一家三级医院子宫肉瘤的存活趋势:牛津经验

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Aakriti Aggarwal, Federico Ferrari, Andreas Zouridis, Sean Kehoe, Sarah Pratap, Elisa Gozzini, Hooman Soleymani Majd
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引用次数: 0

摘要

子宫肉瘤是一种罕见的侵袭性妇科恶性肿瘤。我们对本研究所收治的子宫肉瘤患者的流行病学、治疗效果和存活率进行了评估。我们对 2010 年 2 月至 2022 年 2 月期间在我院接受治疗的组织学证实的子宫肉瘤(包括子宫肌瘤(LMS)、腺肉瘤(ADS)和子宫内膜间质肉瘤(ESS))女性患者的病历进行了分析。共发现 41 例患者。具体而言,60.9%、19.5%、12.1% 和 7.3% 的病例中分别发现了 LMS、ADS 以及高级别和低级别 ESS。大多数受 LMS 影响的妇女(72%)接受了初级手术,其中 40% 还接受了辅助化疗。83%的复发患者首选手术治疗。LMS组的中位OS(总生存期)、DFS(无病生存期)和PFS(无进展生存期)分别为25个月、44.5个月和8个月。LMS组、ADS组和ESS组的5年生存率分别为30.5%、100%和37.5%。发现LMS的5年生存率明显低于其他组织学类型(P = 0.016)。我们的研究为评估这些罕见癌症的治疗策略和生存趋势提供了宝贵的数据。每种亚型的管理和随访计划都需要以患者为中心的多学科讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Survival Trends for Uterine Sarcomas from a Tertiary Center: The Oxford Experience.

Uterine sarcomas are rare and aggressive gynecological malignancies. We evaluated the epidemiology, treatment outcomes and survival rates in uterine sarcoma patients managed in our institute. The medical records of women with histology proven uterine sarcoma, including leiomyosarcoma (LMS), adenosarcoma (ADS), and endometrial stromal sarcoma (ESS), treated at our institution from February 2010 to February 2022, were analyzed. In total, 41 patients were identified. In detail, LMS, ADS, and high-grade and low-grade ESS were identified, respectively, in 60.9%, 19.5%, 12.1%, and 7.3% of the cases. The majority of women affected by LMS (72%) underwent primary surgery and 40% of them also received adjuvant chemotherapy. A surgical approach was the preferred mode of treatment in 83% of the recurrences. The median OS (overall survival), DFS (disease free survival), and PFS (progression free survival) for the LMS group were 25, 44.5, and 8 months, respectively. The 5-year survival rates for LMS, ADS, and ESS groups were 30.5%, 100% and 37.5%, respectively. The 5-year survival for LMS was found to be significantly worse than for other histology types (p = 0.016). Our study provides valuable data for the evaluation of treatment strategies and survival trends among these rare cancers. The management and follow-up planning of each subtype requires a thorough patient-focused multidisciplinary discussion.

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