TY - JOUR
T1 - Status of treatment for advanced gastric carcinoma
AU - Tsai, James Y.
AU - Safran, Howard
N1 - Funding Information:
Dr. Safran has received grant or research support from Eli Lilly and Genentech corporations.
PY - 2003/5
Y1 - 2003/5
N2 - Gastric cancer is the second most common cause of cancer death worldwide. Advanced gastric cancer is incurable. The most widely investigated single-agent chemotherapy is 5-fluorouracil (5-FU), with partial response rates up to 20%. Pilot phase II studies investigating combinations of 5-FU, anthracyclines, mitomycin, methotrexate, and platinums achieved higher response rates; however, the response rates declined in subsequent larger trials. Furthermore, toxicity was substantially higher in confirmatory trials, emphasizing the need to develop well-tolerated regimens prior to multi-institutional testing. Although phase III studies of combination regimens have not achieved a clear worldwide standard, the regimen of epirubicin, cisplatin, and continuous-infusion S-FU achieved a survival benefit, possibly through the increased activity of infusional S-FU combined with cisplatin. The taxanes, irinotecan and oxaliplatin, have recently shown important activity in gastric cancer. Patient accrual to a phase III trial comparing a docetaxel-based combination regimen with the regimen of cisplatin and 5-FU has completed accrual. Whether patients with adenocarcinomas of the proximal stomach and gastroesophageal junction will have the same response rates to these new agents as did patients with classical body and distal gastric cancers is unknown. It is anticipated that the development of these active new agents will ultimately improve survival for patients with advanced gastric cancer. Copyright © 2003 by Current Science Inc.
AB - Gastric cancer is the second most common cause of cancer death worldwide. Advanced gastric cancer is incurable. The most widely investigated single-agent chemotherapy is 5-fluorouracil (5-FU), with partial response rates up to 20%. Pilot phase II studies investigating combinations of 5-FU, anthracyclines, mitomycin, methotrexate, and platinums achieved higher response rates; however, the response rates declined in subsequent larger trials. Furthermore, toxicity was substantially higher in confirmatory trials, emphasizing the need to develop well-tolerated regimens prior to multi-institutional testing. Although phase III studies of combination regimens have not achieved a clear worldwide standard, the regimen of epirubicin, cisplatin, and continuous-infusion S-FU achieved a survival benefit, possibly through the increased activity of infusional S-FU combined with cisplatin. The taxanes, irinotecan and oxaliplatin, have recently shown important activity in gastric cancer. Patient accrual to a phase III trial comparing a docetaxel-based combination regimen with the regimen of cisplatin and 5-FU has completed accrual. Whether patients with adenocarcinomas of the proximal stomach and gastroesophageal junction will have the same response rates to these new agents as did patients with classical body and distal gastric cancers is unknown. It is anticipated that the development of these active new agents will ultimately improve survival for patients with advanced gastric cancer. Copyright © 2003 by Current Science Inc.
KW - Stomach Neoplasms/drug therapy
KW - United States/epidemiology
KW - Humans
KW - Esophagogastric Junction/pathology
KW - Disease Management
KW - Adenocarcinoma/drug therapy
KW - Antinematodal Agents/therapeutic use
KW - Incidence
UR - http://www.scopus.com/inward/record.url?scp=0043237742&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0043237742&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/374575ae-ddcf-3442-bbd1-235bf6bc7465/
U2 - 10.1007/s11912-003-0112-9
DO - 10.1007/s11912-003-0112-9
M3 - Article
C2 - 12667418
SN - 1523-3790
VL - 5
SP - 210
EP - 218
JO - Current Oncology Reports
JF - Current Oncology Reports
IS - 3
ER -