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:Anti-BCMA CAR-T cell-based therapies and bispecific antibodies in the immunotherapy era: are we ready for this?
Anti-BCMA CAR-T cell-based therapies and bispecific antibodies in the immunotherapy era: are we ready for this?
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CAR-T 与 BsAb 抗 BCMA 策略是针对 MM 的突破性疗法。
引言:近几十年来,多发性骨髓瘤(MM)的治疗策略发生了显著演进,治疗领域取得前所未有的成果,近期新型药物也被纳入抗骨髓瘤治疗体系。综述范围:BCMA 是 MM 最具前景的靶点之一,目前已获批或正在积极研究的免疫疗法,正清楚显示出相较标准方案的更大潜力。在此背景下,基于嵌合抗原受体(CAR)工程化 T 细胞和双特异性抗体(BsAb)的免疫疗法已成为焦点,并在临床试验中取得最令人鼓舞的结果。本综述聚焦 BsAb 和 CAR-T 的当前格局,总结最新进展及可能的未来发展。专家观点:抗 BCMA CAR-T 和 BsAb 策略是治疗 MM 的突破性疗法。然而,由于存在相关局限,其纳入临床实践仍令人担忧,本文对此进行了讨论。当前应集中努力,为每位患者制定个体化方案并选择最适合的治疗,同时探索如何联合或序贯应用这些疗法,以提高疗效并尽量降低毒性,尤其是对治疗选择有限的患者。
INTRODUCTION: Therapeutic strategies against multiple myeloma (MM) have evolved dramatically in recent decades, with unprecedent results in the treatment landscape, culminating in the recent incorporation of novel agents in the anti-myeloma armamentarium. AREAS COVERED: BCMA represents one of the most promising targets in MM and currently available immune approaches, either approved or under active investigation, are clearly showing their greater potential over standard regimens.
In this context, immunotherapies based on chimeric antigen receptor (CAR)-engineered T-cells and bispecific antibodies (BsAbs) have taken center stage, being the ones that are yielding the most promising results in clinical trials. This review focuses on the current landscape of BsAbs and CAR-T, summarizing the latest advances and possible future developments. EXPERT OPINION: CAR-T and BsAbs anti-BCMA strategies represent breakthrough therapies against MM.
However, their inclusion in clinical practice is almost feared, due to the associated limitations, some of which have been addressed here. Meanwhile, all the efforts should be focused on individualizing and choosing the most suitable candidates for each treatment and to understand how to combine, or sequence, these therapies to improve efficacy and minimize toxicity, especially for those patients with limited available treatment options.
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