Gynecologic Oncology, Juravinski Cancer Centre, Hamilton, Ontario, Canada
Gynecologic Oncology, Odette Cancer Centre, Toronto, Ontario, Canada.
Int J Gynecol Cancer. 2021 Apr;31(4):545-552. doi: 10.1136/ijgc-2020-001946. Epub 2020 Dec 18.
Ovarian clear cell carcinoma has unique clinical and molecular features compared with other epithelial ovarian cancer histologies. Our objective was to describe the incidence of second primary malignancy in patients with ovarian clear cell carcinoma.
Retrospective cohort study of patients with ovarian clear cell carcinoma at two tertiary academic centers in Toronto, Canada between May 1995 and June 2017. Demographic, histopathologic, treatment, and survival details were obtained from chart review and a provincial cancer registry. We excluded patients with histologies other than pure ovarian clear cell carcinoma (such as mixed clear cell histology), and those who did not have their post-operative follow-up at these institutions.
Of 209 patients with ovarian clear cell carcinoma, 54 patients developed a second primary malignancy (25.8%), of whom six developed two second primary malignancies. Second primary malignancies included: breast (13), skin (9), gastrointestinal tract (9), other gynecologic malignancies (8), thyroid (6), lymphoma (3), head and neck (4), urologic (4), and lung (4). Eighteen second primary malignancies occurred before the index ovarian clear cell carcinoma, 35 after ovarian clear cell carcinoma, and 7 were diagnosed concurrently. Two patients with second primary malignancies were diagnosed with Lynch syndrome. Smoking and radiation therapy were associated with an increased risk of second primary malignancy on multivariable analysis (OR 3.69, 95% CI 1.54 to 9.07, p=0.004; OR 4.39, 95% CI 1.88 to 10.6, p=0.0008, respectively). However, for patients developing second primary malignancies after ovarian clear cell carcinoma, radiation therapy was not found to be a significant risk factor (p=0.17). There was no significant difference in progression-free survival (p=0.85) or overall survival (p=0.38) between those with second primary malignancy and those without.
Patients with ovarian clear cell carcinoma are at increased risk of second primary malignancies, most frequently non-Lynch related. A subset of patients with ovarian clear cell carcinoma may harbor mutations rendering them susceptible to second primary malignancies. Our results may have implications for counseling and consideration for second primary malignancy screening.
与其他上皮性卵巢癌组织学相比,卵巢透明细胞癌具有独特的临床和分子特征。我们的目的是描述卵巢透明细胞癌患者中第二原发性恶性肿瘤的发生率。
对加拿大多伦多两家三级学术中心 1995 年 5 月至 2017 年 6 月间的卵巢透明细胞癌患者进行回顾性队列研究。从病历回顾和省级癌症登记处获得人口统计学、组织病理学、治疗和生存细节。我们排除了组织学不是纯卵巢透明细胞癌(如混合透明细胞组织学)的患者,以及那些不在这些机构进行术后随访的患者。
在 209 例卵巢透明细胞癌患者中,54 例发生了第二原发性恶性肿瘤(25.8%),其中 6 例发生了两种第二原发性恶性肿瘤。第二原发性恶性肿瘤包括:乳腺癌(13 例)、皮肤癌(9 例)、胃肠道癌(9 例)、其他妇科恶性肿瘤(8 例)、甲状腺癌(6 例)、淋巴瘤(3 例)、头颈部癌(4 例)、泌尿科癌(4 例)和肺癌(4 例)。18 例第二原发性恶性肿瘤发生在卵巢透明细胞癌之前,35 例发生在卵巢透明细胞癌之后,7 例与卵巢透明细胞癌同时发生。两名患有第二原发性恶性肿瘤的患者被诊断为林奇综合征。多变量分析显示,吸烟和放疗与第二原发性恶性肿瘤的风险增加相关(OR 3.69,95%CI 1.54 至 9.07,p=0.004;OR 4.39,95%CI 1.88 至 10.6,p=0.0008)。然而,对于卵巢透明细胞癌后发生第二原发性恶性肿瘤的患者,放疗并不是一个显著的危险因素(p=0.17)。第二原发性恶性肿瘤患者与无第二原发性恶性肿瘤患者的无进展生存期(p=0.85)或总生存期(p=0.38)无显著差异。
卵巢透明细胞癌患者发生第二原发性恶性肿瘤的风险增加,最常见的是非林奇相关的。卵巢透明细胞癌患者中有一部分可能携带导致其易发生第二原发性恶性肿瘤的突变。我们的结果可能对咨询和考虑第二原发性恶性肿瘤筛查具有启示意义。