Keane Florence K, Wo Jennifer Y, Ferrone Cristina R, Clark Jeffrey W, Blaszkowsky Lawrence S, Allen Jill N, Kwak Eunice L, Ryan David P, Lillemoe Keith D, Fernandez-Del Castillo Carlos, Hong Theodore S
Harvard Radiation Oncology Program, Harvard Medical School.
Departments of Radiation Oncology.
Am J Clin Oncol. 2018 Jun;41(6):607-612. doi: 10.1097/COC.0000000000000336.
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.
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.
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.
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.
FOLFIRINOX方案或吉西他滨联合纳米白蛋白结合型紫杉醇在转移性胰腺导管腺癌(PDAC)治疗中取得了更好的疗效,促使这些方案被纳入局部晚期不可切除PDAC的新辅助治疗。然而,一些患者在手术探查时仍无法切除,而另一些患者在接受强化新辅助治疗后能够进行切除。我们评估了强化新辅助治疗后联合术中放疗(IORT)并结合切除或剖腹探查的疗效和毒性。
我们回顾性分析了2010年至2015年间在配备IORT的手术室接受强化新辅助治疗(诱导化疗和放化疗)后行剖腹探查的局部晚期不可切除或边界可切除PDAC患者。比较手术结果和总生存期(OS)。
68例患者中,41例(60.3%)接受了切除,18例(26.5%)疾病不可切除,9例(13.2%)有远处转移。41例可切除患者中,22例因术中冰冻切片显示切缘接近/阳性而接受了IORT。切除联合IORT的手术时间或发病率无显著差异。所有接受切除的患者中位OS为26.6个月,接受切除及IORT的患者为35.1个月,单纯接受切除的患者为24.5个月(P=无显著性差异)。18例疾病不可切除的患者中,除1例外均接受了IORT,中位OS为24.8个月。IORT与住院时间延长相关(4天对3.5天),但手术时间或发病率无显著差异。
强化新辅助化疗和放化疗联合IORT用于切除或剖腹探查时,毒性并未增加,且在切缘接近/阳性的患者和疾病不可切除的患者中生存率令人鼓舞。