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Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma
RECIST v1.1 has limitations in evaluating progression. We assessed Dynamic Constrast Enhanced Computed Tomography (DCE-CT) identified Blood Volume (BV) for the evaluation of progressive disease (PD) in patients with metastatic renal cell carcinoma (mRCC). BV was quantified prospectively at baseline,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490379/ https://www.ncbi.nlm.nih.gov/pubmed/34608226 http://dx.doi.org/10.1038/s41598-021-99122-1 |
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author | Drljevic-Nielsen, Aska Rasmussen, Finn Mains, Jill Rachel Thorup, Kennet Donskov, Frede |
author_facet | Drljevic-Nielsen, Aska Rasmussen, Finn Mains, Jill Rachel Thorup, Kennet Donskov, Frede |
author_sort | Drljevic-Nielsen, Aska |
collection | PubMed |
description | RECIST v1.1 has limitations in evaluating progression. We assessed Dynamic Constrast Enhanced Computed Tomography (DCE-CT) identified Blood Volume (BV) for the evaluation of progressive disease (PD) in patients with metastatic renal cell carcinoma (mRCC). BV was quantified prospectively at baseline, after one month, then every three months until PD. Relative changes (ΔBV) were assessed at each timepoint compared with baseline values. The primary endpoint was Time to PD (TTP), the secondary endpoint was Time to the scan prior to PD (PDminus1). Cox proportional hazard models adjusted ΔBV for treatments and International mRCC Database Consortium factors. A total of 62 patients had analyzable scans at the PD timepoint. Median BV was 23.92 mL × 100 g(−1) (range 4.40–399.04) at PD and 26.39 mL × 100 g(−1) (range 8.70–77.44) at PDminus1. In the final multivariate analysis higher ΔBV was statistically significantly associated with shorter Time to PD, HR 1.11 (95% CI 1.07–1.15, P < 0.001). Also assessed at PDminus1, higher ΔBV was significantly associated with shorter time to PD, HR 1.14 (95% CI 1.01–1.28, P = 0.031). In conclusion, DCE-CT identified BV is a new image-based biomarker of therapy progression in patients with mRCC. |
format | Online Article Text |
id | pubmed-8490379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84903792021-10-05 Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma Drljevic-Nielsen, Aska Rasmussen, Finn Mains, Jill Rachel Thorup, Kennet Donskov, Frede Sci Rep Article RECIST v1.1 has limitations in evaluating progression. We assessed Dynamic Constrast Enhanced Computed Tomography (DCE-CT) identified Blood Volume (BV) for the evaluation of progressive disease (PD) in patients with metastatic renal cell carcinoma (mRCC). BV was quantified prospectively at baseline, after one month, then every three months until PD. Relative changes (ΔBV) were assessed at each timepoint compared with baseline values. The primary endpoint was Time to PD (TTP), the secondary endpoint was Time to the scan prior to PD (PDminus1). Cox proportional hazard models adjusted ΔBV for treatments and International mRCC Database Consortium factors. A total of 62 patients had analyzable scans at the PD timepoint. Median BV was 23.92 mL × 100 g(−1) (range 4.40–399.04) at PD and 26.39 mL × 100 g(−1) (range 8.70–77.44) at PDminus1. In the final multivariate analysis higher ΔBV was statistically significantly associated with shorter Time to PD, HR 1.11 (95% CI 1.07–1.15, P < 0.001). Also assessed at PDminus1, higher ΔBV was significantly associated with shorter time to PD, HR 1.14 (95% CI 1.01–1.28, P = 0.031). In conclusion, DCE-CT identified BV is a new image-based biomarker of therapy progression in patients with mRCC. Nature Publishing Group UK 2021-10-04 /pmc/articles/PMC8490379/ /pubmed/34608226 http://dx.doi.org/10.1038/s41598-021-99122-1 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Drljevic-Nielsen, Aska Rasmussen, Finn Mains, Jill Rachel Thorup, Kennet Donskov, Frede Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma |
title | Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma |
title_full | Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma |
title_fullStr | Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma |
title_full_unstemmed | Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma |
title_short | Blood Volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma |
title_sort | blood volume as a new functional image-based biomarker of progression in metastatic renal cell carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490379/ https://www.ncbi.nlm.nih.gov/pubmed/34608226 http://dx.doi.org/10.1038/s41598-021-99122-1 |
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