Department of Radiation Oncology, Cox 3, Massachusetts General Hospital, Boston MA 02114, USA.
J Clin Oncol. 2010 Mar 1;28(7):1106-11. doi: 10.1200/JCO.2009.25.8475. Epub 2010 Feb 1.
PURPOSE To test the hypothesis that increasing radiation dose delivered to men with early-stage prostate cancer improves clinical outcomes. PATIENTS AND METHODS Men with T1b-T2b prostate cancer and prostate-specific antigen </= 15 ng/mL were randomly assigned to a total dose of either 70.2 Gray equivalents (GyE; conventional) or 79.2 GyE (high). No patient received androgen suppression therapy with radiation. Local failure (LF), biochemical failure (BF), and overall survival (OS) were outcomes. Results A total of 393 men were randomly assigned, and median follow-up was 8.9 years. Men receiving high-dose radiation therapy were significantly less likely to have LF, with a hazard ratio of 0.57. The 10-year American Society for Therapeutic Radiology and Oncology BF rates were 32.4% for conventional-dose and 16.7% for high-dose radiation therapy (P < .0001). This difference held when only those with low-risk disease (n = 227; 58% of total) were examined: 28.2% for conventional and 7.1% for high dose (P < .0001). There was a strong trend in the same direction for the intermediate-risk patients (n = 144; 37% of total; 42.1% v 30.4%, P = .06). Eleven percent of patients subsequently required androgen deprivation for recurrence after conventional dose compared with 6% after high dose (P = .047). There remains no difference in OS rates between the treatment arms (78.4% v 83.4%; P = .41). Two percent of patients in both arms experienced late grade >/= 3 genitourinary toxicity, and 1% of patients in the high-dose arm experienced late grade >/= 3 GI toxicity. CONCLUSION This randomized controlled trial shows superior long-term cancer control for men with localized prostate cancer receiving high-dose versus conventional-dose radiation. This was achieved without an increase in grade >/= 3 late urinary or rectal morbidity.
验证提高早期前列腺癌男性的放射剂量可改善临床结局这一假说。
T1b-T2b 期前列腺癌且前列腺特异性抗原(PSA)≤15ng/ml 的男性患者被随机分配接受 70.2 Gray 当量(GyE;常规剂量)或 79.2 GyE(高剂量)的总剂量。所有患者在接受放疗时均未接受雄激素抑制治疗。局部失败(LF)、生化失败(BF)和总体生存(OS)是结局指标。
共 393 例男性患者被随机分配,中位随访时间为 8.9 年。接受高剂量放疗的男性 LF 风险显著降低,风险比为 0.57。美国放射治疗肿瘤学会 10 年 BF 率分别为常规剂量组 32.4%和高剂量组 16.7%(P<0.0001)。当仅检查低危疾病患者(n=227;占总患者的 58%)时,这种差异仍然存在:常规剂量组为 28.2%,高剂量组为 7.1%(P<0.0001)。对于中危患者(n=144;占总患者的 37%;24.1%比 30.4%,P=0.06),也有向同一方向的强烈趋势。与高剂量组相比,常规剂量组有 11%的患者在接受常规剂量治疗后因复发而需要雄激素剥夺治疗,而高剂量组有 6%(P=0.047)。两组的 OS 率没有差异(78.4%比 83.4%;P=0.41)。两组各有 2%的患者发生晚期≥3 级泌尿生殖系统毒性,高剂量组有 1%的患者发生晚期≥3 级胃肠道毒性。
这项随机对照试验显示,接受高剂量与常规剂量放疗的局限性前列腺癌男性患者具有更优的长期癌症控制效果。这一结果在不增加晚期≥3 级泌尿或直肠发病率的情况下实现。