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The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy

BACKGROUND: To evaluate the impact of radiosensitivity on outcomes of spinal metastases treated with stereotactic body radiotherapy (SBRT) and identify the correlated prognostic factors. METHODS: The authors retrospectively reviewed the records of all patients who underwent SBRT with no prior radiat...

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Autores principales: Guo, Lanlan, Xu, Qingqing, Ke, Lixin, Wu, Ziwei, Zeng, Ziyi, Chen, Lei, Chen, Yuanyuan, Lu, Lixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315727/
https://www.ncbi.nlm.nih.gov/pubmed/37162297
http://dx.doi.org/10.1002/cam4.6019
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author Guo, Lanlan
Xu, Qingqing
Ke, Lixin
Wu, Ziwei
Zeng, Ziyi
Chen, Lei
Chen, Yuanyuan
Lu, Lixia
author_facet Guo, Lanlan
Xu, Qingqing
Ke, Lixin
Wu, Ziwei
Zeng, Ziyi
Chen, Lei
Chen, Yuanyuan
Lu, Lixia
author_sort Guo, Lanlan
collection PubMed
description BACKGROUND: To evaluate the impact of radiosensitivity on outcomes of spinal metastases treated with stereotactic body radiotherapy (SBRT) and identify the correlated prognostic factors. METHODS: The authors retrospectively reviewed the records of all patients who underwent SBRT with no prior radiation for spinal metastases between October 2015 and October 2020 at Sun Yat‐sen University Cancer Center. On the basis of radiosensitivity, patients were divided into two groups—radiosensitive and radioresistant. The endpoints included local control (LC), overall survival (OS), pain relief, and time to pain relief. RESULTS: A total of 259 (82.5%) patients with 451 lesions were assessable with a median follow‐up time of 10.53 months. The 1‐, 2‐, and 3‐year OS rates were 59%, 52%, and 44%, respectively. The median survival was 33.17 months. Higher Karnofsky Performance Scale score and shorter time to diagnosis of spinal metastases from primary cancer at consult predicted for better OS (p = 0.02 and p < 0.001, respectively). The presence of other metastases (p = 0.04) and pain at enrollment assessed by the Brief Pain Inventory predicted for worse OS (p = 0.01). The 6‐, 12‐, and 24‐month LC rates were 88%, 86%, and 82%, respectively. Younger age was identified for better LC and pain relief (p < 0.001 and p = 0.04, respectively). There was no variable independently associated with time to pain relief. As for toxicity, no Grade ≥3 toxicity was observed. CONCLUSIONS: Regardless of radiosensitivity, SBRT is feasible and appears to be an effective treatment paradigm for patients with spinal metastases, with limited accepted toxicities.
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spelling pubmed-103157272023-07-04 The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy Guo, Lanlan Xu, Qingqing Ke, Lixin Wu, Ziwei Zeng, Ziyi Chen, Lei Chen, Yuanyuan Lu, Lixia Cancer Med RESEARCH ARTICLES BACKGROUND: To evaluate the impact of radiosensitivity on outcomes of spinal metastases treated with stereotactic body radiotherapy (SBRT) and identify the correlated prognostic factors. METHODS: The authors retrospectively reviewed the records of all patients who underwent SBRT with no prior radiation for spinal metastases between October 2015 and October 2020 at Sun Yat‐sen University Cancer Center. On the basis of radiosensitivity, patients were divided into two groups—radiosensitive and radioresistant. The endpoints included local control (LC), overall survival (OS), pain relief, and time to pain relief. RESULTS: A total of 259 (82.5%) patients with 451 lesions were assessable with a median follow‐up time of 10.53 months. The 1‐, 2‐, and 3‐year OS rates were 59%, 52%, and 44%, respectively. The median survival was 33.17 months. Higher Karnofsky Performance Scale score and shorter time to diagnosis of spinal metastases from primary cancer at consult predicted for better OS (p = 0.02 and p < 0.001, respectively). The presence of other metastases (p = 0.04) and pain at enrollment assessed by the Brief Pain Inventory predicted for worse OS (p = 0.01). The 6‐, 12‐, and 24‐month LC rates were 88%, 86%, and 82%, respectively. Younger age was identified for better LC and pain relief (p < 0.001 and p = 0.04, respectively). There was no variable independently associated with time to pain relief. As for toxicity, no Grade ≥3 toxicity was observed. CONCLUSIONS: Regardless of radiosensitivity, SBRT is feasible and appears to be an effective treatment paradigm for patients with spinal metastases, with limited accepted toxicities. John Wiley and Sons Inc. 2023-05-10 /pmc/articles/PMC10315727/ /pubmed/37162297 http://dx.doi.org/10.1002/cam4.6019 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Guo, Lanlan
Xu, Qingqing
Ke, Lixin
Wu, Ziwei
Zeng, Ziyi
Chen, Lei
Chen, Yuanyuan
Lu, Lixia
The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy
title The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy
title_full The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy
title_fullStr The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy
title_full_unstemmed The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy
title_short The impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy
title_sort impact of radiosensitivity on clinical outcomes of spinal metastases treated with stereotactic body radiotherapy
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315727/
https://www.ncbi.nlm.nih.gov/pubmed/37162297
http://dx.doi.org/10.1002/cam4.6019
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