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:Salvage therapy with "Dara-KDT-P(A)CE" in heavily pretreated, high-risk, proliferative, relapsed/refractory multiple myeloma.
Salvage therapy with "Dara-KDT-P(A)CE" in heavily pretreated, high-risk, proliferative, relapsed/refractory multiple myeloma.
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。
多药联合方案“VDT-PACE”是复发/难治性多发性骨髓瘤(RRMM)的既定治疗方案。在此,我们报告了将新一代抗MM药物daratumumab和carfilzomib纳入“改良VDT-PACE”方案(“Dara-KDT-P(A)CE”)的应用经验。
我们回顾性分析了38例接受“Dara-KDT-P(A)CE”治疗的RRMM患者。中位年龄为62岁(范围45-82岁),患者既往接受过大量治疗,中位既往治疗线数为5线(范围2-12线)。21例(55%)患者为五药难治性MM。31例(81%)患者存在高危细胞遗传学异常。患者接受该方案的中位周期数为2个(范围1-10个),总缓解率(ORR)为70%。五药难治性MM和高危细胞遗传学异常患者的ORR分别为65%和79%,结果相似。中位无进展生存期(PFS)和总生存期分别为4.1个月(95% CI 2.7-5.4)和8.4个月(95% CI 6.7-10.0)。乳酸脱氢酶>250 IU/L的患者与其他患者相比,PFS显著缩短(p = 0.006)。
我们在4例患者中将该方案用作CAR-T 细胞输注前的桥接治疗。总之,“Dara-KDT-P(A)CE”对于既往接受过大量治疗、多药难治、高危且缺乏替代选择的RRMM患者而言,是一种有效的挽救治疗方案。
The multi-agent therapy "VDT-PACE" represents an established regimen in relapsed/refractory multiple myeloma (RRMM).
Here, we report on our experience with a "modified VDT-PACE" incorporating new generation anti-MM agents daratumumab and carfilzomib ("Dara-KDT-P(A)CE").
We retrospectively analyzed 38 patients with RRMM treated with "Dara-KDT-P(A)CE". The median age was 62 (range 45-82) years, and the patients were heavily pretreated with a median of 5 (range 2-12) prior lines of therapy. Twenty-one (55%) patients suffered from penta-refractory MM. High-risk cytogenetics was present in 31 (81%) patients. The patients received a median of 2 (range 1-10) cycles of this therapy, and the overall response rate (ORR) was 70%.
Patients with penta-refractory MM and high-risk cytogenetics showed similar ORR of 65% and 79%, respectively. The median progression-free survival (PFS) and overall survival were 4. 1 (95% CI 2. 7-5. 4) and 8. 4 (95% CI 6. 7-10. 0) months, respectively. Patients with lactate dehydrogenase >250 IU/L showed significantly shorter PFS in comparison with others patients (p = 0. 006).
We used this regimen as bridging therapy prior to chimeric antigen receptor T-cell infusion in four patients.
In conclusion, "Dara-KDT-P(A)CE" is an effective salvage therapy for patients with heavily pretreated, multi-refractory, high-risk RRMM lacking alternative options.
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