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Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity

PURPOSE: To assess acute gastrointestinal (GI) and genitourinary (GU) toxicities of intensity-modulated proton therapy (IMPT) targeting the prostate/seminal vesicles and pelvic lymph nodes for prostate cancer. MATERIALS AND METHODS: A prospective study (ClinicalTrials.gov: NCT02874014), evaluating m...

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Autores principales: Choo, Richard, Hillman, David W., Daniels, Thomas, Vargas, Carlos, Rwigema, Jean Claude, Corbin, Kimberly, Keole, Sameer, Vora, Sujay, Merrell, Kenneth, Stish, Bradley, Pisansky, Thomas, Davis, Brian, Amundson, Adam, Wong, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Particle Therapy Co-operative Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489485/
https://www.ncbi.nlm.nih.gov/pubmed/34722810
http://dx.doi.org/10.14338/IJPT-20-00094.1
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author Choo, Richard
Hillman, David W.
Daniels, Thomas
Vargas, Carlos
Rwigema, Jean Claude
Corbin, Kimberly
Keole, Sameer
Vora, Sujay
Merrell, Kenneth
Stish, Bradley
Pisansky, Thomas
Davis, Brian
Amundson, Adam
Wong, William
author_facet Choo, Richard
Hillman, David W.
Daniels, Thomas
Vargas, Carlos
Rwigema, Jean Claude
Corbin, Kimberly
Keole, Sameer
Vora, Sujay
Merrell, Kenneth
Stish, Bradley
Pisansky, Thomas
Davis, Brian
Amundson, Adam
Wong, William
author_sort Choo, Richard
collection PubMed
description PURPOSE: To assess acute gastrointestinal (GI) and genitourinary (GU) toxicities of intensity-modulated proton therapy (IMPT) targeting the prostate/seminal vesicles and pelvic lymph nodes for prostate cancer. MATERIALS AND METHODS: A prospective study (ClinicalTrials.gov: NCT02874014), evaluating moderately hypofractionated IMPT for high-risk or unfavorable intermediate-risk prostate cancer, accrued a target sample size of 56 patients. The prostate/seminal vesicles and pelvic lymph nodes were treated simultaneously with 6750 and 4500 centigray radiobiologic equivalent (cGyRBE), respectively, in 25 daily fractions. All received androgen-deprivation therapy. Acute GI and GU toxicities were prospectively assessed from 7 GI and 9 GU categories of the Common Terminology Criteria for Adverse Events (version 4), at baseline, weekly during radiotherapy, and 3-month after radiotherapy. Fisher exact tests were used for comparisons of categorical data. RESULTS: Median age was 75 years. Median follow-up was 25 months. Fifty-five patients were available for acute toxicity assessment. Sixty-two percent and 2%, respectively, experienced acute grade 1 and 2 GI toxicity. Grade 2 GI toxicity was proctitis. Sixty-five percent and 35%, respectively, had acute grade 1 and 2 GU toxicity. The 3 most frequent grade 2 GU toxicities were urinary frequency, urgency, and obstructive symptoms. None had acute grade ≥ 3 GI or GU toxicity. The presence of baseline GI and GU symptoms was associated with a greater likelihood of experiencing acute GI and GU toxicity, respectively. Of 45 patients with baseline GU symptoms, 44% experienced acute grade 2 GU toxicity, compared with only 10% among 10 with no baseline GU symptoms (P = 0.07). Although acute grade 1 and 2 GI and GU toxicities were common during radiotherapy, most resolved at 3 months after radiotherapy. CONCLUSION: A moderately hypofractionated IMPT targeting the prostate/seminal vesicles and regional pelvic lymph nodes was well tolerated with no acute grade ≥ 3 GI or GU toxicity. Patients with baseline GU symptoms had a higher rate of acute grade 2 GU toxicity.
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spelling pubmed-84894852021-10-28 Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity Choo, Richard Hillman, David W. Daniels, Thomas Vargas, Carlos Rwigema, Jean Claude Corbin, Kimberly Keole, Sameer Vora, Sujay Merrell, Kenneth Stish, Bradley Pisansky, Thomas Davis, Brian Amundson, Adam Wong, William Int J Part Ther Original Articles PURPOSE: To assess acute gastrointestinal (GI) and genitourinary (GU) toxicities of intensity-modulated proton therapy (IMPT) targeting the prostate/seminal vesicles and pelvic lymph nodes for prostate cancer. MATERIALS AND METHODS: A prospective study (ClinicalTrials.gov: NCT02874014), evaluating moderately hypofractionated IMPT for high-risk or unfavorable intermediate-risk prostate cancer, accrued a target sample size of 56 patients. The prostate/seminal vesicles and pelvic lymph nodes were treated simultaneously with 6750 and 4500 centigray radiobiologic equivalent (cGyRBE), respectively, in 25 daily fractions. All received androgen-deprivation therapy. Acute GI and GU toxicities were prospectively assessed from 7 GI and 9 GU categories of the Common Terminology Criteria for Adverse Events (version 4), at baseline, weekly during radiotherapy, and 3-month after radiotherapy. Fisher exact tests were used for comparisons of categorical data. RESULTS: Median age was 75 years. Median follow-up was 25 months. Fifty-five patients were available for acute toxicity assessment. Sixty-two percent and 2%, respectively, experienced acute grade 1 and 2 GI toxicity. Grade 2 GI toxicity was proctitis. Sixty-five percent and 35%, respectively, had acute grade 1 and 2 GU toxicity. The 3 most frequent grade 2 GU toxicities were urinary frequency, urgency, and obstructive symptoms. None had acute grade ≥ 3 GI or GU toxicity. The presence of baseline GI and GU symptoms was associated with a greater likelihood of experiencing acute GI and GU toxicity, respectively. Of 45 patients with baseline GU symptoms, 44% experienced acute grade 2 GU toxicity, compared with only 10% among 10 with no baseline GU symptoms (P = 0.07). Although acute grade 1 and 2 GI and GU toxicities were common during radiotherapy, most resolved at 3 months after radiotherapy. CONCLUSION: A moderately hypofractionated IMPT targeting the prostate/seminal vesicles and regional pelvic lymph nodes was well tolerated with no acute grade ≥ 3 GI or GU toxicity. Patients with baseline GU symptoms had a higher rate of acute grade 2 GU toxicity. The Particle Therapy Co-operative Group 2021-09-14 /pmc/articles/PMC8489485/ /pubmed/34722810 http://dx.doi.org/10.14338/IJPT-20-00094.1 Text en ©Copyright 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/Distributed under Creative Commons CC-BY (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Original Articles
Choo, Richard
Hillman, David W.
Daniels, Thomas
Vargas, Carlos
Rwigema, Jean Claude
Corbin, Kimberly
Keole, Sameer
Vora, Sujay
Merrell, Kenneth
Stish, Bradley
Pisansky, Thomas
Davis, Brian
Amundson, Adam
Wong, William
Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity
title Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity
title_full Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity
title_fullStr Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity
title_full_unstemmed Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity
title_short Proton Therapy of Prostate and Pelvic Lymph Nodes for High Risk Prostate Cancer: Acute Toxicity
title_sort proton therapy of prostate and pelvic lymph nodes for high risk prostate cancer: acute toxicity
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489485/
https://www.ncbi.nlm.nih.gov/pubmed/34722810
http://dx.doi.org/10.14338/IJPT-20-00094.1
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