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:'Le Roi est mort, vive le Roi': New Roles of Radiotherapy in the Treatment of Lymphomas in Combination With Immunotherapy.
'Le Roi est mort, vive le Roi': New Roles of Radiotherapy in the Treatment of Lymphomas in Combination With Immunotherapy.
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本综述的结果需要在更大规模、最好为前瞻性和随机队列中评估 RT 与免疫治疗的联合应用,以确认这些初步的显著疗效。RT 的最佳剂量、分割方式和时机仍有待明确。
免疫治疗(IT),包括检查点抑制剂(CIs)和CAR-T 细胞疗法(CAR-T),彻底改变了复发/难治性(r/r)淋巴瘤的治疗。若干初步经验评估了放疗与IT的同步给药。
我们进行了一项截至2020年3月30日的当前文献的系统综述。共检索到1090条记录,根据标题和摘要选择了42篇文章,在剔除无原始数据或临床信息不足的分析后,最终纳入28篇论文进行综述。
既往研究多为病例报告/系列或小型队列。尽管如此,放疗与 CIs 或 CAR-T 联合治疗带来了有希望的结果,完全缓解率极高,与近期临床试验数据相比,改善了无进展生存期和总生存期。RT 与 CIs 联合治疗具有可接受的毒性特征,未报告严重副作用。在所检索到的小型队列的局限范围内,与全身治疗相比,RT 似乎是作为 CAR-T“桥接”的更优选择,并且也可能降低严重并发症发生率。放疗可引发针对淋巴瘤的免疫反应,这已由多例远隔效应及其被纳入抗肿瘤疫苗方案所证明。
immunotherapy (IT), including checkpoint inhibitors (CIs) and Chimeric Antigen Receptor T cell therapy (CAR-T) revolutionized the treatment of relapsing or refractory (r/r) lymphoma. Several preliminary experiences evaluated concomitant administration of radiotherapy and IT.
we performed a systematic review of current literature as of March 30, 2020. A total of 1090 records was retrieved, 42 articles were selected on the basis of title and abstract and, after the removal of analyses with no original data or insufficient clinical information, 28 papers were included in the review.
previous studies were mostly represented by case reports/series or small cohorts. Nonetheless, combination of radiotherapy and CIs or CAR-T led to promising outcomes, resulting in extremely high rates of complete response and improving progression free and overall survival compared with data from recent clinical trials. Combination of RT and CIs had a fair toxicity profile with no reports of severe side effects. Within the limits of the small cohorts retrieved, RT seems a superior option compared with systemic treatment as a 'bridge' to CAR-T and could as well reduce severe complications rates. Radiotherapy could elicit immune response against lymphoma, as demonstrated by multiple cases of abscopal effect and its inclusion in anti-neoplastic vaccines protocols.
The results of this review warrant the evaluation of combination of RT and immunotherapy in larger and preferably prospective and randomized cohorts to confirm these preliminary impressive outcomes. The optimal dose, fractionation and timing of RT still have to be clarified.
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