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首页> 外文期刊>Journal of Clinical Oncology >Randomized Trial of Hypofractionated, Dose-Escalated, Intensity-Modulated Radiation Therapy (IMRT) Versus Conventionally Fractionated IMRT for Localized Prostate Cancer
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Randomized Trial of Hypofractionated, Dose-Escalated, Intensity-Modulated Radiation Therapy (IMRT) Versus Conventionally Fractionated IMRT for Localized Prostate Cancer

机译:随机试验的次级次级,剂量升级,强度调节的放射治疗(IMRT)与局部前列腺癌的常规分级IMRT

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摘要

PurposeHypofractionated radiotherapy delivers larger daily doses of radiation and may increase the biologically effective dose delivered to the prostate. We conducted a randomized trial testing the hypothesis that dose-escalated, moderately hypofractionated intensity-modulated radiation therapy (HIMRT) improves prostate cancer control compared with conventionally fractionated IMRT (CIMRT) for men with localized prostate cancer.Patients and MethodsMen were randomly assigned to 75.6 Gy in 1.8-Gy fractions delivered over 8.4 weeks (CIMRT) or 72 Gy in 2.4 Gy fractions delivered over 6 weeks (HIMRT, biologically equivalent to 85 Gy in 1.8-Gy fractions assuming prostate cancer -to- ratio of 1.5). Failure was defined as prostate-specific antigen (PSA) failure (nadir plus 2 ng/mL) or initiation of salvage therapy. Modified Radiation Therapy Oncology Group criteria were used to grade late ( 90 days after completion of radiotherapy) GI and genitourinary toxicity.ResultsMost of the 206 men (72%) had cT1, Gleason score 6 or 7 (99%), and PSA level 10 ng/mL (90%) disease. Androgen deprivation therapy was received by 24%. With a median follow-up of 8.5 years, men treated with HIMRT experienced fewer treatment failures (n = 10) than men treated with CIMRT (n = 21; P = .036). The 8-year failure rate was 10.7% (95% CI, 5.8% to 19.1%) with HIMRT and 15.4% (95% CI, 9.1% to 25.4%) with CIMRT. There was no difference in overall survival (P = .39). There was a nonsignificant increase in late grade 2 or 3 GI toxicity with HIMRT (8-year 5.0% v 12.6%; P = .08). However, GI toxicity was only 8.6% when rectal volume receiving 65 Gy of HIMRT was 15%. Late genitourinary toxicity was similar (P = .84). There was no grade 4 toxicity.ConclusionThe results of this randomized trial demonstrate superior cancer control for men with localized prostate cancer who receive dose-escalated moderately hypofractionation radiotherapy while shortening treatment duration.
机译:目的缺口放射疗法可提供更大的日常辐射剂量,可以增加递送到前列腺的生物有效剂量。我们进行了一项随机试验,该假设剂量升级,中等低位强度调节的放射治疗(HIMRT)与局部前列腺癌的男性的常规分级IMRT(CIMRT)相比,所述前列腺癌控制改善了前列腺癌控制.Patiants和方法被随机分配到75.6 GY在1.8Gy级分中以超过6周(HIMRT)的2.4 GY分数递送了8.4周(CIMRT)或72 GY,假设前列腺癌的前列腺癌为1.5的1.5米的85 GY。失败被定义为前列腺特异性抗原(PSA)衰竭(Nadir加2ng / ml)或开始挽救疗法。修饰的放射治疗肿瘤学群标准用于分级(放疗完成后90天)GI和泌尿族毒性。最多的206名男性(72%)的毒性有CT1,Gleason得分6或7(99%)和PSA等级10 Ng / ml(90%)疾病。雄激素剥夺治疗得到24%。随着8.5年的中位随访,HIMRT治疗的男性经历了更少的治疗失败(n = 10),而不是用CIMRT治疗的男性(n = 21; p = .036)。 8年的失败率为10.7%(95%CI,5.8%至19.1%),HIMRT和15.4%(95%CI,9.1%至25.4%),CIMRT。整体生存没有差异(p = .39)。 HIMRT的晚期2或3次GI毒性有不可显着的增加(8年5.0%V 12.6%; P = .08)。然而,当接收65 GY的直肠体积为15%时,GI毒性仅为8.6%。晚期核心毒性相似(p = .84)。没有4级毒性。结论这种随机试验的结果表明,对局部前列腺癌的男性的优异癌症对照,其在缩短治疗持续时间的同时接受剂量升级的中度低辐射放射治疗。

著录项

  • 来源
    《Journal of Clinical Oncology 》 |2018年第29期| 共10页
  • 作者单位

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Johns Hopkins Univ Hosp Baltimore MD 21287 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Texas Ctr Proton Therapy Irving TX USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Colorado Sch Med Boulder CO 80309 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

    Univ Texas MD Anderson Canc Ctr 1515 Holcombe Blvd Unit 1202 Houston TX 77030 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学 ;
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