Trillo Aliaga Pamela, Trapani Dario, Sandoval José Luis, Crimini Edoardo, Antonarelli Gabriele, Vivanet Grazia, Morganti Stefania, Corti Chiara, Tarantino Paolo, Friedlaender Alex, Belli Carmen, Minchella Ida, Locatelli Marzia, Esposito Angela, Criscitiello Carmen, Curigliano Giuseppe
Division of New Drugs and Early Drug Development, European Institute of Oncology IRCCS, 20141 Milan, Italy.
Department of Oncology and Hematology, University of Milan, 20122 Milan, Italy.
Cancers (Basel). 2021 Nov 20;13(22):5829. doi: 10.3390/cancers13225829.
Pivotal trials of COVID-19 vaccines did not include cancer patients, with questions remaining about their safety and efficacy in this population. Patients enrolled in early-phase clinical trials receive novel treatments with unknown efficacy and safety profiles. Studies on the safety of COVID-19 vaccines in these patients are urgently required. This is a retrospective, real-world, cohort study of patients receiving anticancer treatments and COVID-19 vaccines between 1 February and 25 June 2021 at the Division of New Drugs Development for Innovative Therapies of the European Institute of Oncology. One hundred thirteen patients were enrolled, 40 in early-phase clinical trials, and 20 under novel immunotherapy agents. Nearly three-quarters of the patients experienced at least one adverse event (AE) after the first dose (1D) (74.3%) and second dose (2D) (72.6%). Most of the AEs were local (67.3% 1D and 61.9% after 2D), while 31.8% (1D) and 38.1% (2D) of the patients had systemic AEs. No AEs above grade 2 were observed. Therefore, COVID-19 vaccines appear to be safe in patients enrolled in early-phase clinical trials, including patients receiving novel immunotherapy compounds. All cancer patients should be prioritized for COVID-19 vaccination, regardless of ongoing treatments or enrollment in early-phase trials.
新冠疫苗的关键试验未纳入癌症患者,其在这一人群中的安全性和有效性仍存在疑问。参与早期临床试验的患者接受的是疗效和安全性未知的新型治疗。迫切需要开展关于新冠疫苗在这些患者中安全性的研究。这是一项回顾性、基于真实世界的队列研究,研究对象为2021年2月1日至6月25日期间在欧洲肿瘤研究所创新疗法新药研发部门接受抗癌治疗并接种新冠疫苗的患者。共纳入113名患者,其中40名处于早期临床试验阶段,20名正在接受新型免疫治疗药物治疗。近四分之三的患者在接种第一剂(1D)和第二剂(2D)后至少经历了一次不良事件(AE)(第一剂为74.3%,第二剂为72.6%)。大多数不良事件为局部反应(第一剂为67.3%,第二剂后为61.9%),而31.8%(第一剂)和38.1%(第二剂)的患者出现全身不良事件。未观察到2级以上的不良事件。因此,新冠疫苗在参与早期临床试验的患者中似乎是安全的,包括接受新型免疫治疗化合物的患者。所有癌症患者都应优先接种新冠疫苗,无论其是否正在接受治疗或参与早期试验。