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A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors
BACKGROUND: Regular off‐treatment imaging is often used to assess for recurrence of disease after childhood cancer treatment. It is unclear if this increases survival, or what burden surveillance places on patients, families, or health‐care services. This systematic review examines the impact of rou...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367646/ https://www.ncbi.nlm.nih.gov/pubmed/32431088 http://dx.doi.org/10.1002/cam4.3110 |
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author | Morgan, Jessica E. Walker, Ruth Harden, Melissa Phillips, Robert S. |
author_facet | Morgan, Jessica E. Walker, Ruth Harden, Melissa Phillips, Robert S. |
author_sort | Morgan, Jessica E. |
collection | PubMed |
description | BACKGROUND: Regular off‐treatment imaging is often used to assess for recurrence of disease after childhood cancer treatment. It is unclear if this increases survival, or what burden surveillance places on patients, families, or health‐care services. This systematic review examines the impact of routine surveillance imaging after treatment of pediatric extracranial solid tumors. METHODS: Collaborative patient and public involvement informed the design and interpretation of this work. Thirteen electronic databases, conference proceedings, and trial registries were searched alongside reference list checking and forward citation searching from 1990 onwards. Studies were screened and data were extracted by two researchers. Risk of bias was assessed using a modified ROBINS‐I tool. Relevant outcomes were overall survival, psychological distress indicators, number of imaging tests, cost‐effectiveness, and qualitative data regarding experiences of surveillance programs. PROSPERO (CRD42018103764). RESULTS: Of 17 727 records identified, 55 studies of 10 207 patients were included. All studies used observational methods. Risk of bias for all except one study was moderate, serious, or critical. Data were too few to conduct meta‐analysis; however, narrative synthesis was performed. Surveillance strategies varied, and poorly reported, involving many scans and substantial radiation exposure (eg, neuroblastoma, median 133.5 mSv). For most diseases, surveillance imaging was not associated with increased overall survival, with the probable exception of Wilms tumor. No qualitative or psychological distress data were identified. CONCLUSIONS: At present, there is insufficient evidence to evaluate the effects of routine surveillance imaging on survival in most pediatric extracranial solid tumors. More high‐quality data are required, preferably through randomized controlled trials with well‐conducted qualitative elements. |
format | Online Article Text |
id | pubmed-7367646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73676462020-07-20 A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors Morgan, Jessica E. Walker, Ruth Harden, Melissa Phillips, Robert S. Cancer Med Clinical Cancer Research BACKGROUND: Regular off‐treatment imaging is often used to assess for recurrence of disease after childhood cancer treatment. It is unclear if this increases survival, or what burden surveillance places on patients, families, or health‐care services. This systematic review examines the impact of routine surveillance imaging after treatment of pediatric extracranial solid tumors. METHODS: Collaborative patient and public involvement informed the design and interpretation of this work. Thirteen electronic databases, conference proceedings, and trial registries were searched alongside reference list checking and forward citation searching from 1990 onwards. Studies were screened and data were extracted by two researchers. Risk of bias was assessed using a modified ROBINS‐I tool. Relevant outcomes were overall survival, psychological distress indicators, number of imaging tests, cost‐effectiveness, and qualitative data regarding experiences of surveillance programs. PROSPERO (CRD42018103764). RESULTS: Of 17 727 records identified, 55 studies of 10 207 patients were included. All studies used observational methods. Risk of bias for all except one study was moderate, serious, or critical. Data were too few to conduct meta‐analysis; however, narrative synthesis was performed. Surveillance strategies varied, and poorly reported, involving many scans and substantial radiation exposure (eg, neuroblastoma, median 133.5 mSv). For most diseases, surveillance imaging was not associated with increased overall survival, with the probable exception of Wilms tumor. No qualitative or psychological distress data were identified. CONCLUSIONS: At present, there is insufficient evidence to evaluate the effects of routine surveillance imaging on survival in most pediatric extracranial solid tumors. More high‐quality data are required, preferably through randomized controlled trials with well‐conducted qualitative elements. John Wiley and Sons Inc. 2020-05-19 /pmc/articles/PMC7367646/ /pubmed/32431088 http://dx.doi.org/10.1002/cam4.3110 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 Morgan, Jessica E. Walker, Ruth Harden, Melissa Phillips, Robert S. A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors |
title | A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors |
title_full | A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors |
title_fullStr | A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors |
title_full_unstemmed | A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors |
title_short | A systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors |
title_sort | systematic review of evidence for and against routine surveillance imaging after completing treatment for childhood extracranial solid tumors |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367646/ https://www.ncbi.nlm.nih.gov/pubmed/32431088 http://dx.doi.org/10.1002/cam4.3110 |
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