Viral Infection and Lung Cancer Immunotherapy
Immunotherapy with immune checkpoint inhibitors (mainly anti-PD1 and anti-PDL1 monoclonal antibodies) became a standard of care in non-small cell lung cancer (NSCLC) patients. Most of the clinical trials excluded patients with hepatitis B (HBV), hepatis C (HCV), and human immunodeficiency virus (HIV...
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doaj-ab8d447098664815bc45257d9e720ab12021-08-09T07:15:43ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-08-011110.3389/fonc.2021.577514577514Viral Infection and Lung Cancer ImmunotherapyEwa Kalinka0Izabela Chmielewska1Kamila Wojas-Krawczyk2Department of Oncology, Polish Mother’s Memorial Hospital – Research Institute, Lodz, PolandDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, PolandDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, PolandImmunotherapy with immune checkpoint inhibitors (mainly anti-PD1 and anti-PDL1 monoclonal antibodies) became a standard of care in non-small cell lung cancer (NSCLC) patients. Most of the clinical trials excluded patients with hepatitis B (HBV), hepatis C (HCV), and human immunodeficiency virus (HIV) active infection (1–10). Despite the progress in treatment of these infections, they remain an unresolved clinical problem when lung cancer immunotherapy should be initiated in an NSCLC patient. This manuscript summarizes the data from the literature concerning this subgroup of patients including the rationale for immunotherapy initiation depending on the HBV, HCV, or HIV infection status; the risk of adverse events; and the efficacy compared to non-infected patients. One of the crucial questions is how the candidates to immunotherapy should be screened for HBV, HCV, and HIV infections. The year 2020 brought the world a new but dynamic viral problem—severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2). The incorporation of known data in oncology guidelines became a burning need, and then, which group of the infected patients can be treated with immunotherapy despite the infection. Oncologists should also know if these patients should receive antiviral therapy and what are the safe combinations in these settings. We also indicate which of the adverse events should be monitored carefully during checkpoint inhibitor treatment.https://www.frontiersin.org/articles/10.3389/fonc.2021.577514/fulllung cancerimmunotherapyHBVHCVHIVSARS-Cov-2 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ewa Kalinka Izabela Chmielewska Kamila Wojas-Krawczyk |
spellingShingle |
Ewa Kalinka Izabela Chmielewska Kamila Wojas-Krawczyk Viral Infection and Lung Cancer Immunotherapy Frontiers in Oncology lung cancer immunotherapy HBV HCV HIV SARS-Cov-2 |
author_facet |
Ewa Kalinka Izabela Chmielewska Kamila Wojas-Krawczyk |
author_sort |
Ewa Kalinka |
title |
Viral Infection and Lung Cancer Immunotherapy |
title_short |
Viral Infection and Lung Cancer Immunotherapy |
title_full |
Viral Infection and Lung Cancer Immunotherapy |
title_fullStr |
Viral Infection and Lung Cancer Immunotherapy |
title_full_unstemmed |
Viral Infection and Lung Cancer Immunotherapy |
title_sort |
viral infection and lung cancer immunotherapy |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Oncology |
issn |
2234-943X |
publishDate |
2021-08-01 |
description |
Immunotherapy with immune checkpoint inhibitors (mainly anti-PD1 and anti-PDL1 monoclonal antibodies) became a standard of care in non-small cell lung cancer (NSCLC) patients. Most of the clinical trials excluded patients with hepatitis B (HBV), hepatis C (HCV), and human immunodeficiency virus (HIV) active infection (1–10). Despite the progress in treatment of these infections, they remain an unresolved clinical problem when lung cancer immunotherapy should be initiated in an NSCLC patient. This manuscript summarizes the data from the literature concerning this subgroup of patients including the rationale for immunotherapy initiation depending on the HBV, HCV, or HIV infection status; the risk of adverse events; and the efficacy compared to non-infected patients. One of the crucial questions is how the candidates to immunotherapy should be screened for HBV, HCV, and HIV infections. The year 2020 brought the world a new but dynamic viral problem—severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2). The incorporation of known data in oncology guidelines became a burning need, and then, which group of the infected patients can be treated with immunotherapy despite the infection. Oncologists should also know if these patients should receive antiviral therapy and what are the safe combinations in these settings. We also indicate which of the adverse events should be monitored carefully during checkpoint inhibitor treatment. |
topic |
lung cancer immunotherapy HBV HCV HIV SARS-Cov-2 |
url |
https://www.frontiersin.org/articles/10.3389/fonc.2021.577514/full |
work_keys_str_mv |
AT ewakalinka viralinfectionandlungcancerimmunotherapy AT izabelachmielewska viralinfectionandlungcancerimmunotherapy AT kamilawojaskrawczyk viralinfectionandlungcancerimmunotherapy |
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1721215125132673024 |