COVID-19 vaccination and breakthrough infections in patients with cancer.


Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
03 2022
Historique:
received: 21 09 2021
revised: 14 12 2021
accepted: 16 12 2021
pubmed: 28 12 2021
medline: 19 2 2022
entrez: 27 12 2021
Statut: ppublish

Résumé

Vaccination is an important preventive health measure to protect against symptomatic and severe COVID-19. Impaired immunity secondary to an underlying malignancy or recent receipt of antineoplastic systemic therapies can result in less robust antibody titers following vaccination and possible risk of breakthrough infection. As clinical trials evaluating COVID-19 vaccines largely excluded patients with a history of cancer and those on active immunosuppression (including chemotherapy), limited evidence is available to inform the clinical efficacy of COVID-19 vaccination across the spectrum of patients with cancer. We describe the clinical features of patients with cancer who developed symptomatic COVID-19 following vaccination and compare weighted outcomes with those of contemporary unvaccinated patients, after adjustment for confounders, using data from the multi-institutional COVID-19 and Cancer Consortium (CCC19). Patients with cancer who develop COVID-19 following vaccination have substantial comorbidities and can present with severe and even lethal infection. Patients harboring hematologic malignancies are over-represented among vaccinated patients with cancer who develop symptomatic COVID-19. Vaccination against COVID-19 remains an essential strategy in protecting vulnerable populations, including patients with cancer. Patients with cancer who develop breakthrough infection despite full vaccination, however, remain at risk of severe outcomes. A multilayered public health mitigation approach that includes vaccination of close contacts, boosters, social distancing, and mask-wearing should be continued for the foreseeable future.

Sections du résumé

BACKGROUND
Vaccination is an important preventive health measure to protect against symptomatic and severe COVID-19. Impaired immunity secondary to an underlying malignancy or recent receipt of antineoplastic systemic therapies can result in less robust antibody titers following vaccination and possible risk of breakthrough infection. As clinical trials evaluating COVID-19 vaccines largely excluded patients with a history of cancer and those on active immunosuppression (including chemotherapy), limited evidence is available to inform the clinical efficacy of COVID-19 vaccination across the spectrum of patients with cancer.
PATIENTS AND METHODS
We describe the clinical features of patients with cancer who developed symptomatic COVID-19 following vaccination and compare weighted outcomes with those of contemporary unvaccinated patients, after adjustment for confounders, using data from the multi-institutional COVID-19 and Cancer Consortium (CCC19).
RESULTS
Patients with cancer who develop COVID-19 following vaccination have substantial comorbidities and can present with severe and even lethal infection. Patients harboring hematologic malignancies are over-represented among vaccinated patients with cancer who develop symptomatic COVID-19.
CONCLUSIONS
Vaccination against COVID-19 remains an essential strategy in protecting vulnerable populations, including patients with cancer. Patients with cancer who develop breakthrough infection despite full vaccination, however, remain at risk of severe outcomes. A multilayered public health mitigation approach that includes vaccination of close contacts, boosters, social distancing, and mask-wearing should be continued for the foreseeable future.

Identifiants

pubmed: 34958894
pii: S0923-7534(21)04880-8
doi: 10.1016/j.annonc.2021.12.006
pmc: PMC8704021
pii:
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

340-346

Subventions

Organisme : NCI NIH HHS
ID : U01 CA231840
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001873
Pays : United States

Investigateurs

T K Choueiri (TK)
N Duma (N)
D Farmakiotis (D)
P Grivas (P)
G de Lima Lopes (G)
C A Painter (CA)
S Peters (S)
B I Rini (BI)
D P Shah (DP)
M A Thompson (MA)
J L Warner (JL)

Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure ALS reports non-financial support from Astellas, non-financial support from Pfizer, outside the submitted work. CL reports research support from Genentech/imCORE, outside the submitted work. ZB reports non-financial support from Bristol Myers Squibb, grants from Genentech/imCORE, personal fees from UpToDate, outside the submitted work. CYH reports personal fees from NashBio, outside the submitted work. SAB reports personal fees from Exelixis, personal fees from Seattle Genetics, personal fees from Pfizer, personal fees from Bristol Myers Squibb, outside the submitted work. CRF reports research grants from the Merck Foundation and National Comprehensive Cancer Network (NCCN)/Pfizer, outside the submitted work. EAG reports personal fees and other from Alexion Pharmaceuticals, personal fees and non-financial support from Novartis Pharmaceuticals, personal fees, non-financial support and other from Astex/Otsuka Pharmaceuticals, other from Apellis Pharmaceuticals, personal fees, non-financial support, and other from Celgene/Bristol Myers Squibb, grants and personal fees from AbbVie/Genentech, other from Celldex Therapeutics, personal fees from Boston Biomedical, outside the submitted work. JEH reports research funding paid to her institution from Dendreon Pharmaceuticals LLC, research funding paid to her institution from Regeneron Pharmaceuticals, personal fees from Genzyme, personal fees from Seagen, outside the submitted work. RRM reports grants and personal fees from Bayer, grants from Pfizer, grants from Tempus, personal fees from AVEO, personal fees from Caris, personal fees from Bristol Myers Squib, personal fees from Exelixis, personal fees from Janssen, personal fees from Novartis, personal fees from Pfizer, personal fees from Sanofi, personal fees from Tempus, personal fees from Dendreon, personal fees from Vividion, personal fees from AstraZeneca, personal fees from Calithera, personal fees from Merck, outside the submitted work. OAP reports personal fees from International Consulting Associates, Inc., outside the submitted work. EMW-B reports personal fees from Astellas, personal fees from AVEO Oncology, personal fees from Bristol Myers Squibb, other from Exelixis, grants from Pfizer Global Medical Grants, other from Nektar, other from Immunomedics, outside the submitted work. SM reports personal fees from National Geographic, outside the submitted work. DF reports a grant from Merck to study COVID-19 in immunocompromised patients, outside of the submitted work. YS reports personal fees from Novartis, personal fees from Roche, personal fees from Pfizer, personal fees from Janssen, personal fees from Eisai, personal fees from AstraZeneca, outside of the submitted work. JLW reports personal fees from Westat, personal fees from Roche, personal fees from Melax Tech, personal fees from Flatiron Health, other from HemOnc.org LLC (ownership), outside the submitted work. TKC reports institutional and personal, paid and unpaid support for research, advisory boards, consultancy, and honoraria from AstraZeneca, Aravive, Aveo, Bayer, Bristol Myers Squibb, Eisai, EMD Serono, Exelixis, GlaxoSmithKline, IQVIA, Ipsen, Kanaph, Lilly, Merck, Nikang, Novartis, Pfizer, Roche, Sanofi/Aventis, Takeda, Tempest, UpToDate, CME events (Peerview, OncLive and others), outside the submitted work. All other authors have declared no conflicts of interest.

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Auteurs

A L Schmidt (AL)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA.

C Labaki (C)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA.

C-Y Hsu (CY)

Department of Biostatistics, Vanderbilt University, Nashville, USA.

Z Bakouny (Z)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA.

N Balanchivadze (N)

Hematology and Oncology Fellowship Program, Henry Ford Cancer Institute, Detroit, USA.

S A Berg (SA)

Department of Internal Medicine and Cancer Biology, Division of Hematology and Oncology, Cardinal Bernardin Cancer Centre, Loyola University Chicago, Maywood, USA.

S Blau (S)

Division of Oncology, Northwest Medical Specialties, Tacoma, USA; Division of Hematology, University of Washington, Seattle, USA.

A Daher (A)

Hartford HealthCare Medical Group, Hartford, USA.

T El Zarif (T)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA.

C R Friese (CR)

University of Michigan School of Nursing, School of Public Health, and Rogel Cancer Centre, Ann Arbor, USA.

E A Griffiths (EA)

Leukemia Section, Roswell Park Comprehensive Cancer Centre, Buffalo, USA.

J E Hawley (JE)

Herbert Irving Comprehensive Cancer Centre, Columbia University Irving Medical Centre, New York, USA; University of Washington/Fred Hutchinson Cancer Research Center, Seattle, USA.

B Hayes-Lattin (B)

Division of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health and Science University, Portland, USA.

V Karivedu (V)

Department of Internal Medicine, Division of Medical Oncology, The Ohio State University Wexner Medical Centre, Columbus, USA.

T Latif (T)

Division of Hematology/Medical Oncology, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, USA.

B H Mavromatis (BH)

Department of Cancer, Oncology, Hematology, UPMC Western Maryland, Cumberland, USA.

R R McKay (RR)

Department of Medicine, Division of Hematology/Oncology, University of California San Diego, San Diego, USA.

G Nagaraj (G)

Division of Medical Oncology & Hematology, Department of Medicine, Loma Linda University Cancer Centre, Loma Linda, USA.

R H Nguyen (RH)

Department of Medicine, Division of Hematology and Oncology, University of Illinois at Chicago, Chicago, USA.

O A Panagiotou (OA)

Department of Health Services, Policy & Practice, Brown University School of Public Health, Providence, USA.

A J Portuguese (AJ)

Division of Hematology, University of Washington, Seattle, USA.

M Puc (M)

Department of Surgery, Section of Thoracic Surgery, Virtua Health, Marlton, USA.

M Santos Dutra (M)

Segal Cancer Centre of the Jewish General Hospital, Montréal, Canada.

B A Schroeder (BA)

Virginia Mason Cancer Institute, Seattle, USA.

A Thakkar (A)

Division of Oncology, Montefiore Medical Centre, Bronx, USA.

E M Wulff-Burchfield (EM)

Department of Medicine, Divisions of Medical Oncology and Palliative Medicine, The University of Kansas Health System, Westwood, USA.

S Mishra (S)

Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, USA.

D Farmakiotis (D)

Department of Medicine, Division of Infectious Diseases, The Warren Alpert Medical School of Brown University, Providence, USA.

Yu Shyr (Y)

Department of Biostatistics, Vanderbilt University, Nashville, USA; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, USA.

J L Warner (JL)

Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, USA; Department of Medicine, Division of Hematology/Oncology, Vanderbilt University, Nashville, USA; Department of Biomedical Informatics, Vanderbilt University, Nashville, USA. Electronic address: Jeremy.Warner@vumc.org.

T K Choueiri (TK)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA. Electronic address: Toni_Choueiri@dfci.harvard.edu.

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