Movsas B, Hanlon A L, Pinover W, Hanks G E
Fox Chase Cancer Center, Department of Radiation Oncology, Philadelphia, PA 19111, USA.
Int J Radiat Oncol Biol Phys. 1998 May 1;41(2):251-5. doi: 10.1016/s0360-3016(97)00570-1.
To assess the risk of developing a second primary cancer following prostate irradiation compared to the underlying risk in patients with prostate cancer.
The baseline rate of secondary cancers following prostate cancer was obtained from a study of 18,135 patients from the Connecticut Tumor Registry, of whom only 12.5% received radiotherapy. These patients, with a mean age of 72 and a mean follow-up of 3.9 years, were compared to a cohort of 543 patients (median age 70) with similar follow-up (median 3.9 years), all of whom were treated with definitive radiotherapy at Fox Chase Cancer Center. The possible association between various covariates (age, dose, palpation stage, field size, Gleason score, pretreatment PSA) and the development of a secondary cancer was assessed.
1,053 of 18,135 patients (5.8%) in the Connecticut Tumor Registry developed a second primary cancer compared with 31 of 543 (5.7%) patients treated with prostate radiation (p = 0.99). Although this risk increases gradually over time, it is not significantly different, at any time period, between the two groups of patients. Of the 31 secondary primaries in the irradiated group, 82% had a history of tobacco and/or alcohol use. Only melanomas were significantly increased compared to the expected rate in an age-matched population (p < 0.001). Five of the 31 secondary cancers occurred within the radiation field (four bladder, one colon), four within 3 years and only one occurred 9 years after radiotherapy. No association was found between age (<70 vs. > or =70 and as a continuous variable), dose (<74 vs. > or =74 Gy), palpation stage (
Up to at least 10 years, there is no increased risk of developing a second primary cancer following prostate irradiation compared to the baseline rate from prostate cancer itself. This risk is not higher in younger patients with localized disease (<T2C), who often must choose between surgery and radiation. The vast majority of secondary cancers occurred outside of the radiation field (84%) and/or within 3 years of radiotherapy (97%), suggesting they were not caused by radiation. Most of these patients had lifestyles with predisposing risk factors. Patients with prostate cancer manifested a significantly increased risk of developing melanomas, suggesting that they may benefit from patient education and skin screening examinations.
评估前列腺癌患者接受前列腺放疗后发生第二原发性癌症的风险,并与前列腺癌患者的基础风险进行比较。
前列腺癌后第二原发性癌症的基线发生率来自对康涅狄格肿瘤登记处18135名患者的研究,其中仅12.5%接受了放疗。这些患者的平均年龄为72岁,平均随访时间为3.9年,将其与543名患者(中位年龄70岁)组成的队列进行比较,这些患者具有相似的随访时间(中位3.9年),他们均在福克斯蔡斯癌症中心接受了根治性放疗。评估了各种协变量(年龄、剂量、触诊分期、照射野大小、 Gleason评分、治疗前前列腺特异性抗原)与第二原发性癌症发生之间的可能关联。
康涅狄格肿瘤登记处的18135名患者中有1053名(5.8%)发生了第二原发性癌症,而接受前列腺放疗的543名患者中有31名(5.7%)发生了第二原发性癌症(p = 0.99)。尽管这种风险随时间逐渐增加,但在任何时间段,两组患者之间均无显著差异。在接受放疗的组中,31例第二原发性癌症患者中,82%有吸烟和/或饮酒史。与年龄匹配人群的预期发生率相比,仅黑色素瘤显著增加(p < 0.001)。31例第二原发性癌症中有5例发生在照射野内(4例膀胱癌,1例结肠癌),4例在放疗后3年内发生,仅1例在放疗后9年发生。未发现年龄(<70岁与≥70岁以及作为连续变量)、剂量(<74 Gy与≥74 Gy)、触诊分期(<T2C与≥T2C)、照射野大小(前列腺与盆腔)、放疗技术(传统放疗与适形放疗)、Gleason评分(2 - 6与7 - 10)或治疗前前列腺特异性抗原(<15与≥15以及作为连续变量)与发生第二原发性癌症的风险之间存在关联。尽管较低的放疗剂量(作为连续变量)与发生第二原发性癌症的风险增加相关(p = 0.04),但这种现象可能是由于随访时间的差异所致。
至少在10年内,与前列腺癌本身的基线发生率相比,前列腺放疗后发生第二原发性癌症的风险没有增加。在患有局限性疾病(<T2C)的年轻患者中,这种风险也不更高,这些患者常常必须在手术和放疗之间做出选择。绝大多数第二原发性癌症发生在照射野外(84%)和/或放疗后3年内(97%),这表明它们不是由放疗引起的。这些患者中的大多数具有易患风险因素的生活方式。前列腺癌患者发生黑色素瘤的风险显著增加,这表明他们可能从患者教育和皮肤筛查检查中受益。