Lu Karen H, Dinh Mai, Kohlmann Wendy, Watson Patrice, Green Jane, Syngal Sapna, Bandipalliam Prathap, Chen Lee-May, Allen Brian, Conrad Peggy, Terdiman Jonathan, Sun Charlotte, Daniels Molly, Burke Thomas, Gershenson David M, Lynch Henry, Lynch Patrick, Broaddus Russell R
Department of Gynecologic Oncology, Division of Surgery, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030-4009, USA.
Obstet Gynecol. 2005 Mar;105(3):569-74. doi: 10.1097/01.AOG.0000154885.44002.ae.
Women with hereditary nonpolyposis colorectal cancer syndrome have a 40-60% lifetime risk for colon cancer, a 40-60% lifetime risk for endometrial cancer, and a 12% lifetime risk for ovarian cancer. A number of women with hereditary nonpolyposis colorectal cancer syndrome will have more than one cancer in their lifetime. The purpose of this study was to estimate whether women with hereditary nonpolyposis colorectal cancer syndrome who develop 2 primary cancers present with gynecologic or colon cancer as their "sentinel cancer."
Women whose families fulfilled Amsterdam criteria for hereditary nonpolyposis colorectal cancer syndrome and who developed 2 primary colorectal/gynecologic cancers in their lifetime were identified from 5 large hereditary nonpolyposis colorectal cancer syndrome registries. Information on age at cancer diagnoses and which cancer (colon cancer or endometrial cancer/ovarian cancer) developed first was obtained.
A total of 117 women with dual primary cancers from 223 Amsterdam families were identified. In 16 women, colon cancer and endometrial cancer/ovarian cancer were diagnosed simultaneously. Of the remaining 101 women, 52 (51%) women had an endometrial or ovarian cancer diagnosed first. Forty-nine (49%) women had a colon cancer diagnosed first. For women who developed endometrial cancer/ovarian cancer first, mean age at diagnosis of endometrial cancer/ovarian cancer was 44. For women who developed colon cancer first, the mean age at diagnosis of colon cancer was 40.
In this large series of women with hereditary nonpolyposis colorectal cancer syndrome who developed 2 primary colorectal/gynecologic cancers, endometrial cancer/ovarian cancer was the "sentinel cancer," preceding the development of colon cancer, in half of the cases. Therefore, gynecologists and gynecologic oncologists play a pivotal role in the identification of women with hereditary nonpolyposis colorectal cancer syndrome.
遗传性非息肉病性结直肠癌综合征女性患者一生中患结肠癌的风险为40% - 60%,患子宫内膜癌的风险为40% - 60%,患卵巢癌的风险为12%。许多遗传性非息肉病性结直肠癌综合征女性患者一生中会患不止一种癌症。本研究的目的是评估患有遗传性非息肉病性结直肠癌综合征且发生两种原发性癌症的女性,其“哨兵癌”是妇科癌症还是结肠癌。
从5个大型遗传性非息肉病性结直肠癌综合征登记处中,识别出其家族符合遗传性非息肉病性结直肠癌综合征阿姆斯特丹标准且一生中发生两种原发性结直肠/妇科癌症的女性。获取癌症诊断时的年龄信息以及首先发生的是哪种癌症(结肠癌或子宫内膜癌/卵巢癌)。
共识别出223个阿姆斯特丹家族中的117名患有双原发性癌症的女性。16名女性同时被诊断出患有结肠癌和子宫内膜癌/卵巢癌。在其余101名女性中,52名(51%)女性首先被诊断出患有子宫内膜癌或卵巢癌。49名(49%)女性首先被诊断出患有结肠癌。对于首先发生子宫内膜癌/卵巢癌的女性,子宫内膜癌/卵巢癌的平均诊断年龄为44岁。对于首先发生结肠癌的女性,结肠癌的平均诊断年龄为40岁。
在这一大型系列患有遗传性非息肉病性结直肠癌综合征且发生两种原发性结直肠/妇科癌症的女性中,一半的病例中子宫内膜癌/卵巢癌是先于结肠癌发生的“哨兵癌”。因此,妇科医生和妇科肿瘤学家在识别遗传性非息肉病性结直肠癌综合征女性患者方面起着关键作用。