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:Chidamide and sintilimab combination in diffuse large B-cell lymphoma progressing after chimeric antigen receptor T therapy.
Chidamide and sintilimab combination in diffuse large B-cell lymphoma progressing after chimeric antigen receptor T therapy.
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西达本胺联合信迪利单抗可能成为 CD19 靶向 CAR-T 治疗后进展的 DLBCL 患者的一种选择。
弥漫性大B细胞淋巴瘤(DLBCL)可通过一线化学免疫疗法治愈,但复发/难治性(R/R)DLBCL患者仍面临不良预后。对于R/R DLBCL患者,传统下一线治疗的完全缓解率仅为7%,中位总生存期为6.3个月。近年来,靶向CD19的CAR-T 细胞在临床试验中显示出前景。然而,约50%接受CAR-T 细胞治疗的患者最终进展,且有效的挽救治疗很少。病例总结:本文报告了7例R/R DLBCL患者,其在CAR-T 输注后疾病进展。他们接受了PD-1抑制剂(信迪利单抗)和组蛋白去乙酰化酶抑制剂(西达本胺)治疗。7例患者中有5例耐受治疗,未出现任何严重不良事件。2例患者因肺部感染和皮疹停止治疗。在20个月的随访中,这7例患者的中位总生存期为6个月。值得注意的是,在这种新疗法期间出现了2例完全缓解(CR)和2例部分缓解(PR),总缓解率(ORR)为57.1%,且1例患者获得了持续至少20个月的持久CR。
Diffuse large B-cell lymphoma (DLBCL) is curable with first-line chemoimmunotherapy but patients with relapsed/refractory (R/R) DLBCL still face a poor prognosis. For patients with R/R DLBCL, the complete response rate to traditional next-line therapy is only 7% and the median overall survival is 6.3 mo. Recently, CD19-targeting chimeric antigen receptor T cells (CAR-T) have shown promise in clinical trials. However, approximately 50% of patients treated with CAR-T cells ultimately progress and few salvage therapies are effective. CASE SUMMARY: Here, we report on 7 patients with R/R DLBCL whose disease progressed after CAR-T infusion. They received a PD-1 inhibitor (sintilimab) and a histone deacetylase inhibitor (chidamide). Five of the 7 patients tolerated the treatment without any serious adverse events. Two patients discontinued the treatment due to lung infection and rash. At the 20-mo follow-up, the median overall survival of these 7 patients was 6 mo. Of note, there were 2 complete response rates (CRs) and 2 partial response rates (PRs) during this novel therapy, with an overall response rate (ORR) of 57.1%, and one patient had a durable CR that lasted at least 20 mo.
In conclusion, chidamide combined with sintilimab may be a choice for DLBCL patients progressing after CD19-targeting CAR-T therapy.
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