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Gemcitabine and cisplatin for patients with metastatic or recurrent esophageal carcinoma: a Southwest Oncology Group Study
Experimental data, both in vivo and in vitro, suggest that the combination of gemcitabine and cisplatin acts synergistically. Within the Southwest Oncology Group, we designed a Phase II trial to test this chemotherapy combination for patients with esophageal cancer. Patients with metastatic or recur...
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Published in: | Investigational new drugs 2004-01, Vol.22 (1), p.91-97 |
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creator | Urba, Susan G Chansky, Kari VanVeldhuizen, Peter J Pluenneke, Robert E Benedetti, Jacqueline K Macdonald, John S Abbruzzese, James L |
description | Experimental data, both in vivo and in vitro, suggest that the combination of gemcitabine and cisplatin acts synergistically. Within the Southwest Oncology Group, we designed a Phase II trial to test this chemotherapy combination for patients with esophageal cancer.
Patients with metastatic or recurrent esophageal cancer were treated with gemcitabine 1000 mg/m(2) on days 1, 8, and 15, and cisplatin 100 mg/m(2) on day 15. Cycles were repeated every 28 days. The statistical endpoint was overall survival.
Sixty-four eligible patients were accrued from 37 institutions. Twenty-six percent of patients had prior chemotherapy. The treatment was generally well-tolerated, with the most common toxicity being neutropenia in 31% of patients. All 64 patients have died. Survival at 3 months was 81%, and at 1 year was 20%. Median survival was 7.3 months.
This regimen is tolerable palliative option for patients with metastatic esophageal cancer. |
doi_str_mv | 10.1023/B:DRUG.0000006179.20974.af |
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Patients with metastatic or recurrent esophageal cancer were treated with gemcitabine 1000 mg/m(2) on days 1, 8, and 15, and cisplatin 100 mg/m(2) on day 15. Cycles were repeated every 28 days. The statistical endpoint was overall survival.
Sixty-four eligible patients were accrued from 37 institutions. Twenty-six percent of patients had prior chemotherapy. The treatment was generally well-tolerated, with the most common toxicity being neutropenia in 31% of patients. All 64 patients have died. Survival at 3 months was 81%, and at 1 year was 20%. Median survival was 7.3 months.
This regimen is tolerable palliative option for patients with metastatic esophageal cancer.</description><identifier>ISSN: 0167-6997</identifier><identifier>EISSN: 1573-0646</identifier><identifier>DOI: 10.1023/B:DRUG.0000006179.20974.af</identifier><identifier>PMID: 14707499</identifier><identifier>CODEN: INNDDK</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Adenocarcinoma - drug therapy ; Adenocarcinoma - mortality ; Adenocarcinoma - secondary ; Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Cancer therapies ; Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - secondary ; Chemotherapy ; Cisplatin - administration & dosage ; Creatinine ; Deoxycytidine - administration & dosage ; Deoxycytidine - analogs & derivatives ; Disease ; Esophageal cancer ; Esophageal Neoplasms - drug therapy ; Esophageal Neoplasms - mortality ; Esophageal Neoplasms - pathology ; Female ; Granulocytes ; Humans ; Kinases ; Male ; Medical prognosis ; Metastasis ; Middle Aged ; Neoplasm Recurrence, Local ; Oncology ; Patients ; Radiation ; Response rates ; Survival Rate ; Toxicity</subject><ispartof>Investigational new drugs, 2004-01, Vol.22 (1), p.91-97</ispartof><rights>Copyright Kluwer Academic Publishers Jan 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-25e2703b793e101d43720c5f83c28429baa366c2075172d56220b307497d70013</citedby><cites>FETCH-LOGICAL-c394t-25e2703b793e101d43720c5f83c28429baa366c2075172d56220b307497d70013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/216496509/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/216496509?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,11688,27924,27925,36060,44363,74895</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14707499$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Urba, Susan G</creatorcontrib><creatorcontrib>Chansky, Kari</creatorcontrib><creatorcontrib>VanVeldhuizen, Peter J</creatorcontrib><creatorcontrib>Pluenneke, Robert E</creatorcontrib><creatorcontrib>Benedetti, Jacqueline K</creatorcontrib><creatorcontrib>Macdonald, John S</creatorcontrib><creatorcontrib>Abbruzzese, James L</creatorcontrib><creatorcontrib>Southwest Oncology Group Study</creatorcontrib><title>Gemcitabine and cisplatin for patients with metastatic or recurrent esophageal carcinoma: a Southwest Oncology Group Study</title><title>Investigational new drugs</title><addtitle>Invest New Drugs</addtitle><description>Experimental data, both in vivo and in vitro, suggest that the combination of gemcitabine and cisplatin acts synergistically. Within the Southwest Oncology Group, we designed a Phase II trial to test this chemotherapy combination for patients with esophageal cancer.
Patients with metastatic or recurrent esophageal cancer were treated with gemcitabine 1000 mg/m(2) on days 1, 8, and 15, and cisplatin 100 mg/m(2) on day 15. Cycles were repeated every 28 days. The statistical endpoint was overall survival.
Sixty-four eligible patients were accrued from 37 institutions. Twenty-six percent of patients had prior chemotherapy. The treatment was generally well-tolerated, with the most common toxicity being neutropenia in 31% of patients. All 64 patients have died. Survival at 3 months was 81%, and at 1 year was 20%. Median survival was 7.3 months.
This regimen is tolerable palliative option for patients with metastatic esophageal cancer.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - secondary</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cancer therapies</subject><subject>Carcinoma, Squamous Cell - drug therapy</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - secondary</subject><subject>Chemotherapy</subject><subject>Cisplatin - administration & dosage</subject><subject>Creatinine</subject><subject>Deoxycytidine - administration & dosage</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Disease</subject><subject>Esophageal cancer</subject><subject>Esophageal Neoplasms - drug therapy</subject><subject>Esophageal Neoplasms - mortality</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Female</subject><subject>Granulocytes</subject><subject>Humans</subject><subject>Kinases</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local</subject><subject>Oncology</subject><subject>Patients</subject><subject>Radiation</subject><subject>Response rates</subject><subject>Survival 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Drugs</addtitle><date>2004-01</date><risdate>2004</risdate><volume>22</volume><issue>1</issue><spage>91</spage><epage>97</epage><pages>91-97</pages><issn>0167-6997</issn><eissn>1573-0646</eissn><coden>INNDDK</coden><abstract>Experimental data, both in vivo and in vitro, suggest that the combination of gemcitabine and cisplatin acts synergistically. Within the Southwest Oncology Group, we designed a Phase II trial to test this chemotherapy combination for patients with esophageal cancer.
Patients with metastatic or recurrent esophageal cancer were treated with gemcitabine 1000 mg/m(2) on days 1, 8, and 15, and cisplatin 100 mg/m(2) on day 15. Cycles were repeated every 28 days. The statistical endpoint was overall survival.
Sixty-four eligible patients were accrued from 37 institutions. Twenty-six percent of patients had prior chemotherapy. The treatment was generally well-tolerated, with the most common toxicity being neutropenia in 31% of patients. All 64 patients have died. Survival at 3 months was 81%, and at 1 year was 20%. Median survival was 7.3 months.
This regimen is tolerable palliative option for patients with metastatic esophageal cancer.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>14707499</pmid><doi>10.1023/B:DRUG.0000006179.20974.af</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - drug therapy Adenocarcinoma - mortality Adenocarcinoma - secondary Adult Aged Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Cancer therapies Carcinoma, Squamous Cell - drug therapy Carcinoma, Squamous Cell - mortality Carcinoma, Squamous Cell - secondary Chemotherapy Cisplatin - administration & dosage Creatinine Deoxycytidine - administration & dosage Deoxycytidine - analogs & derivatives Disease Esophageal cancer Esophageal Neoplasms - drug therapy Esophageal Neoplasms - mortality Esophageal Neoplasms - pathology Female Granulocytes Humans Kinases Male Medical prognosis Metastasis Middle Aged Neoplasm Recurrence, Local Oncology Patients Radiation Response rates Survival Rate Toxicity |
title | Gemcitabine and cisplatin for patients with metastatic or recurrent esophageal carcinoma: a Southwest Oncology Group Study |
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