TY - JOUR
T1 - International Multicenter Study Comparing COVID-19 in Patients With Cancer to Patients Without Cancer
T2 - Impact of Risk Factors and Treatment Modalities on Survivorship
AU - Data-Driven Determinants for COVID-19 Oncology Discovery Effort (D3CODE) Team
AU - Raad, Issam
AU - Hachem, Ray
AU - Masayuki, Nigo
AU - Datoguia, Tarcila
AU - Dagher, Hiba
AU - Jiang, Ying
AU - Subbiah, Vivek
AU - Siddiqui, Bilal
AU - Bayle, Arnaud
AU - Somer, Robert
AU - Cruz, Ana Fernández
AU - Gorak, Edward
AU - Bhinder, Arvinder
AU - Mori, Nobuyoshi
AU - Hamerschlak, Nelson
AU - Shelanski, Samuel
AU - Dragivich, Tomislav
AU - Kiat, Yee Elise Vong
AU - Fakhreddine, Suha
AU - Hanna, Pierre Abi
AU - Chemaly, Roy F.
AU - Mulanovich, Victor
AU - Adachi, Javier
AU - Borjan, Jovan
AU - Khawaja, Fareed
AU - Granwehr, Bruno
AU - John, Teny
AU - Guevara, Eduardo Yepez
AU - Torres, Harrys A.
AU - Ammakkanavar, Natraj Reddy
AU - Yibirin, Marcel
AU - Reyes-Gibby, Cielito C.
AU - Pande, Mala
AU - Ali, Noman
AU - Rojo, Raniv Dawey
AU - Ali, Shahnoor M.
AU - Deeba, Rita E.
AU - Chaftari, Patrick
AU - Matsuo, Takahiro
AU - Ishikawa, Kazuhiro
AU - Hasegawa, Ryo
AU - Aguado-Noya, Ramón
AU - García, Álvaro García
AU - Puchol, Cristina Traseira
AU - Lee, Dong Gun
AU - Slavin, Monica
AU - Teh, Benjamin
AU - Arias, Cesar A.
AU - Kontoyiannis, Dimitrios P.
AU - Malek, Alexandre E.
N1 - Publisher Copyright:
© 2023, eLife Sciences Publications Ltd. All rights reserved.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Background: In this international multicenter study we aimed to determine the independent risk factors associated with increased 30-day mortality and the impact of cancer and novel treatment modalities in a large group of patients with and without cancer with COVID-19 from multiple countries. Methods: We retrospectively collected de-identified data on a cohort of patients with and without cancer diagnosed with COVID-19 between January and November 2020, from 16 international centers. Results: We analyzed 3966 COVID-19 confirmed patients, 1115 with cancer and 2851 nwithout cancer patients. Patients with cancer were more likely to be pancytopenic, and have a smoking history, pulmonary disorders, hypertension, diabetes mellitus, and corticosteroid use in the preceding two weeks (p≤0.01). In addition, they were more likely to present with higher inflammatory biomarkers (D-dimer, ferritin and procalcitonin), but were less likely to present with clinical symptoms (p≤0.01). By country-adjusted multivariable logistic regression analyses, cancer was not found to be an independent risk factor for 30-day mortality (p=0.18) whereas lymphopenia was independently associated with increased mortality in all patients, and in patients with cancer. Older age (≥65 years) was the strongest predictor of 30-day mortality in all patients(OR=4.47, p<0.0001). Remdesivir was the only therapeutic agent independently associated with decreased 30-day mortality ()(OR=0.64, p=0.036). Among patients on low-flow oxygen at admission, patients who received remdesivir had a lower 30-day mortality rate than those who did not (5.9% vs 17.6%; p=0.03). Conclusions: Increased 30-day all-cause mortality from COVID-19 was not independently associated with cancer but was independently associated with lymphopenia often observed in hematolgic malignancy. Remdesivir, particularly in patients with cancer receiving low-flow oxygen, can reduce 30-day all-cause mortality. Funding: National Cancer Institute, National Institutes of Health Condensed Abstract In this large multicenter worldwide study of 4015 patients with COVID-19 that included 1115 patients with cancer, we found that cancer is an independent risk factor for increased 30-day allcause mortality. Remdesivir is a promising treatment modality to reduce 30-day all-cause mortality.
AB - Background: In this international multicenter study we aimed to determine the independent risk factors associated with increased 30-day mortality and the impact of cancer and novel treatment modalities in a large group of patients with and without cancer with COVID-19 from multiple countries. Methods: We retrospectively collected de-identified data on a cohort of patients with and without cancer diagnosed with COVID-19 between January and November 2020, from 16 international centers. Results: We analyzed 3966 COVID-19 confirmed patients, 1115 with cancer and 2851 nwithout cancer patients. Patients with cancer were more likely to be pancytopenic, and have a smoking history, pulmonary disorders, hypertension, diabetes mellitus, and corticosteroid use in the preceding two weeks (p≤0.01). In addition, they were more likely to present with higher inflammatory biomarkers (D-dimer, ferritin and procalcitonin), but were less likely to present with clinical symptoms (p≤0.01). By country-adjusted multivariable logistic regression analyses, cancer was not found to be an independent risk factor for 30-day mortality (p=0.18) whereas lymphopenia was independently associated with increased mortality in all patients, and in patients with cancer. Older age (≥65 years) was the strongest predictor of 30-day mortality in all patients(OR=4.47, p<0.0001). Remdesivir was the only therapeutic agent independently associated with decreased 30-day mortality ()(OR=0.64, p=0.036). Among patients on low-flow oxygen at admission, patients who received remdesivir had a lower 30-day mortality rate than those who did not (5.9% vs 17.6%; p=0.03). Conclusions: Increased 30-day all-cause mortality from COVID-19 was not independently associated with cancer but was independently associated with lymphopenia often observed in hematolgic malignancy. Remdesivir, particularly in patients with cancer receiving low-flow oxygen, can reduce 30-day all-cause mortality. Funding: National Cancer Institute, National Institutes of Health Condensed Abstract In this large multicenter worldwide study of 4015 patients with COVID-19 that included 1115 patients with cancer, we found that cancer is an independent risk factor for increased 30-day allcause mortality. Remdesivir is a promising treatment modality to reduce 30-day all-cause mortality.
KW - COVID-19
KW - cancer
KW - coronavirus
UR - http://www.scopus.com/inward/record.url?scp=85147157203&partnerID=8YFLogxK
U2 - 10.7554/eLife.81127
DO - 10.7554/eLife.81127
M3 - Article
C2 - 36715684
AN - SCOPUS:85147157203
SN - 2050-084X
VL - 12
JO - eLife
JF - eLife
M1 - e81127
ER -