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Clinical impact of COVID-19 on patients with cancer (CCC19): a cohort study
- Source :
- Lancet, vol. 395, no. 10241, pp. 1907-1918, The Lancet
- Publication Year :
- 2020
- Publisher :
- Elsevier BV, 2020.
-
Abstract
- Summary Background Data on patients with COVID-19 who have cancer are lacking. Here we characterise the outcomes of a cohort of patients with cancer and COVID-19 and identify potential prognostic factors for mortality and severe illness. Methods In this cohort study, we collected de-identified data on patients with active or previous malignancy, aged 18 years and older, with confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection from the USA, Canada, and Spain from the COVID-19 and Cancer Consortium (CCC19) database for whom baseline data were added between March 17 and April 16, 2020. We collected data on baseline clinical conditions, medications, cancer diagnosis and treatment, and COVID-19 disease course. The primary endpoint was all-cause mortality within 30 days of diagnosis of COVID-19. We assessed the association between the outcome and potential prognostic variables using logistic regression analyses, partially adjusted for age, sex, smoking status, and obesity. This study is registered with ClinicalTrials.gov, NCT04354701, and is ongoing. Findings Of 1035 records entered into the CCC19 database during the study period, 928 patients met inclusion criteria for our analysis. Median age was 66 years (IQR 57–76), 279 (30%) were aged 75 years or older, and 468 (50%) patients were male. The most prevalent malignancies were breast (191 [21%]) and prostate (152 [16%]). 366 (39%) patients were on active anticancer treatment, and 396 (43%) had active (measurable) cancer. At analysis (May 7, 2020), 121 (13%) patients had died. In logistic regression analysis, independent factors associated with increased 30-day mortality, after partial adjustment, were: increased age (per 10 years; partially adjusted odds ratio 1·84, 95% CI 1·53–2·21), male sex (1·63, 1·07–2·48), smoking status (former smoker vs never smoked: 1·60, 1·03–2·47), number of comorbidities (two vs none: 4·50, 1·33–15·28), Eastern Cooperative Oncology Group performance status of 2 or higher (status of 2 vs 0 or 1: 3·89, 2·11–7·18), active cancer (progressing vs remission: 5·20, 2·77–9·77), and receipt of azithromycin plus hydroxychloroquine (vs treatment with neither: 2·93, 1·79–4·79; confounding by indication cannot be excluded). Compared with residence in the US-Northeast, residence in Canada (0·24, 0·07–0·84) or the US-Midwest (0·50, 0·28–0·90) were associated with decreased 30-day all-cause mortality. Race and ethnicity, obesity status, cancer type, type of anticancer therapy, and recent surgery were not associated with mortality. Interpretation Among patients with cancer and COVID-19, 30-day all-cause mortality was high and associated with general risk factors and risk factors unique to patients with cancer. Longer follow-up is needed to better understand the effect of COVID-19 on outcomes in patients with cancer, including the ability to continue specific cancer treatments. Funding American Cancer Society, National Institutes of Health, and Hope Foundation for Cancer Research.
- Subjects :
- Prognostic variable
medicine.medical_specialty
business.industry
Cancer
General Medicine
Odds ratio
Aged
Antiviral Agents/therapeutic use
Azithromycin/therapeutic use
Betacoronavirus
Cause of Death
Comorbidity
Coronavirus Infections/drug therapy
Coronavirus Infections/epidemiology
Coronavirus Infections/mortality
Databases, Factual
Female
Humans
Hydroxychloroquine/therapeutic use
Male
Middle Aged
Neoplasms/epidemiology
Neoplasms/mortality
Neoplasms/therapy
Pandemics
Pneumonia, Viral/drug therapy
Pneumonia, Viral/epidemiology
Pneumonia, Viral/mortality
Prognosis
Risk Factors
030204 cardiovascular system & hematology
medicine.disease
03 medical and health sciences
0302 clinical medicine
Internal medicine
Cohort
Clinical endpoint
Medicine
030212 general & internal medicine
business
Cause of death
Cohort study
Subjects
Details
- ISSN :
- 01406736
- Volume :
- 395
- Database :
- OpenAIRE
- Journal :
- The Lancet
- Accession number :
- edsair.doi.dedup.....21d89f8d57a74fe5fc8b244572e6a776
- Full Text :
- https://doi.org/10.1016/s0140-6736(20)31187-9