Academic Unit and Department of Radiotherapy, Institute of Cancer Research and Royal Marsden Hospital, Sutton, UK.
Clin Oncol (R Coll Radiol). 2010 Apr;22(3):236-44. doi: 10.1016/j.clon.2010.01.005. Epub 2010 Feb 19.
Pelvic irradiation in addition to prostate irradiation may improve outcome in locally advanced prostate cancer, but is associated with dose-limiting bowel toxicity. We report the preliminary results of a dose escalation study using intensity-modulated radiotherapy.
Eligible patients had high-risk (T3, Gleason > or =8 or prostate-specific antigen > or =20 ng/ml) or lymph node-positive disease. Intensity-modulated radiotherapy was inverse planned giving 70 Gy/35 fractions to the prostate and 50 Gy/55 Gy/60 Gy in sequential cohorts to the pelvis with a 5 Gy boost to positive lymph nodes. Acute and late toxicity were recorded with Radiation Therapy Oncology Group (RTOG) and Late Effects Normal Tissue - Subjective Objective Management LENT-SOM scales. Neoadjuvant androgen suppression was given for 3 years. This report concerns the 50 and 55 Gy cohorts.
Seventy-nine men were recruited (25 to 50 Gy/54 to 55 Gy) with a median follow-up of 2 years. Patients were divided into two groups according to the total bowel volume outlined (median 450 cm(3)). Acute RTOG (> or =2) bowel toxicity was 40 and 50% for the 50 and 55 Gy groups and 38 and 51% for bowel volume <450 cm(3) and > or =450 cm(3), respectively, suggesting both volume and dose relationships for acute effects. Late RTOG diarrhoea > or =grade 2 was only seen with bowel volume > or =450 cm(3), but no dose effect was apparent (12%/50 Gy and 10%/55 Gy). LENT-SOM bowel > or =grade 2 toxicity occurred in 22%/50 Gy and 15%/55 Gy. Only one patient had grade 3 toxicity. A dose volume histogram analysis showed increased late RTOG diarrhoea > or =grade 2 with larger bowel volume irradiated, significant for BV40 >124 cm(3) (P=0.04), BV45 >71 cm(3) (P=0.03) and BV60 >2 cm(3) (P=0.01).
Acute and late bowel toxicity was acceptably low using a pelvic dose of up to 55 Gy over 7 weeks. Both relate to total pelvic bowel volume and dose volume constraints have been defined.
在前列腺照射的基础上增加盆腔照射可能改善局部晚期前列腺癌的预后,但会导致剂量限制的肠道毒性。我们报告了使用调强放疗进行剂量递增研究的初步结果。
符合条件的患者为高危(T3、Gleason≥8 或前列腺特异性抗原≥20ng/ml)或淋巴结阳性疾病。调强放疗采用逆向计划,前列腺给予 70Gy/35 次,盆腔分别给予 50Gy、55Gy、60Gy,阳性淋巴结给予 5Gy 加量。采用放射治疗肿瘤学组(RTOG)和晚期效应正常组织主观客观管理 LENT-SOM 量表记录急性和晚期毒性。新辅助雄激素抑制治疗 3 年。本报告涉及 50Gy 和 55Gy 两组。
共招募 79 例患者(25-50Gy/54-55Gy),中位随访时间 2 年。根据勾画的全肠道体积(中位数 450cm³),患者分为两组。50Gy 和 55Gy 组急性 RTOG(≥2 级)肠道毒性分别为 40%和 50%,肠道体积<450cm³和≥450cm³者分别为 38%和 51%,提示急性效应与体积和剂量均相关。只有当肠道体积≥450cm³时才会出现晚期 RTOG 腹泻≥2 级,且无剂量效应(50Gy 组 12%,55Gy 组 10%)。LENT-SOM 肠道≥2 级毒性分别为 22%/50Gy 和 15%/55Gy。仅 1 例患者发生 3 级毒性。剂量体积直方图分析显示,较大的肠道照射体积与晚期 RTOG 腹泻≥2 级相关,具有统计学意义(BV40>124cm³,P=0.04;BV45>71cm³,P=0.03;BV60>2cm³,P=0.01)。
7 周内盆腔给予 55Gy 以下剂量时,急性和晚期肠道毒性可接受。两者均与全盆腔肠道体积相关,已确定剂量体积限制。