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

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 stu...

Full description

Saved in:
Bibliographic Details
Published inInvestigational new drugs Vol. 35; no. 3; pp. 386 - 391
Main Authors Fountzilas, Christos, Stuart, Selena, Hernandez, Brian, Bowhay-Carnes, Elizabeth, Michalek, Joel, Sarantopoulos, John, Karnad, Anand, Patel, Sukeshi, Weitman, Steven, Mahalingam, Devalingam
Format Journal Article
LanguageEnglish
Published New York Springer US 01.06.2017
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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.
ISSN:0167-6997
1573-0646
DOI:10.1007/s10637-017-0425-4