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:Anti-CD19 chimeric antigen receptor T-cell therapy for relapsed or refractory Philadelphia chromosome-positive B cell acute lymphoblastic leukemia: a multicenter retrospective study.
Anti-CD19 chimeric antigen receptor T-cell therapy for relapsed or refractory Philadelphia chromosome-positive B cell acute lymphoblastic leukemia: a multicenter retrospective study.
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CD19 CAR-T 细胞疗法可为 R/R Ph + B-ALL 患者实现高缓解率和长期临床获益,且安全性可控。既往报告声明:初步研究已在 2024 年 12 月 7 日至 10 日于加利福尼亚州圣迭戈举行的第 66 届美国血液学会年会上以壁报形式展示(发布编号:4201)。
尽管无化疗方案已提高了新诊断费城染色体阳性B细胞急性淋巴细胞白血病(Ph + B-ALL)患者的初始缓解率,但复发/难治性(R/R)Ph + B-ALL患者的结局仍然很差。本研究报道了CD19嵌合抗原受体(CAR)T细胞疗法在R/R Ph + B-ALL中的疗效和安全性。
本研究回顾性分析了2015年8月至2024年3月期间在中国接受CD19 CAR-T 细胞治疗的93例R/R Ph + B-ALL患者。我们评估了总缓解率、长期疗效、安全性以及与CD19 CAR-T 细胞治疗相关的预后因素。
完全缓解(CR)或伴血液学恢复不完全的 CR 率为 87.1%(81/93),其中 96.3%(78/81)的缓解者通过流式细胞术达到微小残留病阴性。分子学缓解率为 78.5%(73/93),包括 63.4% 达到完全分子学缓解和 15.1% 达到主要分子学缓解。20 例患者接受了巩固性异基因造血干细胞移植(allo-HSCT)。中位随访 25.4 个月(范围,0.1-68.5)后,中位总生存期(OS)为 20.8 个月,中位无白血病生存期(LFS)为 8.1 个月。较好的 美国东部肿瘤协作组 体能状态和无不良遗传学特征与 OS 和 LFS 改善相关。相反,CAR-T 细胞治疗后行巩固性 allo-HSCT 与 OS 或 LFS 改善无独立相关性。3 级细胞因子释放综合征和神经毒性的发生率分别为 14.0% 和 2.2%。最常见且可预测的不良事件为血液学毒性,主要为血细胞减少,可通过支持治疗进行管理。
Although chemotherapy-free regimens have improved initial remission rates in patients with newly diagnosed Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia (Ph + B-ALL), outcomes for relapsed or refractory (R/R) Ph + B-ALL remain poor. This study reports the efficacy and safety of CD19 chimeric antigen receptor (CAR) T-cell therapy in R/R Ph + B-ALL.
This study retrospectively analyzed 93 patients with R/R Ph + B-ALL who received CD19 CAR T-cell therapy across China between August 2015 and March 2024. We evaluated the overall response rates, long-term efficacy, safety, and prognostic factors associated with CD19 CAR T-cell therapy.
Complete remission (CR) or CR with incomplete hematologic recovery rate was 87.1% (81/93), with 96.3% (78/81) of responders achieving minimal residual disease negativity by flow cytometry. Molecular response rate was 78.5% (73/93), including 63.4% achieving complete molecular remission and 15.1% major molecular remission. Twenty patients underwent consolidative allogeneic hematopoietic stem cell transplantation (allo-HSCT). After a median follow-up of 25.4 months (range, 0.1-68.5), the median overall survival (OS) was 20.8 months, and the median leukemia-free survival (LFS) was 8.1 months. Better Eastern Cooperative Oncology Group performance status and absence of adverse genetic features were associated with improved OS and LFS. In contrast, consolidative allo-HSCT following CAR T-cell therapy was not independently associated with improved OS or LFS. Grade 3 cytokine release syndrome and neurotoxicity occurred in 14.0% and 2.2% of patients, respectively. The most common and predictable adverse events were hematologic, primarily cytopenias, which were manageable with supportive care.
CD19 CAR T-cell therapy can achieve high response rates and long-term clinical benefits for patients with R/R Ph + B-ALL, with a manageable safety profile. STATEMENT OF PRIOR PRESENTATION: The preliminary study was presented as a poster presentation (Publication Number: 4201) at the 66th American Society of Hematology Annual Meeting, San Diego, CA, on December 7-10, 2024.
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