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:Real life clinical outcomes of relapsed/refractory diffuse large B cell lymphoma in the rituximab era: The STRIDER study.
Real life clinical outcomes of relapsed/refractory diffuse large B cell lymphoma in the rituximab era: The STRIDER study.
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我们的发现证实,在利妥昔单抗时代 R/R DLBCL 的结局极差。
弥漫大B细胞淋巴瘤一线R-CHOP后约40%复发、约15%难治。本研究回顾意大利都灵两家大型血液中心403例患者的真实世界结局。
中位随访50个月时,确诊后5年总生存率为66.5%,2年无进展生存率为68%。134例患者对R-CHOP复发或难治。常用挽救治疗包括含铂方案和来那度胺。复发或进展后的中位总生存期和无进展生存期分别仅为6.7和5.1个月;含铂方案与其他方案在总体缓解率及生存方面无显著差异。多变量分析中,60至80岁、来源于生发中心B细胞及结外受累部位少于2处与复发后的较好总生存期相关。讨论:研究证实利妥昔单抗时代复发/难治患者结局仍很差,亟待国家药监机构广泛批准CAR-T 和双特异性抗体等新疗法作为二线方案以改善结局。
Relapse and refractory (R/R) rates after first-line R-CHOP in diffuse large B cell lymphomas (DLBCL) are ~40% and ~15% respectively. AIMS: We conducted a retrospective real-world analysis aimed at evaluating clinical outcomes of R/R DLBCL patients. MATERIAL AND METHODS: Overall, 403 consecutive DLBCL patients treated in two large hematological centers in Torino, Italy were reviewed.
At a median follow up of 50 months, 5-year overall survival from diagnosis (OS-1) was 66.5%, and 2-year progression free survival (PFS-1) was 68%. 134 (34.4%) patients relapsed (n = 46, 11.8%) or were refractory (n = 88, 22.6%) to R-CHOP. Most employed salvage treatments included platinum salt-based regimens in 38/134 (28.4%), lenalidomide in 14 (10.4%). Median OS and PFS after disease relapse or progression (OS-2 and PFS-2) were 6.7 and 5.1 months respectively. No significant difference in overall response rate, OS-2 or PFS-2 in patients treated with platinum-based regimens versus other regimens was observed. By multivariate analysis, age between 60 and 80 years, germinal center B cell type cell of origin and extranodal involvement of <2 sites were associated with better OS-2. DISCUSSION: Our findings confirm very poor outcomes of R/R DLBCL in the rituximab era. Widespread approval by national Medicine Agencies of novel treatments such as CAR-T cells and bispecific antibodies as second-line is eagerly awaited to improve these outcomes.
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