Skip to main content
Journal cover image

A Phase I Pharmacokinetic Study of Trastuzumab Emtansine (T-DM1) in Patients with Human Epidermal Growth Factor Receptor 2-Positive Metastatic Breast Cancer and Normal or Reduced Hepatic Function.

Publication ,  Journal Article
Li, C; Agarwal, P; Gibiansky, E; Jin, JY; Dent, S; Gonçalves, A; Nijem, I; Strasak, A; Harle-Yge, M-L; Chernyukhin, N; LoRusso, P; Girish, S
Published in: Clin Pharmacokinet
September 2017

OBJECTIVE: The aim of this study was to evaluate the pharmacokinetics (PK) of trastuzumab emtansine (T-DM1) and relevant analytes in patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer and hepatic impairment. METHODS: Patients were enrolled in three independent parallel cohorts based on hepatic function per Child-Pugh criteria: normal hepatic function, mild hepatic impairment, and moderate hepatic impairment. Patients received T-DM1 3.6 mg/kg intravenously every 3 weeks. PK samples were collected during cycles 1 and 3, and the PK of T-DM1 and relevant analytes were characterized and compared across cohorts. RESULTS: Compared with patients with normal hepatic function (n = 10), T-DM1 clearance at cycle 1 was 1.8- and 4.0-fold faster in the mild (n = 10) and moderate (n = 8) cohorts, respectively. The trend of faster clearance was less apparent in cycle 3, with similar T-DM1 clearance across cohorts (mean ± standard deviation 8.16 ± 3.27 [n = 9], 9.74 ± 3.62 [n = 7], and 8.99 and 10.2 [individual values, n = 2] mL/day/kg for the normal, mild, and moderate cohorts, respectively). T-DM1 clearance at cycle 1 correlated significantly with baseline albumin, aspartate aminotransferase, and HER2 extracellular domain concentrations (p < 0.05). Plasma concentrations of DM1 and DM1-containing catabolites were low and were comparable across cohorts. CONCLUSIONS: No increase in systemic DM1 concentration was observed in patients with mild or moderate hepatic impairment versus those with normal hepatic function. The faster T-DM1 clearance observed at cycle 1 in patients with hepatic impairment appeared to be transient. After repeated dosing (three cycles), T-DM1 exposure in patients with mild and moderate hepatic impairment was within the range seen in those with normal hepatic function.

Duke Scholars

Published In

Clin Pharmacokinet

DOI

EISSN

1179-1926

Publication Date

September 2017

Volume

56

Issue

9

Start / End Page

1069 / 1080

Location

Switzerland

Related Subject Headings

  • Trastuzumab
  • Receptor, erbB-2
  • Receptor, ErbB-2
  • Pharmacology & Pharmacy
  • Middle Aged
  • Maytansine
  • Liver Neoplasms
  • Liver Diseases
  • Liver
  • Humans
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Li, C., Agarwal, P., Gibiansky, E., Jin, J. Y., Dent, S., Gonçalves, A., … Girish, S. (2017). A Phase I Pharmacokinetic Study of Trastuzumab Emtansine (T-DM1) in Patients with Human Epidermal Growth Factor Receptor 2-Positive Metastatic Breast Cancer and Normal or Reduced Hepatic Function. Clin Pharmacokinet, 56(9), 1069–1080. https://doi.org/10.1007/s40262-016-0496-y
Li, Chunze, Priya Agarwal, Ekaterina Gibiansky, Jin Yan Jin, Susan Dent, Anthony Gonçalves, Ihsan Nijem, et al. “A Phase I Pharmacokinetic Study of Trastuzumab Emtansine (T-DM1) in Patients with Human Epidermal Growth Factor Receptor 2-Positive Metastatic Breast Cancer and Normal or Reduced Hepatic Function.Clin Pharmacokinet 56, no. 9 (September 2017): 1069–80. https://doi.org/10.1007/s40262-016-0496-y.
Li C, Agarwal P, Gibiansky E, Jin JY, Dent S, Gonçalves A, Nijem I, Strasak A, Harle-Yge M-L, Chernyukhin N, LoRusso P, Girish S. A Phase I Pharmacokinetic Study of Trastuzumab Emtansine (T-DM1) in Patients with Human Epidermal Growth Factor Receptor 2-Positive Metastatic Breast Cancer and Normal or Reduced Hepatic Function. Clin Pharmacokinet. 2017 Sep;56(9):1069–1080.
Journal cover image

Published In

Clin Pharmacokinet

DOI

EISSN

1179-1926

Publication Date

September 2017

Volume

56

Issue

9

Start / End Page

1069 / 1080

Location

Switzerland

Related Subject Headings

  • Trastuzumab
  • Receptor, erbB-2
  • Receptor, ErbB-2
  • Pharmacology & Pharmacy
  • Middle Aged
  • Maytansine
  • Liver Neoplasms
  • Liver Diseases
  • Liver
  • Humans