Association of COVID-19 Vaccination With SARS-CoV-2 Infection in Patients With Cancer: A US Nationwide Veterans Affairs Study.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 02 2022
Historique:
pubmed: 3 12 2021
medline: 25 2 2022
entrez: 2 12 2021
Statut: ppublish

Résumé

Patients with cancer are at increased risk for severe COVID-19, but it is unknown whether SARS-CoV-2 vaccination is effective for them. To determine the association between SARS-CoV-2 vaccination and SARS-CoV-2 infections among a population of Veterans Affairs (VA) patients with cancer. Retrospective, multicenter, nationwide cohort study of SARS-CoV-2 vaccination and infection among patients in the VA health care system from December 15, 2020, to May 4, 2021. All adults with solid tumors or hematologic cancer who received systemic cancer-directed therapy from August 15, 2010, to May 4, 2021, and were alive and without a documented SARS-CoV-2 positive result as of December 15, 2020, were eligible for inclusion. Each day between December 15, 2020, and May 4, 2021, newly vaccinated patients were matched 1:1 with unvaccinated or not yet vaccinated controls based on age, race and ethnicity, VA facility, rurality of home address, cancer type, and treatment type/timing. Receipt of a SARS-CoV-2 vaccine. The primary outcome was documented SARS-CoV-2 infection. A proxy for vaccine effectiveness was defined as 1 minus the risk ratio of SARS-CoV-2 infection for vaccinated individuals compared with unvaccinated controls. A total of 184 485 patients met eligibility criteria, and 113 796 were vaccinated. Of these, 29 152 vaccinated patients (median [IQR] age, 74.1 [70.2-79.3] years; 95% were men; 71% were non-Hispanic White individuals) were matched 1:1 to unvaccinated or not yet vaccinated controls. As of a median 47 days of follow-up, 436 SARS-CoV-2 infections were detected in the matched cohort (161 infections in vaccinated patients vs 275 in unvaccinated patients). There were 17 COVID-19-related deaths in the vaccinated group vs 27 COVID-19-related deaths in the unvaccinated group. Overall vaccine effectiveness in the matched cohort was 58% (95% CI, 39% to 72%) starting 14 days after the second dose. Patients who received chemotherapy within 3 months prior to the first vaccination dose were estimated to have a vaccine effectiveness of 57% (95% CI, -23% to 90%) starting 14 days after the second dose vs 76% (95% CI, 50% to 91%) for those receiving endocrine therapy and 85% (95% CI, 29% to 100%) for those who had not received systemic therapy for at least 6 months prior. In this cohort study, COVID-19 vaccination was associated with lower SARS-CoV-2 infection rates in patients with cancer. Some immunosuppressed subgroups may remain at early risk for COVID-19 despite vaccination, and consideration should be given to additional risk reduction strategies, such as serologic testing for vaccine response and a third vaccine dose to optimize outcomes.

Identifiants

pubmed: 34854921
pii: 2786477
doi: 10.1001/jamaoncol.2021.5771
pmc: PMC8640949
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

281-286

Subventions

Organisme : NCI NIH HHS
ID : P01 CA155258
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA124435
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA100707
Pays : United States

Auteurs

Julie Tsu-Yu Wu (JT)

VA Palo Alto Healthcare System, Palo Alto, California.
Stanford University School of Medicine, Stanford, California.

Jennifer La (J)

VA Cooperative Studies Program, VA Boston Healthcare System, Boston, Massachusetts.

Westyn Branch-Elliman (W)

VA Boston Healthcare System, Section of Infectious Diseases, Boston, Massachusetts.
VA Boston Center for Healthcare Organization and Implementation Research (CHOIR), Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.

Linden B Huhmann (LB)

VA Cooperative Studies Program, VA Boston Healthcare System, Boston, Massachusetts.

Summer S Han (SS)

Stanford University School of Medicine, Stanford, California.

Giovanni Parmigiani (G)

Dana-Farber Cancer Institute, Boston, Massachusetts.
Harvard School of Public Health, Boston, Massachusetts.

David P Tuck (DP)

VA Boston Healthcare System, Hematology/Oncology Service, Boston, Massachusetts.
Boston University School of Medicine, Boston, Massachusetts.

Mary T Brophy (MT)

VA Cooperative Studies Program, VA Boston Healthcare System, Boston, Massachusetts.
VA Boston Healthcare System, Hematology/Oncology Service, Boston, Massachusetts.
Boston University School of Medicine, Boston, Massachusetts.

Nhan V Do (NV)

VA Cooperative Studies Program, VA Boston Healthcare System, Boston, Massachusetts.
Boston University School of Medicine, Boston, Massachusetts.

Albert Y Lin (AY)

VA Palo Alto Healthcare System, Palo Alto, California.
Stanford University School of Medicine, Stanford, California.

Nikhil C Munshi (NC)

Harvard Medical School, Boston, Massachusetts.
Dana-Farber Cancer Institute, Boston, Massachusetts.
VA Boston Healthcare System, Hematology/Oncology Service, Boston, Massachusetts.

Nathanael R Fillmore (NR)

VA Cooperative Studies Program, VA Boston Healthcare System, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.
Dana-Farber Cancer Institute, Boston, Massachusetts.

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Classifications MeSH