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Cancer Immunotherapy Trials Underutilize Immune Response Monitoring

Immune‐related radiological and biomarker monitoring in cancer immunotherapy trials permits interrogation of efficacy and reasons for therapeutic failure. We report the results from a cross‐sectional analysis of response monitoring in 685 T‐cell checkpoint‐targeted cancer immunotherapy trials in sol...

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Autores principales: Connell, Claire M., Raby, Sophie E.M., Beh, Ian, Flint, Thomas R., Williams, Edward H., Fearon, Douglas T., Jodrell, Duncan I., Janowitz, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AlphaMed Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759814/
https://www.ncbi.nlm.nih.gov/pubmed/29021379
http://dx.doi.org/10.1634/theoncologist.2017-0226
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author Connell, Claire M.
Raby, Sophie E.M.
Beh, Ian
Flint, Thomas R.
Williams, Edward H.
Fearon, Douglas T.
Jodrell, Duncan I.
Janowitz, Tobias
author_facet Connell, Claire M.
Raby, Sophie E.M.
Beh, Ian
Flint, Thomas R.
Williams, Edward H.
Fearon, Douglas T.
Jodrell, Duncan I.
Janowitz, Tobias
author_sort Connell, Claire M.
collection PubMed
description Immune‐related radiological and biomarker monitoring in cancer immunotherapy trials permits interrogation of efficacy and reasons for therapeutic failure. We report the results from a cross‐sectional analysis of response monitoring in 685 T‐cell checkpoint‐targeted cancer immunotherapy trials in solid malignancies, as registered on the U.S. National Institutes of Health trial registry by October 2016. Immune‐related radiological response criteria were registered for only 25% of clinical trials. Only 38% of trials registered an exploratory immunological biomarker, and registration of immunological biomarkers has decreased over the last 15 years. We suggest that increasing the utilization of immune‐related response monitoring across cancer immunotherapy trials will improve analysis of outcomes and facilitate translational efforts to extend the benefit of immunotherapy to a greater proportion of patients with cancer.
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spelling pubmed-57598142018-01-16 Cancer Immunotherapy Trials Underutilize Immune Response Monitoring Connell, Claire M. Raby, Sophie E.M. Beh, Ian Flint, Thomas R. Williams, Edward H. Fearon, Douglas T. Jodrell, Duncan I. Janowitz, Tobias Oncologist Brief Communications Immune‐related radiological and biomarker monitoring in cancer immunotherapy trials permits interrogation of efficacy and reasons for therapeutic failure. We report the results from a cross‐sectional analysis of response monitoring in 685 T‐cell checkpoint‐targeted cancer immunotherapy trials in solid malignancies, as registered on the U.S. National Institutes of Health trial registry by October 2016. Immune‐related radiological response criteria were registered for only 25% of clinical trials. Only 38% of trials registered an exploratory immunological biomarker, and registration of immunological biomarkers has decreased over the last 15 years. We suggest that increasing the utilization of immune‐related response monitoring across cancer immunotherapy trials will improve analysis of outcomes and facilitate translational efforts to extend the benefit of immunotherapy to a greater proportion of patients with cancer. AlphaMed Press 2017-10-11 2018-01 /pmc/articles/PMC5759814/ /pubmed/29021379 http://dx.doi.org/10.1634/theoncologist.2017-0226 Text en © AlphaMed Press 2017
spellingShingle Brief Communications
Connell, Claire M.
Raby, Sophie E.M.
Beh, Ian
Flint, Thomas R.
Williams, Edward H.
Fearon, Douglas T.
Jodrell, Duncan I.
Janowitz, Tobias
Cancer Immunotherapy Trials Underutilize Immune Response Monitoring
title Cancer Immunotherapy Trials Underutilize Immune Response Monitoring
title_full Cancer Immunotherapy Trials Underutilize Immune Response Monitoring
title_fullStr Cancer Immunotherapy Trials Underutilize Immune Response Monitoring
title_full_unstemmed Cancer Immunotherapy Trials Underutilize Immune Response Monitoring
title_short Cancer Immunotherapy Trials Underutilize Immune Response Monitoring
title_sort cancer immunotherapy trials underutilize immune response monitoring
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759814/
https://www.ncbi.nlm.nih.gov/pubmed/29021379
http://dx.doi.org/10.1634/theoncologist.2017-0226
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