细胞减灭术(CRS)和腹膜内热疗(HIPEC)+/-术中放疗(IORT)治疗腹膜肉瘤的疗效和安全性:真实世界的经验

A. Elashwah, A. Badran, M. Elshenawy, A. Azzam, Rania Naguib, Aisha Alshibani, Reem Alrakaf, A. Eldali, T. Amin
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引用次数: 0

摘要

背景:腹膜肉瘤病(PS)是一种侵袭性疾病;细胞减缩手术(CRS)可以治愈。腹腔高温化疗(HIPEC) +/-术中放射治疗(IORT)是否能克服治疗失败并提高总体生存期?方法:回顾性分析2011-2016年在某综合癌症中心接受CRS、HIPEC和IORT治疗的PS患者的病历。结果:共发现24例患者。其中15人是男性,平均年龄为58岁。脂肪肉瘤是最常见的诊断(50%)。19例患者达到细胞减少完整性(CC)评分0/1,中位病理性腹膜癌指数(pPCI)为12。术中放疗16例。8例患者出现III-IV级Clavien-Dindo术后并发症,1例患者术后5天死亡。9例患者接受辅助化疗。中位随访28.5个月后,中位PFS为20.7个月,而估计的2年和4年PFS分别为37.1%和19.1%。中位OS为176.5个月,估计2年和4年OS分别为95.8%和79.8%。在单变量分析中,PFS仅根据CC评分存在显著差异。CC 0-1患者的中位PFS为23.8个月,CC 2-3患者的中位PFS为8.8个月(p = 0.027)。结论:在CRS基础上加用HIPEC和IORT治疗PS是可行且安全的。将我们的结果与几项研究进行比较,这种多模式方法似乎提高了地方和区域控制率。需要更大的患者队列进行进一步评估并给出具体结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcome and Safety of Cytoreductive Surgery (CRS) and Hyperthermic Intraperitoneal Chemotherapy (HIPEC) +/- Intraoperative Radiation Therapy (IORT) in the Management of Peritoneal Sarcomatosis: A Real-World Experience
Background: Peritoneal sarcomatosis (PS) is an aggressive disease; cytoreductive surgery (CRS) could be curative. Can the addition of hyperthermic intraperitoneal chemotherapy (HIPEC) +/- intraoperative radiation therapy (IORT) overcome treatment failure with an overall survival benefit. Methods: Retrospective review of the medical records of patients with PS treated by CRS, HIPEC and IORT at a comprehensive cancer center in the period between 2011-2016. Results: Twenty-four patients were identified. Fifteen were men and their median age was 58 years. Liposarcoma was the most frequent diagnosis (50%). Cytoreduction completeness (CC) score 0/1 was achieved in 19 patients, with a median pathological peritoneal cancer index (pPCI) of 12. Intraoperative radiation therapy was given in 16 patients. Eight patients developed grade III-IV Clavien-Dindo post-operative complications and 1 patient died 5 days post operative. Adjuvant chemotherapy was received in 9 patients. After a median follow-up of 28.5 months, the median PFS was 20.7 months, while the estimated 2- and 4-year PFS were 37.1% and 19.1%, respectively. The median OS was 176.5 months and the estimated 2- and 4-year OS were 95.8% and 79.8%, respectively. In the univariate analysis, the PFS differed significantly according to the CC score only. The median PFS for patients with CC 0-1 was 23.8 vs. 8.8 months for those with CC 2-3 (p = 0.027). Conclusions: The addition of HIPEC and IORT to CRS in the management of PS is feasible and safe. Comparing our results to several studies, this multimodality approach seems to improve local and regional control rates. A larger cohort of patients is needed for further evaluation and to give a concrete conclusion.
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