Phase II trial of 5-fluorouracil, folinic acid and recombinant α-2a-interferon in patients with advanced colorectal cancer
A clinical trial regimen modulating 5-fluorouracil (5-FU) with both folinic acid (FA) and recombinant α-2a-interferon (rα.-2a-IFN) was noted to have a response rate of 54% and median survival of 16.3 months (Grem ef a/., J Clin Oncol 1993, 111737–45). Reported herein is a phase II trial performed to...
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Veröffentlicht in: | Anti-cancer drugs 1999-07, Vol.10 (6), p.519-524 |
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creator | Ravandi, Farhad Rytting, Michael E Osmon, Carlos Braud, Edward L Roach, Ralph W Edwards, Kimberly Winn, Rodger Abbruzzese, James L Pazdur, Richard |
description | A clinical trial regimen modulating 5-fluorouracil (5-FU) with both folinic acid (FA) and recombinant α-2a-interferon (rα.-2a-IFN) was noted to have a response rate of 54% and median survival of 16.3 months (Grem ef a/., J Clin Oncol 1993, 111737–45). Reported herein is a phase II trial performed to further examine this regimen in metastatic colorectal cancer. Fifty-one patients with histologically proven, measurable advanced colorectal cancer with no prior therapy for metastatic disease were enrolled. rα-2a-IFN, 5 MIU/m/day was given s.c. on days 1–7. FA, 500 mg/m/day, and 5-FU, 370 mg/m/day, were given i.v. on days 2–6. Cycles were repeated at 3 week intervals. Three complete and 12 partial responses were observed for an overall response rate of 29% (95% confidence interval18–45%). The median time to treatment failure and median survival were 4.6 and 15.5 months, respectively. Dose-limiting toxicities encountered were gastrointestinal, and included diarrhea, stomatitis, nausea and vomiting. These results do not support the concept of using concurrent rα-2a-IFN and FA as biochemical modulators of 5-FU. We observed increased toxicity and similar efficacy compared to using either modulator separately with 5-FU. |
doi_str_mv | 10.1097/00001813-199907000-00002 |
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Reported herein is a phase II trial performed to further examine this regimen in metastatic colorectal cancer. Fifty-one patients with histologically proven, measurable advanced colorectal cancer with no prior therapy for metastatic disease were enrolled. rα-2a-IFN, 5 MIU/m/day was given s.c. on days 1–7. FA, 500 mg/m/day, and 5-FU, 370 mg/m/day, were given i.v. on days 2–6. Cycles were repeated at 3 week intervals. Three complete and 12 partial responses were observed for an overall response rate of 29% (95% confidence interval18–45%). The median time to treatment failure and median survival were 4.6 and 15.5 months, respectively. Dose-limiting toxicities encountered were gastrointestinal, and included diarrhea, stomatitis, nausea and vomiting. These results do not support the concept of using concurrent rα-2a-IFN and FA as biochemical modulators of 5-FU. We observed increased toxicity and similar efficacy compared to using either modulator separately with 5-FU.</description><identifier>ISSN: 0959-4973</identifier><identifier>EISSN: 1473-5741</identifier><identifier>DOI: 10.1097/00001813-199907000-00002</identifier><language>eng</language><publisher>Lippincott Williams & Wilkins, Inc</publisher><ispartof>Anti-cancer drugs, 1999-07, Vol.10 (6), p.519-524</ispartof><rights>1999 Lippincott Williams & Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2172-f6b6a8d74dac8cb711f8c4a2003b883aa6ffc01fbbd4e4f5a4a7efdb79b54bd43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Ravandi, Farhad</creatorcontrib><creatorcontrib>Rytting, Michael E</creatorcontrib><creatorcontrib>Osmon, Carlos</creatorcontrib><creatorcontrib>Braud, Edward L</creatorcontrib><creatorcontrib>Roach, Ralph W</creatorcontrib><creatorcontrib>Edwards, Kimberly</creatorcontrib><creatorcontrib>Winn, Rodger</creatorcontrib><creatorcontrib>Abbruzzese, James L</creatorcontrib><creatorcontrib>Pazdur, Richard</creatorcontrib><title>Phase II trial of 5-fluorouracil, folinic acid and recombinant α-2a-interferon in patients with advanced colorectal cancer</title><title>Anti-cancer drugs</title><description>A clinical trial regimen modulating 5-fluorouracil (5-FU) with both folinic acid (FA) and recombinant α-2a-interferon (rα.-2a-IFN) was noted to have a response rate of 54% and median survival of 16.3 months (Grem ef a/., J Clin Oncol 1993, 111737–45). Reported herein is a phase II trial performed to further examine this regimen in metastatic colorectal cancer. Fifty-one patients with histologically proven, measurable advanced colorectal cancer with no prior therapy for metastatic disease were enrolled. rα-2a-IFN, 5 MIU/m/day was given s.c. on days 1–7. FA, 500 mg/m/day, and 5-FU, 370 mg/m/day, were given i.v. on days 2–6. Cycles were repeated at 3 week intervals. Three complete and 12 partial responses were observed for an overall response rate of 29% (95% confidence interval18–45%). The median time to treatment failure and median survival were 4.6 and 15.5 months, respectively. Dose-limiting toxicities encountered were gastrointestinal, and included diarrhea, stomatitis, nausea and vomiting. These results do not support the concept of using concurrent rα-2a-IFN and FA as biochemical modulators of 5-FU. 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Reported herein is a phase II trial performed to further examine this regimen in metastatic colorectal cancer. Fifty-one patients with histologically proven, measurable advanced colorectal cancer with no prior therapy for metastatic disease were enrolled. rα-2a-IFN, 5 MIU/m/day was given s.c. on days 1–7. FA, 500 mg/m/day, and 5-FU, 370 mg/m/day, were given i.v. on days 2–6. Cycles were repeated at 3 week intervals. Three complete and 12 partial responses were observed for an overall response rate of 29% (95% confidence interval18–45%). The median time to treatment failure and median survival were 4.6 and 15.5 months, respectively. Dose-limiting toxicities encountered were gastrointestinal, and included diarrhea, stomatitis, nausea and vomiting. These results do not support the concept of using concurrent rα-2a-IFN and FA as biochemical modulators of 5-FU. We observed increased toxicity and similar efficacy compared to using either modulator separately with 5-FU.</abstract><pub>Lippincott Williams & Wilkins, Inc</pub><doi>10.1097/00001813-199907000-00002</doi><tpages>6</tpages></addata></record> |
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title | Phase II trial of 5-fluorouracil, folinic acid and recombinant α-2a-interferon in patients with advanced colorectal cancer |
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