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:Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy.
Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy.
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。
我们的结果证实了 PET-1 的预后价值。42% 的所有 CMR 患者在 CAR-T 细胞治疗后 1 年仍处于缓解状态。90% 的非 CMR 患者复发,表明需要早期干预。CAR-T 细胞输注前较高的 TMTV 与较低的 CMR 机会相关。
嵌合抗原受体(CAR)-T细胞是复发/难治性(r/r)侵袭性B细胞淋巴瘤患者的一种可行治疗选择。CAR-T 细胞治疗后复发患者的预后不佳,需要确定预测结局的因素。我们的目的是评估FDG-PET/CT在预测患者结局方面的价值。
22例接受tisagenlecleucel(n = 17)或axicabtagene ciloleucel(n = 5)CAR-T 细胞治疗的r/r B细胞淋巴瘤患者,在CAR-T 细胞输注前(PET-0)和输注后1个月(PET-1)接受了定量FDG-PET/CT检查。PET-1被分类为完全代谢缓解(CMR,Deauville评分1-3)或非CMR(Deauville评分4-5)。
在PET-1时,12/22(55%)患者显示CMR,十名(45%)患者为非CMR。7/12(58%)CMR患者在中位223天后复发,其中三名(25%)死亡。9/10(90%)非CMR患者在中位91天后出现复发或疾病进展,其中八名(80%)死亡。CMR患者在PET-0中显示的中位总代谢肿瘤体积(TMTV)显著低于非CMR患者(1 ml vs 225 ml)。
Chimeric antigen receptor (CAR)-T cells are a viable treatment option for patients with relapsed or refractory (r/r) aggressive B-cell lymphomas. The prognosis of patients who relapse after CAR-T cell treatment is dismal and factors predicting outcomes need to be identified. Our aim was to assess the value of FDG-PET/CT in terms of predicting patient outcomes.
Twenty-two patients with r/r B-cell lymphoma who received CAR-T cell treatment with tisagenlecleucel (n = 17) or axicabtagene ciloleucel (n = 5) underwent quantitative FDG-PET/CT before (PET-0) and 1 month after infusion of CAR-T cells (PET-1). PET-1 was classified as complete metabolic response (CMR, Deauville score 1-3) or non-CMR (Deauville score 4-5).
At the time of PET-1, 12/22 (55%) patients showed CMR, ten (45%) patients non-CMR. 7/12 (58%) CMR patients relapsed after a median of 223 days, three of them (25%) died. 9/10 (90%) non-CMR patients developed relapse or progressive disease after a median of 91 days, eight of them (80%) died. CMR patients demonstrated a significantly lower median total metabolic tumor volume (TMTV) in PET-0 (1 ml) than non-CMR patients (225 ml).
Our results confirm the prognostic value of PET-1. 42% of all CMR patients are still in remission 1 year after CAR T-cell treatment. 90% of the non-CMR patients relapsed, indicating the need for early intervention. Higher TMTV before CAR-T cell infusion was associated with lower chances of CMR.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。