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西班牙马德里一家三级医院接受积极治疗的癌症患者队列中,三种剂量的严重急性呼吸综合征冠状病毒 2(SARS-COV-2)mRNA-1273 疫苗的不良反应。

Adverse drug reactions to the three doses of the severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) mRNA-1273 vaccine in a cohort of cancer patients under active treatment of a tertiary hospital in Madrid, Spain.

机构信息

Medical Oncology Department, IdISSC, Hospital Clinico San Carlos, Madrid, Madrid, 28040, Spain.

Bloomberg School of Public Health MD, 21205, USA, Johns Hopkins University, Baltimore, Maryland, 21205, USA.

出版信息

F1000Res. 2022 Apr 19;11:434. doi: 10.12688/f1000research.110268.2. eCollection 2022.

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines efficacy and safety have been tested in phase 3 studies in which cancer patients were not included or were underrepresented. The objective of this study is to evaluate the safety profile of the mRNA-1273 vaccine across cancer patients and its relationship to patients' demographics. We selected from our records all 18-years or older solid cancer patients under active treatment vaccinated with the complete three-dose schedule mRNA-1273 vaccine whose adverse drug reactions (ADRs)  after each dose were recorded. Medical records were reviewed retrospectively to collect data between April 19, 2021, and December 31, 2021. Patients with documented previous infection by SARS-Cov-2 were excluded. A total of 93 patients met the inclusion criteria. Local ADRs were reported more frequently after the first and second dose than after the third (41.9%, 43% and 31.1% of the patients respectively), while systemic ADRs followed the opposite pattern (16.1%, 34.4% and 52.6% of the patients respectively). We found a statistically significant association between sex and systemic adverse reactions after the third dose, p < 0.001 and between systemic adverse reactions after the second dose and systemic adverse reactions after the third dose, p = 0.001 A significant linear trend, = 0.012, with a higher Eastern Cooperative Oncology Group (ECOG) score associated with a lower proportion of patients suffering from systemic side effects was found. Women had 5.79 times higher odds to exhibit systemic ADRs after the third dose (p=0.01) compared to males. Increasing age was associated with a decreased likelihood of exhibiting ADRs (p=0.016).  The mRNA-1273 vaccine shows a tolerable safety profile. The likelihood of ADRs appears to be associated with gender and age. Its association with ECOG scores is less evident. Further studies are needed to elucidate this data in cancer patients.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)疫苗的疗效和安全性已在 3 期研究中得到测试,但这些研究未纳入或代表性不足癌症患者。本研究的目的是评估 mRNA-1273 疫苗在癌症患者中的安全性概况及其与患者人口统计学特征的关系。我们从记录中选择了所有 18 岁或以上正在接受积极治疗的实体癌患者,这些患者接受了完整的三剂 mRNA-1273 疫苗接种,并且记录了每剂后的药物不良反应(ADR)。回顾性审查病历以收集 2021 年 4 月 19 日至 2021 年 12 月 31 日之间的数据。排除有 SARS-CoV-2 既往感染记录的患者。共有 93 名患者符合纳入标准。局部 ADR 在第一剂和第二剂后比第三剂更频繁地报告(分别为 41.9%、43%和 31.1%的患者),而全身 ADR 则相反(分别为 16.1%、34.4%和 52.6%的患者)。我们发现,在第三剂后,性别与全身不良反应之间存在统计学显著关联,p<0.001,在第二剂后和第三剂后全身不良反应之间存在统计学显著关联,p=0.001,具有统计学意义的线性趋势,=0.012,ECOG 评分越高,全身不良反应患者比例越低。与男性相比,女性在第三剂后发生全身 ADR 的几率高 5.79 倍(p=0.01)。年龄越大,发生 ADR 的可能性越低(p=0.016)。mRNA-1273 疫苗具有可耐受的安全性。ADR 的发生似乎与性别和年龄有关。与 ECOG 评分的关系不太明显。需要进一步研究来阐明癌症患者中的这些数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/9816672/1b1dff945c8f/f1000research-11-136429-g0000.jpg

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