Impact of anti-SARS-CoV-2 monoclonal antibodies in the management of patients with lymphoma and COVID19: A retrospective study

被引:6
作者
Assanto, Giovanni Manfredi [1 ]
Di Rocco, Alice [1 ]
Malfona, Francesco [1 ]
Capriata, Marcello [1 ]
Del Giudice, Ilaria [1 ]
Petrucci, Luigi [1 ]
Girardi, Paola [1 ]
D'Elia, Gianna Maria [1 ]
Martelli, Maurizio [1 ]
Gentile, Giuseppe [1 ]
Micozzi, Alessandra [1 ]
Pulsoni, Alessandro [1 ,2 ]
机构
[1] Sapienza Univ Rome, Dept Translat & Precis Med, Hematol, Rome, Italy
[2] Sapienza Univ Rome, Hematol, Via Benevento 6, I-00161 Rome, Italy
关键词
bendamustine; COVID-19; lymphoma; monoclonal antibodies; non hodgkin lymphoma; OUTCOMES; MULTICENTER; CANCER;
D O I
10.1002/hon.3113
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
COVID19 in patients affected by lymphoma represents an important challenge because of the higher mortality rate. Anti-SARS-CoV-2 monoclonal antibodies (anti-S MoAbs) appear promising in this setting. We report a monocentric retrospective study including 176 patients affected by lymphoma which developed SARS-CoV-2 infection since the start of COVID19 pandemic. Overall, mortality was 13.1%, with a decreasing trend between first waves to the last wave of pandemic (18.5% vs. 9.4%, p 0.076). Patients receiving anti-S MoAbs (41.3%) showed inferior mortality rate (overall survival, OS 93.2% vs. 82.7%, p 0.025) with no serious toxicity, reduced documented pneumonia (26% vs. 33%, p 0.005), and reduced need of oxygen support (14.5% vs. 35.7%, p 0.003). Among patients who received 3 doses of vaccine, the employment of anti-COVID MoAbs showed a trend of superior survival versus those who did not receive Anti-S MoAbs (OS rates 97.3% vs. 84.2%, p 0.064). On multivariate analysis, active haematological disease (OS 72% (HR 2.49 CI 1.00-6.41), bendamustine exposure (OS 60% HR 4.2 CI 1.69-10.45) and at least one comorbidity (HR 6.53 CI 1.88-22.60) were independent prognostic factors for death. Our study confirms the adverse prognostic role of COVID-19 in lymphoma patients in presence of active disease, comorbidities and previous exposure to bendamustine. In our experience, anti-S MoAbs represented a therapeutic option in vaccinated patients.
引用
收藏
页码:343 / 353
页数:11
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