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:Outcomes in patients with refractory/relapsed CNS lymphoma treated in complete remission: autologous transplantation vs. CAR-T therapy.
Outcomes in patients with refractory/relapsed CNS lymphoma treated in complete remission: autologous transplantation vs. CAR-T therapy.
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与 CAR-T 疗法相比,ASCT 与达到 CR 的复发 CNSL 患者 PFS 改善相关。
自体造血细胞移植(ASCT)对于已获得完全缓解(CR)并维持CR的化疗敏感的复发中枢神经系统淋巴瘤(CNSL)合格患者而言,是一种合理的巩固治疗。CAR-T 细胞疗法是复发CNSL患者的有效治疗选择,尽管关于获得CR患者结局的证据有限。
比较ASCT与CAR-T 疗法作为巩固治疗在复发CNSL患者再次达到CR后的疗效。
对2021年至2024年期间在北京高博医院淋巴瘤科接受ASCT或CAR-T 治疗的患者进行了回顾性观察性研究。CAR-T 治疗属于临床试验「复发/难治性CNSL的不同B细胞靶向CAR-T 细胞(ChiCTR2200058972)」的一部分。
共纳入60例患者,其中42例(70%)为原发性CNSL,18例(30%)为继发性中枢神经系统受累的弥漫大B细胞淋巴瘤(DLBCL)。中位随访时间为12.1个月(1.28-59.9个月)。与CAR-T 组患者相比,在CR期间接受ASCT的患者具有更优的无进展生存期(PFS)[3年PFS 80%(95% CI:48.4-93.4)vs. 64.8%(95% CI:38.9-81.9);P = 0.026],且复发/进展的累积发生率更低[3年复发率20%(95% CI:4.12-44.39)vs. 30.2%(95% CI:11.0-52.2);P = 0.038]。
Autologous hematopoietic cell transplantation (ASCT) is a reasonable consolidation therapy for eligible patients with chemosensitive relapsed central nervous system lymphoma (CNSL) who have achieved complete remission (CR) and maintained the CR. Chimeric antigen receptor T-cell (CAR-T) therapy is an effective treatment option for patients with relapsed CNSL, although evidence on outcomes in patients who achieve CR is limited. AIM: To compare the efficacy of ASCT versus CAR-T therapy as consolidation therapy in patients with relapsed CNSL once CR had been re-achieved.
A retrospective observational study was conducted on patients who underwent ASCT or CAR-T therapy at the Department of Lymphoma, Beijing Gobroad Hospital, between 2021 and 2024. CAR-T therapy was part of the clinical trial "Different B-cell-targeted CAR-T cells for relapsed/refractory CNSL (ChiCTR2200058972)".
Sixty patients, including 42 (70%) with primary CNSL and 18 (30%) with diffuse large B-cell lymphoma (DLBCL) with secondary CNS involvement, were enrolled. The median follow-up duration was 12.1 months (1.28-59.9 months). Compared with patients in the CAR-T group, patients who received ASCT while in CR had superior progression-free survival (PFS) [3-year PFS 80% (95% CI: 48.4-93.4) vs. 64.8% (95% CI: 38.9-81.9); P = 0.026] and a lower cumulative incidence of relapse/progression [3-year relapse rate 20% (95% CI: 4.12-44.39) vs. 30.2% (95% CI: 11.0-52.2); P = 0.038].
Compared with CAR-T therapy, ASCT was associated with improved PFS in patients with relapsed CNSL who had achieved CR.
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