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Current topics of S-1 at the 74th Japanese Gastric Cancer Congress.

作者信息

Sasaki Tsuneo

机构信息

Department of Chemotherapy, Tokyo Metropolitan Komagome Hospital, 3-18-22 Honkomagome, Bunkyo-ku, Tokyo 113-5677, Japan.

出版信息

Gastric Cancer. 2003;6 Suppl 1:9-12. doi: 10.1007/s10120-003-0229-4.

DOI:10.1007/s10120-003-0229-4
PMID:12775013
Abstract

S-1 (TS-1)-related studies presented at the 74th Japanese Gastric Cancer Congress are reviewed. Of the papers presented at this conference, 35 were related to S-1. In the panel discussion on the therapeutic significance of oral fluoropyrimidines in gastric cancer, 9 papers were related to S-1 (sensitivities to oral fluoropyrimidines, 2 papers; clinical results of treatment with S-1, 5 papers; and combination therapy with S-1, 2 papers). In the general presentations, there were 26 papers on S-1 related-subjects (clinical studies or clinical practice of S-1, 12 papers; case reports, 3 papers; basic studies on animal models of peritoneal metastasis, 2 papers; and combination therapy with S-1, 9 papers). Several studies showed that S-1 was basically as effective against tumors in postmarketing surveillance in clinical practice as in phase II studies at the time of its development, including a report of a patient with complete response to S-1. Some reports suggested the possibility of using S-1 in neoadjuvant chemotherapy and postoperative adjuvant chemotherapy. The usefulness of S-1 in combination chemotherapy was also suggested in several reports. These results indicate that S-1 is a key drug that can be used in first-line treatment of gastric cancer. It will be necessary to accumulate evidence based on data from clinical trials and clinical applications in the future.

摘要

相似文献

1
Current topics of S-1 at the 74th Japanese Gastric Cancer Congress.
Gastric Cancer. 2003;6 Suppl 1:9-12. doi: 10.1007/s10120-003-0229-4.
2
S-1 in gastric cancer: a comprehensive review.胃癌中的S-1:全面综述
Gastric Cancer. 2003;6 Suppl 1:2-8. doi: 10.1007/s10120-003-0232-9.
3
Oral treatment for gastric cancer: new choices, better choices?胃癌的口服治疗:新选择,更好的选择?
Lancet Oncol. 2008 Mar;9(3):188-9. doi: 10.1016/S1470-2045(08)70042-1.
4
Phase II study of S-1, a novel oral derivative of 5-fluorouracil, in advanced gastric cancer. For the S-1 Cooperative Gastric Cancer Study Group.新型口服5-氟尿嘧啶衍生物S-1治疗晚期胃癌的II期研究。S-1协作性胃癌研究组
Oncology. 2000 Apr;58(3):191-7. doi: 10.1159/000012099.
5
Oral fluoropyrimidines in colorectal cancer.结直肠癌中的口服氟嘧啶类药物。
Semin Oncol. 2000 Oct;27(5 Suppl 10):91-5.
6
Feasibility study of adjuvant chemotherapy with S-1 (TS-1; tegafur, gimeracil, oteracil potassium) for gastric cancer.S-1(替吉奥;替加氟、吉美嘧啶、奥替拉西钾)用于胃癌辅助化疗的可行性研究。
Gastric Cancer. 2004;7(2):104-9. doi: 10.1007/s10120-004-0278-3.
7
Other fluorinated pyrimidines in the treatment of solid tumors.其他氟嘧啶类药物在实体瘤治疗中的应用。
Oncology (Williston Park). 2001 Jan;15(1 Suppl 2):65-8.
8
[Tegafur/gimeracil/oteracil (Teysuno), by oral administration].替吉奥(替加氟/吉美嘧啶/奥替拉西钾),口服给药。
J Pharm Belg. 2013 Dec(4):35-6.
9
Just when you thought the fluorouracil debate was over: S-1 and gastric cancer.正当你以为氟尿嘧啶的争论已经结束时:S-1与胃癌。
J Clin Oncol. 2005 Oct 1;23(28):6826-8. doi: 10.1200/JCO.2005.06.006. Epub 2005 Sep 6.
10
[A case of remnant gastric cancer responding to neoadjuvant TS-1 therapy].
Gan To Kagaku Ryoho. 2001 Oct;28(10):1449-52.

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本文引用的文献

1
Possible regulation of 5-fluorouracil-induced neuro- and oral toxicities by two biochemical modulators consisting of S-1, a new oral formulation of 5-fluorouracil.由两种生化调节剂(包括5-氟尿嘧啶的新型口服制剂S-1)对5-氟尿嘧啶诱导的神经毒性和口腔毒性的可能调节作用。
Anticancer Res. 2001 May-Jun;21(3B):1705-12.
2
Phase II study of S-1, a novel oral derivative of 5-fluorouracil, in advanced gastric cancer. For the S-1 Cooperative Gastric Cancer Study Group.新型口服5-氟尿嘧啶衍生物S-1治疗晚期胃癌的II期研究。S-1协作性胃癌研究组
Oncology. 2000 Apr;58(3):191-7. doi: 10.1159/000012099.
3
Late phase II study of novel oral fluoropyrimidine anticancer drug S-1 (1 M tegafur-0.4 M gimestat-1 M otastat potassium) in advanced gastric cancer patients.
S-1作为新辅助化疗给药2周后晚期胃癌出现组织学完全缓解。
Gastric Cancer. 2006;9(2):136-9. doi: 10.1007/s10120-005-0358-z.
新型口服氟嘧啶类抗癌药物S-1(1M替加氟-0.4M吉美嘧啶-1M奥替拉西钾)用于晚期胃癌患者的II期后期研究。
Eur J Cancer. 1998 Oct;34(11):1715-20. doi: 10.1016/s0959-8049(98)00211-1.
4
Preclinical antitumor efficacy of S-1: a new oral formulation of 5-fluorouracil on human tumor xenografts.S-1的临床前抗肿瘤疗效:一种新型口服5-氟尿嘧啶制剂对人肿瘤异种移植模型的作用
Int J Oncol. 1998 Oct;13(4):693-8. doi: 10.3892/ijo.13.4.693.
5
Development of a novel form of an oral 5-fluorouracil derivative (S-1) directed to the potentiation of the tumor selective cytotoxicity of 5-fluorouracil by two biochemical modulators.一种新型口服5-氟尿嘧啶衍生物(S-1)的研发,该衍生物通过两种生化调节剂增强5-氟尿嘧啶的肿瘤选择性细胞毒性。
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6
Antitumor activity of 1 M tegafur-0.4 M 5-chloro-2,4-dihydroxypyridine-1 M potassium oxonate (S-1) against human colon carcinoma orthotopically implanted into nude rats.1 M替加氟-0.4 M 5-氯-2,4-二羟基吡啶-1 M奥替拉西钾(S-1)对原位植入裸鼠的人结肠癌的抗肿瘤活性。
Cancer Res. 1996 Jun 1;56(11):2602-6.
7
Inhibition by oxonic acid of gastrointestinal toxicity of 5-fluorouracil without loss of its antitumor activity in rats.氧嗪酸对大鼠5-氟尿嘧啶胃肠道毒性的抑制作用,且不丧失其抗肿瘤活性。
Cancer Res. 1993 Sep 1;53(17):4004-9.