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[S-1联合香菇多糖用于不可切除或复发性胃癌患者的研究]

[S-1 combined with lentinan in patients with unresectable or recurrent gastric cancer].

作者信息

Nimura Hiroshi, Mitsumori Norio, Takahashi Naoto, Kashimura Hirotaka, Takayama Sumio, Kashiwagi Hideyuki, Yanaga Katsuhiko

机构信息

Dept of Surgery, The Jikei University School of Medicine, Tokyo, Japan.

出版信息

Gan To Kagaku Ryoho. 2006 Jun;33 Suppl 1:106-9.

PMID:16897983
Abstract

Lentinan (LNT) is a beta-glucan known to have a life-prolonging effect in combination with chemotherapy for patients with unresectable or recurrent gastric cancer. Thus, a multi-center trial of chemo-immunotherapy using S-1 combined with LNT may benefit patients with unresectable or recurrent gastric cancer with acceptable toxicity. With such a regimen, the median survival time in 32 patients was 559 days. Regardless of change to second-line chemotherapy, the mean period of using S-1+LNT for patients with long NC above 400 days was 725 days. In subset analyses, the survival period of the patients with G/L ratio of equal to or less than 2 was significantly better than that of the higher one (p<0.0001). The incidence of hematological toxicity (grade 3 leukopenia and thrombocytopenia) was 6.3% (2/32), and non-hematological toxicity (grade 2 dysgeusia) was 6.3% (2/32), while no grade 4 toxicity was observed. S-1 and LNT combination immunotherapy was carried out safely with high QOL and allowed a prolonged administration. S-1+LNT regimen may prolong NC periods in patients with unresectable or recurrent gastric cancer.

摘要

香菇多糖(LNT)是一种β-葡聚糖,已知其与化疗联合使用时,对不可切除或复发性胃癌患者具有延长生存期的作用。因此,一项使用S-1联合LNT进行化学免疫治疗的多中心试验,可能会使不可切除或复发性胃癌患者受益,且毒性可接受。采用这种治疗方案,32例患者的中位生存时间为559天。无论是否改为二线化疗,NC时间超过400天的患者使用S-1+LNT的平均时间为725天。在亚组分析中,G/L比值等于或小于2的患者生存期明显优于比值较高的患者(p<0.0001)。血液学毒性(3级白细胞减少和血小板减少)的发生率为6.3%(2/32),非血液学毒性(2级味觉障碍)为6.3%(2/32),未观察到4级毒性。S-1与LNT联合免疫治疗安全性高,生活质量良好,且可长期给药。S-1+LNT方案可能会延长不可切除或复发性胃癌患者的NC期。

相似文献

1
[S-1 combined with lentinan in patients with unresectable or recurrent gastric cancer].[S-1联合香菇多糖用于不可切除或复发性胃癌患者的研究]
Gan To Kagaku Ryoho. 2006 Jun;33 Suppl 1:106-9.
2
[Pilot study of TS-1 combined with lentinan in patients with unresectable or recurrent advanced gastric cancer].替吉奥联合香菇多糖治疗不可切除或复发性晚期胃癌的初步研究
Gan To Kagaku Ryoho. 2003 Sep;30(9):1289-96.
3
Lentinan with S-1 and paclitaxel for gastric cancer chemotherapy improve patient quality of life.香菇多糖联合S-1和紫杉醇用于胃癌化疗可提高患者生活质量。
Hepatogastroenterology. 2009 Mar-Apr;56(90):547-50.
4
Phase I/II trial of combination therapy with S-1 and weekly paclitaxel in patients with unresectable or recurrent gastric cancer.S-1与每周一次紫杉醇联合治疗不可切除或复发性胃癌的I/II期试验
Cancer Chemother Pharmacol. 2009 Jan;63(2):267-73. doi: 10.1007/s00280-008-0736-4. Epub 2008 Apr 1.
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[Provision for adverse effect of S-1 containing chemotherapy in patients with advanced digestive cancer--combination with superfine dispersed lentinan].[含S-1化疗对晚期消化道癌患者不良反应的防治——与超微香菇多糖联合应用]
Gan To Kagaku Ryoho. 2010 Mar;37(3):457-62.
6
[TS-1 and lentinan combination immunochemotherapy for advanced or recurrent gastric cancer: a preliminary report].
Gan To Kagaku Ryoho. 2003 Oct;30(11):1791-3.
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[TS-1/CDDP/Lentinan combination chemotherapy for inoperable advanced gastric cancer].[替吉奥/顺铂/香菇多糖联合化疗治疗不可切除的晚期胃癌]
Gan To Kagaku Ryoho. 2004 Nov;31(12):1999-2003.
8
[Clinical results of single therapy with TS-1 for advanced/recurrent gastric cancer].[替吉奥单药治疗晚期/复发性胃癌的临床结果]
Gan To Kagaku Ryoho. 2006 Aug;33(8):1105-10.
9
A multi-institutional prospective study of lentinan in advanced gastric cancer patients with unresectable and recurrent diseases: effect on prolongation of survival and improvement of quality of life. Kanagawa Lentinan Research Group.香菇多糖用于不可切除及复发性晚期胃癌患者的多机构前瞻性研究:对延长生存期及改善生活质量的影响。神奈川香菇多糖研究组。
Hepatogastroenterology. 1999 Jul-Aug;46(28):2662-8.
10
[Clinical trial of non-specific immunotherapy using Lentinan in advanced or recurrent gastric cancer].
Gan To Kagaku Ryoho. 2008 Nov;35(12):2239-43.

引用本文的文献

1
Lentinan prolonged survival in patients with gastric cancer receiving S-1-based chemotherapy.香菇多糖可延长接受基于S-1化疗的胃癌患者的生存期。
World J Clin Oncol. 2011 Oct 10;2(10):339-43. doi: 10.5306/wjco.v2.i10.339.