为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Diagnostic performance of [(18)F]FAPI-04 PET/CT in suspected recurrent hepatocellular carcinoma: prospective comparison with contrast-enhanced CT/MRI.
Diagnostic performance of [(18)F]FAPI-04 PET/CT in suspected recurrent hepatocellular carcinoma: prospective comparison with contrast-enhanced CT/MRI.
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[ 18 F]FAPI-04 PET/CT 与 Ce-CT/MRI 联合应用显著提高了鉴别复发性 HCC 与 TILs 的诊断灵敏度、特异度和准确度。[ 18 F]FAPI-04 PET 可能是检测复发性 HCC 的一种有前景的影像学方法。
评估[ 18 F]FAPI-04 PET/CT在鉴别肝细胞癌(HCC)治疗后复发与治疗诱导病灶(TILs)中的诊断效能,并与增强CT/MRI(Ce-CT/MRI)进行比较。
疑似HCC切除或局部区域治疗后复发的患者,接受了Ce-CT/MRI和[18F]FAPI-04 PET/CT检查,被前瞻性纳入研究。对于每位患者或每个病灶,Ce-CT/MRI和[18F]FAPI-04 PET/CT均被赋予三点量表评分(阳性、阴性或可疑)。以组织病理学或影像学随访作为参考标准,通过McNemar检验比较Ce-CT/MRI、[18F]FAPI-04 PET/CT及其联合应用的诊断效能。分析[18F]FAPI-04 PET/CT得出的病灶最大标准化摄取值(SUVmax)和病灶-本底比值(LBR),并计算区分HCC复发与TILs的截断值。
共分析44例患者、129个病灶,其中31例患者(91个病灶)被证实为复发性HCC,38个病灶为TILs。基于病灶的分析显示,与单独Ce-CT/MRI和[18F]FAPI-04 PET/CT相比,[18F]FAPI-04 PET/CT联合Ce-CT/MRI表现出更高的敏感性(86.8% vs. 70.3% vs. 72.5%)、特异性(89.5% vs. 42.1% vs. 52.6%)和准确性(87.6% vs. 62.0% vs. 66.7%)(均P < 0.001)。该联合方案改变了22.7%患者的治疗管理。在半定量分析中,HCC复发灶(n = 91)中[18F]FAPI-04 PET的SUV max和LBR显著高于TILs(n = 38)(SUV max:8.1 vs. 3.65,P < 0.001;LBR:5.4 vs. 1.9,P < 0.001)。使用SUV max截断值5.1和LBR截断值2.3时,[18F]FAPI-04 PET/CT在区分复发性HCC与TILs方面表现出高敏感性和特异性,分别为83.5%、78.9%和96.2%、63.2%。
To evaluate the diagnostic performance of [ 18 F]FAPI-04 PET/CT in differentiating hepatocellular carcinoma (HCC) recurrence from treatment-induced lesions (TILs) after therapy and compare it with contrast-enhanced CT/MRI (Ce-CT/MRI).
Patients with suspected HCC recurrence after resection or local-regional therapy, who underwent Ce-CT/MRI and [ 18 F]FAPI-04 PET/CT, were prospectively enrolled. For each patient or lesion, a three-point-scale (positive, negative, or equivocal) was assigned to Ce-CT/MRI and [ 18 F]FAPI-04 PET/CT. The diagnostic performances of Ce-CT/MRI, [ 18 F]FAPI-04 PET/CT, and their combination were compared by McNemar's test, with histopathology or radiographic follow-up as a reference standard. The maximum standardized uptake value (SUV max ) and lesion-to-background ratio (LBR) of lesions derived from [ 18 F]FAPI-04 PET/CT were analyzed, and the cut-off points for distinguishing between HCC recurrence and TILs were calculated.
A total of 44 patients with 129 lesions were analyzed, of which 31 patients (91 lesions) were proved to be recurrent HCC and 38 lesions were TILs. On lesion-based analysis, the combination of [ 18 F]FAPI-04 PET/CT with Ce-CT/MRI demonstrated superior sensitivity (86.8% vs. 70.3% vs. 72.5%), specificity (89.5% vs. 42.1% vs. 52.6%), and accuracy (87.6% vs. 62.0% vs. 66.7%) compared to Ce-CT/MRI and [ 18 F]FAPI-04 PET/CT alone (all P < 0.001). The combination altered therapy management in 22.7% of patients. On semiquantitative analysis, the SUV max and LBR of [ 18 F]FAPI-04 PET in HCC recurrence (n = 91) were significantly higher than those in TILs (n = 38) (SUV max : 8.1 vs. 3.65, P < 0.001; LBR: 5.4 vs. 1.9, P < 0.001). Using cutoff points of 5.1 for SUV max and 2.3 for LBR, [ 18 F]FAPI-04 PET/CT exhibited high sensitivity and specificity in differentiating recurrent HCC from TILs, with 83.5%, 78.9% and 96.2%, 63.2%, respectively.
The combination of [ 18 F]FAPI-04 PET/CT with Ce-CT/MRI significantly improved diagnostic sensitivity, specificity, and accuracy in differentiating recurrent HCC from TILs. [ 18 F]FAPI-04 PET may be a promising imaging modality in detecting recurrent HCC. TRIAL REGISTRATION: clinicaltrials.gov: NCT05485792.
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