Jenny Kahlmeter Brandell , Antonis Valachis , Henrik Ugge , Daniel Smith , Bengt Johansson
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Biochemical failure-free survival (BFFS), metastasis-free survival (MFS), prostate cancer-specific survival (PCSS), and overall survival (OS) were compared using Kaplan-Meier method and Cox proportional hazards. Toxicity and quality of life measures were also analysed.</p></div><div><h3>Results</h3><p>Among 516 patients (227 PORT, 289 WPRT), 5-year BFFS rates were 77 % (PORT) and 74 % (WPRT), adjusted HR=1.50 (95 % CI=0.88–2.55). No significant differences were found in MFS, PCSS, or OS in main analyses. WPRT was associated with a higher risk of acute grade ≥ 2 and 3 genitourinary toxicities whereas no differences in late toxicities or quality of life between PORT and WPRT were observed.</p></div><div><h3>Conclusion</h3><p>We found no significant differences in oncological outcomes or quality of life when comparing moderately hypofractionated PORT to WPRT. Some differences in toxicity patterns were observed. Despite caveats related to study design, our findings support the need for further research on WPRT’s impact on treatment-related and patient-reported outcomes.</p></div>","PeriodicalId":10342,"journal":{"name":"Clinical and Translational Radiation Oncology","volume":"48 ","pages":"Article 100846"},"PeriodicalIF":2.7000,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S240563082400123X/pdfft?md5=ac075aa12e590c33e0073f55b7bbef0e&pid=1-s2.0-S240563082400123X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Moderately hypofractionated prostate-only versus whole-pelvis radiotherapy for high-risk prostate cancer: A retrospective real-world single-center cohort study\",\"authors\":\"Jenny Kahlmeter Brandell , Antonis Valachis , Henrik Ugge , Daniel Smith , Bengt Johansson\",\"doi\":\"10.1016/j.ctro.2024.100846\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>The benefit of prophylactic whole pelvis radiation therapy (WPRT) in prostate cancer has been debated for decades, with evidence based mainly on conventional fractionation targeting pelvic nodes.</p></div><div><h3>Aim</h3><p>This retrospective cohort study aimed to explore the impact of adding moderately hypofractionated pelvic radiotherapy to prostate-only irradiation (PORT) on prognosis, toxicity, and quality of life in real-world settings.</p></div><div><h3>Materials and methods</h3><p>Patients with high-risk and conventionally staged prostate cancer (cT1-3N0M0) treated with moderately hypofractionated WPRT or PORT, using external beam radiotherapy alone or combined with high-dose-rate brachytherapy, at Örebro University Hospital between 2008 and 2021 were identified. Biochemical failure-free survival (BFFS), metastasis-free survival (MFS), prostate cancer-specific survival (PCSS), and overall survival (OS) were compared using Kaplan-Meier method and Cox proportional hazards. Toxicity and quality of life measures were also analysed.</p></div><div><h3>Results</h3><p>Among 516 patients (227 PORT, 289 WPRT), 5-year BFFS rates were 77 % (PORT) and 74 % (WPRT), adjusted HR=1.50 (95 % CI=0.88–2.55). No significant differences were found in MFS, PCSS, or OS in main analyses. WPRT was associated with a higher risk of acute grade ≥ 2 and 3 genitourinary toxicities whereas no differences in late toxicities or quality of life between PORT and WPRT were observed.</p></div><div><h3>Conclusion</h3><p>We found no significant differences in oncological outcomes or quality of life when comparing moderately hypofractionated PORT to WPRT. Some differences in toxicity patterns were observed. 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引用次数: 0
摘要
这项回顾性队列研究旨在探讨在单纯前列腺照射(PORT)的基础上增加适度低分次盆腔放疗对预后、毒性和生活质量的影响。材料与方法2008年至2021年期间,厄勒布鲁大学医院对高风险、常规分期的前列腺癌患者(cT1-3N0M0)进行了鉴定,这些患者接受了适度低分次的WPRT或PORT治疗,并单独使用或联合使用了高剂量率近距离放射治疗。采用卡普兰-梅耶法(Kaplan-Meier method)和考克斯比例危险法(Cox proportional hazards)比较了无生化失败生存期(BFFS)、无转移生存期(MFS)、前列腺癌特异性生存期(PCSS)和总生存期(OS)。结果516例患者(227例PORT,289例WPRT)中,5年BFFS率分别为77%(PORT)和74%(WPRT),调整后HR=1.50(95% CI=0.88-2.55)。在主要分析中,MFS、PCSS 或 OS 均无明显差异。WPRT与急性≥2级和3级泌尿生殖系统毒性较高的风险相关,而PORT和WPRT在晚期毒性或生活质量方面没有发现差异。我们观察到毒性模式存在一些差异。尽管存在研究设计方面的注意事项,但我们的研究结果支持进一步研究 WPRT 对治疗相关结果和患者报告结果的影响的必要性。
Moderately hypofractionated prostate-only versus whole-pelvis radiotherapy for high-risk prostate cancer: A retrospective real-world single-center cohort study
Background
The benefit of prophylactic whole pelvis radiation therapy (WPRT) in prostate cancer has been debated for decades, with evidence based mainly on conventional fractionation targeting pelvic nodes.
Aim
This retrospective cohort study aimed to explore the impact of adding moderately hypofractionated pelvic radiotherapy to prostate-only irradiation (PORT) on prognosis, toxicity, and quality of life in real-world settings.
Materials and methods
Patients with high-risk and conventionally staged prostate cancer (cT1-3N0M0) treated with moderately hypofractionated WPRT or PORT, using external beam radiotherapy alone or combined with high-dose-rate brachytherapy, at Örebro University Hospital between 2008 and 2021 were identified. Biochemical failure-free survival (BFFS), metastasis-free survival (MFS), prostate cancer-specific survival (PCSS), and overall survival (OS) were compared using Kaplan-Meier method and Cox proportional hazards. Toxicity and quality of life measures were also analysed.
Results
Among 516 patients (227 PORT, 289 WPRT), 5-year BFFS rates were 77 % (PORT) and 74 % (WPRT), adjusted HR=1.50 (95 % CI=0.88–2.55). No significant differences were found in MFS, PCSS, or OS in main analyses. WPRT was associated with a higher risk of acute grade ≥ 2 and 3 genitourinary toxicities whereas no differences in late toxicities or quality of life between PORT and WPRT were observed.
Conclusion
We found no significant differences in oncological outcomes or quality of life when comparing moderately hypofractionated PORT to WPRT. Some differences in toxicity patterns were observed. Despite caveats related to study design, our findings support the need for further research on WPRT’s impact on treatment-related and patient-reported outcomes.