Zighelboim Israel, Babb Sheri, Gao Feng, Powell Matthew A, Mutch David G, Goodfellow Paul J
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University School of Medicine and Siteman Cancer Center, 4911 Barnes Jewish Plaza, Box 8064, St. Louis, MO 63110, USA.
Gynecol Oncol. 2007 May;105(2):390-4. doi: 10.1016/j.ygyno.2006.12.022. Epub 2007 Mar 1.
Determine whether there is an association between uterine cancer and multiple myeloma.
Data on second malignancies were obtained for 368 uterine corpus cancer patients treated between 1992 and 2005. Detailed family histories were devised for 192 probands. Diagnoses of multiple myelomas, lymphomas and leukemias in family members were medical record verified. The frequency of multiple myeloma among uterine cancer patients was compared to the female age-adjusted incidence rate of multiple myeloma obtained from the SEER database. The crude rate of multiple myeloma (as well as Hodgkin's, non-Hodgkin's lymphomas and leukemias) among first-degree relatives of patients with uterine cancer was compared to the age-adjusted incidence rate of multiple myeloma in the general population. Descriptive statistics were used to evaluate disease and cohort characteristics. A P value less than 0.05 was considered statistically significant.
Two of 368 uterine cancer patients were also diagnosed with multiple myeloma, both at age 50. The observed incidence of multiple myeloma in this cohort (543 per 100,000; 95% CI: 66-1962 per 100,000) represents a 120-fold increase based on predicted incidence (P=0.00014). The frequency of multiple myeloma in first-degree relatives was 2/1351 (148 per 100,000; 95% CI: 14.8-533 per 100,000) which represents a 27-fold increase compared to the general population (P=0.0026). The frequencies of leukemias and lymphomas in these family members on the other hand were not significantly increased (P=0.152 and P=0.218).
This specific excess frequency of early onset multiple myeloma in endometrial cancer probands and their relatives suggests shared susceptibility.
确定子宫癌与多发性骨髓瘤之间是否存在关联。
获取了1992年至2005年间接受治疗的368例子宫体癌患者的二次恶性肿瘤数据。为192名先证者制定了详细的家族病史。家庭成员中多发性骨髓瘤、淋巴瘤和白血病的诊断通过病历核实。将子宫癌患者中多发性骨髓瘤的发生率与从监测、流行病学和最终结果(SEER)数据库获得的女性年龄调整后的多发性骨髓瘤发病率进行比较。将子宫癌患者一级亲属中多发性骨髓瘤(以及霍奇金淋巴瘤、非霍奇金淋巴瘤和白血病)的粗发病率与一般人群中年龄调整后的多发性骨髓瘤发病率进行比较。使用描述性统计来评估疾病和队列特征。P值小于0.05被认为具有统计学意义。
368例子宫癌患者中有2例也被诊断出患有多发性骨髓瘤,均为50岁。该队列中观察到的多发性骨髓瘤发病率(每10万人中543例;95%置信区间:每10万人中66 - 1962例)相较于预测发病率增加了120倍(P = 0.00014)。一级亲属中多发性骨髓瘤的发生率为2/1351(每10万人中148例;95%置信区间:每10万人中14.8 - 533例),相较于一般人群增加了27倍(P = 0.0026)。另一方面,这些家庭成员中白血病和淋巴瘤的发生率没有显著增加(P = 0.152和P = 0.218)。
子宫内膜癌先证者及其亲属中这种特定的早发性多发性骨髓瘤高发频率表明存在共同易感性。