Mihaila Romeo Gabriel
Department of Hematology, Faculty of Medicine, Lucian Blaga University of Sibiu, 550169 Sibiu, Romania.
Department of Hematology, Emergency County Clinical Hospital, 550245 Sibiu, Romania.
Oncol Lett. 2021 Aug;22(2):636. doi: 10.3892/ol.2021.12897. Epub 2021 Jul 3.
Oncohematological patients are prone to develop infections due to immunosuppression caused by the disease and chemo-immunotherapy. The aim of this review was to outline the details of the management of patients with chronic lymphocytic leukemia (CLL) during the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. Patients with CLL often exhibit inadequate humoral and cellular immune responses to various infections and vaccinations. Patients under the 'watch and wait' strategy have a lower risk of infections, including with SARS-CoV-2, compared with those undergoing therapeutic interventions, but they still have a higher risk than age-matched controls. Patients with CLL have a high risk of developing severe forms of coronavirus disease-2019 (COVID-19), particularly if they are undergoing chemo-immunotherapy. The total anti-SARS-CoV-2 antibody titer demonstrates a slower increase in patients with CLL infected with the virus, and the antibody levels tend to decrease after reaching a maximum level sooner than in healthy individuals. This leads to a late negativation of the PCR tests and a longer duration of hospitalization. In total, ~1/3 of patients with CLL do not develop a persistent titer of antiviral antibodies, and this is associated with the presence of hypogammaglobulinemia. It appears that patients with CLL have the worst outcomes amongst patients with malignant hemopathies and SARS-CoV-2 infection. Bruton tyrosine kinase inhibitors reduce the hyperinflammatory status of patients with CLL with COVID-19, which is accompanied by decreased levels of serum inflammatory markers, ferritin and D-dimer, and serum levels of pro-inflammatory cytokines, but they increase the risk of infections and impaired humoral immunity. An abrupt discontinuation of these may promote the rapid decompensation of CLL, which may even mimic the clinical manifestations of COVID-I9, including a significant increase in cytokine release. In conclusion, therapeutic decisions must be personalized to each patient with CLL and each at risk patient must be quarantined during the SARS-CoV-2 pandemic to reduce their risk of contraction.
肿瘤血液科患者由于疾病及化疗免疫治疗导致的免疫抑制,容易发生感染。本综述的目的是概述在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)大流行期间慢性淋巴细胞白血病(CLL)患者的管理细节。CLL患者对各种感染和疫苗接种的体液免疫和细胞免疫反应往往不足。与接受治疗干预的患者相比,采取“观察等待”策略的患者感染风险较低,包括感染SARS-CoV-2的风险,但仍高于年龄匹配的对照组。CLL患者发生重症冠状病毒病2019(COVID-19)的风险很高,特别是在接受化疗免疫治疗时。感染该病毒的CLL患者中,抗SARS-CoV-2总抗体滴度升高较慢,且抗体水平在达到最高水平后比健康个体更快下降。这导致PCR检测转阴延迟和住院时间延长。总体而言,约1/3的CLL患者未产生持续的抗病毒抗体滴度,这与低丙种球蛋白血症的存在有关。看来,在恶性血液病和SARS-CoV-2感染患者中,CLL患者的预后最差。布鲁顿酪氨酸激酶抑制剂可降低COVID-19的CLL患者的高炎症状态,这伴随着血清炎症标志物、铁蛋白和D-二聚体水平以及促炎细胞因子血清水平的降低,但会增加感染风险和体液免疫受损。突然停用这些药物可能会促使CLL迅速失代偿,甚至可能模仿COVID-19的临床表现,包括细胞因子释放显著增加。总之,治疗决策必须针对每位CLL患者进行个性化制定,并且在SARS-CoV-2大流行期间,每位有风险的患者都必须进行隔离,以降低其感染风险。