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Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer

PURPOSE: An optimal once-daily radiotherapy (RT) regimen is under investigation for definitive concurrent chemoradiotherapy (CCRT) in limited disease small cell lung cancer (LD-SCLC). We compared the efficacy and safety of dose escalation with intensity-modulated radiotherapy (IMRT). MATERIALS AND M...

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Autores principales: Yang, Eunyeong, Shin, Young Seob, Joo, Ji Hyeon, Choi, Wonsik, Kim, Su Ssan, Choi, Eun Kyung, Lee, Jaeha, Song, Si Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Radiation Oncology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556837/
https://www.ncbi.nlm.nih.gov/pubmed/37793629
http://dx.doi.org/10.3857/roj.2023.00591
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author Yang, Eunyeong
Shin, Young Seob
Joo, Ji Hyeon
Choi, Wonsik
Kim, Su Ssan
Choi, Eun Kyung
Lee, Jaeha
Song, Si Yeol
author_facet Yang, Eunyeong
Shin, Young Seob
Joo, Ji Hyeon
Choi, Wonsik
Kim, Su Ssan
Choi, Eun Kyung
Lee, Jaeha
Song, Si Yeol
author_sort Yang, Eunyeong
collection PubMed
description PURPOSE: An optimal once-daily radiotherapy (RT) regimen is under investigation for definitive concurrent chemoradiotherapy (CCRT) in limited disease small cell lung cancer (LD-SCLC). We compared the efficacy and safety of dose escalation with intensity-modulated radiotherapy (IMRT). MATERIALS AND METHODS: Between January 2016 and March 2021, patients treated with definitive CCRT for LD-SCLC with IMRT were retrospectively reviewed. Patients who received a total dose <50 Gy or those with a history of thoracic RT or surgery were excluded. The patients were divided into two groups (standard and dose-escalated) based on the total biologically effective dose (BED, α/β = 10) of 70 Gy. The chemotherapeutic regimen comprised four cycles of etoposide and cisplatin. RESULTS: One hundred and twenty-two patients were analyzed and the median follow-up was 27.8 months (range, 4.4 to 76.9 months). The median age of the patients was 63 years (range, 35 to 78 years) and the majority had a history of smoking (86.0%). The 1- and 3-year overall survival rates of the escalated dose group were significantly higher than those of the standard group (93.5% and 50.5% vs. 76.7% and 33.3%, respectively; p = 0.008), as were the 1- and 3-year freedom from in-field failure rates (91.4% and 66.5% vs. 73.8% and 46.9%, respectively; p = 0.018). The incidence of grade 2 or higher acute and late pneumonitis was not significantly different between the two groups (p = 0.062, 0.185). CONCLUSION: Dose-escalated once-daily CCRT with IMRT led to improved locoregional control and survival, with no increase in toxicity.
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spelling pubmed-105568372023-10-07 Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer Yang, Eunyeong Shin, Young Seob Joo, Ji Hyeon Choi, Wonsik Kim, Su Ssan Choi, Eun Kyung Lee, Jaeha Song, Si Yeol Radiat Oncol J Original Article PURPOSE: An optimal once-daily radiotherapy (RT) regimen is under investigation for definitive concurrent chemoradiotherapy (CCRT) in limited disease small cell lung cancer (LD-SCLC). We compared the efficacy and safety of dose escalation with intensity-modulated radiotherapy (IMRT). MATERIALS AND METHODS: Between January 2016 and March 2021, patients treated with definitive CCRT for LD-SCLC with IMRT were retrospectively reviewed. Patients who received a total dose <50 Gy or those with a history of thoracic RT or surgery were excluded. The patients were divided into two groups (standard and dose-escalated) based on the total biologically effective dose (BED, α/β = 10) of 70 Gy. The chemotherapeutic regimen comprised four cycles of etoposide and cisplatin. RESULTS: One hundred and twenty-two patients were analyzed and the median follow-up was 27.8 months (range, 4.4 to 76.9 months). The median age of the patients was 63 years (range, 35 to 78 years) and the majority had a history of smoking (86.0%). The 1- and 3-year overall survival rates of the escalated dose group were significantly higher than those of the standard group (93.5% and 50.5% vs. 76.7% and 33.3%, respectively; p = 0.008), as were the 1- and 3-year freedom from in-field failure rates (91.4% and 66.5% vs. 73.8% and 46.9%, respectively; p = 0.018). The incidence of grade 2 or higher acute and late pneumonitis was not significantly different between the two groups (p = 0.062, 0.185). CONCLUSION: Dose-escalated once-daily CCRT with IMRT led to improved locoregional control and survival, with no increase in toxicity. The Korean Society for Radiation Oncology 2023-09 2023-09-26 /pmc/articles/PMC10556837/ /pubmed/37793629 http://dx.doi.org/10.3857/roj.2023.00591 Text en Copyright © 2023 The Korean Society for Radiation Oncology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yang, Eunyeong
Shin, Young Seob
Joo, Ji Hyeon
Choi, Wonsik
Kim, Su Ssan
Choi, Eun Kyung
Lee, Jaeha
Song, Si Yeol
Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer
title Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer
title_full Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer
title_fullStr Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer
title_full_unstemmed Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer
title_short Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer
title_sort outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556837/
https://www.ncbi.nlm.nih.gov/pubmed/37793629
http://dx.doi.org/10.3857/roj.2023.00591
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