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高剂量率近距离放疗对前列腺癌进行强化治疗后的毒性模式:前瞻性I/II期成熟研究结果

Patterns of toxicity following high-dose-rate brachytherapy boost for prostate cancer: mature prospective phase I/II study results.

作者信息

Duchesne Gillian Mary, Williams Scott Garrick, Das Ram, Tai Keen Hun

机构信息

Division of Radiation Oncology, Peter MacCallum Cancer Centre and University of Melbourne, Melbourne, Victoria, Australia.

出版信息

Radiother Oncol. 2007 Aug;84(2):128-34. doi: 10.1016/j.radonc.2007.05.019. Epub 2007 Jun 11.

Abstract

BACKGROUND

To examine the long-term morbidity of high dose rate brachytherapy boost (HDRBB) in prostate cancer.

PATIENTS AND METHODS

A phase I/II HDRBB dose escalation protocol recruited 108 men up to November 1999. Treatment combined 46 Gy external beam radiation to the prostate with four fractions of HDR totalling 16 or 20 Gy. Morbidity data were collected prospectively regarding urological, bowel and erectile dysfunction (ED) symptoms using a validated clinician completed instrument. Actuarial incidence and prevalence of symptoms were estimated; the latter to account for potential recovery.

RESULTS

The median follow-up was 78 months, with 880 questionnaires completed. The respective actuarial cumulative incidence and point prevalence rates of any grade 2 or higher symptom score at 5 years were 24.9% (95% confidence intervals [CI] 16.8-33.5%) and 7.7% (95% CI 1.8-14.5%) for urinary toxicity; and 11.3% (95% CI 5.6-17.1%) and 3.0% (0-7.6%) for rectal toxicity, meaning that most symptom sub-domains showed substantial recovery with time. Corresponding erectile function toxicity figures for the subgroup of men (n=53) with normal erectile function prior to treatment and no androgen deprivation therapy were 77.0% (95% CI 64.9-88.1%) and 45.3% (95% CI 27.2-64.6%). Some late toxicity profiles developed after twelve months, typically with low grade bowel and urinary urgency. These peaked at 12-24 months and stayed relatively stable subsequently. Paradoxically, grade 1 or more nocturia symptoms settle with time, despite the accumulation of grade 2 or more toxicity beyond 24 months.

CONCLUSIONS

HDRBB as a means of dose escalation in prostate cancer is associated with low and relatively stable rates of long-term bowel and urinary morbidity, and compares favourably with external beam results. Actuarial incidence methods overstate the burden of toxicity with substantial recovery noted in most domains.

摘要

背景

研究高剂量率近距离放疗强化(HDRBB)在前列腺癌中的长期发病率。

患者与方法

一项I/II期HDRBB剂量递增方案在1999年11月前招募了108名男性。治疗包括对前列腺进行46 Gy的外照射,联合4次高剂量率放疗,总量为16或20 Gy。使用经过验证的临床医生填写的工具前瞻性收集有关泌尿系统、肠道和勃起功能障碍(ED)症状的发病率数据。估计症状的精算发病率和患病率;后者用于考虑潜在的恢复情况。

结果

中位随访时间为78个月,共完成880份问卷。5年时任何2级或更高症状评分的精算累积发病率和点患病率,泌尿系统毒性分别为24.9%(95%置信区间[CI]16.8 - 33.5%)和7.7%(95% CI 1.8 - 14.5%);直肠毒性分别为11.3%(95% CI 5.6 - 17.1%)和3.0%(0 - 7.6%),这意味着大多数症状子领域随时间有显著恢复。治疗前勃起功能正常且未接受雄激素剥夺治疗的男性亚组(n = 53)的相应勃起功能毒性数据为77.0%(95% CI 64.9 - 88.1%)和45.3%(95% CI 27.2 - 64.6%)。一些晚期毒性情况在12个月后出现,通常表现为轻度肠道和尿急症状。这些症状在12 - 24个月达到峰值,随后相对稳定。矛盾的是,1级或以上夜尿症状随时间缓解,尽管24个月后2级或更高毒性有所累积。

结论

HDRBB作为前列腺癌剂量递增的一种手段,与较低且相对稳定的长期肠道和泌尿系统发病率相关,与外照射结果相比具有优势。精算发病率方法高估了毒性负担,大多数领域有显著恢复。

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