Cancer Prognostics and Health Outcomes Unit, University of Montreal Health Center, Montreal, QC, Canada.
Int J Radiat Oncol Biol Phys. 2010 Feb 1;76(2):342-8. doi: 10.1016/j.ijrobp.2009.02.011.
External-beam radiation therapy (EBRT) may predispose to secondary malignancies that include bladder cancer (BCa), rectal cancer (RCa), and lung cancer (LCa). We tested this hypothesis in a large French Canadian population-based cohort of prostate cancer patients.
Overall, 8,455 radical prostatectomy (RP) and 9,390 EBRT patients treated between 1983 and 2003 were assessed with Kaplan-Meier and Cox regression analyses. Three endpoints were examined: (1) diagnosis of secondary BCa, (2) LCa, or (3) RCa. Covariates included age, Charlson comorbidity index, and year of treatment.
In multivariable analyses that relied on incident cases diagnosed 60 months or later after RP or EBRT, the rates of BCa (hazard ratio [HR], 1.4; p = 0.02), LCa (HR, 2.0; p = 0.004), and RCa (HR 2.1; p <0.001) were significantly higher in the EBRT group. When incident cases diagnosed 120 months or later after RP or EBRT were considered, only the rates of RCa (hazard ratio 2.2; p = 0.003) were significantly higher in the EBRT group. In both analyses, the absolute differences in incident rates ranged from 0.7 to 5.2% and the number needed to harm (where harm equaled secondary malignancies) ranged from 111 to 19, if EBRT was used instead of RP.
EBRT may predispose to clinically meaningfully higher rates of secondary BCa, LCa and RCa. These rates should be included in informed consent consideration.
体外放射治疗(EBRT)可能导致继发性恶性肿瘤,包括膀胱癌(BCa)、直肠癌(RCa)和肺癌(LCa)。我们在一个大型的加拿大法语人群前列腺癌患者队列中对此假说进行了检验。
共评估了 1983 年至 2003 年间接受根治性前列腺切除术(RP)和 EBRT 治疗的 8455 例和 9390 例患者,采用 Kaplan-Meier 和 Cox 回归分析。检查了三个终点:(1)继发性 BCa 的诊断,(2)LCa,或(3)RCa。协变量包括年龄、Charlson 合并症指数和治疗年份。
在多变量分析中,依赖于 RP 或 EBRT 后 60 个月或更长时间诊断的病例,EBRT 组的 BCa(风险比[HR],1.4;p = 0.02)、LCa(HR,2.0;p = 0.004)和 RCa(HR,2.1;p <0.001)的发生率显著更高。当考虑 RP 或 EBRT 后 120 个月或更长时间诊断的病例时,EBRT 组的 RCa 发生率(风险比 2.2;p = 0.003)仍然显著更高。在这两种分析中,如果使用 EBRT 代替 RP,则发生率的绝对差异范围为 0.7%至 5.2%,需要伤害的人数(伤害等于继发性恶性肿瘤)范围为 111 至 19。
EBRT 可能导致临床意义上更高的继发性 BCa、LCa 和 RCa 发生率。这些发生率应纳入知情同意考虑范围。