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女性恶性生殖细胞肿瘤的发病率和生存率。

Incidence and survival rates for female malignant germ cell tumors.

作者信息

Smith Harriet O, Berwick Marianne, Verschraegen Claire F, Wiggins Charles, Lansing Letitia, Muller Carolyn Y, Qualls Clifford R

机构信息

Department of Obstetrics and Gynecology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico 87131-5286, USA.

出版信息

Obstet Gynecol. 2006 May;107(5):1075-85. doi: 10.1097/01.AOG.0000216004.22588.ce.

Abstract

OBJECTIVE

To evaluate 30-year, population-based trends in incidence and survival rates for malignant germ cell tumors originating within the female genital tract.

METHODS

Surveillance, Epidemiology, and End Results data were used to identify malignant germ cell tumors (1973-2002). Overall and 5-year incidence rates, estimated annual percentage change, and survival rates were calculated and compared by age at diagnosis, race, stage, and histology.

RESULTS

Of 1,262 cases, there were 414 (32.8%) dysgerminomas, 449 (35.6%) immature teratomas, 37 (2.9%) mature teratomas with malignant degeneration, and 362 (28.7%) mixed germ cell tumors. The 30-year, age-adjusted incidence rate per 100,000 women-years was 0.338, decreasing by 29.4% for dysgerminomas (P = .18) and by 31.5% for mixed germ cell tumors (P = .22). Other nonwhites had higher rates than whites and blacks, but dysgerminoma rates were higher in whites and other nonwhites than in blacks. Using the registries for expanded races, rates were higher for Asian/Pacific Islanders (P = .059) and Hispanics (P = .07). By age at diagnosis, 15-19 year olds had the highest rates and the only significant change in rates (37.5% increase, P = .008). The 5-year relative survival was 83.9%. Survival rates improved significantly over calendar time and varied by histologic subtype, race, stage of disease, and age at diagnosis.

CONCLUSION

Over the past 30 years, germ cell tumor incidence rates have declined in women and differ from rising trends reported for testicular tumors. Survival rates have improved but were lower for older women and for nondysgerminoma subtypes.

摘要

目的

评估女性生殖道原发性恶性生殖细胞肿瘤30年的人群发病率及生存率趋势。

方法

利用监测、流行病学及最终结果(SEER)数据识别1973 - 2002年的恶性生殖细胞肿瘤。计算总体发病率、5年发病率、估计年百分比变化及生存率,并按诊断时年龄、种族、分期和组织学类型进行比较。

结果

1262例病例中,有414例(32.8%)为无性细胞瘤,449例(35.6%)为未成熟畸胎瘤,37例(2.9%)为成熟畸胎瘤伴恶性变,362例(28.7%)为混合性生殖细胞肿瘤。每100,000女性年的30年年龄调整发病率为0.338,无性细胞瘤下降29.4%(P = 0.18),混合性生殖细胞肿瘤下降31.5%(P = 0.22)。其他非白人的发病率高于白人和黑人,但无性细胞瘤发病率在白人和其他非白人中高于黑人。利用扩展种族登记数据,亚洲/太平洋岛民(P = 0.059)和西班牙裔(P = 0.07)的发病率较高。按诊断时年龄,15 - 19岁年龄组发病率最高且发病率有唯一显著变化(增加37.5%,P = 0.008)。5年相对生存率为83.9%。生存率随时间显著改善,且因组织学亚型、种族、疾病分期和诊断时年龄而异。

结论

在过去30年中,女性生殖细胞肿瘤发病率下降,与睾丸肿瘤报告的上升趋势不同。生存率有所提高,但老年女性和非无性细胞瘤亚型的生存率较低。

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