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Phase II Chemotherapy with Ftorafur for Metastatic Adenocarcinoma of the Colon and Rectum
Basic Trial Information
Objectives I. Determine the efficacy of ftorafur in disseminated adenocarcinoma of the colon and rectum. Entry Criteria Disease Characteristics: See General Eligibility Criteria Patient Characteristics: See General Eligibility Criteria General Eligibility Criteria: Patients with biopsy-proven adenocarcinoma of the colon or rectum with measurable recurrent or disseminated disease, with a life expectancy of at least 8 weeks. Expected Enrollment Protocol closed 09/77. Protocol terminated 02/78. Outline Nonrandomized study. Separately enter patients with and patients without liver metastases. Arm I: Single-agent Chemotherapy. Ftorafur, NSC-148958.Published Results Buroker T, Padilla F, Groppe C, et al.: Phase II evaluation of ftorafur in previously untreated colorectal cancer: a Southwest Oncology Group study. Cancer 44(1): 48-51, 1979. Trial Lead Organizations Southwest Oncology Group
Note: The purpose of most clinical trials listed in this database is to test new cancer treatments, or new methods of diagnosing, screening, or preventing cancer. Because all potentially harmful side effects are not known before a trial is conducted, dose and schedule modifications may be required for participants if they develop side effects from the treatment or test. The therapy or test described in this clinical trial is intended for use by clinical oncologists in carefully structured settings, and may not prove to be more effective than standard treatment. A responsible investigator associated with this clinical trial should be consulted before using this protocol. |
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