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Published in: Investigational New Drugs 3/2017

01-06-2017 | SHORT REPORT

Risks and benefits of phase I liver dysfunction studies: should patients with severe liver dysfunction be included in these trials?

Authors: Christos Fountzilas, Selena Stuart, Brian Hernandez, Elizabeth Bowhay-Carnes, Joel Michalek, John Sarantopoulos, Anand Karnad, Sukeshi Patel, Steven Weitman, Devalingam Mahalingam

Published in: Investigational New Drugs | Issue 3/2017

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Summary

Introduction The goal of organ dysfunction Phase I trials is to characterize the safety and pharmacokinetics of novel agents in cancer patients with liver or kidney dysfunction, but the clinical benefit is not well established. Methods We reviewed 170 patients across 15 liver dysfunction studies at our institution, grouped based on the NCI-Organ Dysfunction Working Group criteria or Child-Pugh Score. Results The median survival for the entire cohort was two months and just one month amongst patients with severe liver dysfunction. Patients with normal or mild liver dysfunction, absence of tumor in liver, good performance status, higher serum albumin and lower bilirubin, aspartate transaminase and alkaline phosphatase had improved survival by univariate analysis. Serum albumin and liver function classification remained significant by multivariate analysis. Conclusion Given poor survival of patients with liver dysfunction, we need better criteria, such as albumin levels, for optimally selecting patients for liver dysfunction studies.
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Metadata
Title
Risks and benefits of phase I liver dysfunction studies: should patients with severe liver dysfunction be included in these trials?
Authors
Christos Fountzilas
Selena Stuart
Brian Hernandez
Elizabeth Bowhay-Carnes
Joel Michalek
John Sarantopoulos
Anand Karnad
Sukeshi Patel
Steven Weitman
Devalingam Mahalingam
Publication date
01-06-2017
Publisher
Springer US
Published in
Investigational New Drugs / Issue 3/2017
Print ISSN: 0167-6997
Electronic ISSN: 1573-0646
DOI
https://doi.org/10.1007/s10637-017-0425-4

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