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:Effectiveness of Paxlovid in the treatment of the SARS-CoV-2 Omicron variant infection in children with hematologic malignancies: a retrospective cohort study.
Effectiveness of Paxlovid in the treatment of the SARS-CoV-2 Omicron variant infection in children with hematologic malignancies: a retrospective cohort study.
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在儿童确诊 SARS-CoV-2 Omicron 变异株感染后 5 天内给予 Paxlovid 可能有效缩短病毒清除时间,但患者仍可能出现检测复阳的结果。
血液系统恶性肿瘤患者接受抗肿瘤治疗后可能处于免疫功能低下状态;若同时感染严重急性呼吸综合征冠状病毒2型(SARS-CoV-2),还会面临包括缺乏有效抗病毒药物在内的多重挑战。本研究旨在考察血液系统恶性肿瘤儿童感染SARS-CoV-2奥密克戎变异株的临床特征及Paxlovid疗效。
开展回顾性、非随机研究,纳入2022年12月1日至2023年3月1日期间在中国上海儿童医学中心住院的SARS-CoV-2奥密克戎变异株感染血液系统恶性肿瘤患儿。Paxlovid治疗组(P组)21例,未治疗组(N组)21例。收集人口学资料、临床特征及治疗结局,并采用统计检验评估疗效和相关因素。
多数患儿奥密克戎感染为非重症(97.6%),仅1例进展为重症(2.4%)。最常见症状为发热(66.7%)和咳嗽(52.4%)。与N组相比,P组患儿临床情况更差,包括既往接受造血干细胞移植(HSCT)或CAR-T 细胞治疗者(71.4%比28.6%,P=0.005)及处于骨髓抑制期者(57.1%比4.8%,P<0.001)。P组多数患儿接受两种以上抗生素治疗(76.2%比42.9%,P=0.02)。确诊后5天内接受Paxlovid治疗者病毒清除时间中位数为5天(四分位距4至8天),显著短于未接受Paxlovid者(P=0.03)。倾向评分匹配分析后,两组临床结局无显著差异。8例(19%)出现复检阳性。二元逻辑回归分析未发现能够显著预测复检阳性的因素。
儿童感染SARS-CoV-2奥密克戎后,确诊5天内给予Paxlovid可能有效缩短病毒清除时间,但患者仍可能出现复检阳性。
Patients with hematologic malignancies (HMs) may be immunocompromised after receiving anti-tumor therapy. Those who also have the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus infection face many challenges, including a lack of effective antiviral drugs. This study aimed to investigate the clinical features of the SARS-CoV-2 Omicron variant infection in children with HMs, and the effectiveness of Paxlovid.
A retrospective, non-randomized study was conducted on pediatric patients with HMs infected with the SARS-CoV-2 Omicron variant who had been admitted to the Shanghai Children's Medical Center, Shanghai, China from December 1, 2022 to March 1, 2023. The Paxlovid-treated group (Group P) comprised 21 patients, and the non-Paxlovid-treated group (Group N) comprised 21 patients. The patients' demographic data, clinical features, and therapeutic outcomes were collected. Statistical tests were used to evaluate the effectiveness of the treatment and related factors.
The clinical course of the SARS-CoV-2 Omicron variant infection for most of the children with HMs was non-severe (97.6%), and only one child progressed to severe disease (2.4%). The most common symptoms were fever (66.7%) and cough (52.4%). Compared with the children in Group N, those in Group P had worse clinical characteristics, including those who previously underwent hematopoietic stem cell transplantation (HSCT) or chimeric antigen receptor T (CAR-T) cell treatment (71.4% vs . 28.6%, P=0.005), and those in the myelosuppressive phase (57.1% vs . 4.8%, P<0.001). Most of the children in Group P were treated with more than two types of antibiotics (76.2% vs . 42.9%, P=0.02). The patients treated with Paxlovid within 5 days of diagnosis had a median viral clearance time of 5 days [interquartile range (IQR), 4-8 days], which was significantly shorter than that of the patients who were not treated with Paxlovid (P=0.03). There were no significant differences in the clinical outcomes between the two groups after the propensity score matching (PSM) analyses. Eight patients (19%) had repeat-positive (re-positive) test results. No factor was found to be statistically significant in predicting re-positive test results based on the binary logistic regression analysis.
Administering Paxlovid within 5 days of the diagnosis of the SARS-CoV-2 Omicron variant infection in children may effectively shorten the clearance time of the virus, but there is still the possibility the patients may have re-positive test results.
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