Challenge for a better combination with basic evidence

被引:25
作者
Yoshida, Kazuhiro [1 ]
Yamaguchi, Kazuya [1 ]
Osada, Shinji [1 ]
Kawaguchi, Yoshihiro [1 ]
Takahashi, Takao [1 ]
Sakashita, Fumio [1 ]
Tanaka, Yoshihiro [1 ]
机构
[1] Gifu Univ, Dept Surg Oncol, Gifu 5011194, Japan
关键词
gastric cancer; chemotherapy; biochemical modulation; TS; DPD; OPRT;
D O I
10.1007/s10147-008-0793-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
5-Fluorouracil (5-FU) has been the most widely accepted and studied chemotherapeutic agent, and many combination chemotherapeutic regimens have been reported. However, until recently, a standard regimen for metastatic gastric cancer had not been established. The combination of S-1 and cisplatin is a good candidate as a standard first-line regimen for metastatic gastric cancer. On the other hand, interest in biochemical modulation has become wide spread recently. The low level of dihydropyrimidine denhydrogenase (DPD), thymidylate synthase (TS) activities, and a high level of orotate phosphoribosyl-transferase (OPRT) activity enhance the antitumor effect of 5-FU and S-1. Docetaxel is one of the agents that modulate these enzyme expressions and activities. Moreover, the response rate of combination therapy of docetaxel and S-1 for metastatic gastric cancer was 56.3% and median survival time was 14.3 months in a phase II study, showing it to be a good candidate for a new standard regimen for gastric cancer. A phase III collaborative study, START (S-1 and Taxotere for advanced gastric cancer randomized phase III trial), is now under way in Japan and Korea.
引用
收藏
页码:212 / 219
页数:8
相关论文
共 55 条
[1]
Identification of TOR signaling complexes: more TORC for the cell growth engine [J].
Abraham, RT .
CELL, 2002, 111 (01) :9-12
[2]
Aogi K, 1997, INT J CANCER, V72, P295
[3]
BOKU N, 2007, CLIN ONCOL, V25
[4]
CHIN K, 2007, J CLIN ONCOL, V25, pS452
[5]
Weekly docetaxel in combination with capecitabine in patients with metastatic gastric cancer [J].
Chun, JH ;
Kim, HK ;
Lee, JS ;
Choi, JY ;
Hwangbo, B ;
Lee, HG ;
Park, SR ;
Choi, IJ ;
Kim, CG ;
Ryu, KW ;
Kim, YW ;
Lee, JS ;
Bae, JM .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2005, 28 (02) :188-194
[6]
Establishment and characterization of 5-fluorouracil-resistant gastric cancer cells [J].
Chung, YM ;
Park, SH ;
Park, JK ;
Kim, YT ;
Kang, YK ;
Yoo, YD .
CANCER LETTERS, 2000, 159 (01) :95-101
[7]
FLUOROURACIL, DOXORUBICIN, AND MITOMYCIN COMBINATION VERSUS PELF CHEMOTHERAPY IN ADVANCED GASTRIC-CANCER - A PROSPECTIVE RANDOMIZED TRIAL OF THE ITALIAN-ONCOLOGY-GROUP-FOR-CLINICAL-RESEARCH [J].
COCCONI, G ;
BELLA, M ;
ZIRONI, S ;
ALGERI, R ;
DICOSTANZO, F ;
DELISI, V ;
LUPPI, G ;
MAZZOCCHI, B ;
RODINO, C ;
SOLDANI, M ;
GILLI, G ;
FINARDI, C .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (12) :2687-2693
[8]
Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer [J].
Cunningham, D ;
Humblet, Y ;
Siena, S ;
Khayat, D ;
Bleiberg, H ;
Santoro, A ;
Bets, D ;
Mueser, M ;
Harstrick, A ;
Verslype, C ;
Chau, I ;
Van Cutsem, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) :337-345
[9]
Capecitabine and oxaliplatin for advanced esophagogastric cancer [J].
Cunningham, David ;
Starling, Naureen ;
Rao, Sheela ;
Iveson, Timothy ;
Nicolson, Marianne ;
Coxon, Fareeda ;
Middleton, Gary ;
Daniel, Francis ;
Oates, Jacqueline ;
Norman, Andrew Richard .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (01) :36-46
[10]
Pharmacogenomics: Translating functional genomics into rational therapeutics [J].
Evans, WE ;
Relling, MV .
SCIENCE, 1999, 286 (5439) :487-491