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:Image-guided interventional radiological delivery of chimeric antigen receptor (CAR) T cells for pleural malignancies in a phase I/II clinical trial.
Image-guided interventional radiological delivery of chimeric antigen receptor (CAR) T cells for pleural malignancies in a phase I/II clinical trial.
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在解剖结构各异的胸膜癌中,采用腔内或瘤内途径进行影像引导的 CAR-T 细胞胸腔内递送是可行、可重复且安全的。
介绍一项Ⅰ/Ⅱ期临床试验中,影像引导下向胸膜恶性肿瘤患者递送间皮素靶向嵌合抗原受体(CAR)T细胞的技术和结果(ClinicalTrials.gov:NCT02414269)。
41例患者中有31例无胸膜导管,或没有积液以供置入导管;介入放射科医师在CT或超声影像引导下为其胸腔内注射CAR-T 细胞。给药方式包括经穿刺针向可及的胸膜分隔积液腔内注射,或在诱导形成局限性人工气胸后注射。若无法腔内输注,则经皮向胸膜结节/增厚周围及/或病灶内部注射(瘤内给药)。评估操作前后的临床、实验室及影像学表现。
31例患者共接受33次胸腔内CAR-T 细胞给药(其中2例接受第二次给药),均成功给予计划剂量(10至186 mL);其中14次(42%)为腔内注射,19次(58%)为瘤内注射。所有操作均在T细胞解冻后2小时内完成。未发生超过1级的操作相关不良事件(3名患者中有1名曾接受同侧胸膜固定术)。最常见影像表现为磨玻璃样阴影伴小叶间隔增厚和/或实变,见于33次操作中的12次(36%)。不同输注方式间,发热、C反应蛋白、IL-6及外周血载体拷贝数峰值的发生或水平没有差异。
根据解剖条件采用腔内或瘤内途径进行影像引导胸腔内CAR-T 细胞递送具有可行性、可重复性,且对解剖结构各异的胸膜癌症均安全。
We describe techniques and results of image-guided delivery of mesothelin-targeted chimeric antigen receptor (CAR) T cells in patients with pleural malignancies in a phase I/II trial (ClinicalTrials.gov: NCT02414269).
Patients without a pleural catheter or who lack effusion for insertion of a catheter (31 of 41) were administered intrapleural CAR T cells by interventional radiologists under image guidance by computed tomography or ultrasound. CAR T cells were administered through a needle in an accessible pleural loculation (intracavitary) or following an induced loculated artificial pneumothorax. In patients where intracavitary infusion was not feasible, CAR T cells were injected via percutaneous approach either surrounding and/or in the pleural nodule/thickening (intratumoral). Pre- and post-procedural clinical, laboratory, and imaging findings were assessed.
CAR T cells were administered intrapleurally in 31 patients (33 procedures, 2 patients were administered a second dose) with successful delivery of planned dose (10-186 mL); 14/33 (42%) intracavitary and 19/33 (58%) intratumoral. All procedures were completed within 2 h of T-cell thawing. There were no procedure-related adverse events greater than grade 1 (1 in 3 patients had prior ipsilateral pleural fusion procedures). The most common imaging finding was ground glass opacities with interlobular septal thickening and/or consolidation, observed in 12/33 (36%) procedures. There was no difference in the incidence of fever, CRP, IL-6, and peak vector copy number in the peripheral blood between infusion methods.
Image-guided intrapleural delivery of CAR T cells using intracavitary or intratumoral routes is feasible, repeatable and safe across anatomically variable pleural cancers.
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