Treatment of fluorouracil-refractory patients with liver metastases from colorectal cancer by using yttrium-90 resin microspheres plus concomitant systemic irinotecan chemotherapy

J Clin Oncol. 2009 Sep 1;27(25):4089-95. doi: 10.1200/JCO.2008.20.8116. Epub 2009 Aug 3.

Abstract

Purpose: Liver metastases are the principal cause of death in patients with advanced colorectal cancer (CRC). Irinotecan is a chemotherapeutic agent used in the treatment of CRC and has demonstrated synergistic potential when used with radiation. Radioembolization with yttrium-90 microspheres has demonstrated increased response and survival rates when given with fluorouracil chemotherapy. This study's goal was to evaluate the maximum-tolerated dose of concomitant irinotecan and radioembolization in fluorouracil-refractory patients with CRC hepatic metastases.

Patients and methods: Twenty-five irinotecan-naive patients who had experienced relapse after previous chemotherapy were enrolled onto three dose-escalating groups. Irinotecan was administered at 50, 75, or 100 mg/m(2) on days 1 and 8 of a 3-week cycle for the first two cycles, and full irinotecan doses (ie, 100 mg/m(2)) were administered during cycles 3 to 9. Radioembolization was administered during the first chemotherapy cycle.

Results: Most patients experienced acute, self-limiting abdominal pain and nausea. Mild lethargy and anorexia were common. Grades 3 to 4 events were seen in three of six patients at 50 mg/m(2) (obstructive jaundice, thrombocytopenia, diarrhea), in five of 13 patients at 75 mg/m(2) (neutropenia, leukopenia, thrombocytopenia, elevated alkaline phosphatase, abdominal pain, ascites, fatigue) and in four of six patients at 100 mg/m(2) (diarrhea, deep vein thrombosis, constipation, leukopenia). Eleven (48%) of 23 patients had a partial response, and nine patients (39%) had stable disease. The median progression-free survival was 6.0 months; the median survival was 12.2 months.

Conclusion: Concomitant use of radioembolization plus irinotecan did not reach a maximum-tolerated dose. The recommended dose of irinotecan in this setting is 100 mg/m(2) on days 1 and 8 of a 3-week cycle.

Publication types

  • Clinical Trial, Phase I
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antimetabolites, Antineoplastic / therapeutic use
  • Australia
  • Brachytherapy*
  • Camptothecin / administration & dosage
  • Camptothecin / adverse effects
  • Camptothecin / analogs & derivatives*
  • Chemotherapy, Adjuvant
  • Colorectal Neoplasms / secondary*
  • Disease-Free Survival
  • Drug Administration Schedule
  • Drug Resistance, Neoplasm*
  • Enzyme Inhibitors / administration & dosage*
  • Enzyme Inhibitors / adverse effects
  • Female
  • Fluorouracil / therapeutic use
  • Humans
  • Infusions, Intravenous
  • Irinotecan
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / radiotherapy*
  • Liver Neoplasms / secondary
  • Male
  • Maximum Tolerated Dose
  • Microspheres
  • Middle Aged
  • Radiopharmaceuticals / administration & dosage*
  • Radiopharmaceuticals / adverse effects
  • Radiotherapy, Adjuvant
  • Time Factors
  • Topoisomerase I Inhibitors
  • Treatment Outcome
  • Yttrium Isotopes / administration & dosage*
  • Yttrium Isotopes / adverse effects

Substances

  • Antimetabolites, Antineoplastic
  • Enzyme Inhibitors
  • Radiopharmaceuticals
  • Topoisomerase I Inhibitors
  • Yttrium Isotopes
  • Irinotecan
  • Fluorouracil
  • Camptothecin