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Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials
BACKGROUND: Patient selection is key in Phase I studies, and prognosis can be difficult to estimate in heavily pre-treated patients. Previous prognostic models like the Royal Marsden Hospital (RMH) score or using the neutrophil–lymphocyte ratio (NLR) have not been validated in current novel therapie...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070409/ https://www.ncbi.nlm.nih.gov/pubmed/36797357 http://dx.doi.org/10.1038/s41416-023-02193-2 |
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author | Loh, Jerold Wu, Jiaxuan Chieng, Jenny Chan, Aurora Yong, Wei-Peng Sundar, Raghav Lee, Soo-Chin Wong, Andrea Lim, Joline S. J. Tan, David S. P. Soo, Ross Goh, Boon-Cher Tai, Bee-Choo Chee, Cheng E. |
author_facet | Loh, Jerold Wu, Jiaxuan Chieng, Jenny Chan, Aurora Yong, Wei-Peng Sundar, Raghav Lee, Soo-Chin Wong, Andrea Lim, Joline S. J. Tan, David S. P. Soo, Ross Goh, Boon-Cher Tai, Bee-Choo Chee, Cheng E. |
author_sort | Loh, Jerold |
collection | PubMed |
description | BACKGROUND: Patient selection is key in Phase I studies, and prognosis can be difficult to estimate in heavily pre-treated patients. Previous prognostic models like the Royal Marsden Hospital (RMH) score or using the neutrophil–lymphocyte ratio (NLR) have not been validated in current novel therapies nor in the Asian Phase I population. METHODS: We conducted a retrospective review of 414 patients with solid tumours participating in Phase I studies at our centre between October 2013 and December 2020. RESULTS: The RMH model showed poorer prognosis with increasing scores [RMH score 1, HR 1.28 (95% CI: 0.96–1.70); RMH score 2, HR 2.27 (95% CI: 1.62–3.17); RMH score 3, HR 4.14 (95% CI: 2.62–6.53)]. NLR did not improve the AUC of the model. Poorer ECOG status (ECOG 1 vs. 0: HR = 1.59 (95% CI = 1.24–2.04), P < 0.001) and primary tumour site (GI vs. breast cancer: HR = 3.06, 95% CI = 2.16–4.35, P < 0.001) were prognostic. CONCLUSIONS: We developed a NCIS prognostic score with excellent prognostic ability for both short-term and longer-term survival (iAUC: 0.71 [95% CI 0.65–0.76]), and validated the RMH model in the largest Asian study to date. |
format | Online Article Text |
id | pubmed-10070409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100704092023-04-05 Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials Loh, Jerold Wu, Jiaxuan Chieng, Jenny Chan, Aurora Yong, Wei-Peng Sundar, Raghav Lee, Soo-Chin Wong, Andrea Lim, Joline S. J. Tan, David S. P. Soo, Ross Goh, Boon-Cher Tai, Bee-Choo Chee, Cheng E. Br J Cancer Article BACKGROUND: Patient selection is key in Phase I studies, and prognosis can be difficult to estimate in heavily pre-treated patients. Previous prognostic models like the Royal Marsden Hospital (RMH) score or using the neutrophil–lymphocyte ratio (NLR) have not been validated in current novel therapies nor in the Asian Phase I population. METHODS: We conducted a retrospective review of 414 patients with solid tumours participating in Phase I studies at our centre between October 2013 and December 2020. RESULTS: The RMH model showed poorer prognosis with increasing scores [RMH score 1, HR 1.28 (95% CI: 0.96–1.70); RMH score 2, HR 2.27 (95% CI: 1.62–3.17); RMH score 3, HR 4.14 (95% CI: 2.62–6.53)]. NLR did not improve the AUC of the model. Poorer ECOG status (ECOG 1 vs. 0: HR = 1.59 (95% CI = 1.24–2.04), P < 0.001) and primary tumour site (GI vs. breast cancer: HR = 3.06, 95% CI = 2.16–4.35, P < 0.001) were prognostic. CONCLUSIONS: We developed a NCIS prognostic score with excellent prognostic ability for both short-term and longer-term survival (iAUC: 0.71 [95% CI 0.65–0.76]), and validated the RMH model in the largest Asian study to date. Nature Publishing Group UK 2023-02-16 2023-04-12 /pmc/articles/PMC10070409/ /pubmed/36797357 http://dx.doi.org/10.1038/s41416-023-02193-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Loh, Jerold Wu, Jiaxuan Chieng, Jenny Chan, Aurora Yong, Wei-Peng Sundar, Raghav Lee, Soo-Chin Wong, Andrea Lim, Joline S. J. Tan, David S. P. Soo, Ross Goh, Boon-Cher Tai, Bee-Choo Chee, Cheng E. Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials |
title | Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials |
title_full | Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials |
title_fullStr | Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials |
title_full_unstemmed | Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials |
title_short | Clinical outcome and prognostic factors for Asian patients in Phase I clinical trials |
title_sort | clinical outcome and prognostic factors for asian patients in phase i clinical trials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070409/ https://www.ncbi.nlm.nih.gov/pubmed/36797357 http://dx.doi.org/10.1038/s41416-023-02193-2 |
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