Choueiri Toni K, Labaki Chris, Bakouny Ziad, Hsu Chih-Yuan, Schmidt Andrew L, de Lima Lopes Gilberto, Hwang Clara, Singh Sunny R K, Jani Chinmay, Weissmann Lisa B, Griffiths Elizabeth A, Halabi Susan, Wu Ulysses, Berg Stephanie, O'Connor Timothy E, Wise-Draper Trisha M, Panagiotou Orestis A, Klein Elizabeth J, Joshi Monika, Yared Fares, Dutra Miriam Santos, Gatson Na Tosha N, Blau Sibel, Singh Harpreet, Nanchal Rahul, McKay Rana R, Nonato Taylor K, Quinn Ryann, Rubinstein Samuel M, Puc Matthew, Mavromatis Blanche H, Vikas Praveen, Faller Bryan, Zaren Howard A, Del Prete Salvatore, Russell Karen, Reuben Daniel Y, Accordino Melissa K, Singh Harpreet, Friese Christopher R, Mishra Sanjay, Rivera Donna R, Shyr Yu, Farmakiotis Dimitrios, Warner Jeremy L
Dana-Farber Cancer Institute, Boston, MA, USA.
Brigham and Women's Hospital, Boston, MA, USA.
Lancet Reg Health Am. 2023 Mar;19:100445. doi: 10.1016/j.lana.2023.100445. Epub 2023 Feb 13.
Breakthrough SARS-CoV-2 infections following vaccination against COVID-19 are of international concern. Patients with cancer have been observed to have worse outcomes associated with COVID-19 during the pandemic. We sought to evaluate the clinical characteristics and outcomes of patients with cancer who developed breakthrough SARS-CoV-2 infections after 2 or 3 doses of mRNA vaccines.
We evaluated the clinical characteristics of patients with cancer who developed breakthrough infections using data from the multi-institutional COVID-19 and Cancer Consortium (CCC19; NCT04354701). Analysis was restricted to patients with laboratory-confirmed SARS-CoV-2 diagnosed in 2021 or 2022, to allow for a contemporary unvaccinated control population; potential differences were evaluated using a multivariable logistic regression model after inverse probability of treatment weighting to adjust for potential baseline confounding variables. Adjusted odds ratios (aOR) and 95% confidence intervals (CI) are reported. The primary endpoint was 30-day mortality, with key secondary endpoints of hospitalization and ICU and/or mechanical ventilation (ICU/MV).
The analysis included 2486 patients, of which 564 and 385 had received 2 or 3 doses of an mRNA vaccine prior to infection, respectively. Hematologic malignancies and recent receipt of systemic anti-neoplastic therapy were more frequent among vaccinated patients. Vaccination was associated with improved outcomes: in the primary analysis, 2 doses (aOR: 0.62, 95% CI: 0.44-0.88) and 3 doses (aOR: 0.20, 95% CI: 0.11-0.36) were associated with decreased 30-day mortality. There were similar findings for the key secondary endpoints of ICU/MV (aOR: 0.60, 95% CI: 0.45-0.82 and 0.37, 95% CI: 0.24-0.58) and hospitalization (aOR: 0.60, 95% CI: 0.48-0.75 and 0.35, 95% CI: 0.26-0.46) for 2 and 3 doses, respectively. Importantly, Black patients had higher rates of hospitalization (aOR: 1.47, 95% CI: 1.12-1.92), and Hispanic patients presented with higher rates of ICU/MV (aOR: 1.61, 95% CI: 1.06-2.44).
Vaccination against COVID-19, especially with additional doses, is a fundamental strategy in the prevention of adverse outcomes including death, among patients with cancer.
This study was partly supported by grants from the National Cancer Institute grant number P30 CA068485 to C-YH, YS, SM, JLW; T32-CA236621 and P30-CA046592 to C.R.F; CTSA 2UL1TR001425-05A1 to TMW-D; ACS/FHI Real-World Data Impact Award, P50 MD017341-01, R21 CA242044-01A1, Susan G. Komen Leadership Grant Hunt to MKA. REDCap is developed and supported by Vanderbilt Institute for Clinical and Translational Research grant support (UL1 TR000445 from NCATS/NIH).
接种新冠疫苗后出现的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)突破性感染受到国际关注。在疫情期间,观察到癌症患者感染新冠病毒后的预后较差。我们试图评估在接种2剂或3剂信使核糖核酸(mRNA)疫苗后出现SARS-CoV-2突破性感染的癌症患者的临床特征和预后。
我们使用来自多机构新冠与癌症联盟(CCC19;NCT04354701)的数据,评估出现突破性感染的癌症患者的临床特征。分析仅限于2021年或2022年实验室确诊SARS-CoV-2的患者,以便有一个同期未接种疫苗的对照人群;在采用治疗权重逆概率调整潜在基线混杂变量后,使用多变量逻辑回归模型评估潜在差异。报告调整后的优势比(aOR)和95%置信区间(CI)。主要终点是30天死亡率,关键次要终点是住院、入住重症监护病房(ICU)和/或机械通气(ICU/MV)。
分析纳入2486例患者,其中564例和385例在感染前分别接种了2剂或3剂mRNA疫苗。血液系统恶性肿瘤和近期接受全身抗肿瘤治疗在接种疫苗的患者中更为常见。接种疫苗与改善预后相关:在初步分析中,2剂(aOR:0.62,95%CI:0.44-0.88)和3剂(aOR:0.20,95%CI:0.11-0.36)与30天死亡率降低相关。对于ICU/MV(aOR:0.60,95%CI:0.45-0.82和0.37,95%CI:0.24-0.58)和住院(aOR:0.60,95%CI:0.48-0.75和0.35,95%CI:0.26-0.46)这两个关键次要终点,2剂和3剂疫苗分别有类似的结果。重要的是,黑人患者住院率较高(aOR:1.47,95%CI:1.12-1.92),西班牙裔患者ICU/MV率较高(aOR:1.61,95%CI:1.06-2.44)。
接种新冠疫苗,尤其是额外接种几剂,是预防癌症患者包括死亡在内的不良后果的基本策略。
本研究部分得到了美国国立癌症研究所的资助,编号分别为P30 CA068485给C-YH、YS、SM、JLW;T32-CA236621和P30-CA046592给C.R.F;CTSA 2UL1TR001425-05A1给TMW-D;美国癌症协会/家庭健康国际真实世界数据影响奖、P50 MD017341-01、R21 CA242044-01A1、苏珊·G·科门领导力资助亨特给MKA。REDCap由范德比尔特临床与转化研究所以及美国国立转化医学推进中心/美国国立卫生研究院(NCATS/NIH)的UL1 TR000445资助开发和支持。