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:Polatuzumab-based regimen or CAR T cell for patients with refractory/relapsed DLBCL-a matched cohort analysis.
Polatuzumab-based regimen or CAR T cell for patients with refractory/relapsed DLBCL-a matched cohort analysis.
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。
基于Polatuzumab(Pola)的方案和CAR-T(CAR-T)细胞在复发/难治性弥漫性大B细胞淋巴瘤(R/R DLBCL)患者中相比传统化学免疫治疗提供了更优的结局。在这些策略之间进行选择仍存在争议。在一项回顾性“真实世界”研究中,比较了CAR-T 与Pola-利妥昔单抗(R)/Pola-苯达莫司汀(B)-R在2线治疗失败后的R/R DLBCL患者中的疗效。应用倾向性评分匹配,针对年龄、淋巴瘤类别(原发/转化)、既往治疗线数、东部肿瘤协作组体能状态和乳酸脱氢酶水平,以控制患者特征的差异。分析了缓解率、无进展生存期(PFS)和总生存期(OS)。
共纳入82例患者,接受CAR-T(n=41)或基于Pola的方案(n=41)治疗。CAR-T 未发生治疗相关死亡,而Pola为3例(7.3%)。CAR-T 的总体缓解率和完全缓解率分别为83%和58%,而基于Pola的方案为66%和44%(分别为p=0.077和p=0.18)。CAR-T 组和Pola组的中位随访时间分别为9个月(范围1-19.2)和16个月(范围0.7-25.3),CAR-T 的中位PFS尚未达到,而Pola为5.6个月(95% CI 3.6-7.6,p=0.014)。CAR-T 的中位OS尚未达到,而Pola为10.8个月(95% CI 2.2-19.4)(p=0.026)。
总之,在真实世界环境中,与基于Pola的方案相比,CAR-T 治疗在R/R DLBCL患者中实现了更优的PFS和OS。
Polatuzumab (Pola)-based regimens and chimeric antigen receptor T (CAR T) cells provide superior outcome compared to conventional chemoimmunotherapy in patients with relapsed/refractory diffuse large B cell lymphoma (R/R DLBCL). Choosing between these strategies remains controversial. The efficacy of CAR T versus Pola-rituximab(R) /Pola-bendamustine(B)-R in R/R DLBCL patients after failing 2 lines of treatment was compared in a retrospective, 'real-world' study. Propensity score matching, for age, lymphoma category (de-novo/transformed), number of prior lines, Eastern Cooperative Oncology Group performance status and lactate dehydrogenase level, was applied to control for differences in patients' characteristics. Response rate, progression-free survival (PFS) and overall survival (OS) were analyzed.
A total of 82 patients, treated with CAR T (n=41) or Pola-based regimens (n=41), were included. No treatment-related deaths occurred with CAR T vs. 3 (7. 3%) with Pola. The overall and complete response rates were 83% and 58% with CAR T vs. 66% and 44% with Pola-based-regimens (p=0. 077 and p=0. 18, respectively). At a median follow-up of 9 months (range 1-19. 2) and 16 months (range 0. 7-25.
3) for the CAR T and Pola arm respectively, the median PFS has not been reached for CAR T vs. 5. 6 months for Pola (95% CI 3. 6-7. 6, p=0. 014). Median OS has not been reached for CAR T vs. 10. 8 months (95% CI 2. 2-19. 4) for Pola (p=0. 026). To conclude, in a real-world setting, treatment with CAR T achieved superior PFS and OS compared to Pola-based regimens in patients with R/R DLBCL.
MEMBER ACCOUNT
登录成功会直接打开下一页。