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CD19 靶向 CAR T 细胞治疗中转植状态的影响:系统评价和荟萃分析。

Effect of transplant status in CD19-targeted CAR T-cell therapy: a systematic review and meta-analysis.

机构信息

Department of Health Informatics, School of Health Professions, Rutgers, The State University of New Jersey, 65 Bergen Street, Newark, NJ, 07107, USA.

Department of Interdisciplinary Studies, School of Health Professions, Rutgers, The State University of New Jersey, 65 Bergen Street, Room 353A, Newark, NJ, 07107, USA.

出版信息

Med Oncol. 2018 Sep 11;35(11):144. doi: 10.1007/s12032-018-1204-6.

Abstract

Chimeric antigen receptor (CAR) T-cell therapy has shown promise for relapsed/refractory malignancies. Many patients have undergone prior hematopoietic stem cell transplant (HSCT), yet effects of transplant status on CAR T-cell therapy efficacy and safety have not been reported. The purpose of the study is to systematically evaluate the likelihood of achieving optimum response, severe cytokine release syndrome (sCRS), and neurotoxicity in the context of CAR T-cell therapy for HSCT-naïve patients versus those with prior HSCT. Trials were identified in ClinicalTrials.gov, Cochrane Library, and PubMed, and through reference pearl growing. Included studies used CD19-directed CAR T-cells for relapsed/refractory B-lineage Acute Lymphoblastic Leukemia and B cell Chronic Lymphocytic Leukemia, enrolled both HSCT-naïve and prior-HSCT patients, and denoted transplant status with outcomes. Six studies were included for optimum response, five for sCRS incidence, and four for neurotoxicity incidence. The pooled odds ratio for optimum response was 1.57 favoring HSCT-naïve patients (95% CI 0.54-4.61), whereas the pooled odds ratios for sCRS and neurotoxicity were 1.41 (95% CI 0.51-3.94) and 1.37 (95% CI 0.28-6.77), respectively, toward HSCT-naïve patients. Odds ratios were non-statistically significant. Overall risk of bias was moderate. While pooled estimates showed an advantage among HSCT-naïve patients for achieving optimum response and increased likelihood for sCRS and neurotoxicity, findings were not statistically significant. Any differences in efficacy and safety of CAR T-cell therapy cannot be verifiably attributed to transplant status, and additional controlled trials with increased sample sizes are needed to determine whether suggestive patterns favoring HSCT-naïve patients are validated.

摘要

嵌合抗原受体 (CAR) T 细胞疗法在复发/难治性恶性肿瘤方面显示出良好的疗效。许多患者已接受过造血干细胞移植 (HSCT),但移植状态对 CAR T 细胞治疗疗效和安全性的影响尚未报道。本研究的目的是系统评估 CAR T 细胞治疗在 HSCT 初治患者与既往 HSCT 患者中的最佳反应、严重细胞因子释放综合征 (sCRS) 和神经毒性的可能性。通过在 ClinicalTrials.gov、Cochrane 图书馆和 PubMed 以及参考文献中进行检索,确定了研究方案。纳入的研究使用 CD19 定向 CAR T 细胞治疗复发/难治性 B 细胞急性淋巴细胞白血病和 B 细胞慢性淋巴细胞白血病,同时纳入 HSCT 初治和既往 HSCT 患者,并根据结局标记移植状态。纳入了 6 项研究用于最佳反应,5 项研究用于 sCRS 发生率,4 项研究用于神经毒性发生率。最佳反应的汇总优势比为 1.57,有利于 HSCT 初治患者 (95%CI 0.54-4.61),而 sCRS 和神经毒性的汇总优势比分别为 1.41 (95%CI 0.51-3.94) 和 1.37 (95%CI 0.28-6.77),有利于 HSCT 初治患者。优势比无统计学意义。整体偏倚风险为中度。尽管汇总估计显示 HSCT 初治患者在获得最佳反应方面具有优势,并且发生 sCRS 和神经毒性的可能性增加,但无统计学意义。CAR T 细胞治疗的疗效和安全性差异不能可靠地归因于移植状态,需要更多的具有更大样本量的对照试验来确定是否存在有利于 HSCT 初治患者的验证性模式。

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