Literature DB >> 18525298

Phase I dose escalation study with irinotecan, capecitabine, epirubicin, and granulocyte colony-stimulating factor support for patients with solid malignancies.

Carlos R Becerra1, Udit N Verma, Hia T Tran, Denise Tavana, Noelle S Williams, Eugene P Frenkel.   

Abstract

OBJECTIVES: Preclinical studies using sequences of topoisomerase I and II inhibitors suggested synergism; preliminary clinical studies, resulting in enhanced antitumor responses, confirm this in selected malignancies. This study determined the maximum-tolerated dose (MTD), toxicity, and pharmacokinetics of irinotecan (CPT-11), capecitabine, and epirubicin in patients with metastatic adenocarcinoma of lung, breast, or gastrointestinal tract. Correlation of topoisomerase IIbeta was also done.
METHODS: Eligibility criteria included the following: documented adenocarcinoma of the lung, breast, or gastrointestinal tract, <3 prior chemotherapy regimens, Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2, age > or =18 years, adequate organ function, and signed informed consent. Irinotecan was administered at 250 mg/m2 intravenously day 1 every 21-day cycle, but was reduced to 180 mg/m2 in cohort 2 due to toxicity. Capecitabine was administered at 750 mg/m2 twice daily days 2 to 14 in cohort 1 but only on days 2 to 7 from cohort 2 due to early neutropenia and to allow for prophylactic granulocyte colony-stimulating factor (GCSF) support. Epirubicin was administered at 40 mg/m2 in cohort 1, but reduced to 30 mg/m2 in cohort 2, then reescalated until the MTD was reached.
RESULTS: Toxicity was assessed in 21 patients; response was assessed in 17 patients. The most common grade 3 to 4 toxicities included neutropenia (57.1%) and anemia (28.6%). The MTD of epirubicin was 50 mg/m2. In evaluable patients, there were 2 partial responses (11.8%) and 13 stable disease (76.5%); these correlated well with topoisomerase IIbeta.
CONCLUSIONS: The recommended doses for phase II studies: irinotecan 180 mg/m2 day 1, epirubicin 50 mg/m2 day 2, and capecitabine 750 mg/m2 twice daily days 2 to 7 of each 21-day cycle. This combination is reasonably active and warrants evaluation in the phase II setting.

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Year:  2008        PMID: 18525298     DOI: 10.1097/COC.0b013e31815a438f

Source DB:  PubMed          Journal:  Am J Clin Oncol        ISSN: 0277-3732            Impact factor:   2.339


  2 in total

1.  Synergistic interactions between aminoflavone, paclitaxel and camptothecin in human breast cancer cells.

Authors:  Kathryn E Reinicke; Mary J Kuffel; Matthew P Goetz; Matthew M Ames
Journal:  Cancer Chemother Pharmacol       Date:  2009-12-11       Impact factor: 3.333

2.  Cytotoxicity and genotoxicity of capecitabine in head and neck cancer and normal cells.

Authors:  Maria Wisniewska-Jarosinska; Tomasz Sliwinski; Jacek Kasznicki; Dariusz Kaczmarczyk; Renata Krupa; Karolina Bloch; Jozef Drzewoski; Jan Chojnacki; Janusz Blasiak; Alina Morawiec-Sztandera
Journal:  Mol Biol Rep       Date:  2010-11-24       Impact factor: 2.316

  2 in total

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