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Prevalence and Clinical Impact of SARS-CoV-2 Silent Carriers Among Actively Treated Patients with Cancer During the COVID-19 Pandemic

机译:SARS-COV-2在Covid-19大流行期间的SARS-COV-2患者中SARS-COV-2患者中的患病率和临床影响

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Introduction In Europe, the SARS-CoV-2 pandemic had its first epicenter in Italy. Despite a significant mortality rate, the severity of most cases of COVID-19 infection ranges from asymptomatic to mildly symptomatic, and silent infection affects a still-unknown proportion of the general population. No information is available on the prevalence and clinical impact of SARS-CoV-2 silent infection among patients with cancer receiving anticancer treatment during the pandemic. Materials and Methods From April 1, 2020, to the end of the same month, 560 consecutive patients with cancer, asymptomatic for COVID-19 and on anticancer treatment at Papa Giovanni XXIII Hospital in Bergamo, were evaluated and tested for SARS-CoV-2. We implemented a two-step diagnostics, including the rapid serological immunoassay for anti–SARS-CoV-2 immunoglobulin (Ig) G/IgM and the nasopharyngeal swab reverse transcriptase-polymerase chain reaction (RT-PCR) test in case of seropositivity to identify SARS-CoV-2 silent carriers. Results In 560 patients, 172 (31%) resulted positive for anti–SARS-CoV-2 IgM/IgG antibodies, regardless of different type of cancer, stage, and treatment. The Ig-seropositive patients were then tested with RT-PCR nasopharyngeal swabs, and 38% proved to be SARS-CoV-2 silent carriers. At an early follow-up, in the 97 SARS-CoV-2–seropositive/RT-PCR–negative patients who continued their anticancer therapies, only one developed symptomatic COVID-19 illness. Conclusion Among patients with cancer, the two-step diagnostics is feasible and effective for SARS-CoV-2 silent carriers detection and might support optimal cancer treatment strategies at both the individual and the population level. The early safety profile of the different anticancer therapies, in patients previously exposed to SARS-CoV-2, supports the recommendation to continue the active treatment, at least in cases of RT-PCR–negative patients. Implications for Practice This is the first study evaluating the prevalence and clinical impact of SARS-CoV-2 silent infection in actively treated patients with cancer, during the epidemic peak in one of the worst areas of the COVID-19 pandemic. Lacking national and international recommendations for the detection of asymptomatic SARS-CoV-2 infection, a pragmatic and effective two-step diagnostics was implemented to ascertain SARS-CoV-2 silent carriers. In this series, consisting of consecutive and unselected patients with cancer, the prevalence of both SARS-CoV-2–seropositive patients and silent carriers is substantial (31% and 10%, respectively). The early safety profile of the different anticancer therapies, in patients previously exposed to SARS-CoV-2, supports the recommendation to continue the active treatment, at least in case of RT-PCR–negative patients.
机译:在欧洲介绍,SARS-COV-2 PANDEMAMED在意大利的第一家震中。尽管死亡率显着,但大多数Covid-19感染病例的严重程度范围从无症状到轻微的症状,无声感染影响一般人群的仍有不当的比例。在大流行期间患有抗癌治疗的癌症患者中SARS-COV-2无声感染的患病率和临床影响没有任何信息。从2020年4月1日到同月底,560名连续癌症患者,Covid-19和贝加莫帕帕·朱瓦氏XXIII医院的抗癌患者进行了评估,并对SARS-COV-2进行了评估和测试。我们实施了两步的诊断,包括用于抗SARS-COV-2免疫球蛋白(Ig)G / IgM的快速血清学免疫测定和在血液呈阳性的情况下识别的情况下的鼻咽拭子逆转录酶链反应(RT-PCR)测试SARS-COV-2无声载体。结果560名患者,172名(31%)导致抗SARS-COV-2 IgM / IgG抗体阳性,无论不同类型的癌症,阶段和治疗如何。然后用RT-PCR鼻咽拭子测试Ig-血清阳性患者,并证明是SARS-COV-2无声载体的38%。在早期的随访中,在97个SARS-COV-2 - 血清阳性/ RT-PCR阴性患者中,持续抗癌疗法,只有一个突出的症状性Covid-19疾病。结论癌症患者,两步诊断对于SARS-COV-2无声载体检测是可行的,有效,并且可能支持个人和人口水平的最佳癌症治疗策略。在先前暴露于SARS-COV-2的患者中,不同抗癌疗法的早期安全性曲线支持至少在RT-PCR阴性患者的情况下继续活跃治疗的建议。对实践的影响这是第一项研究评估SARS-COV-2在Covid-19大流行的最差地区之一的流行病峰期间SARS-COV-2无声感染的患病率和临床影响。缺乏用于检测无症状SARS-COV-2感染的国家和国际建议,实施了务实和有效的两步诊断,以确定SARS-COV-2无声载体。在本系列中,由连续和未选择的癌症患者组成,SARS-COV-2血清阳性患者和静音载体的患病率显着(分别为31%和10%)。在先前暴露于SARS-COV-2的患者中,不同抗癌疗法的早期安全性曲线支持至少在RT-PCR阴性患者的情况下继续进行活性治疗的建议。

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