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Selection of Treatment Regimens for Recurrent Cervical Cancer

OBJECTIVE: The selection of individualized treatment for recurrent cervical cancer is challenging. This study aimed to investigate the impact of various therapies on survival outcomes after recurrence. METHODS: Eligible patients were diagnosed with recurrent cervical cancer between March 2012 and Ap...

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Autores principales: Chao, Xiaopei, Song, Xiaochen, Wu, Huanwen, You, Yan, Wu, Ming, Li, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884815/
https://www.ncbi.nlm.nih.gov/pubmed/33604304
http://dx.doi.org/10.3389/fonc.2021.618485
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author Chao, Xiaopei
Song, Xiaochen
Wu, Huanwen
You, Yan
Wu, Ming
Li, Lei
author_facet Chao, Xiaopei
Song, Xiaochen
Wu, Huanwen
You, Yan
Wu, Ming
Li, Lei
author_sort Chao, Xiaopei
collection PubMed
description OBJECTIVE: The selection of individualized treatment for recurrent cervical cancer is challenging. This study aimed to investigate the impact of various therapies on survival outcomes after recurrence. METHODS: Eligible patients were diagnosed with recurrent cervical cancer between March 2012 and April 2018. Postrecurrence progression-free survival (PFS) and overall survival (OS) were investigated in the whole cohort and in subgroups, categorized by recurrence site and prior radiotherapy history, using a multivariate model that incorporated treatment for primary and recurrent tumors, histological pathology, and FIGO staging. RESULTS: Two hundred and sixty recurrent cervical cancer patients were included. As of March 1, 2020, the median postrecurrence PFS and OS were 7.0 (range 0-94) and 24.0 (1.8-149.1) months, respectively. In a multivariate model measured by PFS, radiotherapy was superior to other therapies for the whole cohort (p=0.029) and recurrence only within the pelvic cavity (p=0.005), but the advantages of radiotherapy disappeared in patients with a history of radiotherapy (p values >0.05). For recurrence only beyond the pelvic cavity, combination therapy resulted in improved PFS (p=0.028). For recurrence both within and beyond the pelvic cavity, no therapy regimen provided additional PFS benefits (p values >0.05). Radiotherapy and combination therapy were also associated with improved postrecurrence OS for recurrence within the pelvic cavity (p=0.034) and only beyond the pelvic cavity (p=0.017), respectively. CONCLUSIONS: In cervical cancer patients, postrecurrence radiotherapy can improve PFS and OS for patients with recurrence within the pelvic cavity and without prior radiotherapy. For recurrence beyond the pelvic cavity or cases with a history of radiotherapy, combination or individualized therapy may provide potential survival benefits.
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spelling pubmed-78848152021-02-17 Selection of Treatment Regimens for Recurrent Cervical Cancer Chao, Xiaopei Song, Xiaochen Wu, Huanwen You, Yan Wu, Ming Li, Lei Front Oncol Oncology OBJECTIVE: The selection of individualized treatment for recurrent cervical cancer is challenging. This study aimed to investigate the impact of various therapies on survival outcomes after recurrence. METHODS: Eligible patients were diagnosed with recurrent cervical cancer between March 2012 and April 2018. Postrecurrence progression-free survival (PFS) and overall survival (OS) were investigated in the whole cohort and in subgroups, categorized by recurrence site and prior radiotherapy history, using a multivariate model that incorporated treatment for primary and recurrent tumors, histological pathology, and FIGO staging. RESULTS: Two hundred and sixty recurrent cervical cancer patients were included. As of March 1, 2020, the median postrecurrence PFS and OS were 7.0 (range 0-94) and 24.0 (1.8-149.1) months, respectively. In a multivariate model measured by PFS, radiotherapy was superior to other therapies for the whole cohort (p=0.029) and recurrence only within the pelvic cavity (p=0.005), but the advantages of radiotherapy disappeared in patients with a history of radiotherapy (p values >0.05). For recurrence only beyond the pelvic cavity, combination therapy resulted in improved PFS (p=0.028). For recurrence both within and beyond the pelvic cavity, no therapy regimen provided additional PFS benefits (p values >0.05). Radiotherapy and combination therapy were also associated with improved postrecurrence OS for recurrence within the pelvic cavity (p=0.034) and only beyond the pelvic cavity (p=0.017), respectively. CONCLUSIONS: In cervical cancer patients, postrecurrence radiotherapy can improve PFS and OS for patients with recurrence within the pelvic cavity and without prior radiotherapy. For recurrence beyond the pelvic cavity or cases with a history of radiotherapy, combination or individualized therapy may provide potential survival benefits. Frontiers Media S.A. 2021-02-02 /pmc/articles/PMC7884815/ /pubmed/33604304 http://dx.doi.org/10.3389/fonc.2021.618485 Text en Copyright © 2021 Chao, Song, Wu, You, Wu and Li http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Chao, Xiaopei
Song, Xiaochen
Wu, Huanwen
You, Yan
Wu, Ming
Li, Lei
Selection of Treatment Regimens for Recurrent Cervical Cancer
title Selection of Treatment Regimens for Recurrent Cervical Cancer
title_full Selection of Treatment Regimens for Recurrent Cervical Cancer
title_fullStr Selection of Treatment Regimens for Recurrent Cervical Cancer
title_full_unstemmed Selection of Treatment Regimens for Recurrent Cervical Cancer
title_short Selection of Treatment Regimens for Recurrent Cervical Cancer
title_sort selection of treatment regimens for recurrent cervical cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884815/
https://www.ncbi.nlm.nih.gov/pubmed/33604304
http://dx.doi.org/10.3389/fonc.2021.618485
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