Nuzzo Amedeo, Manacorda Simona, Sammarco Enrico, Sbrana Andrea, Bazzurri Serena, Paolieri Federico, Manfredi Fiorella, Mercinelli Chiara, Ferrari Marco, Massaro Giulia, Bonato Adele, Salfi Alessia, Galli Luca, Morganti Riccardo, Antonuzzo Andrea, Cremolini Chiara, Masi Gianluca
Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Santa Chiara Hospital, 56125 Pisa, Italy.
Department of Surgical, Medical and Molecular Pathology and Critical Area Medicine, Azienda Ospedaliero-Universitaria Pisana, 56125 Pisa, Italy.
Vaccines (Basel). 2022 Jun 2;10(6):892. doi: 10.3390/vaccines10060892.
Severe acute respiratory syndrome coronavirus 2 disease (COVID-19) has caused a worldwide challenging and threatening pandemic. Multinational, placebo-controlled, observer-blinded trials were conducted since the beginning of pandemic because safe and effective vaccines were needed urgently. In most trials of COVID-19 vaccines patients affected by malignancies or on treatment with immunosuppressive drugs were excluded.
A retrospective monocentric study was conducted at Medical Oncological Unit of Santa Chiara Hospital (Pisa, Italy) in this subset of population to investigate safety and tolerability of COVID-19 vaccines; 377 patients with solid tumor on treatment were enrolled. Vaccine-related adverse events were recorded using a face-to-face questionnaire including a toxicity grading scale. Most of the patients (94%) received mRNA vaccine as indicated by Italian health ministry guidelines. Mean age was 66 years (range 27-87), 62% of the patients were older than 65 years and 68% had at least one additional comorbidity. The majority (86%) of patients were in a metastatic setting and 29% received immunotherapy-based treatment. For statistical analysis, multivariate binary logistic regression models were performed and linear regression models were applied.
Adverse events were mild and transient and ended in a few days without any sequelae. No severe or uncommon adverse events were recorded. In multivariate analysis, we found that the female sex was associated with a greater risk of more severe and longer lasting adverse events, and a higher risk of adverse events was found for patients treated with immunotherapy.
Our results demonstrate that COVID-19 vaccines were safe and well-tolerated in this population of patients being treated for solid tumors.
严重急性呼吸综合征冠状病毒2疾病(COVID-19)已引发一场具有全球挑战性和威胁性的大流行。自疫情开始以来,开展了多项跨国、安慰剂对照、观察者盲法试验,因为迫切需要安全有效的疫苗。在大多数COVID-19疫苗试验中,患有恶性肿瘤或正在接受免疫抑制药物治疗的患者被排除在外。
在意大利比萨圣基亚拉医院医学肿瘤科室对这一亚组人群进行了一项回顾性单中心研究,以调查COVID-19疫苗的安全性和耐受性;纳入了377例正在接受治疗的实体瘤患者。使用包括毒性分级量表的面对面问卷记录与疫苗相关的不良事件。按照意大利卫生部指南,大多数患者(94%)接种了mRNA疫苗。平均年龄为66岁(范围27 - 87岁),62%的患者年龄超过65岁,68%的患者至少有一种合并症。大多数患者(86%)处于转移状态,29%接受了基于免疫疗法的治疗。进行统计分析时,采用了多变量二元逻辑回归模型并应用了线性回归模型。
不良事件轻微且短暂,数天内结束,无任何后遗症。未记录到严重或罕见的不良事件。在多变量分析中,我们发现女性发生更严重、持续时间更长的不良事件的风险更高,接受免疫疗法治疗的患者发生不良事件的风险更高。
我们的结果表明,COVID-19疫苗在这一接受实体瘤治疗的患者群体中是安全且耐受性良好的。