Treatment patterns and survival outcomes according to histologic subtype in malignant ovarian germ cell tumors: a nationwide real-world cohort study.

IF 4.2 2区 医学 Q1 OBSTETRICS & GYNECOLOGY
Journal of Gynecologic Oncology Pub Date : 2026-07-01 Epub Date: 2026-02-02 DOI:10.3802/jgo.2026.37.e60
Jaekyung Bae, Byeong-Chan Oh, Uisuk Kim, Junyoung Shin, Sokbom Kang
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引用次数: 0

Abstract

Objective: To investigate real-world treatment patterns and survival outcomes by histologic subtype in patients with malignant ovarian germ cell tumors (MOGCTs) in Korea.

Methods: Using the Cancer Public Library Database, a retrospective cohort study was conducted including adult patients newly diagnosed with MOGCTs between 2013 and 2018. Patients were categorized into 3 histologic subtypes: dysgerminoma, non-dysgerminomatous germ cell tumors (ND-GCTs; yolk sac tumor, embryonal carcinoma, and mixed germ cell tumor [GCT]), and malignant teratomatous germ cell tumors (immature teratoma and teratocarcinoma). Initial treatment patterns, including surgery and chemotherapy, were examined. Overall survival (OS) was assessed by histologic subtype using the Kaplan-Meier method. In localized-stage patients, OS and time to first subsequent therapy or death (TFST) were estimated by adjuvant chemotherapy use, with subgroup analysis by histology.

Results: A total of 332 patients were included (27.7% dysgerminomas, 33.4% ND-GCTs, 38.9% malignant teratomatous GCTs). In localized disease, surgery alone was common in dysgerminomas (57.6%), while adjuvant chemotherapy was frequently used in ND-GCTs (88.5%) and malignant teratomatous GCTs (60.0%). Adjuvant chemotherapy was associated with longer TFST overall (p<0.01), but no OS benefit (p=0.22). In subgroup analysis, adjuvant chemotherapy was associated with longer TFST in ND-GCTs (p<0.01) and malignant teratomatous GCTs (p=0.04), but not in dysgerminomas. No significant differences in OS were observed in any group.

Conclusion: This study highlights distinct treatment patterns and outcomes by histologic subtype in MOGCTs. These findings support the value of large population-based data in guiding treatment decisions for rare ovarian tumor subtypes.

恶性卵巢生殖细胞瘤的组织学亚型的治疗模式和生存结果:一项全国性的现实世界队列研究。
目的:探讨韩国恶性卵巢生殖细胞瘤(mogct)患者的实际治疗模式和组织学亚型的生存结果。方法:利用癌症公共图书馆数据库,对2013年至2018年新诊断为mogct的成年患者进行回顾性队列研究。患者分为3个组织学亚型:异常生殖细胞瘤、非异常生殖细胞瘤生殖细胞瘤(nd -GCT;卵黄囊瘤、胚胎癌和混合性生殖细胞瘤[GCT])和恶性畸胎瘤生殖细胞瘤(未成熟畸胎瘤和畸胎癌)。研究人员检查了包括手术和化疗在内的初始治疗模式。总生存期(OS)采用Kaplan-Meier法按组织学亚型评估。在局部期患者中,通过辅助化疗的使用估计OS和到首次后续治疗或死亡的时间(TFST),并通过组织学进行亚组分析。结果:共纳入332例患者(27.7%为无生殖细胞瘤,33.4%为nd - gct, 38.9%为恶性畸胎瘤gct)。在局限性疾病中,生殖细胞异常瘤多采用单纯手术治疗(57.6%),而nd - gct(88.5%)和恶性畸胎瘤gct(60.0%)常采用辅助化疗。总体而言,辅助化疗与更长的TFST相关(结论:本研究强调了mogct中不同组织学亚型的不同治疗模式和结果。这些发现支持了基于大量人群的数据在指导罕见卵巢肿瘤亚型治疗决策中的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Gynecologic Oncology
Journal of Gynecologic Oncology ONCOLOGY-OBSTETRICS & GYNECOLOGY
CiteScore
6.00
自引率
2.60%
发文量
84
审稿时长
>12 weeks
期刊介绍: The Journal of Gynecologic Oncology (JGO) is an official publication of the Asian Society of Gynecologic Oncology. Abbreviated title is ''J Gynecol Oncol''. It was launched in 1990. The JGO''s aim is to publish the highest quality manuscripts dedicated to the advancement of care of the patients with gynecologic cancer. It is an international peer-reviewed periodical journal that is published bimonthly (January, March, May, July, September, and November). Supplement numbers are at times published. The journal publishes editorials, original and review articles, correspondence, book review, etc.
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