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Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades

BACKGROUND: Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) are heterogenous malignancies that require well-designed trials to develop effective management strategies. This cross-sectional study aimed to illustrate the current landscape of clinical trials in GEP-NENs to provide insights f...

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Autores principales: Yang, Kaili, Li, Jiarui, Cheng, Yuejuan, Bai, Chunmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083666/
https://www.ncbi.nlm.nih.gov/pubmed/36724047
http://dx.doi.org/10.1530/EC-22-0441
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author Yang, Kaili
Li, Jiarui
Cheng, Yuejuan
Bai, Chunmei
author_facet Yang, Kaili
Li, Jiarui
Cheng, Yuejuan
Bai, Chunmei
author_sort Yang, Kaili
collection PubMed
description BACKGROUND: Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) are heterogenous malignancies that require well-designed trials to develop effective management strategies. This cross-sectional study aimed to illustrate the current landscape of clinical trials in GEP-NENs to provide insights for future research. MATERIALS AND METHODS: We reviewed all clinical trials registered on ClinicalTrials.gov between 1 January 2000 and 31 December 2021 with GEP-NEN in the ‘condition or disease’ field. RESULTS: We included 206 eligible trials. Most trials enrolled less than 50 patients (59.8%) and were sponsored by institutions other than government or industry (67.0%). Most trials were conducted in high-income countries (86.6%) and countries located in Europe (30.1%) or Northern America (29.6%). The overall result reporting rates of GEP-NEN trials was 41.4%, and the median time from primary completion to result reporting was 101 months. Characteristics that improved the reporting of results included larger sample size, tumor differentiation specification for inclusion, progression-free survival as primary endpoint, industry sponsorship, and multicenter or multinational participation (all P < 0.05). Compared with trials registered between 2000 and 2011 (n = 28), trials registered between 2012 and 2021 (n = 178) were more likely to specify the Ki-67 index for inclusion (68.0% vs 35.7%, P = 0.002) and to be conducted outside Europe or Northern America (16.4% vs 3.7%, P = 0.02), while the sample size and the sponsorship did not change significantly. CONCLUSIONS: Novel management options have been explored for GEP-NENs with more specific inclusion criteria during the past two decades. More efforts are needed to promote international collaborations in clinical trials and enhance timely result dissemination.
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spelling pubmed-100836662023-04-11 Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades Yang, Kaili Li, Jiarui Cheng, Yuejuan Bai, Chunmei Endocr Connect Research BACKGROUND: Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) are heterogenous malignancies that require well-designed trials to develop effective management strategies. This cross-sectional study aimed to illustrate the current landscape of clinical trials in GEP-NENs to provide insights for future research. MATERIALS AND METHODS: We reviewed all clinical trials registered on ClinicalTrials.gov between 1 January 2000 and 31 December 2021 with GEP-NEN in the ‘condition or disease’ field. RESULTS: We included 206 eligible trials. Most trials enrolled less than 50 patients (59.8%) and were sponsored by institutions other than government or industry (67.0%). Most trials were conducted in high-income countries (86.6%) and countries located in Europe (30.1%) or Northern America (29.6%). The overall result reporting rates of GEP-NEN trials was 41.4%, and the median time from primary completion to result reporting was 101 months. Characteristics that improved the reporting of results included larger sample size, tumor differentiation specification for inclusion, progression-free survival as primary endpoint, industry sponsorship, and multicenter or multinational participation (all P < 0.05). Compared with trials registered between 2000 and 2011 (n = 28), trials registered between 2012 and 2021 (n = 178) were more likely to specify the Ki-67 index for inclusion (68.0% vs 35.7%, P = 0.002) and to be conducted outside Europe or Northern America (16.4% vs 3.7%, P = 0.02), while the sample size and the sponsorship did not change significantly. CONCLUSIONS: Novel management options have been explored for GEP-NENs with more specific inclusion criteria during the past two decades. More efforts are needed to promote international collaborations in clinical trials and enhance timely result dissemination. Bioscientifica Ltd 2023-02-01 /pmc/articles/PMC10083666/ /pubmed/36724047 http://dx.doi.org/10.1530/EC-22-0441 Text en © the author(s) https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Research
Yang, Kaili
Li, Jiarui
Cheng, Yuejuan
Bai, Chunmei
Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades
title Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades
title_full Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades
title_fullStr Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades
title_full_unstemmed Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades
title_short Evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades
title_sort evolving landscape of clinical trials in gastroenteropancreatic neuroendocrine neoplasms in the past two decades
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083666/
https://www.ncbi.nlm.nih.gov/pubmed/36724047
http://dx.doi.org/10.1530/EC-22-0441
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