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:FDG-PET/CT is a powerful tool to predict and evaluate response to chimeric antigen receptor (CAR) T-cell therapy in Non-Hodgkin-Lymphoma (NHL).
FDG-PET/CT is a powerful tool to predict and evaluate response to chimeric antigen receptor (CAR) T-cell therapy in Non-Hodgkin-Lymphoma (NHL).
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
嵌合抗原受体(CAR)T细胞治疗显著改变了非霍奇金淋巴瘤(NHL)的治疗格局。本研究评估氟脱氧葡萄糖(FDG)正电子发射断层显像/计算机断层扫描(PET/CT)在CAR-T 治疗NHL中的疗效评估和预后判断价值。研究纳入2019年8月至2022年7月接受CAR-T 治疗的34例NHL患者。所有患者均在治疗前6天接受FDG-PET/CT(PET-0),并在CAR-T 治疗后34天接受复查(PET-1)。采用Deauville评分(DS)评估疗效,并与至少5个月的随访结果比较。19/34例(55.9%)患者PET-1的DS为3,另15例(44.1%)DS>3。PET-1时DS为3的患者中,14/19例无复发/难治性(r/r)疾病,且在末次随访时仍存活;其余5例为r/r疾病,其中4例死亡。DS>3患者中,除2例无r/r疾病外,其余13/15例均为r/r疾病,其中12例随后死亡。与PET-1时DS>3患者相比,DS=3患者无进展生存期(PFS;HR=5.7;p<0.01)和总生存期(OS;HR=5.0;p<0.01)显著更好。
此外,PET-0时DS=4的患者PFS较长呈趋势(HR=3.6;p=0.05)。CAR-T 治疗后早期采用既定DS标准开展FDG-PET/CT,是有力的治疗应答评估工具。
Chimeric antigen receptor (CAR) T-cell therapy has dramatically shifted the landscape of treatment especially for Non-Hodgkin-Lymphoma (NHL).
This study evaluates the role of fluorodeoxyglucose (FDG)-positron emission tomography/computed tomography (PET/CT) in NHL treated with CAR T-cell therapy concerning response assessment and prognosis.
We evaluated 34 patients with NHL who received a CAR T-cell therapy between August 2019 and July 2022. All patients underwent a pre-therapeutic FDG-PET/CT (PET-0) 6 days prior and a post-therapeutic FDG-PET/CT (PET-1) 34 days after CAR T-cell therapy. Deauville score (DS) was used for evaluation of response to therapy and compared to a minimum follow-up of 5 months. 19/34 (55. 9%) patients achieved DS 3 on PET-1, the remaining 15 (44. 1%) patients had DS > 3 on PET-1.
14/19 patients with DS 3 on PET-1 had no relapsed or refractory (r/r)-disease and were still alive at last follow-up. The other 5 patients had r/r-disease and 4 of these died. Except for two patients who had no r/r-disease, all other patients (13/15) with DS > 3 on PET-1 had r/r-disease and 12 of these subsequently died. Patients with DS 3 on PET-1 had significantly better progression free survival (PFS; HR: 5. 7; p < 0. 01) and overall survival (OS; HR: 5. 0; p < 0. 01) compared to patients with DS > 3 on PET-1.
In addition, we demonstrated that patients with DS 4 on PET-0 tended to have longer PFS (HR: 3. 6; p = 0. 05). Early FDG-PET/CT using the established DS after CAR T-cell therapy is a powerful tool to evaluate response to therapy.
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