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Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer

Background: To assess the efficacy and toxicity profiles of palliative radiation therapy (RT) for macroscopic hematuria (MH) caused by urothelial cancer. Methods: A total of 25 urothelial cancer patients with MH who underwent palliative RT between 2008 and 2018 were analyzed in this retrospective st...

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Autores principales: Zhang, Haiqin, Hojo, Hidehiro, Parshuram Raturi, Vijay, Nakamura, Naoki, Nakamura, Masaki, Okumura, Masayuki, Hirano, Yasuhiro, Motegi, Atsushi, Kageyama, Shun-Ichiro, Zenda, Sadamoto, Akimoto, Tetsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241331/
https://www.ncbi.nlm.nih.gov/pubmed/34223477
http://dx.doi.org/10.1089/pmr.2020.0027
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author Zhang, Haiqin
Hojo, Hidehiro
Parshuram Raturi, Vijay
Nakamura, Naoki
Nakamura, Masaki
Okumura, Masayuki
Hirano, Yasuhiro
Motegi, Atsushi
Kageyama, Shun-Ichiro
Zenda, Sadamoto
Akimoto, Tetsuo
author_facet Zhang, Haiqin
Hojo, Hidehiro
Parshuram Raturi, Vijay
Nakamura, Naoki
Nakamura, Masaki
Okumura, Masayuki
Hirano, Yasuhiro
Motegi, Atsushi
Kageyama, Shun-Ichiro
Zenda, Sadamoto
Akimoto, Tetsuo
author_sort Zhang, Haiqin
collection PubMed
description Background: To assess the efficacy and toxicity profiles of palliative radiation therapy (RT) for macroscopic hematuria (MH) caused by urothelial cancer. Methods: A total of 25 urothelial cancer patients with MH who underwent palliative RT between 2008 and 2018 were analyzed in this retrospective study. The hematuria-free survival (HFS) time was defined as the period from complete resolution of MH to the recurrence of MH, death, or the last follow-up examination. Adverse events were classified according to the Common Terminology Criteria for Adverse Events version 4.0. Results: By the end of the median follow-up duration of 90 days (11–886 days), complete resolution of MH had been achieved in 22 patients (88%), and the median interval between the start of RT and resolution of MH was 9 days (2–179 days). Of the 22 patients in whom the symptom resolved, 9 (41%) developed recurrent MH, and the median time to relapse of MH was 129 days (30–692 days). The median RT dose was 30 Gy (20–40 Gy). Nine (36%) patients received a blood transfusion before the RT. The three-month HFS rate was 52.1%. There was a significant difference in the three-month HFS rate between patients with and without a history of pretreatment blood transfusion (HFS rate: 34.6% vs. 61.5%, p = 0.03). Grade 2 urinary tract pain and grade 3 diarrhea were seen in one patient each. Conclusion: Palliative RT appeared to be effective with limited toxicities for urothelial cancer patients with MH.
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spelling pubmed-82413312021-07-02 Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer Zhang, Haiqin Hojo, Hidehiro Parshuram Raturi, Vijay Nakamura, Naoki Nakamura, Masaki Okumura, Masayuki Hirano, Yasuhiro Motegi, Atsushi Kageyama, Shun-Ichiro Zenda, Sadamoto Akimoto, Tetsuo Palliat Med Rep Original Article Background: To assess the efficacy and toxicity profiles of palliative radiation therapy (RT) for macroscopic hematuria (MH) caused by urothelial cancer. Methods: A total of 25 urothelial cancer patients with MH who underwent palliative RT between 2008 and 2018 were analyzed in this retrospective study. The hematuria-free survival (HFS) time was defined as the period from complete resolution of MH to the recurrence of MH, death, or the last follow-up examination. Adverse events were classified according to the Common Terminology Criteria for Adverse Events version 4.0. Results: By the end of the median follow-up duration of 90 days (11–886 days), complete resolution of MH had been achieved in 22 patients (88%), and the median interval between the start of RT and resolution of MH was 9 days (2–179 days). Of the 22 patients in whom the symptom resolved, 9 (41%) developed recurrent MH, and the median time to relapse of MH was 129 days (30–692 days). The median RT dose was 30 Gy (20–40 Gy). Nine (36%) patients received a blood transfusion before the RT. The three-month HFS rate was 52.1%. There was a significant difference in the three-month HFS rate between patients with and without a history of pretreatment blood transfusion (HFS rate: 34.6% vs. 61.5%, p = 0.03). Grade 2 urinary tract pain and grade 3 diarrhea were seen in one patient each. Conclusion: Palliative RT appeared to be effective with limited toxicities for urothelial cancer patients with MH. Mary Ann Liebert, Inc., publishers 2020-09-29 /pmc/articles/PMC8241331/ /pubmed/34223477 http://dx.doi.org/10.1089/pmr.2020.0027 Text en © Haiqin Zhang et al., 2020; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by/4.0/This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zhang, Haiqin
Hojo, Hidehiro
Parshuram Raturi, Vijay
Nakamura, Naoki
Nakamura, Masaki
Okumura, Masayuki
Hirano, Yasuhiro
Motegi, Atsushi
Kageyama, Shun-Ichiro
Zenda, Sadamoto
Akimoto, Tetsuo
Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer
title Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer
title_full Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer
title_fullStr Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer
title_full_unstemmed Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer
title_short Palliative Radiation Therapy for Macroscopic Hematuria Caused by Urothelial Cancer
title_sort palliative radiation therapy for macroscopic hematuria caused by urothelial cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241331/
https://www.ncbi.nlm.nih.gov/pubmed/34223477
http://dx.doi.org/10.1089/pmr.2020.0027
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