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:Indicators describing the tumor lesion aggregation and dissemination and their impact on the prognosis of patients with diffuse large B cell lymphoma receiving chimeric antigen receptor T cell therapy.
Indicators describing the tumor lesion aggregation and dissemination and their impact on the prognosis of patients with diffuse large B cell lymphoma receiving chimeric antigen receptor T cell therapy.
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肿瘤病灶的相对位置显著影响接受 CAR-T 细胞治疗的 DLBCL 患者的预后。理想情况是肿瘤播散极少且无聚集。
嵌合抗原受体(CAR)T细胞疗法显著改善了弥漫性大B细胞淋巴瘤(DLBCL)患者的预后。淋巴瘤肿瘤病灶的相对位置在患者之间存在差异,表现为聚集(成团聚集)或播散(遍布全身)。在CAR-T 细胞疗法中,提示肿瘤病灶相对位置的因素其预后意义仍未被充分探索。对于聚集,既往研究提出了肿瘤体积表面积比(TVSR),并将其与化疗预后相关联。对于播散,临床实践中常用的疾病分期或结外受累等指标,在CAR-T 细胞疗法中尚未显示出预后意义。本研究旨在分析当前用于评估肿瘤聚集或播散的指标,并引入一种新指标,以评估接受CAR-T 细胞疗法的DLBCL患者中肿瘤病灶相对位置的预后价值。
这项回顾性研究纳入42例接受CAR-T 细胞治疗的患者。从CAR-T 细胞输注前最后一次PET/CT扫描获取病灶影像信息,包括总代谢肿瘤体积、总肿瘤表面积、淋巴瘤肿块直径及肿瘤病灶部位。我们评估了TVSR和巨块型病变作为肿瘤聚集的描述指标。我们对现有指标(III&IV期和>1处结外受累)进行优化,提炼出一个新指标,称为“extra stage”,以更好地代表肿瘤播散。本研究考察了肿瘤聚集和播散的预后意义。
我们的研究结果表明,TVSR 在化疗中具有预后价值,但在 CAR-T 细胞治疗中缺乏实际预后价值。相反,大包块疾病成为肿瘤聚集的最佳预后指标。大包块疾病和结外分期均与不良预后相关,并在 CAR-T 细胞治疗中表现出协同预后影响。
This retrospective study included 42 patients receiving CAR T cell therapy. Lesion image information was obtained from the last PET/CT scan prior to CAR T cell infusion, including total metabolic tumor volume, total tumor surface, diameter of lymphoma masses, and the sites of tumor lesions. We evaluated TVSR and bulky disease as descriptors of tumor aggregation. We refined existing indicators, stage III&IV and >1 site extranodal involvement, to distill a new indicator, termed 'extra stage', to better represent tumor dissemination. The study examined the prognostic significance of tumor aggregation and dissemination.
Our findings indicate that TVSR, while prognostically valuable in chemotherapy, lacks practical prognostic value in CAR T cell therapy. Conversely, bulky disease emerged as an optimal prognostic indicator of tumor aggregation. Both bulky disease and extra stage were associated with poor prognosis and exhibiting synergistic prognostic impact in CAR T cell therapy.
Overall, the relative positioning of tumor lesions significantly influences the prognosis of patients with DLBCL receiving CAR T cell therapy. The ideal scenario involves tumors with minimal dissemination and no aggregation.
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