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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A retrospective cohort study of chimeric antigen receptor T-Cell therapy in follicular lymphoma patients with or without histological transformation.
A retrospective cohort study of chimeric antigen receptor T-Cell therapy in follicular lymphoma patients with or without histological transformation.
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CAR-T 疗法治疗复发/难治性滤泡性淋巴瘤和转化型淋巴瘤显示出显著的疗效和安全性。
滤泡性淋巴瘤(FL)是最常见的惰性淋巴瘤之一,目前仍被归为不可治愈疾病。FL患者的不良结局常见于早期复发或组织学转化为侵袭性淋巴瘤者。CAR-T 细胞疗法已获批用于复发/难治性B细胞淋巴瘤。
本回顾性研究报告了接受CAR-T 治疗的26例转化型或复发/难治性FL患者的临床特征和治疗随访情况,并评估CAR-T 疗效以及治疗线数、乳酸脱氢酶(LDH)水平、治疗前缓解状态和组织学转化对预后的影响。
14例转化型FL患者中,发生1例治疗相关死亡;总缓解率(ORR)为92.0%,2年无进展生存率(PFS)为66.7%,总生存率(OS)为73.3%。12例复发/难治性FL患者的ORR为100.0%,2年PFS为75.0%,OS为100.0%,均高于转化型FL患者。CAR-T 治疗前缓解状态较好与PFS改善相关(P=0.009)。与转化型患者相比,复发/难治性FL患者接受CAR-T 治疗后的OS更佳(P=0.04)。
CAR-T 疗法治疗复发/难治性滤泡性淋巴瘤及转化型淋巴瘤显示出显著疗效和安全性。后续研究应着重识别预后因素、延长缓解持续时间并预防复发。
Follicular lymphoma (FL), one of the most common indolent lymphomas, is still classified as an incurable disease. Adverse outcomes in FL frequently occur in patients who experience early relapse or histological transformation to aggressive lymphoma. Chimeric antigen receptor T-cell therapy (CAR-T) has received approval for the treatment of relapsed/refractory B-cell lymphoma.
This retrospective study presents the clinical characteristics and treatment follow-up of 26 patients with transformed or relapsed/refractory FL who received CAR-T therapy. It evaluates the efficacy of CAR-T and assesses treatment lines, LDH levels, remission status before treatment, and the histological transformation of their prognostic impact.
Among the 14 transformed FL patients, there was one treatment-related death, the overall response rate (ORR) was 92.0%, with a 2-year progression-free survival (PFS) rate of 66.7% and an overall survival (OS) rate of 73.3%. For the 12 relapsed/refractory FL patients, the ORR was 100.0%, with a 2-year PFS rate of 75.0% and an OS rate of 100.0%, which is higher than that for transformed FL. A favorable remission state before CAR-T treatment correlated with improved PFS (P = 0.009). Compared to transformed patients, those with relapsed/refractory FL exhibited better OS following CAR-T treatment (P = 0.04).
CAR-T therapy shows significant efficacy and safety for treating relapsed/refractory follicular lymphoma and transformed lymphoma. Further research should focus on identifying prognostic factors, extending remission duration, and preventing recurrence.
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