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:Geographic and Racial Disparities in Chimeric Antigen Receptor-T Cells and Bispecific Antibodies Trials Access for Diffuse Large B-Cell Lymphoma.
Geographic and Racial Disparities in Chimeric Antigen Receptor-T Cells and Bispecific Antibodies Trials Access for Diffuse Large B-Cell Lymphoma.
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应制定策略以解决观察到的差异并改善可及性。
我们研究在获取针对DLBCL的CAR-T 和双特异性抗体试验中存在的地区和种族差异。
检索了ClinicalTrials.gov,纳入了至少在美国有1个开放中心的75项试验。使用2020年美国人口普查局数据获取种族和族裔数据。使用SPSS 26版进行分析。
共有62项CAR-T 和13项双特异性抗体试验,已入组或预计入组6221例患者。85%的临床试验仅在美国开放,其中大多数(64%)由制药公司资助。共有126个独特的研究中心分布在31个州,每个州的平均试验数为11(0-51),每个中心的CAR-T 和双特异性抗体试验平均数量分别为4.5(1-26)和4.4(1-24)。南部各州的试验数量最多,占31%,其次是中西部25%、东北部24%和西部20%。研究地点数量最多的是加利福尼亚州13个、纽约州9个和宾夕法尼亚州9个,而开放研究数量最多的是加利福尼亚州51项、德克萨斯州32项和纽约州23项。有20个州没有开放的CAR-T 或双特异性抗体试验。只有33%的非裔美国人(AA)居住在有试验的县,而在非裔美国人居民比例最高的10个州中(18.6%-41.4%),有7个州没有或少于4个试验中心。在分析的62个县中,92%以白人为主,而只有8%以非裔美国人为主(P = .009)。
We investigate the geographical and racial disparities in accessing CAR-T and bispecific antibodies trials for DLBCL.
ClinicalTrials.gov was searched, and 75 trials with at least 1 open site in the US were included. 2020 US Census Bureau data was used to obtain data on race and ethnicity. SPSS version 26 was used for analysis.
There were 62 CAR-T and 13 bispecific antibodies trials with 6221 enrolled or expected to enroll patients. Eighty-five percent of the clinical trials were only open in the US, and the majority 64% were pharmaceutical-funded. There were 126 unique study sites distributed over 31 states with 11 (0-51) mean number of trials per state and 4.5 (1-26) and 4.4 (1-24) mean number of CAR-T and bispecific antibodies trials per site, respectively. Southern states had the most number of trials 31%, followed by Midwestern 25%, Northeastern 24%, and Western 20%. The highest number of study locations were in California 13, New York 9, and Pennsylvania 9, while the highest number of open studies were in California 51, Texas 32, and New York 23. Twenty states had no open CAR-T or bispecific antibodies trials. Only 33% of African Americans (AA) lived in a county with a trial, and 7 out of 10 states with the highest proportion of AA residents (18.6%-41.4%) have no or less than 4 trial sites. Of the 62 counties analyzed, 92% were White predominant, while only 8% were AA predominant (P = .009).
Strategies should be framed to address the observed disparities and to improve access.
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