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Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients

Although immune checkpoint inhibitors (ICIs) can induce durable responses in non-small-cell lung cancer (NSCLC) patients, a significant proportion of responders still experience progressive disease after a period of response. Limited data are available on the clinical patterns of acquired resistance...

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Autores principales: Heo, Ja Yoon, Yoo, Shin Hye, Suh, Koung Jin, Kim, Se Hyun, Kim, Yu Jung, Ock, Chan-Young, Kim, Miso, Keam, Bhumsuk, Kim, Tae Min, Kim, Dong-Wan, Heo, Dae Seog, Lee, Jong Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844257/
https://www.ncbi.nlm.nih.gov/pubmed/33510255
http://dx.doi.org/10.1038/s41598-021-81666-x
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author Heo, Ja Yoon
Yoo, Shin Hye
Suh, Koung Jin
Kim, Se Hyun
Kim, Yu Jung
Ock, Chan-Young
Kim, Miso
Keam, Bhumsuk
Kim, Tae Min
Kim, Dong-Wan
Heo, Dae Seog
Lee, Jong Seok
author_facet Heo, Ja Yoon
Yoo, Shin Hye
Suh, Koung Jin
Kim, Se Hyun
Kim, Yu Jung
Ock, Chan-Young
Kim, Miso
Keam, Bhumsuk
Kim, Tae Min
Kim, Dong-Wan
Heo, Dae Seog
Lee, Jong Seok
author_sort Heo, Ja Yoon
collection PubMed
description Although immune checkpoint inhibitors (ICIs) can induce durable responses in non-small-cell lung cancer (NSCLC) patients, a significant proportion of responders still experience progressive disease after a period of response. Limited data are available on the clinical patterns of acquired resistance (AR) to ICIs. Clinical and radiologic data from 125 NSCLC patients treated with anti-PD-1 or PD-L1 antibodies between 2011 and 2018 at two tertiary academic institutions were retrospectively reviewed. Overall, 63 (50.4%) patients experienced AR after ICI treatment in a median of 10.7 months. Among the 13 patients with a partial response with ICI, 12 (32.4%) had only lymph node progression. Most patients (n = 52, 82.5%) had one or two sites with progression (oligo-progression). The median overall survival (OS) after progression was significantly longer in the extrathoracic group than in the thoracic and liver progression groups (30.2 months [95% confidence interval (CI), 13.4 to not reached (NR)], 11.7 months [95% CI, 9.5–21.1], and 5.4 months [95% CI, 2.6-NR], respectively, P < 0.001). Patients with oligo-progression had significantly longer OS after AR than did the multi-progression patients (18.9 months [95% CI, 10.6-NR] vs. 8.8 months [95% CI, 5.7-NR], P = 0.04). No significant difference in progression-free survival was observed between the subsequent chemotherapy and the ICI after AR groups (P = 0.723). Patients with AR after ICI treatment had a unique progression pattern with oligo-progression and high rates of progression only in the lymph nodes. Local treatment and/or continuation of ICIs beyond AR might be an effective option.
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spelling pubmed-78442572021-02-01 Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients Heo, Ja Yoon Yoo, Shin Hye Suh, Koung Jin Kim, Se Hyun Kim, Yu Jung Ock, Chan-Young Kim, Miso Keam, Bhumsuk Kim, Tae Min Kim, Dong-Wan Heo, Dae Seog Lee, Jong Seok Sci Rep Article Although immune checkpoint inhibitors (ICIs) can induce durable responses in non-small-cell lung cancer (NSCLC) patients, a significant proportion of responders still experience progressive disease after a period of response. Limited data are available on the clinical patterns of acquired resistance (AR) to ICIs. Clinical and radiologic data from 125 NSCLC patients treated with anti-PD-1 or PD-L1 antibodies between 2011 and 2018 at two tertiary academic institutions were retrospectively reviewed. Overall, 63 (50.4%) patients experienced AR after ICI treatment in a median of 10.7 months. Among the 13 patients with a partial response with ICI, 12 (32.4%) had only lymph node progression. Most patients (n = 52, 82.5%) had one or two sites with progression (oligo-progression). The median overall survival (OS) after progression was significantly longer in the extrathoracic group than in the thoracic and liver progression groups (30.2 months [95% confidence interval (CI), 13.4 to not reached (NR)], 11.7 months [95% CI, 9.5–21.1], and 5.4 months [95% CI, 2.6-NR], respectively, P < 0.001). Patients with oligo-progression had significantly longer OS after AR than did the multi-progression patients (18.9 months [95% CI, 10.6-NR] vs. 8.8 months [95% CI, 5.7-NR], P = 0.04). No significant difference in progression-free survival was observed between the subsequent chemotherapy and the ICI after AR groups (P = 0.723). Patients with AR after ICI treatment had a unique progression pattern with oligo-progression and high rates of progression only in the lymph nodes. Local treatment and/or continuation of ICIs beyond AR might be an effective option. Nature Publishing Group UK 2021-01-28 /pmc/articles/PMC7844257/ /pubmed/33510255 http://dx.doi.org/10.1038/s41598-021-81666-x Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Heo, Ja Yoon
Yoo, Shin Hye
Suh, Koung Jin
Kim, Se Hyun
Kim, Yu Jung
Ock, Chan-Young
Kim, Miso
Keam, Bhumsuk
Kim, Tae Min
Kim, Dong-Wan
Heo, Dae Seog
Lee, Jong Seok
Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients
title Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients
title_full Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients
title_fullStr Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients
title_full_unstemmed Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients
title_short Clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients
title_sort clinical pattern of failure after a durable response to immune check inhibitors in non-small cell lung cancer patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844257/
https://www.ncbi.nlm.nih.gov/pubmed/33510255
http://dx.doi.org/10.1038/s41598-021-81666-x
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