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Phase-I trial of combination therapy with continuous-infusion MMPR and continuous-infusion 5-FU

  • Original Articles
  • MMPR Infusion, 5-F Infusion
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Summary

Fourty-four evaluable patients were treated with 6-methylmercaptopurine riboside (MMPR) at a dose of 20 mg/m2/day x 5 by continuous IV infusion (days 1–5) and 5-fluorouracil (5-FU) on an escalating dose schedule of 300–1519 mg/m2/day x 5 by continuous IV infusion (days 2–6). Dose-limiting oral mucositis occured at a 5-FU dose of 1,381 mg/m2/day; other toxicities included nausea, vomiting, diarrhea, skin rash, and occasional myelosuppression. A partial and a complete response were observed in two previously untreated patients with metastatic colon carcinoma given the highest 5-FU doses (1,381 and 1,519 mg/m2/day). Bone marrow phosphoribosyl pyrophosphate (PRPP) levels monitored after 24 h of MMPR treatment indicated increases of 7.8- and 9.2-fold those found prior to therapy.

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Peters, W.P., Weiss, G. & Kufe, D.W. Phase-I trial of combination therapy with continuous-infusion MMPR and continuous-infusion 5-FU. Cancer Chemother. Pharmacol. 13, 136–138 (1984). https://doi.org/10.1007/BF00257131

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  • DOI: https://doi.org/10.1007/BF00257131

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