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Mayo Clinic, Mayo Foundation, Rochester, Minnesota 55901
Thirty-six patients with advanced gastrointestinal carcinoma were treated sequentially with full therapeutic doses of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea followed by 5-fluorouracil. 5-Fluorouracil could be safely administered at 6 weeks although patients still demonstrated peripheral hematological depression secondary to the earlier 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea therapy. Of the 36 patients, 8.3% showed an objective response to 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea therapy. Of the 21 patients who were able to receive sequential 5-fluorouracil, 19% showed objective response. Only 8.3% of all patients entered into this trial showed objective response after completion of the sequential therapy, and this program must be judged as ineffective treatment for gastrointestinal cancer.
1 Supported by Grant NIH 70-2066 from the National Cancer Institute, NIH, Bethesda, Md.
Received 2/14/72. Accepted 3/ 7/72.
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