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癌症免疫细胞治疗评价组(CITEG)对恶性肿瘤免疫细胞治疗的安全性评价

英文原题:Safety evaluation of immune-cell therapy for malignant tumor in the Cancer Immune-cell Therapy Evaluation Group (CITEG).

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Safety evaluation of immune-cell therapy for malignant tumor in the Cancer Immune-cell Therapy Evaluation Group (CITEG).

PubMed 2023/07/22(内容时间) Cytotherapy Q1 · IF 4.5(JCR 2025)

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研究概要

癌症免疫细胞治疗曾被认为是一种不会发生严重不良事件的安全治疗。

中文摘要

为加强癌症免疫细胞治疗的科学证据并进一步评估其安全性,本院于2015年10月与全国39家医疗机构共同成立癌症免疫细胞治疗评估组(CITEG)。

CITEG收集、分析和评估各机构提供的患者背景特征、临床疗效和治疗细胞类型等医疗信息。本前瞻性研究分析截至2022年9月底免疫细胞治疗相关不良事件,并报告阶段性安全性评估。

共有3,839名恶性肿瘤患者接受免疫细胞治疗,中位年龄64岁(范围13至97岁),男女比例为1:1.08(1,846:1,993)。首次就诊时大多数患者体能状态评分为0或1(86.8%);3,234例(84.2%)为晚期或复发病例,占多数。CITEG报告的治疗总次数为31,890次,其中960次(3.0%)出现不良事件。T细胞治疗19,661次中有363次(1.8%)出现治疗相关不良事件;其他T细胞治疗845次中有9次(1.1%),NK 细胞治疗626次中有10次(1.6%)。树突状细胞(DC)疫苗治疗10,748次中有578次(5.4%)出现不良事件,显著高于其他治疗。多变量分析显示,T细胞治疗中体能状态评分≥1与不良事件风险显著升高相关;DC疫苗治疗中,年龄小于64岁、女性或接受辅助免疫细胞治疗者不良事件风险较高。最常报告的不良事件为注射部位反应,共449例,主要与DC疫苗治疗相关。其他常见事件包括发热228例、疲劳141例和瘙痒131例。另有3名患者出现需住院处理的不良事件(发热、腹痛和间质性肺炎),但其与该疗法关联较弱,更可能与原发疾病治疗有关。

癌症免疫细胞治疗被认为是一种安全治疗,未见严重不良事件。

展开英文摘要原文

Medical information, such as patients' background characteristics, clinical efficacy and therapeutic cell types obtained from each facility, has been accumulated, analyzed and evaluated by CITEG. In this prospective study, we analyzed the adverse events associated with immune-cell therapy until the end of September 2022, and we presented our interim safety evaluation.

A total of 3839 patients with malignant tumor were treated with immune-cell therapy, with a median age of 64 years (range, 13-97 years) and a male-to-female ratio of 1:1.08 (1846:1993). Most patients' performance status was 0 or 1 (86.8%) at the first visit, and 3234 cases (84.2%) were advanced or recurrent cases, which accounted for the majority. The total number of administrations reported in CITEG was 31890, of which 960 (3.0%) showed adverse events. The numbers of adverse events caused by treatment were 363 (1.8%) of 19661 administrations of T cell therapy, 9 of 845 administrations of T-cell therapy (1.1%) and 10 of 626 administrations of natural killer cell therapy (1.6%). The number of adverse events caused by dendritic cell (DC) vaccine therapy was 578 of 10748 administrations (5.4%), which was significantly larger than those for other treatments. Multivariate analysis revealed that T cell therapy had a significantly greater risk of adverse events at performance status 1 or higher, and patients younger than 64 years, women or adjuvant immune-cell therapy had a greater risk of adverse events in DC vaccine therapy. Injection-site reactions were the most frequently reported adverse events, with 449 events, the majority of which were associated with DC vaccine therapy. Among all other adverse events, fever (228 events), fatigue (141 events) and itching (131 events) were frequently reported. In contrast, three patients had adverse events (fever, abdominal pain and interstitial pneumonia) that required hospitalization, although they were weakly related to this therapy; rather, it was considered to be the effect of treatment for the primary disease.

Immune-cell therapy for cancer was considered to be a safe treatment without serious adverse events.

论文信息

作者
Takimoto R、Kamigaki T、Ito H、Saito M、Takizawa K、Soejima K、Yasuda H、Ohgino K
单位
Seta Clinic Group, Tokyo, Japan; Next Generation Cell and Immunotherapy, Advanced Research Institute for Health Science, Juntendo University, Tokyo, Japan; LSI Sapporo Clinic, Sapporo, Japan; Cancer Immune-cell Therapy Evaluation Group (CITEG), Tokyo, Japan. Electronic address: takimoto@j-immunother.com.Japan
期刊
Cytotherapy2023 Nov
原文标识
PubMed 37486281 · DOI 10.1016/j.jcyt.2023.06.007