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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Antibody-drug conjugates, bispecific antibodies and CAR-T cells therapy in multiple myeloma.
Antibody-drug conjugates, bispecific antibodies and CAR-T cells therapy in multiple myeloma.
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引言:现代免疫疗法正革新复发/难治性(RR)多发性骨髓瘤(MM)患者的治疗格局,为实现深度缓解和延长生存带来机会。综述范围:抗体药物偶联物(ADC)及 T 细胞重定向疗法,包括双特异性抗体(BsAb)和嵌合抗原受体(CAR)T 细胞疗法,近期已用于 RRMM 治疗。部分药物已获监管批准,更新型构建体、新联合方案及更早治疗线中的应用仍在探索。本综述讨论 ADC、BsAb 和 CAR-T 细胞免疫疗法的现状及潜在发展。专家观点:ADC、BsAb 和 CAR-T 疗法在既往接受大量治疗、暴露于三类药物(TCE)的 MM 患者中均显示出显著活性;T 细胞重定向疗法已成为三线(欧洲药品管理局,EMA)或四线(美国食品药品监督管理局,FDA)治疗后的新标准。三类免疫疗法各有利弊,其可及性不同,并带来需要妥善管理的新毒性。多项正在进行的研究项目包括联合治疗及向更早治疗线拓展,同时开发新药或新构建体,以提高效力、降低毒性并简化给药。治疗顺序仍是一项挑战,现有数据有限,耐药机制也尚待阐明。
INTRODUCTION: Modern immunotherapy approaches are revolutionizing the treatment scenario of relapsed/refractory (RR) multiple myeloma (MM) patients, providing an opportunity to reach deep level of responses and extend survival outcomes. AREAS COVERED: Antibody-drug conjugates (ADCs) and T-cell redirecting treatments, including bispecific antibodies (BsAbs) and chimeric antigen receptor (CAR) T cells therapy, have been recently introduced in the treatment of RRMM. Some agents have already received regulatory approval, while newer constructs, novel combinations, and applications in earlier lines of therapy are currently being explored. This review discusses the current landscape and possible development of ADCs, BsAbs and CAR-T cells immunotherapies.
EXPERT OPINION: ADCs, BsAbs, and CAR-T therapy have demonstrated substantial activity in heavily pretreated, triple-class exposed (TCE) MM patients, and T-cell redirecting treatments represent new standards of care after third (European Medicines Agency, EMA), or fourth (Food and Drug Administration, FDA), line of therapy. All these three immunotherapies carry advantages and disadvantages, with different accessibility and new toxicities that require appropriate management and guidelines.
Multiple on-going programs include combinations therapies and applications in earlier lines of treatment, as well as the development of novel agents or construct to enhance potency, reduce toxicity and facilitate administration. Sequencing is a challenge, with few data available and mechanisms of resistance still to be unraveled.
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