霍奇金淋巴瘤幸存者与乳腺癌相关的乳腺癌家族史

Sarah Colonna, Karen Curtin, Eric Johnson, Wendy Kohlmann, Jennifer Wright, Anne Kirchhoff, Sean Tavtigian, Joshua Schiffman
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引用次数: 5

摘要

霍奇金淋巴瘤(HL)治疗的进展显著提高了儿童和成人患者的生存率;然而,HL幸存者死亡的主要原因是HL治疗后继发恶性肿瘤[1,2]。在HL治疗的女性中,乳腺癌(BC)是最常见的继发性恶性肿瘤[3]。我们探讨了HL和BC在家族中是否存在关联。方法:利用犹他州人口数据库和犹他州癌症登记处,我们确定了988名患有HL的女性,在HL之前没有BC病史,从1966年到2014年在犹他州诊断。我们检查了患有HL的女性是否有更大的患BC的风险,这取决于是否有BC家族史。我们还使用Cox回归方法检查了患有HL和BC的女性fdr中BC的家族性复发风险。结果:在988例女性HL患者中,42例(4.3%)被诊断为后续BC,而在9676例匹配的对照组中,280例(2.8%)被诊断为BC (P < 0.05)。我们观察到,与对照组的FDR相比,女性HL患者继发BC的一级亲属(父母、全兄妹或子女)患BC的风险显著增加3倍(HR = 2.8, 95%CI 1.4-5.6;P = 0.005)。有BC家族史的女性HL患者发生BC的可能性明显高于亲属中无BC家族史的HL患者(HR = 3.3, 95%CI 1.6-7.1;P = 0.002)。结论:患有HL且有BC家族史的女性患BC的风险甚至高于预期,其女性亲属也是如此。对于准备接受HL治疗的女性,获得完整的家族史对于HL的治疗决策非常重要,随着时间的推移,保持最新的家族史对于管理女性持续的癌症风险和HL生存后的监测策略也很重要。
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Family History of Breast Cancer Associated with Breast Cancer in Survivors of Hodgkin Lymphoma.

Introduction: Advances in treatments for Hodgkin Lymphoma (HL) have significantly increased survival of childhood and adult patients; however, the leading cause of death in HL survivors is due to secondary malignancy following HL treatment [1,2]. Among women treated for HL, breast cancer (BC) is the most common secondary malignancy [3]. We explored if an association exists between HL and BC exists within families.

Methods: Utilizing the Utah Population Database and the Utah Cancer Registry, we identified 988 women with HL, and no history of BC prior to HL, diagnosed in Utah from 1966-2014. We examined if women with HL were at greater risk of developing BC based on the presence or absence of family history of BC. We also examined the familial recurrence risk of BC among female FDRs of women with HL and BC using Cox regression methods.

Result: Among 988 female HL patients, 42 (4.3%) were diagnosed with subsequent BC while among 9,876 matched controls, 280 controls (2.8%) were diagnosed with BC from 1966-2014 (P < 0.05). We observed a significant 3-fold increased risk of BC in the first-degree relatives (parent, full sibling, or child of patient) of female HL patients with subsequent BC, compared to FDR in controls (HR = 2.8, 95%CI 1.4-5.6; P = 0.005). Female HL patients who had a family history of BC were significantly more likely to develop BC, compared to HL patients with no history of BC among relatives (HR = 3.3, 95%CI 1.6-7.1; P = 0.002).

Conclusion: Women with HL and a family history of BC are at even higher than anticipated risk of BC, as are their female relatives. Obtaining a thorough family history for a woman preparing to undergo therapy for HL is important for treatment decisions for HL and maintaining an up to date family history over time is also important for the management of a woman's ongoing cancer risks and her surveillance strategy following survival of HL.

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