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:COVID-19 outcomes in children, adolescents and young adults with cancer.
COVID-19 outcomes in children, adolescents and young adults with cancer.
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儿童肿瘤患者发生呼吸道病毒感染时,结局不佳风险较高。需要了解儿童和青年癌症患者COVID-19结局;有关肥胖/超重患者及青少年和青年成人亚组的数据仍有限。
本研究在单中心队列中考察25岁以下癌症患者COVID-19结局,并通过单变量和多变量分析评估住院候选危险因素。共识别87名患癌且感染COVID-19的患者,多数为西班牙裔/拉丁裔(n=63,72%);42人(48%)超重或肥胖。抗癌治疗包括单纯化疗64人(74%)、CAR-T 7人、造血干细胞移植(HSCT)12人,以及CAR-T 联合HSCT 4人。未发生COVID-19相关死亡。26人(30%)因COVID-19住院,其中4人多次住院;9人(10%)发生重症/危重感染,6人需重症监护。正在接受治疗的64名患者中,22人(34%)因COVID-19延迟抗癌治疗,中位延迟14天。住院相关因素包括感染前2周内使用类固醇、淋巴细胞减少、既往严重非COVID感染及COVID-19 PCR循环阈值较低。CAR-T 后B细胞缺如者更易出现重症/危重感染(7人中3人)。32人中有14人(44%)检测到COVID-19抗体应答。相当比例的儿童和青年癌症患者感染COVID-19后需住院;B细胞免疫缺陷患者发病风险可能较高。
不过,多数患者仍可继续化疗,且治疗延迟不长。病毒载量可能是儿童癌症患者COVID-19结局的预测指标。
Pediatric oncology patients are at risk for poor outcomes with respiratory viral infections. Outcome data for COVID-19 in children and young adults with cancer are needed; data are sparse for obese/overweight and adolescent and young adult subgroups.
We conducted a single center cohort study of COVID-19 outcomes in patients younger than 25 years with cancer. Candidate hospitalization risk factors were analyzed via univariable and multivariable analyses. Eighty-seven patients with cancer and COVID-19 were identified. Most were Hispanic/Latinx (n = 63, 72%). Forty-two (48%) were overweight/obese. Anticancer therapy included chemotherapy only (n = 64, 74%), chimeric antigen receptor T-cells (CAR-T, n = 7), hematopoietic stem cell transplantation (HSCT, n = 12), or CAR-T and HSCT (n = 4). There was no COVID-19 related mortality. Twenty-six patients (30%) required COVID-19 related hospitalization; 4 required multiple hospitalizations.
Nine (10%) had severe/critical infection; 6 needed intensive care. COVID-19 resulted in anticancer therapy delays in 22 (34%) of 64 patients on active therapy (median delay = 14 days). Factors associated with hospitalization included steroids within 2 weeks prior to infection, lymphopenia, previous significant non-COVID infection, and low COVID-19 PCR cycle threshold value.
CAR-T recipients with B-cell aplasia tended to have severe/critical infection (3 of 7 patients). A COVID-19 antibody response was detected in 14 of 32 patients (44%). A substantial proportion of COVID-19 infected children and young adults with cancer require inpatient management; morbidity may be high in B-cell immunodeficiency.
However, a majority of patients can be taken through chemotherapy without prolonged therapy delays. Viral load is a potential outcome predictor in COVID-19 in pediatric cancer.
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