Tate Keisei, Watanabe Reiko, Yoshida Hiroshi, Shimizu Hanako, Uehara Takashi, Ishikawa Mitsuya, Ikeda Shun-Ichi, Hiraoka Nobuyoshi, Kato Tomoyasu
Department of Gynecology, National Cancer Center Hospital, Chuo-ku, Tokyo, Japan.
Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, Chuo-ku, Tokyo, Japan.
Asia Pac J Clin Oncol. 2018 Aug;14(4):318-325. doi: 10.1111/ajco.12859. Epub 2018 Feb 14.
Uterine adenosarcoma is a rare malignancy with limited cohort data in Asian countries. This study evaluated the clinicopathologic features of Japanese patients with uterine adenosarcoma and their potential treatment challenges.
A retrospective chart review was performed at the National Cancer Center Hospital, Japan from 2000 to 2016. A literature search for Japanese cases of uterine adenosarcoma was conducted using PubMed, Japanese Central Review of Medicine, and the Annual of Pathological Autopsy Cases in Japan. Only histologically confirmed cases of uterine adenosarcoma were included. All collected data were analyzed.
A total of 110 cases was identified (6 from our hospital and 104 from the literature review). Most baseline characteristics were similar to those reported in western countries. Death due to the disease was observed in 34% (29/86) of patients, whereas patients with stage IA disease showed a 13% (4/30) recurrence rate and a 3.3% (1/30) mortality rate. Preoperative radiological and pathological examinations occasionally failed to help reach the correct diagnosis. In cases of sarcomatous overgrowth, the recurrence and mortality rates were 45% (9/20) and 35% (7/20), respectively. Distant recurrence occurred in 44% (12/27) of cases, 75% of which included lung metastasis.
This study showed the clinicopathologic features of Japanese patients with uterine adenosarcoma and suggested potential solutions for improving prognosis including early treatment based on a timely diagnosis, the development of effective adjuvant therapy for patients at high risk of recurrence, and optimal follow-up focusing on late recurrence and lung metastasis.
子宫腺肉瘤是一种罕见的恶性肿瘤,亚洲国家的相关队列数据有限。本研究评估了日本子宫腺肉瘤患者的临床病理特征及其潜在的治疗挑战。
对日本国立癌症中心医院2000年至2016年的病例进行回顾性图表审查。使用PubMed、日本医学中央杂志和日本病理尸检病例年鉴对日本子宫腺肉瘤病例进行文献检索。仅纳入组织学确诊的子宫腺肉瘤病例。对所有收集的数据进行分析。
共确定110例病例(6例来自我们医院,104例来自文献综述)。大多数基线特征与西方国家报道的相似。34%(29/86)的患者死于该疾病,而IA期疾病患者的复发率为13%(4/30),死亡率为3.3%(1/30)。术前放射学和病理学检查偶尔无法帮助做出正确诊断。在肉瘤过度生长的病例中,复发率和死亡率分别为45%(9/20)和35%(7/20)。44%(12/27)的病例发生远处复发,其中75%包括肺转移。
本研究显示了日本子宫腺肉瘤患者的临床病理特征,并提出了改善预后的潜在解决方案,包括基于及时诊断的早期治疗、为复发高危患者开发有效的辅助治疗,以及针对晚期复发和肺转移的最佳随访。