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Clinical significance of post‐progression survival in lung cancer

Progression‐free survival (PFS) and overall survival (OS) are two common endpoints in cancer trials. OS is usually preferred, because it is reliable, precise, meaningful, and can easily be documented. However, subsequent lines of therapy might confound the effects of first‐line treatment on OS. Whet...

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Autores principales: Imai, Hisao, Kaira, Kyoichi, Minato, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582459/
https://www.ncbi.nlm.nih.gov/pubmed/28627767
http://dx.doi.org/10.1111/1759-7714.12463
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author Imai, Hisao
Kaira, Kyoichi
Minato, Koichi
author_facet Imai, Hisao
Kaira, Kyoichi
Minato, Koichi
author_sort Imai, Hisao
collection PubMed
description Progression‐free survival (PFS) and overall survival (OS) are two common endpoints in cancer trials. OS is usually preferred, because it is reliable, precise, meaningful, and can easily be documented. However, subsequent lines of therapy might confound the effects of first‐line treatment on OS. Whether PFS or OS is the more appropriate endpoint in clinical trials of metastatic cancer remains controversial. Previous reports on lung cancer have shown that an increase in PFS does not necessarily result in an increase in OS; however, post‐progression survival (PPS) is strongly associated with OS after early‐line treatment. The significance of PPS after first and second‐line therapy at the individual level in patients with advanced lung cancer has also recently been reported. Findings of previous reports indicate that PPS is highly associated with OS after first and second‐line chemotherapy in patients with advanced non‐small cell lung cancer and small cell lung cancer, whereas PFS is only moderately associated with OS. Therefore, subsequent treatment after disease progression following early‐line treatments may greatly influence OS. This review demonstrates that even in advanced lung cancer, PPS, rather than PFS, has become more strongly associated with OS over the years, potentially because of intensive post‐study treatments. As a result of the increasing impact of PPS on OS, a PFS‐related advantage does not necessarily indicate an OS‐related advantage. Thus, the prolongation of PPS might limit the classical role of OS for assessing true efficacy derived from early‐line chemotherapy in future clinical trials.
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spelling pubmed-55824592017-09-06 Clinical significance of post‐progression survival in lung cancer Imai, Hisao Kaira, Kyoichi Minato, Koichi Thorac Cancer Mini Review Progression‐free survival (PFS) and overall survival (OS) are two common endpoints in cancer trials. OS is usually preferred, because it is reliable, precise, meaningful, and can easily be documented. However, subsequent lines of therapy might confound the effects of first‐line treatment on OS. Whether PFS or OS is the more appropriate endpoint in clinical trials of metastatic cancer remains controversial. Previous reports on lung cancer have shown that an increase in PFS does not necessarily result in an increase in OS; however, post‐progression survival (PPS) is strongly associated with OS after early‐line treatment. The significance of PPS after first and second‐line therapy at the individual level in patients with advanced lung cancer has also recently been reported. Findings of previous reports indicate that PPS is highly associated with OS after first and second‐line chemotherapy in patients with advanced non‐small cell lung cancer and small cell lung cancer, whereas PFS is only moderately associated with OS. Therefore, subsequent treatment after disease progression following early‐line treatments may greatly influence OS. This review demonstrates that even in advanced lung cancer, PPS, rather than PFS, has become more strongly associated with OS over the years, potentially because of intensive post‐study treatments. As a result of the increasing impact of PPS on OS, a PFS‐related advantage does not necessarily indicate an OS‐related advantage. Thus, the prolongation of PPS might limit the classical role of OS for assessing true efficacy derived from early‐line chemotherapy in future clinical trials. John Wiley & Sons Australia, Ltd 2017-06-19 2017-09 /pmc/articles/PMC5582459/ /pubmed/28627767 http://dx.doi.org/10.1111/1759-7714.12463 Text en © 2017 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 Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Mini Review
Imai, Hisao
Kaira, Kyoichi
Minato, Koichi
Clinical significance of post‐progression survival in lung cancer
title Clinical significance of post‐progression survival in lung cancer
title_full Clinical significance of post‐progression survival in lung cancer
title_fullStr Clinical significance of post‐progression survival in lung cancer
title_full_unstemmed Clinical significance of post‐progression survival in lung cancer
title_short Clinical significance of post‐progression survival in lung cancer
title_sort clinical significance of post‐progression survival in lung cancer
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582459/
https://www.ncbi.nlm.nih.gov/pubmed/28627767
http://dx.doi.org/10.1111/1759-7714.12463
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