Mauro Francesca R, Giannarelli Diana, Galluzzo Clementina M, Visentin Andrea, Frustaci Anna M, Sportoletti Paolo, Vitale Candida, Reda Gianluigi, Gentile Massimo, Levato Luciano, Murru Roberta, Armiento Daniele, Molinari Maria C, Proietti Giulia, Pepe Sara, De Falco Filomena, Mattiello Veronica, Barabino Luca, Amici Roberta, Coscia Marta, Tedeschi Alessandra, Girmenia Corrado, Trentin Livio, Baroncelli Silvia
Hematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Design and Analysis of Clinical Trials Unit, Scientific Directorate, IRCS Fondazione Policlinico Universitario A. Gemelli, 00168 Rome, Italy.
Cancers (Basel). 2023 May 30;15(11):2993. doi: 10.3390/cancers15112993.
High morbidity and mortality due to COVID-19 were described in the pre-vaccination era in patients with chronic lymphocytic leukemia (CLL). To evaluate COVID-19 morbidity after the SARS-CoV-2 vaccine, we carried out a prospective study in 200 CLL patients. The median age of patients was 70 years; 35% showed IgG levels ≤ 550 mg/dL, 61% unmutated IGHV, and 34% showed 53 disruption. Most patients, 83.5%, were previously treated, including 36% with ibrutinib and 37.5% with venetoclax. The serologic response rates to the second and third dose of the vaccine were 39% and 53%, respectively. With a median follow-up of 23.4 months, 41% of patients experienced COVID-19, 36.5% during the Omicron pandemic, and 10% had subsequent COVID-19 events. Severe COVID-19 requiring hospitalization was recorded in 26% of patients, and 4% died. Significant and independent factors associated with the response to the vaccine and vulnerability to COVID-19 were age (OR: 0.93; HR: 0.97) and less than 18 months between the start of targeted agents and vaccine (OR: 0.17; HR: 0.31). 53 mutation and ≥two prior treatments also emerged as significant and independent factors associated with an increased risk of developing COVID-19 (HR: 1.85; HR: 2.08). No statistical difference in COVID-19 morbidity was found in patients with or without antibody response to the vaccine (47.5% vs. 52.5%; = 0.21). Given the persistent risk of infection due to the continuous emergence of SARS-CoV-2 variants, our results support the importance of new vaccines and protective measures to prevent and mitigate COVID-19 in CLL patients.
在慢性淋巴细胞白血病(CLL)患者的疫苗接种前时代,曾描述过因新冠病毒病(COVID-19)导致的高发病率和高死亡率。为评估接种严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗后的COVID-19发病率,我们对200例CLL患者进行了一项前瞻性研究。患者的中位年龄为70岁;35%的患者免疫球蛋白G(IgG)水平≤550毫克/分升,61%的患者免疫球蛋白重链可变区(IGHV)未发生突变,34%的患者显示有53号染色体易位。大多数患者(83.5%)曾接受过治疗,其中36%接受过伊布替尼治疗,37.5%接受过维奈克拉治疗。疫苗第二剂和第三剂的血清学应答率分别为39%和53%。中位随访23.4个月时,41%的患者感染了COVID-19,其中36.5%是在奥密克戎大流行期间感染的,10%的患者随后又发生了COVID-19事件。26%的患者出现了需要住院治疗的重症COVID-19,4%的患者死亡。与疫苗应答和对COVID-19易感性相关的显著且独立的因素是年龄(比值比:0.93;风险比:0.97)以及在开始使用靶向药物与接种疫苗之间间隔不到18个月(比值比:0.17;风险比:0.31)。53号染色体突变以及既往接受过≥两次治疗也成为与发生COVID-19风险增加相关的显著且独立的因素(风险比:1.85;风险比:2.08)。在对疫苗有或没有抗体应答的患者中,COVID-19发病率未发现统计学差异(47.5%对52.5%;P = 0.21)。鉴于由于SARS-CoV-2变异株不断出现而持续存在的感染风险,我们的结果支持新型疫苗和预防措施对于预防和减轻CLL患者COVID-19的重要性。