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Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer

Atezolizumab was the first immune checkpoint inhibitor (ICI) to be introduced as a first‐line treatment option for extensive‐stage small cell lung cancer (ES‐SCLC), in combination with carboplatin and etoposide (CE) chemotherapy. However, SCLC treatment options after progression to first‐line chemot...

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Autores principales: Kataoka, Nobutaka, Kunimatsu, Yusuke, Tachibana, Yusuke, Sugimoto, Takumi, Sato, Izumi, Tani, Nozomi, Ogura, Yuri, Hirose, Kazuki, Takeda, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471014/
https://www.ncbi.nlm.nih.gov/pubmed/32706170
http://dx.doi.org/10.1111/1759-7714.13588
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author Kataoka, Nobutaka
Kunimatsu, Yusuke
Tachibana, Yusuke
Sugimoto, Takumi
Sato, Izumi
Tani, Nozomi
Ogura, Yuri
Hirose, Kazuki
Takeda, Takayuki
author_facet Kataoka, Nobutaka
Kunimatsu, Yusuke
Tachibana, Yusuke
Sugimoto, Takumi
Sato, Izumi
Tani, Nozomi
Ogura, Yuri
Hirose, Kazuki
Takeda, Takayuki
author_sort Kataoka, Nobutaka
collection PubMed
description Atezolizumab was the first immune checkpoint inhibitor (ICI) to be introduced as a first‐line treatment option for extensive‐stage small cell lung cancer (ES‐SCLC), in combination with carboplatin and etoposide (CE) chemotherapy. However, SCLC treatment options after progression to first‐line chemotherapy are limited, warranting the readministration of previously used drugs. In combination with atezolizumab, CE readministration may theoretically be effective, based on two tentative mechanisms: its additive and synergistic effects on cytotoxic chemotherapy. The additive effect is based on the IFCT‐1603 trial in which the Kaplan‐Meier estimates of both progression‐free survival (PFS) and overall survival (OS) in the atezolizumab group exhibited a tail plateau in the selected population. Conversely, an anti‐PD‐L1 antibody synergistic effect on platinum compounds was assessed in a preclinical study, which was reinforced by clinical data. Thus, atezolizumab in combination with CE may be a treatment option in heavily treated patients. Here, we describe the first case of a heavily treated ES‐SCLC patient treated with chemoimmunotherapy, resulting in a partial response and a durable PFS. KEY POINTS: SIGNIFICANT FINDINGS OF THE STUDY AND WHAT THIS STUDY ADDS: CE readministration with atezolizumab may be effective based on two tentative mechanisms. Additive and synergistic effects of atezolizumab on CE have been previously suggested via a clinical trial and preclinical study, respectively. This is reflected in the current case in clinical settings.
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spelling pubmed-74710142020-09-09 Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer Kataoka, Nobutaka Kunimatsu, Yusuke Tachibana, Yusuke Sugimoto, Takumi Sato, Izumi Tani, Nozomi Ogura, Yuri Hirose, Kazuki Takeda, Takayuki Thorac Cancer Case Reports Atezolizumab was the first immune checkpoint inhibitor (ICI) to be introduced as a first‐line treatment option for extensive‐stage small cell lung cancer (ES‐SCLC), in combination with carboplatin and etoposide (CE) chemotherapy. However, SCLC treatment options after progression to first‐line chemotherapy are limited, warranting the readministration of previously used drugs. In combination with atezolizumab, CE readministration may theoretically be effective, based on two tentative mechanisms: its additive and synergistic effects on cytotoxic chemotherapy. The additive effect is based on the IFCT‐1603 trial in which the Kaplan‐Meier estimates of both progression‐free survival (PFS) and overall survival (OS) in the atezolizumab group exhibited a tail plateau in the selected population. Conversely, an anti‐PD‐L1 antibody synergistic effect on platinum compounds was assessed in a preclinical study, which was reinforced by clinical data. Thus, atezolizumab in combination with CE may be a treatment option in heavily treated patients. Here, we describe the first case of a heavily treated ES‐SCLC patient treated with chemoimmunotherapy, resulting in a partial response and a durable PFS. KEY POINTS: SIGNIFICANT FINDINGS OF THE STUDY AND WHAT THIS STUDY ADDS: CE readministration with atezolizumab may be effective based on two tentative mechanisms. Additive and synergistic effects of atezolizumab on CE have been previously suggested via a clinical trial and preclinical study, respectively. This is reflected in the current case in clinical settings. John Wiley & Sons Australia, Ltd 2020-07-24 2020-09 /pmc/articles/PMC7471014/ /pubmed/32706170 http://dx.doi.org/10.1111/1759-7714.13588 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, 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 Case Reports
Kataoka, Nobutaka
Kunimatsu, Yusuke
Tachibana, Yusuke
Sugimoto, Takumi
Sato, Izumi
Tani, Nozomi
Ogura, Yuri
Hirose, Kazuki
Takeda, Takayuki
Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer
title Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer
title_full Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer
title_fullStr Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer
title_full_unstemmed Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer
title_short Atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer
title_sort atezolizumab in combination with carboplatin and etoposide for heavily treated small cell lung cancer
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471014/
https://www.ncbi.nlm.nih.gov/pubmed/32706170
http://dx.doi.org/10.1111/1759-7714.13588
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