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The frequency of assessment of progression in randomized oncology clinical trials
BACKGROUND: Progression in tumor assessments is often detected at a follow‐up appointment rather than when actual change in progression has occurred, which can bias PFS outcomes. AIM: We sought to evaluate the frequency of tumor assessment scans in clinical trials of anti‐cancer interventions and to...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327664/ https://www.ncbi.nlm.nih.gov/pubmed/34821077 http://dx.doi.org/10.1002/cnr2.1527 |
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author | Haslam, Alyson Gill, Jennifer Prasad, Vinay |
author_facet | Haslam, Alyson Gill, Jennifer Prasad, Vinay |
author_sort | Haslam, Alyson |
collection | PubMed |
description | BACKGROUND: Progression in tumor assessments is often detected at a follow‐up appointment rather than when actual change in progression has occurred, which can bias PFS outcomes. AIM: We sought to evaluate the frequency of tumor assessment scans in clinical trials of anti‐cancer interventions and to compare this to recommended (National Comprehensive Cancer Network) and real‐world frequencies of tumor assessments. METHODS: In a cross‐sectional analysis, we searched for articles published in the three top oncology journals between July 2017 and June 2020. We included articles that were RCTs of patients that had unresectable or metastatic solid tumors and used an intervention that was designed to be anti‐tumor. We abstracted median PFS survival for each group, the PFS hazard ratio, frequency of tumor assessment scans, tumor type, intervention type, and information regarding the study. RESULTS: We found that, in the 182 comparisons (163 articles), less frequent tumor assessment (occurring more than 9 weeks between assessments) was associated with higher median PFS values for both the intervention group (p < .0001) and the control group (p < .0001). PFS hazard ratios for studies scanning for tumors every 10 or more weeks were no different than for studies scanning for tumors more frequently (p = .88). Data on the frequency of tumor assessments in the real world is sparse. CONCLUSION: We found that less frequent tumor assessment frequency was associated with longer median PFS in both intervention and control groups of clinical oncology trials but was not associated with differences in PFS hazard ratios. Future research is needed to compare real world to trial assessment. |
format | Online Article Text |
id | pubmed-9327664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93276642022-07-30 The frequency of assessment of progression in randomized oncology clinical trials Haslam, Alyson Gill, Jennifer Prasad, Vinay Cancer Rep (Hoboken) Original Articles BACKGROUND: Progression in tumor assessments is often detected at a follow‐up appointment rather than when actual change in progression has occurred, which can bias PFS outcomes. AIM: We sought to evaluate the frequency of tumor assessment scans in clinical trials of anti‐cancer interventions and to compare this to recommended (National Comprehensive Cancer Network) and real‐world frequencies of tumor assessments. METHODS: In a cross‐sectional analysis, we searched for articles published in the three top oncology journals between July 2017 and June 2020. We included articles that were RCTs of patients that had unresectable or metastatic solid tumors and used an intervention that was designed to be anti‐tumor. We abstracted median PFS survival for each group, the PFS hazard ratio, frequency of tumor assessment scans, tumor type, intervention type, and information regarding the study. RESULTS: We found that, in the 182 comparisons (163 articles), less frequent tumor assessment (occurring more than 9 weeks between assessments) was associated with higher median PFS values for both the intervention group (p < .0001) and the control group (p < .0001). PFS hazard ratios for studies scanning for tumors every 10 or more weeks were no different than for studies scanning for tumors more frequently (p = .88). Data on the frequency of tumor assessments in the real world is sparse. CONCLUSION: We found that less frequent tumor assessment frequency was associated with longer median PFS in both intervention and control groups of clinical oncology trials but was not associated with differences in PFS hazard ratios. Future research is needed to compare real world to trial assessment. John Wiley and Sons Inc. 2021-11-24 /pmc/articles/PMC9327664/ /pubmed/34821077 http://dx.doi.org/10.1002/cnr2.1527 Text en © 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Haslam, Alyson Gill, Jennifer Prasad, Vinay The frequency of assessment of progression in randomized oncology clinical trials |
title | The frequency of assessment of progression in randomized oncology clinical trials |
title_full | The frequency of assessment of progression in randomized oncology clinical trials |
title_fullStr | The frequency of assessment of progression in randomized oncology clinical trials |
title_full_unstemmed | The frequency of assessment of progression in randomized oncology clinical trials |
title_short | The frequency of assessment of progression in randomized oncology clinical trials |
title_sort | frequency of assessment of progression in randomized oncology clinical trials |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327664/ https://www.ncbi.nlm.nih.gov/pubmed/34821077 http://dx.doi.org/10.1002/cnr2.1527 |
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