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后疫情时代多发性骨髓瘤合并 COVID-19 患者的管理:欧洲骨髓瘤网络(EMN)共识文件

英文原题:Management of patients with multiple myeloma and COVID-19 in the post pandemic era: a consensus paper from the European Myeloma Network (EMN).

PubMed 2023/05/04(内容时间) Leukemia Q1 · IF 8.8(JCR 2025)

研究概要

在后疫情COVID-19时期,人类活动已恢复正常,COVID-19病例通常症状轻微。

中文摘要

在后疫情COVID-19时期,人类活动已恢复正常,COVID-19病例通常症状轻微。然而,多发性骨髓瘤(MM)患者出现突破性感染和重症COVID-19结局(包括住院和死亡)的风险增加。欧洲骨髓瘤网络提供了专家共识,以指导该时代的患者管理。随着新变异株出现并在社区中成为优势株,接种针对变异株的加强疫苗(如针对祖先武汉株和Omicron BA.4/5株的二价疫苗)至关重要。应在末次疫苗接种或确诊COVID-19感染(混合免疫)后每6-12个月接种一次加强针。加强针似乎可以克服抗CD38单克隆抗体对体液反应的负面影响;然而,抗BCMA治疗仍然是体液免疫反应的不良预测因素。评估疫苗接种后的免疫反应可能识别出特别脆弱的一部分患者,他们可能需要额外的加强针、预防性治疗和预防措施。使用tixagevimab/cilgavimab进行暴露前预防对新的优势变异株无效,因此不再推荐。口服抗病毒药物(nirmatrelvir/ritonavir和molnupiravir)和remdesivir对Omicron亚变异株BA.2.12.1、BA.4、BA.5、BQ.1.1和/或XBB.1.5有效,应在MM患者COVID-19检测阳性时或症状出现后5天内给药。恢复期血浆在后疫情时代似乎价值较低。在SARS-CoV-2暴发期间,MM患者继续采取预防措施(包括佩戴口罩和避免前往拥挤场所)似乎是审慎的。

展开英文摘要原文

In the post-pandemic COVID-19 period, human activities have returned to normal and COVID-19 cases are usually mild. However, patients with multiple myeloma (MM) present an increased risk for breakthrough infections and severe COVID-19 outcomes, including hospitalization and death. The European Myeloma Network has provided an expert consensus to guide patient management in this era. Vaccination with variant-specific booster vaccines, such as the bivalent vaccine for the ancestral Wuhan strain and the Omicron BA.4/5 strains, is essential as novel strains emerge and become dominant in the community. Boosters should be administered every 6-12 months after the last vaccine shot or documented COVID-19 infection (hybrid immunity). Booster shots seem to overcome the negative effect of anti-CD38 monoclonal antibodies on humoral responses; however, anti-BCMA treatment remains an adverse predictive factor for humoral immune response. Evaluation of the immune response after vaccination may identify a particularly vulnerable subset of patients who may need additional boosters, prophylactic therapies and prevention measures. Pre-exposure prophylaxis with tixagevimab/cilgavimab is not effective against the new dominant variants and thus is no longer recommended. Oral antivirals (nirmatrelvir/ritonavir and molnupiravir) and remdesivir are effective against Omicron subvariants BA.2.12.1, BA.4, BA.5, BQ.1.1 and/or XBB.1.5 and should be administered in MM patients at the time of a positive COVID-19 test or within 5 days post symptoms onset. Convalescent plasma seems to have low value in the post-pandemic era. Prevention measures during SARS-CoV-2 outbreaks, including mask wearing and avoiding crowded places, seem prudent to continue for MM patients.

论文信息

作者
Terpos E、Musto P、Engelhardt M、Delforge M、Cook G、Gay F、van de Donk NWCJ、Ntanasis-Stathopoulos I
单位
Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece. eterpos@med.uoa.gr.Greece
文献类型
综述 · 共识声明
期刊
Leukemia2023 Jun
原文标识
PubMed 37142661 · DOI 10.1038/s41375-023-01920-1