胰腺癌强化新辅助化疗和放化疗时代的术中放疗。

Florence K Keane, Jennifer Y Wo, Cristina R Ferrone, Jeffrey W Clark, Lawrence S Blaszkowsky, Jill N Allen, Eunice L Kwak, David P Ryan, Keith D Lillemoe, Carlos Fernandez-Del Castillo, Theodore S Hong
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引用次数: 34

摘要

目的:FOLFIRINOX或吉西他滨联合nab-紫杉醇治疗转移性胰腺腺癌(PDAC)的改善结果促使这些方案被纳入局部晚期不可切除的PDAC的新辅助治疗。然而,一些患者在手术探查时仍然无法切除,而另一些患者在强化新辅助治疗后能够切除。我们评估了强化新辅助治疗后术中放疗(IORT)联合手术切除或剖腹探查的结果和毒性。方法:我们回顾性分析了2010年至2015年间在iort设备的手术室中接受强化新辅助治疗的局部晚期不可切除或边缘可切除的PDAC患者,这些患者接受了诱导化疗和放化疗,然后进行了剖腹探查。比较手术结果和总生存期(OS)。结果:68例患者中,41例(60.3%)行手术切除,18例(26.5%)无法切除,9例(13.2%)远处转移。在41例可切除的患者中,22例接受IORT术中冷冻切面闭合/阳性切除边缘。在切除的基础上增加IORT,手术时间和发病率没有显著差异。所有切除患者的中位OS为26.6个月,切除和IORT患者的中位OS为35.1个月,单独切除患者的中位OS为24.5个月(P=NS)。在18例不可切除的患者中,除1例外,其余患者均接受了IORT,中位生存期为24.8个月。IORT与住院时间增加有关(4天vs. 3.5天),但在手术时间或发病率方面无显著差异。结论:IORT除强化新辅助化疗和放化疗外,与切除或剖腹探查术联合使用时毒性增加无关,并且与切缘闭合/阳性患者和不可切除疾病患者的生存率提高相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intraoperative Radiotherapy in the Era of Intensive Neoadjuvant Chemotherapy and Chemoradiotherapy for Pancreatic Adenocarcinoma.

Objectives: Improved outcomes with FOLFIRINOX or gemcitabine with nab-paclitaxel in the treatment of metastatic pancreatic adenocarcinoma (PDAC) have prompted incorporation of these regimens into neoadjuvant treatment of locally advanced unresectable PDAC. Whereas some patients remain unresectable on surgical exploration, others are able to undergo resection after intensive neoadjuvant treatment. We evaluated outcomes and toxicity associated with use of intensive neoadjuvant treatment followed by intraoperative radiotherapy (IORT) in combination with resection or exploratory laparotomy.

Methods: We retrospectively analyzed patients with locally advanced unresectable or borderline-resectable PDAC who received intensive neoadjuvant treatment with induction chemotherapy and chemoradiotherapy followed by exploratory laparotomy in an IORT-equipped operating suite between 2010 and 2015. Surgical outcomes and overall survival (OS) were compared.

Results: Of 68 patients, 41 (60.3%) underwent resection, 18 (26.5%) had unresectable disease, and 9 (13.2%) had distant metastases. Of 41 resectable patients, 22 received IORT for close/positive resection margins on intraoperative frozen section. There was no significant difference in operative times or morbidity with addition of IORT to resection. Median OS was 26.6 months for all patients who underwent resection, 35.1 months for patients who underwent resection and IORT, and 24.5 months for patients who underwent resection alone (P=NS). Of 18 patients with unresectable disease, all but 1 received IORT, with median OS of 24.8 months. IORT was associated with increased hospital stay (4 vs. 3.5 d), but no significant difference in operative times or morbidity.

Conclusions: IORT in addition to intensive neoadjuvant chemotherapy and chemoradiotherapy was not associated with increased toxicity when used with resection or exploratory laparotomy, and was associated with encouraging survival rates in patients with close/positive margins and patients with unresectable disease.

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