A phase I trial of intrahepatic Verapamil and doxorubicin. Regional therapy to overcome multidrug resistance

Leonard Saltz, Barbara Murphy, Nancy Kemeny, Joseph Bertino, William Tong, Deborah Keefe, Yao Tzy‐Jun, Yue Tao, David Kelsen, James P. O'Brien

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Background. Verapamil can modulate multidrug resistance in vitro, but only at levels that are not tolerable when administered systemically. Regional strategies of drug administration may permit the delivery of high concentrations of a drug to specific areas with lower systemic levels. Colorectal cancers typically express the multidrug resistance phenotype. Methods. A Phase I trial was performed to determine the maximum tolerable dose (MTD) and dose limiting toxicities of verapamil by hepatic artery infusion, together with doxorubicin, to patients with hepatic metastases of colorectal cancer. Fourteen patients with metastatic colorectal cancer received a 14‐hour intrahepatic infusion of verapamil. Six hours after the start of the infusion, a fixed dose of doxorubicin (50 mg/m2) was given, also via the hepatic artery, over a 30‐minute period. Patients were followed by cardiac telemetry but were not in an intensive care setting, and no invasive monitoring was used. All patients had received prior intrahepatic chemotherapy. Results. The MTD of intrahepatic verapamil on this schedule in this patient population was 1.2 mg/kg/hour. Hypotension was the dose limiting toxicity. No major objective responses were noted in this heavily pretreated patient population. A dose of 1.0 mg/kg/hour is recommended for Phase II trials. Conclusions. Based on estimations of normal hepatic artery blood flow, the estimated concentration of verapamil delivered to the hepatic tumors at 1.0 mg/kg/hour is 3.6 μg/ml (7.3 μM), which is comparable to concentrations at which an in vitro reversal of MDR is seen. This study demonstrates that the systemic toxicities of an MDR reversal agent can be overcome by regional drug delivery, establishing this approach as an important model system for further study of MDR modulation.

Original languageEnglish (US)
Pages (from-to)2757-2764
Number of pages8
JournalCancer
Volume74
Issue number10
DOIs
StatePublished - Nov 15 1994

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

Keywords

  • intrahepatic
  • multidrug resistance
  • verapamil

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