Kaiser Permanente乳腺癌幸存者队列中女性第二原发癌的风险

Cody Ramin, Lene H S Veiga, Jacqueline B Vo, Rochelle E Curtis, Clara Bodelon, Erin J Aiello Bowles, Diana S M Buist, Sheila Weinmann, Heather Spencer Feigelson, Gretchen L Gierach, Amy Berrington de Gonzalez
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引用次数: 0

摘要

背景:由于早期发现和治疗的进步,乳腺癌幸存者的寿命更长,患第二原发癌症的风险增加。对近几十年来接受治疗的患者第二癌风险的综合评价缺乏。方法:在1990年至2016年期间(随访至2017年),在科罗拉多州、西北部和华盛顿州凯撒医疗机构(KP)确诊为第一原发性I-III期乳腺癌的16,004名女性患者存活≥1年。第二癌被定义为在第一原发性乳腺癌后≥12个月确诊的浸润性原发性癌症。采用标准化发病率比(SIRs)评估所有癌症(不包括同侧乳腺癌)的第二种癌症风险,并采用竞争风险方法评估累积发病率和危险比(hr),根据KP中心、治疗、年龄和首次癌症诊断年份进行调整。结果:在6.2年的中位随访中,1562名女性患上了第二种癌症。与一般人群相比,乳腺癌幸存者患任何癌症的风险高出70% (95%CI = 1.62-1.79),非乳腺癌的风险高出45% (95%CI = 1.37-1.54)。腹膜恶性肿瘤(SIR = 3.44, 95%CI = 1.65-6.33)、软组织恶性肿瘤(SIR = 3.32, 95%CI = 2.51-4.30)、对侧乳腺恶性肿瘤(SIR = 3.10, 95%CI = 2.82-3.40)和急性髓性白血病(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SIRs最高。女性患口腔癌、结肠癌、胰腺癌、肺癌和子宫癌、黑色素瘤和非霍奇金淋巴瘤的风险也较高(SIR范围= 1.31-1.97)。放疗与所有第二癌(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(HR = 0.87, 95%CI = 0.78-0.98)的风险降低相关,骨髓增生异常综合征(HR = 3.01, 95%CI = 1.01-8.94)的风险增加相关,内分泌治疗与对侧乳腺癌风险降低相关(HR = 0.48, 95%CI = 0.38-0.60)。在存活≥1年的女性中,大约每9名女性中就有1名患上第二种癌症,每13名女性中就有1名患上第二种非乳腺癌,每30名女性中就有1名在10年内患上对侧乳腺癌。对侧乳腺癌的累积发病率呈下降趋势,但第二种非乳腺癌没有下降趋势。结论:近几十年来接受治疗的乳腺癌幸存者中二次癌的风险增加,这表明有必要加强监测,并继续努力减少二次癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Risk of second primary cancer among women in the Kaiser Permanente Breast Cancer Survivors Cohort.

Risk of second primary cancer among women in the Kaiser Permanente Breast Cancer Survivors Cohort.

Risk of second primary cancer among women in the Kaiser Permanente Breast Cancer Survivors Cohort.

Risk of second primary cancer among women in the Kaiser Permanente Breast Cancer Survivors Cohort.

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

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