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Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis

BACKGROUND: No standard radiotherapy regimens have been established for the treatment of de novo metastatic nasopharyngeal carcinoma (mNPC) with bone-only metastasis. The current study aimed to investigate the efficacy of palliative chemotherapy (PCT) plus locoregional radiotherapy (LRRT) with or wi...

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Autores principales: Lin, Cheng, Lin, Sheng, Zhu, Lili, Lin, Shaojun, Pan, Jianji, Xu, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8729074/
https://www.ncbi.nlm.nih.gov/pubmed/34983459
http://dx.doi.org/10.1186/s12885-021-09152-1
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author Lin, Cheng
Lin, Sheng
Zhu, Lili
Lin, Shaojun
Pan, Jianji
Xu, Yun
author_facet Lin, Cheng
Lin, Sheng
Zhu, Lili
Lin, Shaojun
Pan, Jianji
Xu, Yun
author_sort Lin, Cheng
collection PubMed
description BACKGROUND: No standard radiotherapy regimens have been established for the treatment of de novo metastatic nasopharyngeal carcinoma (mNPC) with bone-only metastasis. The current study aimed to investigate the efficacy of palliative chemotherapy (PCT) plus locoregional radiotherapy (LRRT) with or without local radiotherapy (RT) for metastatic bone lesions in mNPC. METHODS: We retrospectively analysed 131 de novo patients with mNPC who had bone-only metastasis and received at least two cycles of PCT with LRRT. The difference in survival was evaluated by the log-rank test. Univariable and multivariable analyses were performed by Cox regression. RESULTS: The median overall survival (OS) and progression-free survival (PFS) were 33.0 months and 24.0 months, respectively. Patients with five or fewer metastatic bone lesions had significantly longer OS (72.0 months vs. 23.0 months, Hazard ratios (HR) = 0.45, p <  0.001) and PFS (48.0 months vs. 15.0 months, HR = 0.52, p = 0.004) than those who had more than five metastatic bone lesions. Patients who received four or more cycles of chemotherapy were associated with significantly longer OS (unreached vs. 19.0 months, HR = 0.27, p <  0.001) and PFS (66 months vs. 16.0 months, HR = 0.32, p <  0.001). Multivariate analysis confirmed that fewer bone metastases (≤ 5) and more chemotherapy cycles (≥ 4) were favourable prognostic factors for OS. Subgroup analysis revealed that RT to metastatic bone lesions tended to prolong OS (83.0 months vs. 45.0 months) and PFS (60 months vs. 36.5 months) in patients with five or fewer metastatic bone lesions than in those without RT to metastatic bone lesions (p > 0.05). Patients who received a RT dose > 30 Gy had neither better OS (63.5 months vs. 32.0 months, p = 0.299) nor PFS (48.0 months vs. 28.0 months, p = 0.615) than those who received a RT dose ≤30 Gy. CONCLUSIONS: Local RT to bone metastases may not significantly improve survival in patients with de novo mNPC with bone-only metastasis who have already received PCT plus LRRT. Receiving four or more cycles of chemotherapy can significantly prolong survival and is a favourable independent protective factor. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-09152-1.
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spelling pubmed-87290742022-01-07 Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis Lin, Cheng Lin, Sheng Zhu, Lili Lin, Shaojun Pan, Jianji Xu, Yun BMC Cancer Research BACKGROUND: No standard radiotherapy regimens have been established for the treatment of de novo metastatic nasopharyngeal carcinoma (mNPC) with bone-only metastasis. The current study aimed to investigate the efficacy of palliative chemotherapy (PCT) plus locoregional radiotherapy (LRRT) with or without local radiotherapy (RT) for metastatic bone lesions in mNPC. METHODS: We retrospectively analysed 131 de novo patients with mNPC who had bone-only metastasis and received at least two cycles of PCT with LRRT. The difference in survival was evaluated by the log-rank test. Univariable and multivariable analyses were performed by Cox regression. RESULTS: The median overall survival (OS) and progression-free survival (PFS) were 33.0 months and 24.0 months, respectively. Patients with five or fewer metastatic bone lesions had significantly longer OS (72.0 months vs. 23.0 months, Hazard ratios (HR) = 0.45, p <  0.001) and PFS (48.0 months vs. 15.0 months, HR = 0.52, p = 0.004) than those who had more than five metastatic bone lesions. Patients who received four or more cycles of chemotherapy were associated with significantly longer OS (unreached vs. 19.0 months, HR = 0.27, p <  0.001) and PFS (66 months vs. 16.0 months, HR = 0.32, p <  0.001). Multivariate analysis confirmed that fewer bone metastases (≤ 5) and more chemotherapy cycles (≥ 4) were favourable prognostic factors for OS. Subgroup analysis revealed that RT to metastatic bone lesions tended to prolong OS (83.0 months vs. 45.0 months) and PFS (60 months vs. 36.5 months) in patients with five or fewer metastatic bone lesions than in those without RT to metastatic bone lesions (p > 0.05). Patients who received a RT dose > 30 Gy had neither better OS (63.5 months vs. 32.0 months, p = 0.299) nor PFS (48.0 months vs. 28.0 months, p = 0.615) than those who received a RT dose ≤30 Gy. CONCLUSIONS: Local RT to bone metastases may not significantly improve survival in patients with de novo mNPC with bone-only metastasis who have already received PCT plus LRRT. Receiving four or more cycles of chemotherapy can significantly prolong survival and is a favourable independent protective factor. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-09152-1. BioMed Central 2022-01-04 /pmc/articles/PMC8729074/ /pubmed/34983459 http://dx.doi.org/10.1186/s12885-021-09152-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Lin, Cheng
Lin, Sheng
Zhu, Lili
Lin, Shaojun
Pan, Jianji
Xu, Yun
Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis
title Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis
title_full Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis
title_fullStr Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis
title_full_unstemmed Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis
title_short Optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis
title_sort optimizing the treatment mode for de novo metastatic nasopharyngeal carcinoma with bone-only metastasis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8729074/
https://www.ncbi.nlm.nih.gov/pubmed/34983459
http://dx.doi.org/10.1186/s12885-021-09152-1
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