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Interplay of Immunosuppression and Immunotherapy Among Patients With Cancer and COVID-19.
Bakouny, Ziad; Labaki, Chris; Grover, Punita; Awosika, Joy; Gulati, Shuchi; Hsu, Chih-Yuan; Alimohamed, Saif I; Bashir, Babar; Berg, Stephanie; Bilen, Mehmet A; Bowles, Daniel; Castellano, Cecilia; Desai, Aakash; Elkrief, Arielle; Eton, Omar E; Fecher, Leslie A; Flora, Daniel; Galsky, Matthew D; Gatti-Mays, Margaret E; Gesenhues, Alicia; Glover, Michael J; Gopalakrishnan, Dharmesh; Gupta, Shilpa; Halfdanarson, Thorvardur R; Hayes-Lattin, Brandon; Hendawi, Mohamed; Hsu, Emily; Hwang, Clara; Jandarov, Roman; Jani, Chinmay; Johnson, Douglas B; Joshi, Monika; Khan, Hina; Khan, Shaheer A; Knox, Natalie; Koshkin, Vadim S; Kulkarni, Amit A; Kwon, Daniel H; Matar, Sara; McKay, Rana R; Mishra, Sanjay; Moria, Feras A; Nizam, Amanda; Nock, Nora L; Nonato, Taylor K; Panasci, Justin; Pomerantz, Lauren; Portuguese, Andrew J; Provenzano, Destie; Puc, Matthew.
  • Bakouny Z; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Labaki C; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Grover P; Division of Hematology/Oncology, University of Cincinnati Cancer Center, Cincinnati, Ohio.
  • Awosika J; Division of Hematology/Oncology, University of Cincinnati Cancer Center, Cincinnati, Ohio.
  • Gulati S; Division of Hematology/Oncology, University of Cincinnati Cancer Center, Cincinnati, Ohio.
  • Hsu CY; Vanderbilt University Medical Center, Nashville, Tennessee.
  • Alimohamed SI; Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, North Carolina.
  • Bashir B; Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania.
  • Berg S; Loyola University Medical Center, Maywood, Illinois.
  • Bilen MA; Winship Cancer Institute, Emory University, Atlanta, Georgia.
  • Bowles D; University of Colorado, Denver.
  • Castellano C; Winship Cancer Institute, Emory University, Atlanta, Georgia.
  • Desai A; Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
  • Elkrief A; Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
  • Eton OE; Hartford Healthcare Cancer Institute, Hartford, Connecticut.
  • Fecher LA; University of Michigan Rogel Cancer Center, Ann Arbor.
  • Flora D; St. Elizabeth Health Care, Edgewood, Kentucky.
  • Galsky MD; Tisch Cancer Institute, Mount Sinai, New York.
  • Gatti-Mays ME; Division of Medical Oncology, The Ohio State University, Columbus.
  • Gesenhues A; St. Elizabeth Health Care, Edgewood, Kentucky.
  • Glover MJ; Stanford University, Stanford, California.
  • Gopalakrishnan D; Roswell Park Comprehensive Cancer Center, Buffalo, New York.
  • Gupta S; Cleveland Clinic, Cleveland, Ohio.
  • Halfdanarson TR; Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
  • Hayes-Lattin B; Knight Cancer Institute, Oregon Health and Science University, Portland.
  • Hendawi M; Aurora Cancer Center, Advocate Aurora Health, Milwaukee, Wisconsin.
  • Hsu E; Hartford Healthcare Cancer Institute, Hartford, Connecticut.
  • Hwang C; Henry Ford Cancer Institute, Detroit, Michigan.
  • Jandarov R; Division of Hematology/Oncology, University of Cincinnati Cancer Center, Cincinnati, Ohio.
  • Jani C; Mt. Auburn Hospital, Boston, Massachusetts.
  • Johnson DB; Vanderbilt University Medical Center, Nashville, Tennessee.
  • Joshi M; Penn State Cancer Institute, Hershey, Pennsylvania.
  • Khan H; Brown University and Lifespan Cancer Institute, Providence, Rhode Island.
  • Khan SA; Herbert Irving Comprehensive Cancer Center, Columbia University, New York, New York.
  • Knox N; Loyola University Medical Center, Maywood, Illinois.
  • Koshkin VS; UCSF, Helen Diller Comprehensive Cancer Center, San Francisco.
  • Kulkarni AA; Masonic Cancer Center, University of Minnesota, Minneapolis.
  • Kwon DH; UCSF, Helen Diller Comprehensive Cancer Center, San Francisco.
  • Matar S; Hollings Cancer Center, MUSC, Charleston.
  • McKay RR; Moores Cancer Center, UCSD, San Diego, California.
  • Mishra S; Vanderbilt University Medical Center, Nashville, Tennessee.
  • Moria FA; McGill University Health Centre, Montreal, Quebec, Canada.
  • Nizam A; Cleveland Clinic, Cleveland, Ohio.
  • Nock NL; Case Comprehensive Cancer Center, Department of Population and Quantitative Health Sciences, Cleveland, Ohio.
  • Nonato TK; Moores Cancer Center, UCSD, San Diego, California.
  • Panasci J; Jewish General Hospital, McGill University, Montreal, Quebec, Canada.
  • Pomerantz L; Penn State Cancer Institute, Hershey, Pennsylvania.
  • Portuguese AJ; Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Provenzano D; George Washington University, Washington, DC.
  • Puc M; Virtua Health, Marlton, New Jersey.
JAMA Oncol ; 2022 Nov 03.
Article in English | MEDLINE | ID: covidwho-2227862
ABSTRACT
Importance Cytokine storm due to COVID-19 can cause high morbidity and mortality and may be more common in patients with cancer treated with immunotherapy (IO) due to immune system activation.

Objective:

To determine the association of baseline immunosuppression and/or IO-based therapies with COVID-19 severity and cytokine storm in patients with cancer. Design, Setting, and

Participants:

This registry-based retrospective cohort study included 12 046 patients reported to the COVID-19 and Cancer Consortium (CCC19) registry from March 2020 to May 2022. The CCC19 registry is a centralized international multi-institutional registry of patients with COVID-19 with a current or past diagnosis of cancer. Records analyzed included patients with active or previous cancer who had a laboratory-confirmed infection with SARS-CoV-2 by polymerase chain reaction and/or serologic findings. Exposures Immunosuppression due to therapy; systemic anticancer therapy (IO or non-IO). Main Outcomes and

Measures:

The primary outcome was a 5-level ordinal scale of COVID-19 severity no complications; hospitalized without requiring oxygen; hospitalized and required oxygen; intensive care unit admission and/or mechanical ventilation; death. The secondary outcome was the occurrence of cytokine storm.

Results:

The median age of the entire cohort was 65 years (interquartile range [IQR], 54-74) years and 6359 patients were female (52.8%) and 6598 (54.8%) were non-Hispanic White. A total of 599 (5.0%) patients received IO, whereas 4327 (35.9%) received non-IO systemic anticancer therapies, and 7120 (59.1%) did not receive any antineoplastic regimen within 3 months prior to COVID-19 diagnosis. Although no difference in COVID-19 severity and cytokine storm was found in the IO group compared with the untreated group in the total cohort (adjusted odds ratio [aOR], 0.80; 95% CI, 0.56-1.13, and aOR, 0.89; 95% CI, 0.41-1.93, respectively), patients with baseline immunosuppression treated with IO (vs untreated) had worse COVID-19 severity and cytokine storm (aOR, 3.33; 95% CI, 1.38-8.01, and aOR, 4.41; 95% CI, 1.71-11.38, respectively). Patients with immunosuppression receiving non-IO therapies (vs untreated) also had worse COVID-19 severity (aOR, 1.79; 95% CI, 1.36-2.35) and cytokine storm (aOR, 2.32; 95% CI, 1.42-3.79). Conclusions and Relevance This cohort study found that in patients with cancer and COVID-19, administration of systemic anticancer therapies, especially IO, in the context of baseline immunosuppression was associated with severe clinical outcomes and the development of cytokine storm. Trial Registration ClinicalTrials.gov Identifier NCT04354701.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article