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:Patients With Relapsed Large B-Cell Lymphoma After 12 Months Have a Similarly Poor Prognosis to Those Relapsing Within 12 Months.
Patients With Relapsed Large B-Cell Lymphoma After 12 Months Have a Similarly Poor Prognosis to Those Relapsing Within 12 Months.
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CAR-T 细胞疗法(CAR-T)已取代挽救性免疫化疗后行大剂量化疗和自体干细胞移植(HDT-ASCT),成为早期复发(< 12个月)大B细胞淋巴瘤(LBCL)的首选二线治疗。
然而,对于晚期复发(> 12个月)的患者,CAR-T 直到三线才可及。我们分析了HemoBase注册研究中的877例患者(诊断于2005-2020年),以评估二线治疗中早期与晚期复发在长期结局方面的差异。早期复发发生于120/654例(18%)完成一线治疗的患者中,2年和5年总生存期(OS)分别为22%和18%。晚期复发发生于70例(11%)患者中,2年OS略好,为36%,但5年OS同样较差,为20%。仅13%的早期复发和16%的晚期复发患者完成了HDT-ASCT,5年OS分别为71%和49%。大多数启动挽救性免疫化疗的患者未能达到HDT-ASCT,且生存极差(5年OS早期8%,晚期18%),与不适合HDT-ASCT的患者(早期10%,晚期14%)相当。这些真实世界数据突显了既往二线治疗的不良结局,并支持在早期复发(< 12个月)和晚期复发(> 12个月)LBCL患者中采用CAR-T 等二线替代策略。
Chimeric antigen receptor T-cell therapy (CART) has replaced salvage immunochemotherapy followed by high-dose chemotherapy and autologous stem cell transplantation (HDT-ASCT) as the preferred second-line treatment for early relapsed (< 12 months) large B-cell lymphoma (LBCL).
However, for patients with a late relapse (> 12 months), CART is inaccessible until third line.
We analyzed 877 patients from the HemoBase registry (diagnosed 2005-2020) to assess differences in long-term outcomes of early versus late relapse in second line. Early relapse occurred in 120/654 patients (18%) who completed first-line treatment, with 2- and 5-year overall survival (OS) of 22% and 18%. Late relapse occurred in 70 patients (11%), showing slightly better 2-year OS of 36% but similarly poor 5-year OS of 20%. Only 13% of early and 16% of late relapsed patients completed HDT-ASCT, achieving 5-year OS of 71% and 49%, respectively.
Most patients initiating salvage immunochemotherapy did not reach HDT-ASCT and had dismal survival (5-year OS 8% early, 18% late), comparable to HDT-ASCT-ineligible patients (10% early, 14% late). These real-world data highlight poor outcomes with previous second-line therapies and support alternative strategies like CART in second line for patients with both early relapsing (< 12 months) and late relapsing (> 12 months) LBCL.
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