Department of Clinical and Radiation Oncology, Multiscan and Pardubice Regional Hospital, Pardubice, Czech Republic.
Int J Urol. 2010 Sep;17(9):784-90. doi: 10.1111/j.1442-2042.2010.02592.x. Epub 2010 Jul 6.
To retrospectively compare late toxicity of conventional-dose three-dimensional conformal radiation therapy (3D-CRT) and high-dose intensity-modulated radiation therapy (IMRT) for prostate cancer.
A total of 340 patients with T1-3 prostate cancer were treated with 3D-CRT (n = 228) and IMRT (n = 112). The median follow-up time was 5.9 years and 3.0 years, respectively. The prescription dose was 70 Gy for 3D-CRT and 78 Gy for IMRT. Late gastrointestinal (GI) and genitourinary (GU) toxicities were graded according to the Fox Chase modification of the Radiation Therapy Oncology Group and Late Effects Normal Tissue Task Force criteria.
There was no difference between 3D-CRT and IMRT in the incidence of GI and GU toxicity at 3 years. On multivariate analysis, transurethral resection of prostate/open transvesical prostatectomy (TURP/TVPE) for benign prostatic hyperplasia, carried out before radiotherapy, significantly increased the risk of Grade >or=2 GU toxicity (risk ratio 1.88). Among patients who experienced TURP/TVPE, the 5-year actuarial likelihood of Grade 2-3 urinary incontinence was 23%, compared with 9% for those without prostate surgery (P = 0.01).
Tolerance of 3D-CRT and IMRT was similar, despite the use of high radiation dose with IMRT. Previous TURP/TVPE increased the risk of GU toxicity.
回顾性比较常规剂量三维适形放疗(3D-CRT)和高剂量调强放疗(IMRT)治疗前列腺癌的晚期毒性。
共有 340 例 T1-3 期前列腺癌患者接受 3D-CRT(n=228)和 IMRT(n=112)治疗。中位随访时间分别为 5.9 年和 3.0 年。处方剂量为 3D-CRT 为 70Gy,IMRT 为 78Gy。根据 Fox Chase 改良版放射治疗肿瘤学组和晚期效应正常组织工作组标准对晚期胃肠道(GI)和泌尿生殖系统(GU)毒性进行分级。
3D-CRT 和 IMRT 在 3 年时 GI 和 GU 毒性的发生率无差异。多因素分析显示,放疗前经尿道前列腺切除术/经膀胱前列腺切除术(TURP/TVPE)治疗良性前列腺增生显著增加了 GU 毒性≥2 级的风险(风险比 1.88)。在接受 TURP/TVPE 的患者中,5 年时尿失禁 2-3 级的累积发生率为 23%,而未行前列腺手术者为 9%(P=0.01)。
尽管 IMRT 采用了高剂量放疗,但 3D-CRT 和 IMRT 的耐受性相似。既往 TURP/TVPE 增加了 GU 毒性的风险。