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Utilization of COVID-19 Treatments and Clinical Outcomes among Patients with Cancer: A COVID-19 and Cancer Consortium (CCC19) Cohort Study.
Rivera, Donna R; Peters, Solange; Panagiotou, Orestis A; Shah, Dimpy P; Kuderer, Nicole M; Hsu, Chih-Yuan; Rubinstein, Samuel M; Lee, Brendan J; Choueiri, Toni K; de Lima Lopes, Gilberto; Grivas, Petros; Painter, Corrie A; Rini, Brian I; Thompson, Michael A; Arcobello, Jonathan; Bakouny, Ziad; Doroshow, Deborah B; Egan, Pamela C; Farmakiotis, Dimitrios; Fecher, Leslie A; Friese, Christopher R; Galsky, Matthew D; Goel, Sanjay; Gupta, Shilpa; Halfdanarson, Thorvardur R; Halmos, Balazs; Hawley, Jessica E; Khaki, Ali Raza; Lemmon, Christopher A; Mishra, Sanjay; Olszewski, Adam J; Pennell, Nathan A; Puc, Matthew M; Revankar, Sanjay G; Schapira, Lidia; Schmidt, Andrew; Schwartz, Gary K; Shah, Sumit A; Wu, Julie T; Xie, Zhuoer; Yeh, Albert C; Zhu, Huili; Shyr, Yu; Lyman, Gary H; Warner, Jeremy L.
  • Rivera DR; Division of Cancer Control and Population Sciences, NCI, Rockville, Maryland.
  • Peters S; Department of Oncology, University of Lausanne, Lausanne, Switzerland.
  • Panagiotou OA; Department of Health Services, Policy and Practice, Brown University, Providence, Rhode Island.
  • Shah DP; Department of Population Health Sciences, Mays Cancer Center, UT Health San Antonio MD Anderson, San Antonio, Texas.
  • Kuderer NM; Advanced Cancer Research Group, LLC, Kirkland, Washington.
  • Hsu CY; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Rubinstein SM; Deparment of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Lee BJ; Deparment of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Choueiri TK; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • de Lima Lopes G; Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida.
  • Grivas P; Department of Medicine, Division of Oncology, University of Washington, Seattle, Washington.
  • Painter CA; Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Rini BI; Count Me In, Cambridge, Massachusetts.
  • Thompson MA; Deparment of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Arcobello J; Advocate Aurora Health, Milwaukee, Wisconsin.
  • Bakouny Z; Karmanos Cancer Institute, Detroit, Michigan.
  • Doroshow DB; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Egan PC; Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Farmakiotis D; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Fecher LA; Department of Medicine, Division of Hematology/Oncology, The Warren Alpert Medical School of Brown University, Providence, Rhode Island.
  • Friese CR; Department of Medicine, Division of Infectious Diseases, The Warren Alpert Medical School of Brown University, Providence, Rhode Island.
  • Galsky MD; Department of Internal Medicine, Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
  • Goel S; School of Nursing, University of Michigan, Ann Arbor, Michigan.
  • Gupta S; Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Halfdanarson TR; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Halmos B; Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
  • Hawley JE; Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, Ohio.
  • Khaki AR; Department of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
  • Lemmon CA; Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
  • Mishra S; Department of Medicine, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York.
  • Olszewski AJ; Department of Medicine, Division of Oncology, University of Washington, Seattle, Washington.
  • Pennell NA; Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, Ohio.
  • Puc MM; Vanderbilt-Ingram Cancer Center, Nashville, Tennessee.
  • Revankar SG; Department of Medicine, Division of Hematology/Oncology, The Warren Alpert Medical School of Brown University, Providence, Rhode Island.
  • Schapira L; Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, Ohio.
  • Schmidt A; Department of Surgery, Section of Thoracic Surgery, Virtua Health, Marlton, New Jersey.
  • Schwartz GK; Karmanos Cancer Institute, Detroit, Michigan.
  • Shah SA; Department of Medicine, Division of Oncology, Stanford University, Palo Alto, California.
  • Wu JT; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Xie Z; Department of Medicine, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York.
  • Yeh AC; Department of Medicine, Division of Oncology, Stanford University, Palo Alto, California.
  • Zhu H; Department of Medicine, Division of Oncology, Stanford University, Palo Alto, California.
  • Shyr Y; Department of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
  • Lyman GH; Department of Medicine, Division of Oncology, University of Washington, Seattle, Washington.
  • Warner JL; Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Cancer Discov ; 10(10): 1514-1527, 2020 10.
Article in English | MEDLINE | ID: covidwho-981743
ABSTRACT
Among 2,186 U.S. adults with invasive cancer and laboratory-confirmed SARS-CoV-2 infection, we examined the association of COVID-19 treatments with 30-day all-cause mortality and factors associated with treatment. Logistic regression with multiple adjustments (e.g., comorbidities, cancer status, baseline COVID-19 severity) was performed. Hydroxychloroquine with any other drug was associated with increased mortality versus treatment with any COVID-19 treatment other than hydroxychloroquine or untreated controls; this association was not present with hydroxychloroquine alone. Remdesivir had numerically reduced mortality versus untreated controls that did not reach statistical significance. Baseline COVID-19 severity was strongly associated with receipt of any treatment. Black patients were approximately half as likely to receive remdesivir as white patients. Although observational studies can be limited by potential unmeasured confounding, our findings add to the emerging understanding of patterns of care for patients with cancer and COVID-19 and support evaluation of emerging treatments through inclusive prospective controlled trials.

SIGNIFICANCE:

Evaluating the potential role of COVID-19 treatments in patients with cancer in a large observational study, there was no statistically significant 30-day all-cause mortality benefit with hydroxychloroquine or high-dose corticosteroids alone or in combination; remdesivir showed potential benefit. Treatment receipt reflects clinical decision-making and suggests disparities in medication access.This article is highlighted in the In This Issue feature, p. 1426.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Drug Utilization / Healthcare Disparities / Neoplasms Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Country/Region as subject: North America Language: English Journal: Cancer Discov Year: 2020 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Drug Utilization / Healthcare Disparities / Neoplasms Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Country/Region as subject: North America Language: English Journal: Cancer Discov Year: 2020 Document Type: Article