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:When Chinese patients with plasma cell disorders encountered the nationwide Omicron outbreak (December 2022): a real-world multicenter and multiregional study.
When Chinese patients with plasma cell disorders encountered the nationwide Omicron outbreak (December 2022): a real-world multicenter and multiregional study.
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与普通人群相比,最新一轮 Omicron 疫情导致中国 PCD 患者的重症感染率和死亡率更高,凸显出在大流行期间保护这一脆弱人群的必要性。
评估 2022 年 12 月全国 Omicron 疫情对中国浆细胞疾病(PCD)患者的影响,重点关注 COVID-19 感染 PCD 患者的临床特征,以及导致不良临床过程(疾病严重程度和住院)及结局的危险因素。
开展多中心回顾性研究,研究时间为 2022 年 12 月 1 日至 2023 年 1 月 19 日。共纳入 404 例 PCD 患者,分为 COVID-19 组(n = 342)和未感染组(n = 62)。
COVID-19 感染率为 84.7%(342/404),其中 16.4%(56/342)为重症 COVID-19。在完成随访的 277 例患者中,报告 2 例死亡(0.7%),231 例(83.4%)从 COVID-19 中康复。年龄 >65 岁(P = 0.02)及过去 6 个月内接受抗 CD38 单克隆抗体(mAb)治疗(P = 0.03)是重症感染的独立危险因素。此外,过去 6 个月内接受CAR-T 细胞治疗与住院风险增加(P = 0.04)和康复时间延长(P = 0.03)相关。未观察到疫苗接种对感染或重症感染的显著保护作用(P > 0.05)。
与中国一般人群相比,最新一轮 Omicron 疫情中 PCD 患者重症感染率和死亡率更高,凸显疫情期间保护这一脆弱人群的必要性。近期接受抗 CD38 mAb 或 CAR-T 治疗与 PCD 患者 COVID-19 临床过程和结局较差相关。
This study aims to assess the impact of the nationwide Omicron outbreak in December 2022 on Chinese patients with plasma cell disorders (PCD), focusing on the clinical characteristics of PCD patients with COVID-19 and the risk factors contributing to adverse clinical courses (severity and hospitalization) and outcomes.
A multicenter retrospective study was performed from December 1, 2022, to January 19, 2023. The study population includes 404 PCD patients, divided into a COVID-19 group ( n = 342) and an uninfected group ( n = 62).
The frequency of COVID-19 infection was 84.7% (342/404), and 16.4% (56/342) were severe COVID-19. Among the 277 patients with complete follow-up, 2 deaths (0.7%) were reported, while 231 (83.4%) recovered from COVID-19. Age > 65 ( P = 0.02) and prior anti-CD38 monoclonal antibody (mAb) treatment within six months ( P = 0.03) were independent risk factors for severe infection. Additionally, previous chimeric antigen receptor T-cell (CAR-T) therapy within six months was correlated with a higher risk of hospitalization ( P = 0.04) and prolonged recovery time ( P = 0.03). No significant protective effect of vaccination on infection or severe infection was observed ( P > 0.05).
The latest Omicron outbreak results in higher rates of severe infection and mortality in PCD patients compared with the general population in China, highlighting the need to protect this vulnerable population during the pandemic. Recent use of anti-CD38 mAb and CAR-T therapy are associated with poorer clinical courses and outcomes of PCD patients with COVID-19.
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