Division of Cancer Epidemiology and Genetics, National Cancer Institute, 9609 Medical Center Drive, Bethesda, MD, USA.
Cancer Research Center for Health Equity, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Breast Cancer Res. 2023 May 3;25(1):50. doi: 10.1186/s13058-023-01647-y.
Breast cancer survivors are living longer due to early detection and advances in treatment and are at increased risk for second primary cancers. Comprehensive evaluation of second cancer risk among patients treated in recent decades is lacking.
We identified 16,004 females diagnosed with a first primary stage I-III breast cancer between 1990 and 2016 (followed through 2017) and survived ≥ 1 year at Kaiser Permanente (KP) Colorado, Northwest, and Washington. Second cancer was defined as an invasive primary cancer diagnosed ≥ 12 months after the first primary breast cancer. Second cancer risk was evaluated for all cancers (excluding ipsilateral breast cancer) using standardized incidence ratios (SIRs), and a competing risk approach for cumulative incidence and hazard ratios (HRs) adjusted for KP center, treatment, age, and year of first cancer diagnosis.
Over a median follow-up of 6.2 years, 1,562 women developed second cancer. Breast cancer survivors had a 70% higher risk of any cancer (95%CI = 1.62-1.79) and 45% higher risk of non-breast cancer (95%CI = 1.37-1.54) compared with the general population. SIRs were highest for malignancies of the peritoneum (SIR = 3.44, 95%CI = 1.65-6.33), soft tissue (SIR = 3.32, 95%CI = 2.51-4.30), contralateral breast (SIR = 3.10, 95%CI = 2.82-3.40), and acute myeloid leukemia (SIR = 2.11, 95%CI = 1.18-3.48)/myelodysplastic syndrome (SIR = 3.25, 95%CI = 1.89-5.20). Women also had elevated risks for oral, colon, pancreas, lung, and uterine corpus cancer, melanoma, and non-Hodgkin lymphoma (SIR range = 1.31-1.97). Radiotherapy was associated with increased risk for all second cancers (HR = 1.13, 95%CI = 1.01-1.25) and soft tissue sarcoma (HR = 2.36, 95%CI = 1.17-4.78), chemotherapy with decreased risk for all second cancers (HR = 0.87, 95%CI = 0.78-0.98) and increased myelodysplastic syndrome risk (HR = 3.01, 95%CI = 1.01-8.94), and endocrine therapy with lower contralateral breast cancer risk (HR = 0.48, 95%CI = 0.38-0.60). Approximately 1 in 9 women who survived ≥ 1 year developed second cancer, 1 in 13 developed second non-breast cancer, and 1 in 30 developed contralateral breast cancer by 10 years. Trends in cumulative incidence declined for contralateral breast cancer but not for second non-breast cancers.
Elevated risks of second cancer among breast cancer survivors treated in recent decades suggests that heightened surveillance is warranted and continued efforts to reduce second cancers are needed.
由于早期发现和治疗的进步,乳腺癌幸存者的寿命更长,并且患第二原发癌的风险增加。最近几十年接受治疗的患者的第二癌症风险综合评估还很缺乏。
我们确定了 1990 年至 2016 年期间(随访至 2017 年)在 Kaiser Permanente(KP)科罗拉多州、西北部和华盛顿州诊断为 1 期至 3 期 I 期乳腺癌且生存时间≥1 年的 16004 名女性。第二癌被定义为首次原发性乳腺癌诊断后≥12 个月诊断出的侵袭性原发性癌症。使用标准化发病率比(SIR)评估所有癌症(不包括同侧乳腺癌)的第二癌风险,并使用累积发病率和风险比(HR)的竞争风险方法进行调整,以纳入 KP 中心、治疗、年龄和首次癌症诊断年份。
在中位随访 6.2 年期间,有 1562 名女性发生了第二癌。与普通人群相比,乳腺癌幸存者的任何癌症风险增加了 70%(95%CI=1.62-1.79),非乳腺癌风险增加了 45%(95%CI=1.37-1.54)。腹膜(SIR=3.44,95%CI=1.65-6.33)、软组织(SIR=3.32,95%CI=2.51-4.30)、对侧乳房(SIR=3.10,95%CI=2.82-3.40)和急性髓系白血病(SIR=2.11,95%CI=1.18-3.48)/骨髓增生异常综合征(SIR=3.25,95%CI=1.89-5.20)的恶性肿瘤的 SIR 最高。女性也存在口腔、结肠、胰腺、肺和子宫体癌、黑色素瘤和非霍奇金淋巴瘤(SIR 范围为 1.31-1.97)的风险增加。放疗与所有第二癌症(HR=1.13,95%CI=1.01-1.25)和软组织肉瘤(HR=2.36,95%CI=1.17-4.78)的风险增加相关,化疗与所有第二癌症(HR=0.87,95%CI=0.78-0.98)和骨髓增生异常综合征风险增加(HR=3.01,95%CI=1.01-8.94)相关,而内分泌治疗与对侧乳腺癌风险降低(HR=0.48,95%CI=0.38-0.60)相关。大约 1/9 的≥1 年生存的女性患有第二癌症,1/13 的女性患有第二非乳腺癌,1/30 的女性在 10 年内患有对侧乳腺癌。对侧乳腺癌的累积发病率趋势下降,但第二非乳腺癌的累积发病率趋势没有下降。
最近几十年接受治疗的乳腺癌幸存者第二癌风险增加表明需要进行强化监测,需要继续努力降低第二癌的风险。