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本文引用的文献

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Neoadjuvant chemoradiation with Gemcitabine for locally advanced pancreatic cancer.吉西他滨新辅助放化疗治疗局部进展期胰腺癌。
Radiat Oncol. 2012 Mar 2;7:28. doi: 10.1186/1748-717X-7-28.
2
Long-term outcomes of neoadjuvant chemotherapy before chemoradiation for locally advanced pancreatic cancer.新辅助化疗联合放化疗治疗局部进展期胰腺癌的长期疗效。
Cancer. 2012 Jun 15;118(12):3026-35. doi: 10.1002/cncr.26633. Epub 2011 Oct 21.
3
Survival and quality of life of patients with resected pancreatic adenocarcinoma treated with adjuvant interferon-based chemoradiation: a phase II trial.接受辅助基于干扰素的放化疗的胰腺腺癌切除患者的生存和生活质量:一项 II 期试验。
Ann Surg Oncol. 2011 Dec;18(13):3615-22. doi: 10.1245/s10434-011-1847-4. Epub 2011 Jun 24.
4
Neoadjuvant GTX chemotherapy and IMRT-based chemoradiation for borderline resectable pancreatic cancer.新辅助 GTX 化疗和基于调强放疗的放化疗治疗局部进展期胰腺癌。
J Surg Oncol. 2011 Aug 1;104(2):155-61. doi: 10.1002/jso.21954. Epub 2011 Apr 25.
5
Borderline resectable pancreatic cancer: definitions and the importance of multimodality therapy.可切除边缘的胰腺癌:定义及多模式治疗的重要性
Ann Surg Oncol. 2010 Nov;17(11):2803-5. doi: 10.1245/s10434-010-1285-8.
6
Multicenter phase II trial of adjuvant therapy for resected pancreatic cancer using cisplatin, 5-fluorouracil, and interferon-alfa-2b-based chemoradiation: ACOSOG Trial Z05031.多中心 II 期临床试验:使用顺铂、5-氟尿嘧啶和干扰素-α-2b 的基于放化疗的辅助治疗可切除胰腺癌:ACOSOG 试验 Z05031。
Ann Oncol. 2011 Feb;22(2):348-54. doi: 10.1093/annonc/mdq384. Epub 2010 Jul 29.
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Cancer statistics, 2010.癌症统计数据,2010 年。
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7.
8
Pretreatment assessment of resectable and borderline resectable pancreatic cancer: expert consensus statement.可切除及边缘可切除胰腺癌的术前评估:专家共识声明
Ann Surg Oncol. 2009 Jul;16(7):1727-33. doi: 10.1245/s10434-009-0408-6. Epub 2009 Apr 24.
9
Combined modality treatment of resectable and borderline resectable pancreas cancer: expert consensus statement.可切除及边缘可切除胰腺癌的综合治疗:专家共识声明
Ann Surg Oncol. 2009 Jul;16(7):1751-6. doi: 10.1245/s10434-009-0413-9. Epub 2009 Apr 24.
10
Preoperative gemcitabine and cisplatin followed by gemcitabine-based chemoradiation for resectable adenocarcinoma of the pancreatic head.术前使用吉西他滨和顺铂,随后对可切除的胰头腺癌进行以吉西他滨为基础的放化疗。
J Clin Oncol. 2008 Jul 20;26(21):3487-95. doi: 10.1200/JCO.2007.15.8642.

新辅助放化疗很少能使局部晚期胰腺癌在影像学上显示肿瘤退缩。

Neoadjuvant chemoradiotherapy for locally advanced pancreas cancer rarely leads to radiological evidence of tumour regression.

机构信息

Department of Surgery, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

HPB (Oxford). 2013 Sep;15(9):661-7. doi: 10.1111/hpb.12015. Epub 2012 Dec 2.

DOI:10.1111/hpb.12015
PMID:23458352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3948532/
Abstract

BACKGROUND

Neo-adjuvant chemo-radiotherapy has been proposed to improve resectability of locally-advanced pancreatic cancer (LAPC). However, the ability of neo-adjuvant therapy to induce radiological tumour regression has not been reported.

METHODS

Pre- and post-treatment computed tomography (CT) scans of patients undergoing neo-adjuvant chemo-radiotherapy for LAPC were reviewed. LAPC was sub-classified into borderline resectable disease [≤ 180° involvement of the superior mesenteric artery (SMA); short-segment encasement/abutment of the common hepatic artery; or tumour-associated deformity, abutment or short-segment occlusion of the superior mesenteric vein (SMV)/ portal vein (PV) that was amenable to vascular resection and reconstruction] and locally advanced un-resectable pancreatic cancer (vascular involvement more than that described for borderline resectable pancreatic cancer). The radiological response and surgical resection rates were assessed.

RESULTS

Sixteen patients received neo-adjuvant therapy for LAPC during 2005-2008. Regression of major vascular involvement, i.e. un-encasement or regression of abutment of any involved vessels was not observed in any patient. Pre- and post-treatment tumour densities were not statistically different. Fifty per cent of patients with borderline resectable disease and none of the patients with locally advanced un-resectable pancreatic cancer eventually underwent surgical resection.

CONCLUSION

Neo-adjuvant treatment does not induce radiological tumour regression of LAPC with major vascular involvement. Patient selection for neo-adjuvant trial enrollment should remain focused on borderline disease which may have a potential for surgical resection.

摘要

背景

新辅助化疗放疗被提议用于提高局部晚期胰腺癌(LAPC)的可切除性。然而,新辅助治疗诱导肿瘤退缩的能力尚未被报道。

方法

对接受新辅助化疗放疗的 LAPC 患者的治疗前后计算机断层扫描(CT)进行了回顾性研究。将 LAPC 分为可边界切除疾病[≤ 180°肠系膜上动脉(SMA)受累;肝总动脉短段包绕/毗邻;或肿瘤相关变形、毗邻或短段闭塞肠系膜上静脉(SMV)/门静脉(PV),可进行血管切除和重建]和局部晚期不可切除的胰腺癌(血管受累程度超过可边界切除胰腺癌)。评估了影像学反应和手术切除率。

结果

2005 年至 2008 年期间,有 16 名患者接受了新辅助治疗 LAPC。在任何患者中,主要血管受累的退缩,即任何受累血管的无包绕或退缩都没有观察到。治疗前后肿瘤密度无统计学差异。50%的边界可切除疾病患者和局部晚期不可切除胰腺癌患者均未进行手术切除。

结论

新辅助治疗不能诱导 LAPC 伴有主要血管受累的影像学肿瘤退缩。新辅助试验入组患者的选择应继续集中在可能具有手术切除潜力的边界疾病上。