CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Anti-SARS-CoV-2 antibody-containing plasma improves outcome in patients with hematologic or solid cancer and severe COVID-19: a randomized clinical trial.
Anti-SARS-CoV-2 antibody-containing plasma improves outcome in patients with hematologic or solid cancer and severe COVID-19: a randomized clinical trial.
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癌症患者是2019冠状病毒病(COVID-19)重症的高危人群,发病率和死亡率均较高。此外,体液免疫应答受损使严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗效力降低,且治疗选择匮乏。针对高危患者,目前尚缺乏使用恢复期血浆的随机试验。
在此,我们在134例住院的重症COVID-19患者中开展了一项随机、开放标签、多中心试验(https://www.clinicaltrialsregister.eu/ctr-search/trial/2020-001632-10/DE),将患者分为四个风险组:(1)癌症(n = 56);(2)免疫抑制(n = 16);(3)基于实验室的风险因素(n = 36);(4)高龄(n = 26),随机分配至标准治疗(对照组)或标准治疗联合恢复期/疫苗接种后抗SARS-CoV-2血浆(血浆组)。未观察到与血浆治疗相关的严重不良事件。主要结局为临床改善,采用七分序数量表评估。次要结局为至出院时间和总生存期。四个组合并分析,接受血浆治疗的患者与对照组相比临床改善无差异(风险比(HR)= 1.29;P = 0.205)。
然而,癌症患者接受血浆治疗后,至改善的中位时间缩短(HR = 2.50;P = 0.003),生存优于对照组(HR = 0.28;P = 0.042)。癌症患者血浆组中和抗体活性升高,而对照组未升高(P = 0.001)。
综上所述,恢复期/疫苗接种后血浆可能改善无法自身产生足够免疫应答的癌症患者的COVID-19结局。
Patients with cancer are at high risk of severe coronavirus disease 2019 (COVID-19), with high morbidity and mortality.
Furthermore, impaired humoral response renders severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines less effective and treatment options are scarce. Randomized trials using convalescent plasma are missing for high-risk patients.
Here, we performed a randomized, open-label, multicenter trial ( https://www. clinicaltrialsregister. eu/ctr-search/trial/2020-001632-10/DE ) in hospitalized patients with severe COVID-19 (n = 134) within four risk groups ((1) cancer (n = 56); (2) immunosuppression (n = 16); (3) laboratory-based risk factors (n = 36); and (4) advanced age (n = 26)) randomized to standard of care (control arm) or standard of care plus convalescent/vaccinated anti-SARS-CoV-2 plasma (plasma arm).
No serious adverse events were observed related to the plasma treatment. Clinical improvement as the primary outcome was assessed using a seven-point ordinal scale. Secondary outcomes were time to discharge and overall survival. For the four groups combined, those receiving plasma did not improve clinically compared with those in the control arm (hazard ratio (HR) = 1. 29; P = 0. 205).
However, patients with cancer experienced a shortened median time to improvement (HR = 2. 50; P = 0. 003) and superior survival with plasma treatment versus the control arm (HR = 0. 28; P = 0. 042). Neutralizing antibody activity increased in the plasma cohort but not in the control cohort of patients with cancer (P = 0. 001). Taken together, convalescent/vaccinated plasma may improve COVID-19 outcomes in patients with cancer who are unable to intrinsically generate an adequate immune response.
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