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Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer

机译:低分割质子助推结合外照射治疗局部前列腺癌

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Proton boost of 20 Gy in daily 5 Gy fractions followed by external beam radiotherapy (EBRT) of 50 Gy in daily 2 Gy fractions were given to 278 patients with prostate cancer with T1b to T4N0M0 disease. Fifty-three percent of the patients received neoadjuvant androgen deprivation therapy (N-ADT). The medium followup was 57 months. The 5-year PSA progression-free survival was 100%, 95%, and 74% for low-, intermediate-, and high-risk patients, respectively. The toxicity evaluation was supported by a patient-reported questionnaire before every consultant visit. Cumulative probability and actuarial prevalence of genitourinary (GU) and gastrointestinal (GI) toxicities are presented according to the RTOG classification. N-ADT did not influence curability. Mild pretreatment GU-symptoms were found to be a strong predictive factor for GU-toxicity attributable to treatment. The actuarial prevalence declined over 3 to 5 years for both GU and GI toxicities, indicating slow resolution of epithelial damage to the genitourinary and gastrointestinal tract. Bladder toxicities rather than gastrointestinal toxicities seem to be dose limiting. More than 5-year followup is necessary to reveal any sign of true progressive late side effects of the given treatment. Hypofractionated proton-boost combined with EBRT is associated with excellent curability of localized PC and acceptable frequencies of treatment toxicity.
机译:278名患有T1b至T4N0M0疾病的前列腺癌患者接受了每天5 Gy分数的20 Gy质子刺激,随后每天2 Gy分数的50%Gy的体外束放射疗法(EBRT)。 53%的患者接受了新辅助雄激素剥夺治疗(N-ADT)。中等随访时间为57个月。低,中,高风险患者的5年PSA无进展生存率分别为100%,95%和74%。在每次顾问拜访之前,均应通过患者报告调查表来支持毒性评估。根据RTOG分类,列出了泌尿生殖道(GU)和胃肠道(GI)毒性的累积概率和精算发生率。 N-ADT不影响可固化性。发现轻度的预处理GU症状是归因于治疗的GU毒性的重要预测因素。 GU和GI毒性的精算患病率在3至5年内下降,表明上皮对泌尿生殖系统和胃肠道损伤的缓解速度较慢。膀胱毒性而非胃肠道毒性似乎是剂量限制。必须进行5年以上的随访,以揭示给定治疗的任何真正进展性晚期副作用的迹象。与EBRT结合使用的低级质子升压技术与出色的局部PC固化性和可接受的治疗毒性频率相关。

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