials (RCT), and this further complicates treatment decision-making. In RRMM patients, the choice of previously unused drugs and the number and duration of previous therapeutic regimens until progression has a greater impact on treatment efficacy than the adverse biological characteristics of MM itself.
In addition to proteasome inhibitors, immunomodulatory drugs, anti-CD38 antibodies and corticosteroids, a new generation of drugs such as XPO inhibitors, BCL-2 inhibitors, new alkylators and, above all, immunotherapy based on conjugated anti-BCMA antibodies and CAR-T cells, have been developed to fight RRMM. This comprehensive review addresses the fundamentals and controversies regarding RRMM, and discusses the main aspects of management and treatment.
The basis for the clinical management of RRMM (complexity of clinical scenarios, key factors to consider before choosing an appropriate treatment, or when to treat), the arsenal of new drugs with no cross resistance with previously administered standard first line regimens (main phase 3 clinical trials), the future outlook including the usefulness of abandoned resources, together with the controversies surrounding the clinical management of RRMM patients will be reviewed in detail.
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