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Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer

Achieving systemic tumor control across metastases is vital for long-term patient survival but remains intractable in many patients. High lesion-level response heterogeneity persists, conferring many dissociated responses across metastatic lesions. Most studies of metastatic disease focus on tumor m...

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Autores principales: Zhou, Jiawei, Cipriani, Amber, Liu, Yutong, Fang, Gang, Li, Quefeng, Cao, Yanguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876906/
https://www.ncbi.nlm.nih.gov/pubmed/36697416
http://dx.doi.org/10.1038/s41467-023-36121-y
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author Zhou, Jiawei
Cipriani, Amber
Liu, Yutong
Fang, Gang
Li, Quefeng
Cao, Yanguang
author_facet Zhou, Jiawei
Cipriani, Amber
Liu, Yutong
Fang, Gang
Li, Quefeng
Cao, Yanguang
author_sort Zhou, Jiawei
collection PubMed
description Achieving systemic tumor control across metastases is vital for long-term patient survival but remains intractable in many patients. High lesion-level response heterogeneity persists, conferring many dissociated responses across metastatic lesions. Most studies of metastatic disease focus on tumor molecular and cellular features, which are crucial to elucidating the mechanisms underlying lesion-level variability. However, our understanding of lesion-specific heterogeneity on the macroscopic level, such as lesion dynamics in growth, response, and progression during treatment, remains rudimentary. This study investigates lesion-specific response heterogeneity through analyzing 116,542 observations of 40,612 lesions in 4,308 metastatic colorectal cancer (mCRC) patients. Despite significant differences in their response and progression dynamics, metastatic lesions converge on four phenotypes that vary with anatomical site. Importantly, we find that organ-level progression sequence is closely associated with patient long-term survival, and that patients with the first lesion progression in the liver often have worse survival. In conclusion, our study provides insights into lesion-specific response and progression heterogeneity in mCRC and creates impetus for metastasis-specific therapeutics.
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spelling pubmed-98769062023-01-27 Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer Zhou, Jiawei Cipriani, Amber Liu, Yutong Fang, Gang Li, Quefeng Cao, Yanguang Nat Commun Article Achieving systemic tumor control across metastases is vital for long-term patient survival but remains intractable in many patients. High lesion-level response heterogeneity persists, conferring many dissociated responses across metastatic lesions. Most studies of metastatic disease focus on tumor molecular and cellular features, which are crucial to elucidating the mechanisms underlying lesion-level variability. However, our understanding of lesion-specific heterogeneity on the macroscopic level, such as lesion dynamics in growth, response, and progression during treatment, remains rudimentary. This study investigates lesion-specific response heterogeneity through analyzing 116,542 observations of 40,612 lesions in 4,308 metastatic colorectal cancer (mCRC) patients. Despite significant differences in their response and progression dynamics, metastatic lesions converge on four phenotypes that vary with anatomical site. Importantly, we find that organ-level progression sequence is closely associated with patient long-term survival, and that patients with the first lesion progression in the liver often have worse survival. In conclusion, our study provides insights into lesion-specific response and progression heterogeneity in mCRC and creates impetus for metastasis-specific therapeutics. Nature Publishing Group UK 2023-01-26 /pmc/articles/PMC9876906/ /pubmed/36697416 http://dx.doi.org/10.1038/s41467-023-36121-y 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
Zhou, Jiawei
Cipriani, Amber
Liu, Yutong
Fang, Gang
Li, Quefeng
Cao, Yanguang
Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer
title Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer
title_full Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer
title_fullStr Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer
title_full_unstemmed Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer
title_short Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer
title_sort mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876906/
https://www.ncbi.nlm.nih.gov/pubmed/36697416
http://dx.doi.org/10.1038/s41467-023-36121-y
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