Department of Medical Oncology, Trophoblastic Tumour Screening and Treatment Centre, Charing Cross Hospital, Imperial Hospitals NHS Trust, London, UK.
Sheffield Trophoblastic Disease Centre, Weston Park Cancer Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
BJOG. 2020 Aug;127(9):1102-1107. doi: 10.1111/1471-0528.16202. Epub 2020 Apr 3.
To investigate the demographics, natural history and treatment outcomes of non-molar gestational choriocarcinoma.
A retrospective national population-based study.
UK 1995-2015.
A total of 234 women with a diagnosis of gestational choriocarcinoma, in the absence of a prior molar pregnancy, managed at the UKs two gestational trophoblast centres in London and Sheffield.
Retrospective review of the patient's demographic and clinical data. Comparison with contemporary UK birth and pregnancy statistics.
Incidence statistics for non-molar choriocarcinoma across the maternal age groups. Cure rates for patients by FIGO prognostic score group.
Over the 21-year study period, there were 234 cases of non-molar gestational choriocarcinoma, giving an incidence of 1:66 775 relative to live births and 1:84 226 to viable pregnancies. For women aged under 20, the incidence relative to viable pregnancies was 1:223 494, for ages 30-34, 1:80 227, and for ages 40-45, 1:41 718. Treatment outcomes indicated an overall 94.4% cure rate. Divided by FIGO prognostic groups, the cure rates were low-risk group 100%, high-risk group 96% and ultra-high-risk group 80.5%.
Non-molar gestational choriocarcinoma is a very rare diagnosis with little prior detailed information on the demographics and natural history. The data in this study give age-related incidence data based on a large national population study. The results also demonstrated the widely varying natural history of this rare malignancy and the marked correlation of disease incidence with rising maternal age.
National gestational choriocarcinoma database indicates a close association between increasing maternal age and incidence.
研究非葡萄胎性妊娠绒癌的人口统计学、自然史和治疗结局。
一项回顾性全国人群研究。
英国,1995-2015 年。
在英国伦敦和谢菲尔德的两个妊娠滋养细胞肿瘤中心接受治疗的,无既往葡萄胎妊娠的 234 例妊娠绒癌患者。
回顾性分析患者的人口统计学和临床数据。与同期英国出生和妊娠统计数据进行比较。
各年龄组非葡萄胎性绒癌的发病率统计。按 FIGO 预后评分组比较患者的治愈率。
在 21 年的研究期间,共有 234 例非葡萄胎性妊娠绒癌,活产儿相对发病率为 1:66775,活胎相对发病率为 1:84226。年龄小于 20 岁的患者,活胎相对发病率为 1:223494;年龄在 30-34 岁的患者,为 1:80227;年龄在 40-45 岁的患者,为 1:41718。治疗结果表明总治愈率为 94.4%。按 FIGO 预后分组,低危组治愈率为 100%,高危组为 96%,超高危组为 80.5%。
非葡萄胎性妊娠绒癌是一种非常罕见的诊断,此前对其人口统计学和自然史的详细信息知之甚少。本研究中的数据基于一项大型全国人群研究提供了与年龄相关的发病率数据。结果还表明,这种罕见恶性肿瘤的自然史差异很大,疾病的发生与产妇年龄的增加密切相关。
全国妊娠绒癌数据库表明,产妇年龄的增加与发病率密切相关。