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Patients Recently Treated for B-lymphoid Malignancies Show Increased Risk of Severe COVID-19.
Rubinstein, Samuel M; Bhutani, Divaya; Lynch, Ryan C; Hsu, Chih-Yuan; Shyr, Yu; Advani, Shailesh; Mesa, Ruben A; Mishra, Sanjay; Mundt, Daniel P; Shah, Dimpy P; Sica, R Alejandro; Stockerl-Goldstein, Keith E; Stratton, Catherine; Weiss, Matthias; Beeghly-Fadiel, Alicia; Accordino, Melissa; Assouline, Sarit E; Awosika, Joy; Bakouny, Ziad; Bashir, Babar; Berg, Stephanie; Bilen, Mehmet Asim; Castellano, Cecilia A; Cogan, Jacob C; Kc, Devendra; Friese, Christopher R; Gupta, Shilpa; Hausrath, Daniel; Hwang, Clara; Johnson, Nathalie A; Joshi, Monika; Kasi, Anup; Klein, Elizabeth J; Koshkin, Vadim S; Kuderer, Nicole M; Kwon, Daniel H; Labaki, Chris; Latif, Tahir; Lau, Eric; Li, Xuanyi; Lyman, Gary H; McKay, Rana R; Nagaraj, Gayathri; Nizam, Amanda; Nonato, Taylor K; Olszewski, Adam J; Polimera, Hyma V; Portuguese, Andrew J; Puc, Matthew M; Razavi, Pedram.
  • Rubinstein SM; Division of Hematology, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina.
  • Bhutani D; Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York.
  • Lynch RC; Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, Washington.
  • Hsu CY; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Shyr Y; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Advani S; Department of Health Policy, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Mesa RA; Cancer Prevention and Control, Department of Oncology, Georgetown University School of Medicine, Georgetown University, Washington D.C.
  • Mishra S; Mays Cancer Center, UT Health San Antonio MD Anderson, San Antonio, Texas.
  • Mundt DP; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Shah DP; Aurora Cancer Care, Advocate Aurora Health, Milwaukee, Wisconsin.
  • Sica RA; Mays Cancer Center, UT Health San Antonio MD Anderson, San Antonio, Texas.
  • Stockerl-Goldstein KE; Division of Hematology and Oncology, Montefiore Medical Center/Albert Einstein College of Medicine, New York, New York.
  • Stratton C; Division of Oncology, Washington University, Saint Louis, Missouri.
  • Weiss M; Division of Hematology and Oncology, Yale University, New Haven, Connecticut.
  • Beeghly-Fadiel A; Thedacare, Appleton, Wisconsin.
  • Accordino M; Department of Health Policy, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Assouline SE; Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York.
  • Awosika J; Division of Hematology, McGill University, Jewish General Hospital, Montreal, Quebec, Canada.
  • Bakouny Z; University of Cincinnati Cancer Center, Cincinnati, Ohio.
  • Bashir B; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Berg S; Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania.
  • Bilen MA; Division of Hematology and Oncology, Loyola University Medical Center, Hines, Illinois.
  • Castellano CA; Winship Cancer Institute of Emory University, Atlanta, Georgia.
  • Cogan JC; Winship Cancer Institute of Emory University, Atlanta, Georgia.
  • Kc D; Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York.
  • Friese CR; Hartford HealthCare Cancer Institute, Hartford, Connecticut.
  • Gupta S; University of Michigan Rogel Cancer Center, Ann Arbor, Michigan.
  • Hausrath D; Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.
  • Hwang C; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Johnson NA; Henry Ford Cancer Institute, Henry Ford Hospital, Detroit, Michigan.
  • Joshi M; Division of Hematology, McGill University, Jewish General Hospital, Montreal, Quebec, Canada.
  • Kasi A; Penn State Health/Penn State Cancer Institute/St. Joseph Cancer Center, Philadelphia, Pennsylvania.
  • Klein EJ; The University of Kansas Cancer Center, Kansas City, Kansas.
  • Koshkin VS; Brown University and Lifespan Cancer Institute, Providence, Rhode Island.
  • Kuderer NM; Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, San Francisco, California.
  • Kwon DH; Advanced Cancer Research Group, Seattle, Washington.
  • Labaki C; Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, San Francisco, California.
  • Latif T; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Lau E; University of Cincinnati Cancer Center, Cincinnati, Ohio.
  • Li X; Division of Medical Oncology and Hematology, Loma Linda University, Loma Linda, California.
  • Lyman GH; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee.
  • McKay RR; Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Nagaraj G; Moores Comprehensive Cancer Center, University of California, San Diego, San Diego, California.
  • Nizam A; Division of Medical Oncology and Hematology, Loma Linda University, Loma Linda, California.
  • Nonato TK; Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.
  • Olszewski AJ; Moores Comprehensive Cancer Center, University of California, San Diego, San Diego, California.
  • Polimera HV; Brown University and Lifespan Cancer Institute, Providence, Rhode Island.
  • Portuguese AJ; Penn State Health/Penn State Cancer Institute/St. Joseph Cancer Center, Philadelphia, Pennsylvania.
  • Puc MM; Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, Washington.
  • Razavi P; Virtua Health, Marlton, New Jersey.
Blood Cancer Discov ; 3(3): 181-193, 2022 05 05.
Article in English | MEDLINE | ID: covidwho-1883342
ABSTRACT
Patients with B-lymphoid malignancies have been consistently identified as a population at high risk of severe COVID-19. Whether this is exclusively due to cancer-related deficits in humoral and cellular immunity, or whether risk of severe COVID-19 is increased by anticancer therapy, is uncertain. Using data derived from the COVID-19 and Cancer Consortium (CCC19), we show that patients treated for B-lymphoid malignancies have an increased risk of severe COVID-19 compared with control populations of patients with non-B-lymphoid malignancies. Among patients with B-lymphoid malignancies, those who received anticancer therapy within 12 months of COVID-19 diagnosis experienced increased COVID-19 severity compared with patients with non-recently treated B-lymphoid malignancies, after adjustment for cancer status and several other prognostic factors. Our findings suggest that patients recently treated for a B-lymphoid malignancy are at uniquely high risk for severe COVID-19.

SIGNIFICANCE:

Our study suggests that recent therapy for a B-lymphoid malignancy is an independent risk factor for COVID-19 severity. These findings provide rationale to develop mitigation strategies targeted at the uniquely high-risk population of patients with recently treated B-lymphoid malignancies. This article is highlighted in the In This Issue feature, p. 171.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Lymphatic Diseases / Neoplasms Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Blood Cancer Discov Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Lymphatic Diseases / Neoplasms Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Blood Cancer Discov Year: 2022 Document Type: Article