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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Bridging the gap: cancer scientific equity, global child health, and distribution of CAR T-cell therapy clinical trials in childhood cancer.
Bridging the gap: cancer scientific equity, global child health, and distribution of CAR T-cell therapy clinical trials in childhood cancer.
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嵌合抗原受体(CAR)T细胞疗法已改变了儿童癌症的治疗格局。然而,其全球分布仍不均衡,在疾病负担沉重的地区可及性有限。这一状况引发了关于全球儿科肿瘤学研究科学公平性的关键关切。迄今为止,尚无研究系统性地考察儿童健康需求、全球健康指标与儿童癌症CAR-T 细胞疗法临床试验频率之间的科学一致性。这一空白代表了文献中的重大缺口,对全球健康公平和癌症研究优先排序具有影响。采用混合方法分析,使用全球健康指标、儿童癌症指标以及来自全球健康研究与发展观察站的数据。共识别出30个国家中的414项CAR-T 细胞疗法临床试验参与,高度集中于中国(n = 161)和美国(n = 84)。高收入国家占参与者的73.3%。多元线性回归仅识别出一个显著的临床试验参与预测因子:青年死亡率(<15岁)(Coef. = 161.53;p = 0.045)。Lasso模型揭示了关键预测因子,如5-14岁儿童中因酒精使用(Coef. = 29.99)和肥胖(Coef. = 9.62)导致的死亡。研究结果揭示了儿童癌症疾病负担与先进疗法研究活动之间的结构性错位。临床试验集中于科学基础设施较强的国家,而非健康需求最大的国家,加剧了生物医学知识生产和分布中的癌症科学不公平。
Chimeric antigen receptor (CAR) T-cell therapy has transformed the treatment land-scape for childhood cancer.
However, its global distribution remains unequal, with limited access in regions bearing a high burden of disease. This situation raises critical concerns about scientific equity in pediatric oncology research worldwide. To date, no study has systematically examined the scientific coherence between child health needs, global health indicators, and the frequency of CAR T-cell therapy clinical trials for childhood cancer. This omission represents a significant gap in the literature, with im-plications for global health equity and cancer research prioritization. A mixed-method analysis was conducted using global health metrics, child cancer indicators, and data from the Global Observatory on Health Research and Development. A total of 414 CAR T-cell therapy clinical trial participations across 30 countries were identified, with a heavy concentration in China ( n = 161) and the United States ( n = 84).
High-income countries represented 73. 3% of those participating. Multiple linear regression identified only one significant predictor for clinical trials participation: youth mortality (<15 years) (Coef. = 161. 53; p = 0. 045). The Lasso model revealed key predictors such as deaths due to alcohol use (Coef. = 29. 99) and obesity (Coef. = 9. 62) in children aged 5-14.
Findings reveal a structural misalignment between childhood cancer disease burden and research activity in advanced therapies. Clinical trials are concentrated in countries with stronger scientific infrastructure rather than those with the greatest health needs, reinforcing cancer scientific inequities in the production and distribution of biomedical knowledge.
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