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A phase I pharmacodynamic trial of bortezomib in combination with doxorubicin in patients with advanced cancer

  • Noelle K. LoConte
  • , James P. Thomas
  • , Dona Alberti
  • , Jennifer Heideman
  • , Kimberly Binger
  • , Rebecca Marnocha
  • , Kyle Utecht
  • , Peter Geiger
  • , Jens Eickhoff
  • , George Wilding
  • , Jill Kolesar

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Purpose: This phase I trial sought to define the toxicity, maximally tolerated dose (MTD) and pharmacodynamics of a combination of bortezomib and doxorubicin in patients with advanced malignancies. Patients and methods: Twenty-six patients were treated with bortezomib intravenously on days 1, 4, 8 and 11, with doxorubicin also administered intravenously on days 1 and 8, both in a 21-day cycle. Dosing ranged from 1.0 mg/m2 of bortezomib with 15 mg/m2 of doxorubicin to 1.5 mg/m2 of bortezomib with 20 mg/m2 of doxorubicin. Pharmacodynamic studies performed included assessment of levels of 20S proteasome activity and ubiquitin-protein conjugates. Results: The combination of bortezomib and doxorubicin was generally well tolerated. There were two dose limiting toxicities (DLT) at dose cohort 3 (1.3 mg/m2 bortezomib, 20 mg/m2 doxorubicin) and 2 DLT at dose cohort 3a (1.5 mg/m2 bortezomib, 15 mg/m2 doxorubicin). DLT seen included neutropenia, thrombocytopenia, and neuropathy. In addition, one patient developed grade 3 central nervous system toxicity in cycle 2 (not a DLT). One patient with hormone refractory prostate cancer had a partial response. Proteasome inhibition in whole blood was demonstrated and an increase in ubiquitin-protein conjugates was observed in peripheral blood mononuclear cells of most patients. Conclusions: Bortezomib and doxorubicin can be administered safely. The recommended phase II dose for this 21-day cycle is bortezomib 1.3 mg/m2 intravenously on days 1, 4, 8 and 11, and doxorubicin 20 mg/m2 intravenously on days 1 and 8. This combination may be of special interest in multiple myeloma, given the activity of both drugs in that disease.

Original languageEnglish
Pages (from-to)109-115
Number of pages7
JournalCancer Chemotherapy and Pharmacology
Volume63
Issue number1
DOIs
StatePublished - Dec 2008

Bibliographical note

Funding Information:
Supported by grant: U01 CA062491 “Early Clinical Trials of AntiCancer Agents With Phase I Emphasis, NCI” and M01 RR03186 “General Clinical Research Center Program of The National Center for Research Resources, NIH”.

Funding

Supported by grant: U01 CA062491 “Early Clinical Trials of AntiCancer Agents With Phase I Emphasis, NCI” and M01 RR03186 “General Clinical Research Center Program of The National Center for Research Resources, NIH”.

FundersFunder number
National Institutes of Health (NIH)
National Childhood Cancer Registry – National Cancer InstituteK12CA087718, M01 RR03186
National Center for Research Resources

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Bortezomib
    • Doxorubicin
    • Proteasome inhibition
    • Ubiquitination

    ASJC Scopus subject areas

    • Oncology
    • Toxicology
    • Pharmacology
    • Cancer Research
    • Pharmacology (medical)

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