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1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients

BACKGROUND: Immune checkpoint inhibitors (ICI) therapy has ushered cancer treatment into a potentially curative era. However, infectious complications remain largely unknown and the few studies that described infectious complications associated with ICI had no comparative control groups. We assessed...

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Autores principales: Malek, Alexandre, Fares, Johny, Khalil, Melissa, Hachem, Ray Y, Chaftari, Anne-Marie, Jiang, Ying, Kontoyiannis, Dimitrios P, Fossella, Frank, Chaftari, Patrick, Mulanovich, Victor E, Viola, George, Raad, Issam I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809399/
http://dx.doi.org/10.1093/ofid/ofz360.1632
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author Malek, Alexandre
Fares, Johny
Khalil, Melissa
Hachem, Ray Y
Chaftari, Anne-Marie
Jiang, Ying
Kontoyiannis, Dimitrios P
Fossella, Frank
Chaftari, Patrick
Mulanovich, Victor E
Viola, George
Raad, Issam I
author_facet Malek, Alexandre
Fares, Johny
Khalil, Melissa
Hachem, Ray Y
Chaftari, Anne-Marie
Jiang, Ying
Kontoyiannis, Dimitrios P
Fossella, Frank
Chaftari, Patrick
Mulanovich, Victor E
Viola, George
Raad, Issam I
author_sort Malek, Alexandre
collection PubMed
description BACKGROUND: Immune checkpoint inhibitors (ICI) therapy has ushered cancer treatment into a potentially curative era. However, infectious complications remain largely unknown and the few studies that described infectious complications associated with ICI had no comparative control groups. We assessed the rate of infections in patients with non-small cell lung cancer (NSCLC) treated with ICI plus conventional chemotherapy (CC) vs. CC alone. METHODS: We performed a comparative single-center retrospective cohort study of patients with NSCLC who received de novo treatment with either Pembrolizumab or Nivolumab, and/or Ipilimumab combined with CC including Pemetrexed and Carboplatin vs. patients treated with CC alone between August 2016 and January 2019. We excluded all patients who were switched from CC to ICI or vice-versa. We evaluated patients’ characteristics, treatment modality, immune-related adverse events (irAEs), and outcome. Infections were defined by clinical signs and symptoms, microbiologic documentation, and/or imaging studies. RESULTS: A group of 126 patients who received ICI concurrently with CC were compared with 126 patients who received CC alone (control group). Patients in the ICI group were more likely to have stage IV NSCLC compared with the control group (P < 0.0001). Pembrolizumab was most commonly used as a single ICI agent in 107 patients (85%), followed by Ipilimumab and Nivolumab as dual therapy (9%). Confirmed infections were identified in 20 (16%) patients in the ICI group and 18 (14%) in the control group (P = 0.7). The control group had a higher rate of multiple infections at different times compared with the ICI group (P = 0.014). However, there was no significant difference in the types of infections (bacterial, fungal or viral) that occurred between the two groups. The irAEs were reported in 14 (11%) patients, 13 of them received corticosteroids with a median duration of 32 days (range, 15–64 days). Out of these patients, three (21%) developed confirmed infections of which two were viral upper respiratory tract infections and one was a bacterial urinary tract infection. CONCLUSION: Patients with NSCLC treated with the combination of Immune Checkpoint Inhibitors plus Conventional Chemotherapy have comparable risk of developing infections compared with those on Conventional Chemotherapy alone. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68093992019-10-28 1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients Malek, Alexandre Fares, Johny Khalil, Melissa Hachem, Ray Y Chaftari, Anne-Marie Jiang, Ying Kontoyiannis, Dimitrios P Fossella, Frank Chaftari, Patrick Mulanovich, Victor E Viola, George Raad, Issam I Open Forum Infect Dis Abstracts BACKGROUND: Immune checkpoint inhibitors (ICI) therapy has ushered cancer treatment into a potentially curative era. However, infectious complications remain largely unknown and the few studies that described infectious complications associated with ICI had no comparative control groups. We assessed the rate of infections in patients with non-small cell lung cancer (NSCLC) treated with ICI plus conventional chemotherapy (CC) vs. CC alone. METHODS: We performed a comparative single-center retrospective cohort study of patients with NSCLC who received de novo treatment with either Pembrolizumab or Nivolumab, and/or Ipilimumab combined with CC including Pemetrexed and Carboplatin vs. patients treated with CC alone between August 2016 and January 2019. We excluded all patients who were switched from CC to ICI or vice-versa. We evaluated patients’ characteristics, treatment modality, immune-related adverse events (irAEs), and outcome. Infections were defined by clinical signs and symptoms, microbiologic documentation, and/or imaging studies. RESULTS: A group of 126 patients who received ICI concurrently with CC were compared with 126 patients who received CC alone (control group). Patients in the ICI group were more likely to have stage IV NSCLC compared with the control group (P < 0.0001). Pembrolizumab was most commonly used as a single ICI agent in 107 patients (85%), followed by Ipilimumab and Nivolumab as dual therapy (9%). Confirmed infections were identified in 20 (16%) patients in the ICI group and 18 (14%) in the control group (P = 0.7). The control group had a higher rate of multiple infections at different times compared with the ICI group (P = 0.014). However, there was no significant difference in the types of infections (bacterial, fungal or viral) that occurred between the two groups. The irAEs were reported in 14 (11%) patients, 13 of them received corticosteroids with a median duration of 32 days (range, 15–64 days). Out of these patients, three (21%) developed confirmed infections of which two were viral upper respiratory tract infections and one was a bacterial urinary tract infection. CONCLUSION: Patients with NSCLC treated with the combination of Immune Checkpoint Inhibitors plus Conventional Chemotherapy have comparable risk of developing infections compared with those on Conventional Chemotherapy alone. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6809399/ http://dx.doi.org/10.1093/ofid/ofz360.1632 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Malek, Alexandre
Fares, Johny
Khalil, Melissa
Hachem, Ray Y
Chaftari, Anne-Marie
Jiang, Ying
Kontoyiannis, Dimitrios P
Fossella, Frank
Chaftari, Patrick
Mulanovich, Victor E
Viola, George
Raad, Issam I
1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients
title 1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients
title_full 1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients
title_fullStr 1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients
title_full_unstemmed 1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients
title_short 1769. The Impact of Checkpoint Inhibitor Immunotherapy on Infections in Lung Cancer Patients
title_sort 1769. the impact of checkpoint inhibitor immunotherapy on infections in lung cancer patients
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809399/
http://dx.doi.org/10.1093/ofid/ofz360.1632
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