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PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence

BACKGROUND: Immune checkpoint inhibitors (ICIs) have provided new therapeutic options for non‐small cell lung cancer(NSCLC) patients. However, due to concerning increases in immune‐related adverse events, clinical trials usually exclude patients with special issues such as viral hepatitis, tuberculo...

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Autores principales: Byeon, Seonggyu, Cho, Jang Ho, Jung, Hyun Ae, Sun, Jong‐Mu, Lee, Se‐Hoon, Ahn, Jin Seok, Park, Keunchil, Ahn, Myung‐Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131857/
https://www.ncbi.nlm.nih.gov/pubmed/32027780
http://dx.doi.org/10.1002/cam4.2868
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author Byeon, Seonggyu
Cho, Jang Ho
Jung, Hyun Ae
Sun, Jong‐Mu
Lee, Se‐Hoon
Ahn, Jin Seok
Park, Keunchil
Ahn, Myung‐Ju
author_facet Byeon, Seonggyu
Cho, Jang Ho
Jung, Hyun Ae
Sun, Jong‐Mu
Lee, Se‐Hoon
Ahn, Jin Seok
Park, Keunchil
Ahn, Myung‐Ju
author_sort Byeon, Seonggyu
collection PubMed
description BACKGROUND: Immune checkpoint inhibitors (ICIs) have provided new therapeutic options for non‐small cell lung cancer(NSCLC) patients. However, due to concerning increases in immune‐related adverse events, clinical trials usually exclude patients with special issues such as viral hepatitis, tuberculosis (Tbc), interstitial lung disease (ILD) and autoimmune disease. METHODS: We retrospectively reviewed the medical records of NSCLC patients who received ICIs, and analyzed the clinical outcomes of patients with special issues. RESULTS: Between January 2015 and October 2018, 237 patients received ICIs. Of these patients, 26% (61/237) had special issues: 32 had hepatitis B viral (HBV) infections, 20 Tbc, six ILD, one HIV infection, one Behçet's disease and a past HBV infection, and one rheumatoid arthritis. The incidence of hepatitis tended to be higher in patients with HBV infections than in those without (18.8% vs 8.91%, P = .082). Severe hepatitis (grade 3 or higher) was more common in HBV‐infected patients (12.5% vs 1.9%, P = .0021), but the AEs were well‐managed. During ICI treatment, three of the 20 patients with a history of pulmonary Tbc developed active pulmonary Tbc, considered reactivations. No aggravation of ILD was noted. One RA patient experienced a disease flare and was treated with a low‐dose steroid. There was no significant difference in the overall response rate or progression‐free survival between patients with and without special issues. CONCLUSION: Given the relatively low incidence of immune‐related AEs and the comparability of clinical outcomes, ICIs can be treatment option of NSCLC patients with special issues.
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spelling pubmed-71318572020-04-06 PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence Byeon, Seonggyu Cho, Jang Ho Jung, Hyun Ae Sun, Jong‐Mu Lee, Se‐Hoon Ahn, Jin Seok Park, Keunchil Ahn, Myung‐Ju Cancer Med Clinical Cancer Research BACKGROUND: Immune checkpoint inhibitors (ICIs) have provided new therapeutic options for non‐small cell lung cancer(NSCLC) patients. However, due to concerning increases in immune‐related adverse events, clinical trials usually exclude patients with special issues such as viral hepatitis, tuberculosis (Tbc), interstitial lung disease (ILD) and autoimmune disease. METHODS: We retrospectively reviewed the medical records of NSCLC patients who received ICIs, and analyzed the clinical outcomes of patients with special issues. RESULTS: Between January 2015 and October 2018, 237 patients received ICIs. Of these patients, 26% (61/237) had special issues: 32 had hepatitis B viral (HBV) infections, 20 Tbc, six ILD, one HIV infection, one Behçet's disease and a past HBV infection, and one rheumatoid arthritis. The incidence of hepatitis tended to be higher in patients with HBV infections than in those without (18.8% vs 8.91%, P = .082). Severe hepatitis (grade 3 or higher) was more common in HBV‐infected patients (12.5% vs 1.9%, P = .0021), but the AEs were well‐managed. During ICI treatment, three of the 20 patients with a history of pulmonary Tbc developed active pulmonary Tbc, considered reactivations. No aggravation of ILD was noted. One RA patient experienced a disease flare and was treated with a low‐dose steroid. There was no significant difference in the overall response rate or progression‐free survival between patients with and without special issues. CONCLUSION: Given the relatively low incidence of immune‐related AEs and the comparability of clinical outcomes, ICIs can be treatment option of NSCLC patients with special issues. John Wiley and Sons Inc. 2020-02-06 /pmc/articles/PMC7131857/ /pubmed/32027780 http://dx.doi.org/10.1002/cam4.2868 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Byeon, Seonggyu
Cho, Jang Ho
Jung, Hyun Ae
Sun, Jong‐Mu
Lee, Se‐Hoon
Ahn, Jin Seok
Park, Keunchil
Ahn, Myung‐Ju
PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence
title PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence
title_full PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence
title_fullStr PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence
title_full_unstemmed PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence
title_short PD‐1 inhibitors for non‐small cell lung cancer patients with special issues: Real‐world evidence
title_sort pd‐1 inhibitors for non‐small cell lung cancer patients with special issues: real‐world evidence
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131857/
https://www.ncbi.nlm.nih.gov/pubmed/32027780
http://dx.doi.org/10.1002/cam4.2868
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