Cesaro Simone, Ljungman Per, Mikulska Malgorzata, Hirsch Hans H, Navarro David, Cordonnier Catherine, Mehra Varun, Styczynski Jan, Marchesi Francesco, Pinana Jose Luis, Beutel Gernot, Einsele Herman, Maertens Johan, de la Camara Rafael
Pediatric Haematology Oncology, Department of Mother and Child, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Division of Haematology, Department of Medicine, Huddinge, Karolinska Institute, Stockholm, Sweden.
Leukemia. 2025 Jun 2. doi: 10.1038/s41375-025-02649-9.
In the post-pandemic years, SARS-CoV-2 morbidity and mortality declined due to less pathogenic variants, active and passive immunization, and antiviral therapies. However, patients with hematological malignancies and/or undergoing hematopoietic cell transplantation (HCT) remain at increased risk for poor outcomes. Therefore, adherence to contact and droplet precautions is essential to avoid transmission, especially during epidemic waves. Detection of viral RNA by nucleic acid testing of naso-oro-pharyngeal samples is the gold standard for diagnosis due to its high sensitivity and specificity. Direct antigen testing allows for rapid management decisions if positive, but has a low sensitivity, especially in asymptomatic patients. Active immunisation is the key to prevention and may require annual matching to circulating variants. Passive immunization with SARS-CoV-2 neutralizing anti-antibodies lost its indication due to the emergence of immune escape variants. Convalescent plasma has been proposed for passive immunization but is not readily available in most centres. For symptomatic patients, early antiviral treatment with nirmatrelvir/ritonavir or remdesivir may reduce the risk of progression to severe-critical COVID-19. Prolonged administration, repeated courses, and a combination of antivirals are considered for patients with clinical or virological failure to antiviral monotherapy. In severe-critical COVID-19, dexamethasone or drugs downregulating the inflammatory cytokine responses (anti-Il-6/anti-IL-2 agents, Janus kinase inhibitor) are recommended, together with the best supportive and intensive care, but care should be exercised in immunosuppressed patients. Deferral of intensive chemotherapy, HCT conditioning, T-cell-based immunotherapy, or T-cell engaging antibodies are considered for patients with COVID-19, whereas deferral decisions are taken on a case-by-case basis for asymptomatic patients with confirmed SARS-CoV-2 infection.
在疫情后的几年里,由于致病性较低的变异株、主动和被动免疫以及抗病毒治疗,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的发病率和死亡率有所下降。然而,血液系统恶性肿瘤患者和/或接受造血细胞移植(HCT)的患者预后不良的风险仍然增加。因此,坚持接触和飞沫预防措施对于避免传播至关重要,尤其是在疫情流行期间。通过鼻咽口咽样本的核酸检测来检测病毒RNA,因其高灵敏度和特异性,是诊断的金标准。直接抗原检测如果呈阳性可做出快速管理决策,但灵敏度较低,尤其是在无症状患者中。主动免疫是预防的关键,可能需要每年根据流行的变异株进行匹配。由于免疫逃逸变异株的出现,用SARS-CoV-2中和抗抗体进行被动免疫已不再适用。康复期血浆已被提议用于被动免疫,但在大多数中心不易获得。对于有症状的患者,早期使用奈玛特韦/利托那韦或瑞德西韦进行抗病毒治疗可能会降低进展为重症-危重症2019冠状病毒病(COVID-19)的风险。对于抗病毒单药治疗临床或病毒学失败的患者,考虑延长给药时间、重复疗程以及联合使用抗病毒药物。在重症-危重症COVID-19中,推荐使用地塞米松或下调炎症细胞因子反应的药物(抗白细胞介素-6/抗白细胞介素-2药物、Janus激酶抑制剂),同时给予最佳的支持性和重症监护,但对于免疫抑制患者应谨慎使用。对于COVID-19患者,考虑推迟强化化疗、HCT预处理、基于T细胞的免疫治疗或T细胞接合抗体,而对于确诊SARS-CoV-2感染的无症状患者,则根据具体情况做出推迟决策。