Circulating Tumour Cell Release after Cement Augmentation of Vertebral Metastases
Abstract Cement augmentation via percutaneous vertebroplasty or kyphoplasty for treatment of spinal metastasis is a well-established treatment option. We assessed whether elevated intrametastatic pressure during cement augmentation results in an increased dissemination of tumour cells into the vascu...
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2017
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oai:doaj.org-article:91d6cac1f9e843848dfa4e20a239fc072021-12-02T16:07:01ZCirculating Tumour Cell Release after Cement Augmentation of Vertebral Metastases10.1038/s41598-017-07649-z2045-2322https://doaj.org/article/91d6cac1f9e843848dfa4e20a239fc072017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-07649-zhttps://doaj.org/toc/2045-2322Abstract Cement augmentation via percutaneous vertebroplasty or kyphoplasty for treatment of spinal metastasis is a well-established treatment option. We assessed whether elevated intrametastatic pressure during cement augmentation results in an increased dissemination of tumour cells into the vascular circulation. We prospectively collected blood from patients with osteolytic spinal column metastases and analysed the prevalence of circulating tumour cells (CTCs) at three time-points: preoperatively, 20 minutes after cement augmentation, and 3–5 days postoperatively. Enrolling 21 patients, including 13 breast- (61.9%), 5 lung- (23.8%), and one (4.8%) colorectal-, renal-, and prostate-carcinoma patient each, we demonstrate a significant 1.8-fold increase of EpCAM+/K+ CTCs in samples taken 20 minutes post-cement augmentation (P < 0.0001). Despite increased mechanical CTC dissemination due to cement augmentation, follow-up blood draws demonstrated that no long-term increase of CTCs was present. Array-CGH analysis revealed a specific profile of the CTC collected 20 minutes after cement augmentation. This is the first study to report that peripheral CTCs are temporarily increased due to vertebral cement augmentation procedures. Our findings provide a rationale for the development of new prophylactic strategies to reduce the increased release of CTC after cement augmentation of osteolytic spinal metastases.Malte MohmeSabine RiethdorfMarc DreimannStefan WernerCecile L. MaireSimon A. JoosseFrederic BludauVolkmar MuellerRui P. L. NevesNikolas H. StoeckleinKatrin LamszusManfred WestphalKlaus PantelHarriet WikmanSven O. EickerNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017) |
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Medicine R Science Q Malte Mohme Sabine Riethdorf Marc Dreimann Stefan Werner Cecile L. Maire Simon A. Joosse Frederic Bludau Volkmar Mueller Rui P. L. Neves Nikolas H. Stoecklein Katrin Lamszus Manfred Westphal Klaus Pantel Harriet Wikman Sven O. Eicker Circulating Tumour Cell Release after Cement Augmentation of Vertebral Metastases |
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Abstract Cement augmentation via percutaneous vertebroplasty or kyphoplasty for treatment of spinal metastasis is a well-established treatment option. We assessed whether elevated intrametastatic pressure during cement augmentation results in an increased dissemination of tumour cells into the vascular circulation. We prospectively collected blood from patients with osteolytic spinal column metastases and analysed the prevalence of circulating tumour cells (CTCs) at three time-points: preoperatively, 20 minutes after cement augmentation, and 3–5 days postoperatively. Enrolling 21 patients, including 13 breast- (61.9%), 5 lung- (23.8%), and one (4.8%) colorectal-, renal-, and prostate-carcinoma patient each, we demonstrate a significant 1.8-fold increase of EpCAM+/K+ CTCs in samples taken 20 minutes post-cement augmentation (P < 0.0001). Despite increased mechanical CTC dissemination due to cement augmentation, follow-up blood draws demonstrated that no long-term increase of CTCs was present. Array-CGH analysis revealed a specific profile of the CTC collected 20 minutes after cement augmentation. This is the first study to report that peripheral CTCs are temporarily increased due to vertebral cement augmentation procedures. Our findings provide a rationale for the development of new prophylactic strategies to reduce the increased release of CTC after cement augmentation of osteolytic spinal metastases. |
format |
article |
author |
Malte Mohme Sabine Riethdorf Marc Dreimann Stefan Werner Cecile L. Maire Simon A. Joosse Frederic Bludau Volkmar Mueller Rui P. L. Neves Nikolas H. Stoecklein Katrin Lamszus Manfred Westphal Klaus Pantel Harriet Wikman Sven O. Eicker |
author_facet |
Malte Mohme Sabine Riethdorf Marc Dreimann Stefan Werner Cecile L. Maire Simon A. Joosse Frederic Bludau Volkmar Mueller Rui P. L. Neves Nikolas H. Stoecklein Katrin Lamszus Manfred Westphal Klaus Pantel Harriet Wikman Sven O. Eicker |
author_sort |
Malte Mohme |
title |
Circulating Tumour Cell Release after Cement Augmentation of Vertebral Metastases |
title_short |
Circulating Tumour Cell Release after Cement Augmentation of Vertebral Metastases |
title_full |
Circulating Tumour Cell Release after Cement Augmentation of Vertebral Metastases |
title_fullStr |
Circulating Tumour Cell Release after Cement Augmentation of Vertebral Metastases |
title_full_unstemmed |
Circulating Tumour Cell Release after Cement Augmentation of Vertebral Metastases |
title_sort |
circulating tumour cell release after cement augmentation of vertebral metastases |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/91d6cac1f9e843848dfa4e20a239fc07 |
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