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:Value of CT-Textural Features and Volume-Based PET Parameters in Comparison to Serologic Markers for Response Prediction in Patients with Diffuse Large B-Cell Lymphoma Undergoing CD19-CAR-T Cell Therapy.
Value of CT-Textural Features and Volume-Based PET Parameters in Comparison to Serologic Markers for Response Prediction in Patients with Diffuse Large B-Cell Lymphoma Undergoing CD19-CAR-T Cell Therapy.
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本研究旨在探讨CT纹理特征和基于体积的PET参数与血清学标志物相比,在接受分化簇19(CD19)嵌合抗原受体(CAR)-T细胞治疗的弥漫性大B细胞淋巴瘤(DLBCL)患者中对反应预测的价值。
我们回顾性分析了21例DLBCL患者(57.7±14.7岁;7例女性)在CAR-T 细胞治疗前后的全身(WB)-代谢肿瘤体积(MTV)、WB-总病灶糖酵解(TLG)以及源自18F-FDG-PET/CT的一阶纹理特征,以及血清学参数(C反应蛋白[CRP]和乳酸脱氢酶[LDH]、白细胞)。在治疗开始后监测白细胞介素6(IL-6)和IL-2受体峰值,并与通过随访18F-FDG-PET/CT判断的患者结局进行比较。在12/21例患者(57%)中观察到完全缓解(CR),而9/21例患者(43%)显示部分缓解(PR)。
在基线时,达到CR的患者WB-MTV和WB-TLG低于达到PR的患者(35±38 mL和319±362 vs 88±110 mL和1487±2254;p < 0.05)。与PR患者相比,CR患者的熵更低(1.81±0.09),均匀性更高(0.33±0.02)(2.08±0.22和0.28±0.47;p < 0.05)。与达到PR的患者相比,达到CR的患者在基线时CRP、LDH和白细胞水平更低(p < 0.05)。在整个队列中,WB-MTV和WB-TLG在治疗开始后下降(p < 0.01),在CR组中变得不可测量。白细胞和CRP在治疗后显著下降(p < 0.01)。与PR患者相比,CR患者治疗后IL-6和IL-2R峰值更低(p > 0.05)。
总之,基于体积的PET参数(源自PET/CT)和CT纹理特征有潜力预测接受CAR-T 细胞治疗的DLBCL患者的治疗反应。
The goal of this study was to investigate the value of CT-textural features and volume-based PET parameters in comparison to serologic markers for response prediction in patients with diffuse large B-cell lymphoma (DLBCL) undergoing cluster of differentiation (CD19)-chimeric antigen receptor (CAR)-T cell therapy.
We retrospectively analyzed the whole-body (WB)-metabolic tumor volume (MTV), the WB-total lesion glycolysis (TLG) and first order textural features derived from 18F-FDG-PET/CT, as well as serologic parameters (C-reactive protein [CRP] and lactate dehydrogenase [LDH], leucocytes) prior and after CAR-T cell therapy in 21 patients with DLBCL (57. 7 14. 7 year; 7 female). Interleukin 6 (IL-6) and IL-2 receptor peaks were monitored after treatment onset and compared with patient outcome judged by follow-up 18F-FDG-PET/CT. In 12/21 patients (57%), complete remission (CR) was observed, whereas 9/21 patients (43%) showed partial remission (PR).
At baseline, WB-MTV and WB-TLG were lower in patients achieving CR (35 38 mL and 319 362) compared to patients achieving PR (88 110 mL and 1487 2254; p < 0. 05). The entropy proved lower (1. 81 0. 09) and uniformity higher (0. 33 0. 02) in patients with CR compared to PR (2. 08 0. 22 and 0. 28 0. 47; p < 0. 05).
Patients achieving CR had lower levels of CRP, LDH and leucocytes at baseline compared to patients achieving PR (p < 0. 05). In the entire cohort, WB-MTV and WB-TLG decreased after therapy onset (p < 0. 01) becoming not measurable in the CR-group. Leucocytes and CRP significantly dropped after therapy (p < 0. 01). The IL-6 and IL-2R peaks after therapy were lower in patients with CR compared to PR (p > 0. 05).
In conclusion, volume-based PET parameters derived from PET/CT and CT-textural features have the potential to predict therapy response in patients with DLBCL undergoing CAR-T cell therapy.
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