决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Efficacy and safety of natural killer cell therapy in patients with solid tumors: a systematic review and meta-analysis.
NK 细胞疗法是实体瘤有前景的治疗选择,为 CAR-T 等基因修饰细胞疗法提供了可行的替代方案。
引言:2020年全球癌症统计数据显示,每年新增癌症病例1,930万例、死亡1,000万例,凸显了对有效疗法的迫切需求。手术、放疗和化疗等现有疗法在全面治疗实体瘤方面存在局限。包括CAR-T细胞疗法在内的癌症生物学和肿瘤免疫学近期进展显示出前景,但用于实体瘤时仍面临疗效挑战。 方法:本荟萃分析系统综述截至2024年5月PubMed、Embase、Cochrane和ClinicalTrials.gov数据库中的研究,以评估未改造NK细胞疗法治疗实体瘤的临床疗效和安全性。纳入的试验须报告客观缓解率(ORR)。 结果:共分析31项试验,涉及600例不同癌症患者(如非小细胞肺癌、肝细胞癌、乳腺癌和卵巢癌)。NK细胞疗法显示出令人鼓舞的ORR,其中肝细胞癌患者ORR尤高,达72.3%;治疗通常与局部疗法联合使用。安全性良好,最常见的不良事件为疲劳。 讨论:NK细胞疗法是实体瘤的一种有前景的治疗选择,可作为CAR-T等基因修饰细胞疗法的可行替代方案。仍需进一步研究以优化NK细胞疗法的临床应用价值,并将其有效纳入标准癌症治疗方案。 系统综述注册: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42023438410,注册号CRD42023438410。
INTRODUCTION: In 2020, global cancer statistics reported 19.3 million new cases and 10 million deaths annually, highlighting the urgent need for effective treatments. Current therapies, such as surgery, radiation, and chemotherapy, have limitations in comprehensively addressing solid tumor. Recent advances in cancer biology and immuno-oncology, including CAR-T cell therapy, show promise but face efficacy challenges against solid tumors. METHODS: This meta-analysis systematically reviewed studies from PubMed, Embase, Cochrane, and ClinicalTrials.gov databases up to May 2024 to evaluate the clinical efficacy and safety of unmodified NK cell therapies in solid tumors. The included trials focused on reporting objective response rates (ORR). RESULTS: Thirty-one trials involving 600 patients across various cancers (e.g., NSCLC, HCC, breast, ovarian) were analyzed. NK cell therapies demonstrated promising ORRs, particularly 72.3% in hepatocellular carcinoma, often in combination with local therapies. Safety profiles were favorable, with fatigue being the most common adverse event. DISCUSSION: NK cell therapies represent a promising treatment option for solid tumors, offering a viable alternative to genetically modified cell therapies like CAR-T. Further research is needed to optimize the clinical utility of NK cell therapy and integrate it effectively into standard cancer treatment regimens. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42023438410, identifier CRD42023438410.
MEMBER ACCOUNT
登录成功会直接打开下一页。