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A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy

PURPOSE/OBJECTIVE: The primary objective is to examine patient self‐assessment of breast pain and cosmesis between three‐dimensional (3D‐CRT) versus intensity‐modulated radiotherapy (IMRT). The secondary objective is to evaluate any relationship of treatment planning conformality of both cohorts to...

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Autores principales: Leonard, Charles E., Wang, Yunfei, Asmar, Lina, Lei, Rachel Y., Howell, Kathryn T., Henkenberns, Phyllis L., Johnson, Timothy K., Hobart, Tracy L., Tole, Shannon P., Kercher, Jane M., Widner, Jodi L., Barke, Lora, Kaske, Terese, Carter, Dennis L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525102/
https://www.ncbi.nlm.nih.gov/pubmed/34469056
http://dx.doi.org/10.1002/cam4.4242
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author Leonard, Charles E.
Wang, Yunfei
Asmar, Lina
Lei, Rachel Y.
Howell, Kathryn T.
Henkenberns, Phyllis L.
Johnson, Timothy K.
Hobart, Tracy L.
Tole, Shannon P.
Kercher, Jane M.
Widner, Jodi L.
Barke, Lora
Kaske, Terese
Carter, Dennis L.
author_facet Leonard, Charles E.
Wang, Yunfei
Asmar, Lina
Lei, Rachel Y.
Howell, Kathryn T.
Henkenberns, Phyllis L.
Johnson, Timothy K.
Hobart, Tracy L.
Tole, Shannon P.
Kercher, Jane M.
Widner, Jodi L.
Barke, Lora
Kaske, Terese
Carter, Dennis L.
author_sort Leonard, Charles E.
collection PubMed
description PURPOSE/OBJECTIVE: The primary objective is to examine patient self‐assessment of breast pain and cosmesis between three‐dimensional (3D‐CRT) versus intensity‐modulated radiotherapy (IMRT). The secondary objective is to evaluate any relationship of treatment planning conformality of both cohorts to patient‐assessed pain. Assessments were performed at interim 12, 24, 36, and 48 months with a final 5‐year assessment. MATERIALS/METHODS: In total, 656 patients (3D‐CRT n = 328; IMRT n = 328) were randomly assigned to either IMRT or 3D‐CRT accelerated partial breast radiotherapy to 38.5 Gy in 10 BID 3.85 Gy fractions. RESULTS: Median follow‐up was 3 years. Multivariate analysis showed that pain severity significantly decreased from baseline to the 12‐month follow‐up visit (<0.001 for both 3D‐CRT and IMRT) in each cohort. There was significantly less pain at 2 (p = 0.002) and 3 years (0.045) in the IMRT arm versus the 3D‐CRT arm when compared to the baseline pain level. There was no difference in patient‐assessed cosmesis at any follow‐up point; however, although MD‐assessed cosmesis showed no difference from years 1 to 4, there was significantly better cosmesis for 3D‐CRT versus IMRT (p = 0.047) at 5 years. There was a significant correlation between a maximum pain score and an increase in the CI(100) (indicating less conformity) in the IMRT cohort (p < 0.01) and in the IMRT subgroup when the CI(100) was ≤0.37 cohort arm (p = 0.01). CONCLUSION: In the analysis of our primary objective we found that at 2 years, IMRT resulted in more interval improvement in breast pain after baseline when compared to patients treated with 3D‐CRT planning. As seen in our secondary analysis, this may be due to the ability of IMRT to achieve higher conformality (as evidenced by lower CI values) resulting in less fibrosis. There were no differences in patient‐assessed cosmesis or MD‐assessed cosmesis for years 1–4; however, physician‐assessed 5‐year cosmesis was better with 3D‐CRT.
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spelling pubmed-85251022021-10-26 A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy Leonard, Charles E. Wang, Yunfei Asmar, Lina Lei, Rachel Y. Howell, Kathryn T. Henkenberns, Phyllis L. Johnson, Timothy K. Hobart, Tracy L. Tole, Shannon P. Kercher, Jane M. Widner, Jodi L. Barke, Lora Kaske, Terese Carter, Dennis L. Cancer Med Clinical Cancer Researcher PURPOSE/OBJECTIVE: The primary objective is to examine patient self‐assessment of breast pain and cosmesis between three‐dimensional (3D‐CRT) versus intensity‐modulated radiotherapy (IMRT). The secondary objective is to evaluate any relationship of treatment planning conformality of both cohorts to patient‐assessed pain. Assessments were performed at interim 12, 24, 36, and 48 months with a final 5‐year assessment. MATERIALS/METHODS: In total, 656 patients (3D‐CRT n = 328; IMRT n = 328) were randomly assigned to either IMRT or 3D‐CRT accelerated partial breast radiotherapy to 38.5 Gy in 10 BID 3.85 Gy fractions. RESULTS: Median follow‐up was 3 years. Multivariate analysis showed that pain severity significantly decreased from baseline to the 12‐month follow‐up visit (<0.001 for both 3D‐CRT and IMRT) in each cohort. There was significantly less pain at 2 (p = 0.002) and 3 years (0.045) in the IMRT arm versus the 3D‐CRT arm when compared to the baseline pain level. There was no difference in patient‐assessed cosmesis at any follow‐up point; however, although MD‐assessed cosmesis showed no difference from years 1 to 4, there was significantly better cosmesis for 3D‐CRT versus IMRT (p = 0.047) at 5 years. There was a significant correlation between a maximum pain score and an increase in the CI(100) (indicating less conformity) in the IMRT cohort (p < 0.01) and in the IMRT subgroup when the CI(100) was ≤0.37 cohort arm (p = 0.01). CONCLUSION: In the analysis of our primary objective we found that at 2 years, IMRT resulted in more interval improvement in breast pain after baseline when compared to patients treated with 3D‐CRT planning. As seen in our secondary analysis, this may be due to the ability of IMRT to achieve higher conformality (as evidenced by lower CI values) resulting in less fibrosis. There were no differences in patient‐assessed cosmesis or MD‐assessed cosmesis for years 1–4; however, physician‐assessed 5‐year cosmesis was better with 3D‐CRT. John Wiley and Sons Inc. 2021-09-01 /pmc/articles/PMC8525102/ /pubmed/34469056 http://dx.doi.org/10.1002/cam4.4242 Text en © 2021 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 Clinical Cancer Researcher
Leonard, Charles E.
Wang, Yunfei
Asmar, Lina
Lei, Rachel Y.
Howell, Kathryn T.
Henkenberns, Phyllis L.
Johnson, Timothy K.
Hobart, Tracy L.
Tole, Shannon P.
Kercher, Jane M.
Widner, Jodi L.
Barke, Lora
Kaske, Terese
Carter, Dennis L.
A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy
title A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy
title_full A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy
title_fullStr A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy
title_full_unstemmed A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy
title_short A prospective Phase III trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐D versus intensity‐modulated radiotherapy
title_sort prospective phase iii trial evaluating patient self‐reported pain and cosmesis in accelerated partial breast irradiation utilizing 3‐d versus intensity‐modulated radiotherapy
topic Clinical Cancer Researcher
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525102/
https://www.ncbi.nlm.nih.gov/pubmed/34469056
http://dx.doi.org/10.1002/cam4.4242
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