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Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050)

Objectives: The COVID-19 pandemic has disrupted timely medical care, including receipt of anticancer therapy. Gynecologic oncology (GO) patients (pts), who are often comorbid and require a range of therapies, may have varied responses to COVID-19 infection. Our study aimed to describe outcomes for G...

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Autores principales: Glaser, Gretchen, Lara, Olivia, Pothuri, Bhavana, Grimaldi, Carolina Gomez, Prescott, Lauren, Mastroyannis, Spyridon, Kim, Sarah, ElNaggar, Adam, Torres, Diogo, Conrad, Lesley, McGree, Michaela, Weaver, Amy, Huh, Warner, Cohn, David, Fader, Amanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462874/
http://dx.doi.org/10.1016/S0090-8258(22)01269-0
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author Glaser, Gretchen
Lara, Olivia
Pothuri, Bhavana
Grimaldi, Carolina Gomez
Prescott, Lauren
Mastroyannis, Spyridon
Kim, Sarah
ElNaggar, Adam
Torres, Diogo
Conrad, Lesley
McGree, Michaela
Weaver, Amy
Huh, Warner
Cohn, David
Fader, Amanda
author_facet Glaser, Gretchen
Lara, Olivia
Pothuri, Bhavana
Grimaldi, Carolina Gomez
Prescott, Lauren
Mastroyannis, Spyridon
Kim, Sarah
ElNaggar, Adam
Torres, Diogo
Conrad, Lesley
McGree, Michaela
Weaver, Amy
Huh, Warner
Cohn, David
Fader, Amanda
author_sort Glaser, Gretchen
collection PubMed
description Objectives: The COVID-19 pandemic has disrupted timely medical care, including receipt of anticancer therapy. Gynecologic oncology (GO) patients (pts), who are often comorbid and require a range of therapies, may have varied responses to COVID-19 infection. Our study aimed to describe outcomes for GO pts with concurrent COVID-19 infection in the United States. Methods: The Society of Gynecologic Oncology COVID-19 and Gynecologic Cancer Registry was developed as a web-based data entry platform to capture the clinical courses and cancer treatment-related effects in GO pts with confirmed COVID-19 infection. Demographics, clinical manifestations, outcomes, treatment type, and disease severity were analyzed. Results: Data were available for 312 GO pts across eight institutions. The median age was 63 years, and most pts were identified as White (70%), Black/African American (17%), or Asian (2%). GO diagnosis included low-grade endometrial (31%), high-grade ovarian (22%), cervical (14%), high-grade endometrial (13%), vulvar (3%), and other (16%). At the time of COVID-19 diagnosis, 37% of pts had active malignancy, with 25% receiving anticancer therapy. The most common anticancer treatments included chemotherapy (51%, n=39), targeted agents (25%, n = 27), and surgery (27%, n = 21), whereas 12 pts (16%) received multi-modal therapy. Delay or discontinuation of treatment due to COVID-19 infection occurred in 28% of patients (median 3-4 weeks delay). Chemotherapy was most frequently delayed (43%), followed by surgery (27%). In total, 19% of GO pts required supplemental oxygen, and 29% were hospitalized (5% in the intensive care setting). Ten pts (3%) required ventilator support, and 30% of pts receiving chemotherapy were hospitalized. Older age, having more than two comorbid conditions, and non-White race were associated (p<0.05) with a higher likelihood of being hospitalized or admitted to the intensive care unit. Patients who required hospitalization were disproportionately Black/African American, Asian, or other non-Whites (p = 0.003). On multivariable analysis, pts of non-White race (aOR: 2.86, 95% CI: 1.64-5.00; p<0.001) and advancing age (aOR: 1.28, 95% CI: 1.16-1.42; p<0.001) had a higher risk of hospitalization. In terms of mortality, 8% of hospitalized pts died of COVID-19 complications, and 4% of the entire cohort was not alive 30 days after COVID-19 diagnosis. Patients who died were more likely to be older (OR: 1.25 per 5-year increase, 95% CI: 1.01-1.55), had active malignancy (OR: 3.86, 95% CI: 1.16-12.85), or be of the non-White race (death rate of 3% White, 8% Black/African American, 25% Asian). Conclusions: GO pts diagnosed with COVID-19 are at high risk of hospitalization, delay of anticancer treatments, and death. Approximately one in 23 GO pts who contracted COVID-19 were not alive 30 days after diagnosis. Racial disparities exist in pt hospitalizations and mortality rates. Additional studies are needed to determine the long-term oncologic and mortality outcomes and the impact of race in this pt cohort.
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spelling pubmed-94628742022-09-10 Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050) Glaser, Gretchen Lara, Olivia Pothuri, Bhavana Grimaldi, Carolina Gomez Prescott, Lauren Mastroyannis, Spyridon Kim, Sarah ElNaggar, Adam Torres, Diogo Conrad, Lesley McGree, Michaela Weaver, Amy Huh, Warner Cohn, David Fader, Amanda Gynecol Oncol Focused Plenary III: Inequities During the Pandemic and Beyond Objectives: The COVID-19 pandemic has disrupted timely medical care, including receipt of anticancer therapy. Gynecologic oncology (GO) patients (pts), who are often comorbid and require a range of therapies, may have varied responses to COVID-19 infection. Our study aimed to describe outcomes for GO pts with concurrent COVID-19 infection in the United States. Methods: The Society of Gynecologic Oncology COVID-19 and Gynecologic Cancer Registry was developed as a web-based data entry platform to capture the clinical courses and cancer treatment-related effects in GO pts with confirmed COVID-19 infection. Demographics, clinical manifestations, outcomes, treatment type, and disease severity were analyzed. Results: Data were available for 312 GO pts across eight institutions. The median age was 63 years, and most pts were identified as White (70%), Black/African American (17%), or Asian (2%). GO diagnosis included low-grade endometrial (31%), high-grade ovarian (22%), cervical (14%), high-grade endometrial (13%), vulvar (3%), and other (16%). At the time of COVID-19 diagnosis, 37% of pts had active malignancy, with 25% receiving anticancer therapy. The most common anticancer treatments included chemotherapy (51%, n=39), targeted agents (25%, n = 27), and surgery (27%, n = 21), whereas 12 pts (16%) received multi-modal therapy. Delay or discontinuation of treatment due to COVID-19 infection occurred in 28% of patients (median 3-4 weeks delay). Chemotherapy was most frequently delayed (43%), followed by surgery (27%). In total, 19% of GO pts required supplemental oxygen, and 29% were hospitalized (5% in the intensive care setting). Ten pts (3%) required ventilator support, and 30% of pts receiving chemotherapy were hospitalized. Older age, having more than two comorbid conditions, and non-White race were associated (p<0.05) with a higher likelihood of being hospitalized or admitted to the intensive care unit. Patients who required hospitalization were disproportionately Black/African American, Asian, or other non-Whites (p = 0.003). On multivariable analysis, pts of non-White race (aOR: 2.86, 95% CI: 1.64-5.00; p<0.001) and advancing age (aOR: 1.28, 95% CI: 1.16-1.42; p<0.001) had a higher risk of hospitalization. In terms of mortality, 8% of hospitalized pts died of COVID-19 complications, and 4% of the entire cohort was not alive 30 days after COVID-19 diagnosis. Patients who died were more likely to be older (OR: 1.25 per 5-year increase, 95% CI: 1.01-1.55), had active malignancy (OR: 3.86, 95% CI: 1.16-12.85), or be of the non-White race (death rate of 3% White, 8% Black/African American, 25% Asian). Conclusions: GO pts diagnosed with COVID-19 are at high risk of hospitalization, delay of anticancer treatments, and death. Approximately one in 23 GO pts who contracted COVID-19 were not alive 30 days after diagnosis. Racial disparities exist in pt hospitalizations and mortality rates. Additional studies are needed to determine the long-term oncologic and mortality outcomes and the impact of race in this pt cohort. Elsevier Inc. 2022-08 2022-09-10 /pmc/articles/PMC9462874/ http://dx.doi.org/10.1016/S0090-8258(22)01269-0 Text en Copyright © 2022 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Focused Plenary III: Inequities During the Pandemic and Beyond
Glaser, Gretchen
Lara, Olivia
Pothuri, Bhavana
Grimaldi, Carolina Gomez
Prescott, Lauren
Mastroyannis, Spyridon
Kim, Sarah
ElNaggar, Adam
Torres, Diogo
Conrad, Lesley
McGree, Michaela
Weaver, Amy
Huh, Warner
Cohn, David
Fader, Amanda
Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050)
title Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050)
title_full Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050)
title_fullStr Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050)
title_full_unstemmed Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050)
title_short Impact of COVID-19 on gynecologic oncology patients: an SGO COVID-19 and Gynecologic Cancer Registry study (050)
title_sort impact of covid-19 on gynecologic oncology patients: an sgo covid-19 and gynecologic cancer registry study (050)
topic Focused Plenary III: Inequities During the Pandemic and Beyond
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462874/
http://dx.doi.org/10.1016/S0090-8258(22)01269-0
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