Gansu Provincial Academy of Medical Sciences, Gansu Provincial Cancer Hospital, Lanzhou, China.
Dis Esophagus. 2012 Aug;25(6):505-11. doi: 10.1111/j.1442-2050.2011.01273.x. Epub 2011 Nov 8.
The introduction of new treatments for esophageal cancer including surgery, chemotherapy, radiotherapy, or a combination of these modalities has not only improved patient survival, but may also increase the risk of the second primary cancers. The available evidence is conflicting with most risk estimates based on sparse numbers. Here we estimated standardized incidence ratios (SIRs) of second cancer among 24,557 esophageal cancer survivors (at least 2 months) in the Surveillance, Epidemiology, and End Results (SEER) Program between 1973 and 2007, who had been followed up for median 6.5 years (range 2 months-29.3 years). Second cancer risk was statistically significantly elevated (SIR = 1.34, 95% confidence interval [CI]= 1.25-1.42) among the survivors compared with the general population; the SIRs for cancers of oral and pharynx, stomach, small intestine, larynx, lung and bronchus, thyroid and prostate cancer were 8.64 (95% CI = 7.36-10.07), 2.87 (95% CI = 2.10-3.82), 3.80 (95% CI = 1.82-7.00), 3.19 (95% CI = 2.12-4.61), 1.68 (95% CI = 1.46-1.93), 2.50 (95% CI = 1.25-4.47), and 0.77 (95% CI = 0.65-0.90), respectively. Radiotherapy raised cancer risk of larynx (SIR = 3.98, 95% CI = 2.43-6.14) and thyroid (SIR = 3.57, 95% CI = 1.54-7.03) among all esophageal cancer survivors. For patients who had 5-9 years of follow up after radiotherapy, the SIR for lung cancer was 3.46 (95% CI = 2.41-4.82). Patients with esophageal cancer are at increased risks of second cancers of oral and pharynx, larynx, lung, and thyroid, while at a decreased risk for prostate cancer. These findings indicate that radiotherapy for esophageal cancer patients may increase risk of developing second cancers of larynx, lung, and thyroid. Thus, randomized clinical trials to address the association of radiotherapy and the risk of secondary cancer are warranted.
食管癌的新治疗方法,包括手术、化疗、放疗或这些方法的联合应用,不仅提高了患者的生存率,而且可能增加第二原发癌的风险。现有证据与大多数基于稀疏数据的风险估计存在冲突。在这里,我们估计了 1973 年至 2007 年间在监测、流行病学和最终结果(SEER)计划中至少有 2 个月的 24557 例食管癌幸存者(随访中位数为 6.5 年,范围为 2 个月至 29.3 年)中第二癌症的标准化发病比(SIR)。与普通人群相比,幸存者的第二癌症风险显著升高(SIR = 1.34,95%置信区间[CI] = 1.25-1.42);口腔和咽、胃、小肠、喉、肺和支气管、甲状腺和前列腺癌的 SIR 分别为 8.64(95%CI = 7.36-10.07)、2.87(95%CI = 2.10-3.82)、3.80(95%CI = 1.82-7.00)、3.19(95%CI = 2.12-4.61)、1.68(95%CI = 1.46-1.93)、2.50(95%CI = 1.25-4.47)和 0.77(95%CI = 0.65-0.90)。所有食管癌幸存者中,放疗均增加了喉(SIR = 3.98,95%CI = 2.43-6.14)和甲状腺(SIR = 3.57,95%CI = 1.54-7.03)癌症的风险。对于放疗后随访 5-9 年的患者,肺癌的 SIR 为 3.46(95%CI = 2.41-4.82)。食管癌患者患口腔和咽、喉、肺和甲状腺第二原发癌的风险增加,而患前列腺癌的风险降低。这些发现表明,放疗可能会增加食管癌患者发生喉、肺和甲状腺第二原发癌的风险。因此,有必要进行随机临床试验来解决放疗与继发性癌症风险的关系。