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胃癌新辅助治疗后的手术问题。

Surgical issues after neoadjuvant treatment for gastric cancer.

机构信息

1st Surgical Division, Department of Surgery, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

Eur Rev Med Pharmacol Sci. 2010 Apr;14(4):315-9.

PMID:20496541
Abstract

Gastric carcinoma is one of the most frequent malignancies in the world and its clinical behavior depends on the metastatic potential of the tumour. Particularly, lymphatic metastasis is one of the main predictor of tumour recurrence and survival and current pathologic staging systems reflect the concept that lymphatic spread is the most relevant prognostic factor in patients resected with curative intent. This is deducted by the observation that two thirds of gastric cancers in the western world present at an advanced stage, with nearly 85% of tumors accompanied by lymph node metastasis at diagnosis. To date most therapeutic efforts are directed toward individualization of therapeutic protocols, tailoring the extent of resection integrated by the administration of preoperative and postoperative treatment. The goal of such strategies is to improve prognosis towards the achievement of a curative resection (R0-resection) with minimal morbidity and mortality, with better postoperative quality of life. A brief review of literature about preoperative therapy for gastric carcinoma will be herein illustrated. The rationale and the general drawbacks of preoperative treatments will be both discussed in order to demonstrate its value in terms of safety and efficacy.

摘要

胃癌是世界上最常见的恶性肿瘤之一,其临床行为取决于肿瘤的转移潜能。特别是,淋巴转移是肿瘤复发和生存的主要预测因素之一,目前的病理分期系统反映了这样一种概念,即对于有治愈意图进行切除的患者,淋巴扩散是最相关的预后因素。这可以从观察到的结果中推断出来,即在西方世界,三分之二的胃癌处于晚期,近 85%的肿瘤在诊断时伴有淋巴结转移。迄今为止,大多数治疗努力都集中在治疗方案的个体化上,通过术前和术后治疗来调整切除的范围。这些策略的目标是改善预后,实现根治性切除(R0 切除),同时最大限度地降低发病率和死亡率,并提高术后生活质量。本文将简要综述胃癌的术前治疗。将讨论术前治疗的原理和一般缺点,以证明其在安全性和疗效方面的价值。

相似文献

1
Surgical issues after neoadjuvant treatment for gastric cancer.胃癌新辅助治疗后的手术问题。
Eur Rev Med Pharmacol Sci. 2010 Apr;14(4):315-9.
2
Adjuvant and neoadjuvant therapy for gastric cancer.胃癌的辅助治疗和新辅助治疗。
Semin Oncol. 1996 Jun;23(3):379-89.
3
Current status and future perspectives in gastric cancer management.胃癌治疗的现状与未来展望
Cancer Treat Rev. 2000 Aug;26(4):243-55. doi: 10.1053/ctrv.2000.0164.
4
[The value of adjuvant and neoadjuvant chemotherapy in treatment of stomach carcinoma].[辅助和新辅助化疗在胃癌治疗中的价值]
Wien Klin Wochenschr. 1996;108(16):496-504.
5
R0 resection in the treatment of gastric cancer: room for improvement.胃癌的 R0 切除术:仍有改进空间。
World J Gastroenterol. 2010 Jul 21;16(27):3358-70. doi: 10.3748/wjg.v16.i27.3358.
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Outcome of patients with known metastatic gastric cancer undergoing resection with therapeutic intent.已知有转移性胃癌且接受根治性切除手术患者的治疗结果。
Ann Surg Oncol. 2007 Feb;14(2):365-72. doi: 10.1245/s10434-006-9059-z.
7
Prognostic indicators in locally advanced gastric cancer (LAGC) treated with preoperative chemotherapy and D2-gastrectomy.术前化疗联合D2胃切除术治疗局部进展期胃癌(LAGC)的预后指标
J Surg Oncol. 2005 Mar 15;89(4):227-36; discussion 237-8. doi: 10.1002/jso.20207.
8
[Utilization of multimodal therapy concepts in stomach carcinoma in Germany].[德国胃癌多模式治疗理念的应用]
Zentralbl Chir. 2000;125(4):341-7.
9
[Stomach carcinoma. Optimizing therapy by neoadjuvant or adjuvant therapy?].[胃癌。通过新辅助治疗或辅助治疗优化治疗方案?]
Zentralbl Chir. 1999;124(5):387-93.
10
[Preoperative (neoadjuvant) chemotherapy in multimodality treatment concept of stomach carcinoma].[胃癌多模式治疗理念中的术前(新辅助)化疗]
Zentralbl Chir. 1995;120(2):128-34.

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Molecules. 2018 Jan 30;23(2):279. doi: 10.3390/molecules23020279.
2
Clinicopathologic Implications of Eukaryotic Initiation Factor 3f and Her-2/neu Expression in Gastric Cancer.真核生物起始因子3f和Her-2/neu在胃癌中的表达及其临床病理意义
Clin Transl Sci. 2015 Aug;8(4):320-5. doi: 10.1111/cts.12263. Epub 2015 Feb 14.
3
G-protein coupled receptor 34 knockdown impairs the proliferation and migration of HGC-27 gastric cancer cells in vitro.
G蛋白偶联受体34基因敲低会损害HGC-27胃癌细胞在体外的增殖和迁移能力。
Chin Med J (Engl). 2015 Feb 20;128(4):545-9. doi: 10.4103/0366-6999.151114.
4
Decreased expression of eukaryotic initiation factor 3f is an adverse prognostic factor for stage I-III gastric cancer.真核生物起始因子3f表达降低是I-III期胃癌的不良预后因素。
World J Surg Oncol. 2014 Mar 28;12:72. doi: 10.1186/1477-7819-12-72.
5
Down-regulation of miR-622 in gastric cancer promotes cellular invasion and tumor metastasis by targeting ING1 gene.胃癌中 miR-622 的下调通过靶向 ING1 基因促进细胞侵袭和肿瘤转移。
World J Gastroenterol. 2011 Apr 14;17(14):1895-902. doi: 10.3748/wjg.v17.i14.1895.