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Published in: Cancer Chemotherapy and Pharmacology 4/2016

01-04-2016 | Original Article

Population pharmacokinetics and exposure–response relationship of amatuximab, an anti-mesothelin monoclonal antibody, in patients with malignant pleural mesothelioma and its application in dose selection

Authors: Anubha Gupta, Ziad Hussein, Raffit Hassan, Jason Wustner, Julia D. Maltzman, Bruce A. Wallin

Published in: Cancer Chemotherapy and Pharmacology | Issue 4/2016

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Abstract

Purpose

To characterize amatuximab pharmacokinetics (PK) and the relationship of amatuximab exposure with response in patients with unresectable malignant pleural mesothelioma (MPM) receiving amatuximab with pemetrexed and cisplatin.

Methods

A nonlinear mixed effects PK model was built using data from all of the amatuximab studies conducted to date. Patients received amatuximab alone or in combination with chemotherapy. The influence of demographic, laboratory and disease characteristics on PK parameters was assessed. Exposure–response analyses explored relationships between amatuximab exposure and overall survival (OS), progression-free survival (PFS) and safety. Alternative amatuximab dosing regimens were explored with simulations using population PK and parametric survival models.

Results

Amatuximab PK was best described by a two-compartment model with parallel linear and nonlinear elimination pathways. Body weight and an antidrug antibodies reaction with the titer >64 affected volume of distribution and clearance, respectively. Exposure–response analyses demonstrated that the amatuximab exposure (C min) showed a significant effect on OS (log-rank test, P = 0.0202). For patients with amatuximab C min above the median (38.2 μg/mL), the median OS was 583 days (90 % CI 418 –NE). For patients with C min ≤ 38.2 μg/mL, the median OS was 375 days (90 % CI 325–486). The amatuximab exposure showed similar significant effect on PFS. Exposure–response analysis for adverse events did not reveal any relationship.

Conclusions

In patients with MPM, higher amatuximab exposure in combination with chemotherapy was shown to be associated with longer OS, supporting evaluation of more frequent dosing in future trials to achieve higher exposure and subsequently longer OS.
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Literature
1.
go back to reference Sugarbaker DJ, Garcia JP, Richards WG et al (1996) Extrapleural pneumonectomy in the multimodality therapy of malignant pleural mesothelioma—Results in 120 consecutive patients. Ann Surg 224:288–294CrossRefPubMedPubMedCentral Sugarbaker DJ, Garcia JP, Richards WG et al (1996) Extrapleural pneumonectomy in the multimodality therapy of malignant pleural mesothelioma—Results in 120 consecutive patients. Ann Surg 224:288–294CrossRefPubMedPubMedCentral
2.
go back to reference Vogelzang NJ, Rusthoven JJ, Symanowski J et al (2003) Phase III study of pemetrexed in combination with cisplatin versus cisplatin alone in patients with malignant pleural mesothelioma. J Clin Oncol 21:2636–2644CrossRefPubMed Vogelzang NJ, Rusthoven JJ, Symanowski J et al (2003) Phase III study of pemetrexed in combination with cisplatin versus cisplatin alone in patients with malignant pleural mesothelioma. J Clin Oncol 21:2636–2644CrossRefPubMed
3.
go back to reference Manzini VD, Brollo A, Franceschi S et al (1993) Prognostic factors of malignant mesothelioma of the pleura. Cancer 72:410–417CrossRef Manzini VD, Brollo A, Franceschi S et al (1993) Prognostic factors of malignant mesothelioma of the pleura. Cancer 72:410–417CrossRef
4.
go back to reference Chang K, Pastan I, Willingham MC (1992) Isolation and characterization of a monoclonal antibody, K1, reactive with ovarian cancers and normal mesothelium. Int J Cancer 50:373–381CrossRefPubMed Chang K, Pastan I, Willingham MC (1992) Isolation and characterization of a monoclonal antibody, K1, reactive with ovarian cancers and normal mesothelium. Int J Cancer 50:373–381CrossRefPubMed
5.
go back to reference Ordonez NG (2003) Value of mesothelin immunostaining in the diagnosis of mesothelioma. Mod Pathol 16:192–197CrossRefPubMed Ordonez NG (2003) Value of mesothelin immunostaining in the diagnosis of mesothelioma. Mod Pathol 16:192–197CrossRefPubMed
6.
go back to reference Hassan R, Laszik ZG, Lerner M et al (2005) Mesothelin is overexpressed in pancreaticobiliary adenocarcinomas but not in normal pancreas and chronic pancreatitis. Am J Clin Pathol 124:838–845CrossRefPubMed Hassan R, Laszik ZG, Lerner M et al (2005) Mesothelin is overexpressed in pancreaticobiliary adenocarcinomas but not in normal pancreas and chronic pancreatitis. Am J Clin Pathol 124:838–845CrossRefPubMed
7.
go back to reference Argani P, Iacobuzio-Donahue C, Ryu B et al (2001) Mesothelin is overexpressed in the vast majority of ductal adenocarcinomas of the pancreas: identification of a new pancreatic cancer marker by serial analysis of gene expression (SAGE). Clin Cancer Res 7:3862–3868PubMed Argani P, Iacobuzio-Donahue C, Ryu B et al (2001) Mesothelin is overexpressed in the vast majority of ductal adenocarcinomas of the pancreas: identification of a new pancreatic cancer marker by serial analysis of gene expression (SAGE). Clin Cancer Res 7:3862–3868PubMed
8.
go back to reference Hassan R, Kreitman RJ, Pastan I, Willingham MC (2005) Localization of mesothelin in epithelial ovarian cancer. Appl Immunohistochem Mol Morphol 13:243–247CrossRefPubMed Hassan R, Kreitman RJ, Pastan I, Willingham MC (2005) Localization of mesothelin in epithelial ovarian cancer. Appl Immunohistochem Mol Morphol 13:243–247CrossRefPubMed
9.
go back to reference Miettinen M, Sarlomo-Rikala M (2003) Expression of calretinin, thrombomodulin, keratin 5, and mesothelin in lung carcinomas of different types: an immunohistochemical analysis of 596 tumors in comparison with epithelioid mesotheliomas of the pleura. Am J Surg Pathol 27:150–158CrossRefPubMed Miettinen M, Sarlomo-Rikala M (2003) Expression of calretinin, thrombomodulin, keratin 5, and mesothelin in lung carcinomas of different types: an immunohistochemical analysis of 596 tumors in comparison with epithelioid mesotheliomas of the pleura. Am J Surg Pathol 27:150–158CrossRefPubMed
10.
go back to reference Hassan R, Schweizer C, Lu KF et al (2010) Inhibition of mesothelin-CA125 interaction in patients with mesothelioma by the anti-mesothelin monoclonal antibody MORAb-009: implications for cancer therapy. Lung Cancer 68:455–459CrossRefPubMedPubMedCentral Hassan R, Schweizer C, Lu KF et al (2010) Inhibition of mesothelin-CA125 interaction in patients with mesothelioma by the anti-mesothelin monoclonal antibody MORAb-009: implications for cancer therapy. Lung Cancer 68:455–459CrossRefPubMedPubMedCentral
11.
go back to reference Kelly RJ, Sharon E, Pastan I, Hassan R (2012) Mesothelin-targeted agents in clinical trials and in preclinical development. Mol Cancer Ther 11:517–525CrossRefPubMedPubMedCentral Kelly RJ, Sharon E, Pastan I, Hassan R (2012) Mesothelin-targeted agents in clinical trials and in preclinical development. Mol Cancer Ther 11:517–525CrossRefPubMedPubMedCentral
12.
go back to reference Hassan R, Ebel W, Routhier EL et al (2007) Preclinical evaluation of MORAb-009, a chimeric antibody targeting tumor-associated mesothelin. Cancer Immun 7:20PubMedPubMedCentral Hassan R, Ebel W, Routhier EL et al (2007) Preclinical evaluation of MORAb-009, a chimeric antibody targeting tumor-associated mesothelin. Cancer Immun 7:20PubMedPubMedCentral
13.
go back to reference Hassan R, Cohen SJ, Phillips M et al (2010) Phase I clinical trial of the chimeric anti-mesothelin monoclonal antibody MORAb-009 in patients with mesothelin-expressing cancers. Clin Cancer Res 16:6132–6138CrossRefPubMedPubMedCentral Hassan R, Cohen SJ, Phillips M et al (2010) Phase I clinical trial of the chimeric anti-mesothelin monoclonal antibody MORAb-009 in patients with mesothelin-expressing cancers. Clin Cancer Res 16:6132–6138CrossRefPubMedPubMedCentral
14.
go back to reference Hassan R, Jahan T, Kindler HL et al (2014) Amatuximab, a chimeric monoclonal antibody to mesothelin in combination with pemetrexed and cisplatin in patients with unresectable pleural mesothelioma: results of a multi-center phase II clinical trial. Clin Cancer Res 20:5927–5936CrossRefPubMedPubMedCentral Hassan R, Jahan T, Kindler HL et al (2014) Amatuximab, a chimeric monoclonal antibody to mesothelin in combination with pemetrexed and cisplatin in patients with unresectable pleural mesothelioma: results of a multi-center phase II clinical trial. Clin Cancer Res 20:5927–5936CrossRefPubMedPubMedCentral
15.
go back to reference Fujisaka Y, Kurata T, Tanaka K et al (2015) Phase I study of amatuximab, a novel monoclonal antibody to mesothelin, in Japanese patients with advanced solid tumors. Invest New Drugs 33:380–388CrossRefPubMedPubMedCentral Fujisaka Y, Kurata T, Tanaka K et al (2015) Phase I study of amatuximab, a novel monoclonal antibody to mesothelin, in Japanese patients with advanced solid tumors. Invest New Drugs 33:380–388CrossRefPubMedPubMedCentral
16.
go back to reference Beal SL (2001) Ways to fit a PK model with some data below the quantification limit. J Pharmacokinet Pharmacodyn 28:481–504CrossRefPubMed Beal SL (2001) Ways to fit a PK model with some data below the quantification limit. J Pharmacokinet Pharmacodyn 28:481–504CrossRefPubMed
17.
go back to reference Dirks NL, Meibohm B (2010) Population pharmacokinetics of therapeutic monoclonal antibodies. Clin Pharmacokinet 49:633–659CrossRefPubMed Dirks NL, Meibohm B (2010) Population pharmacokinetics of therapeutic monoclonal antibodies. Clin Pharmacokinet 49:633–659CrossRefPubMed
18.
19.
go back to reference Bergstrand M, Hooker AC, Wallin JE, Karlsson MO (2011) Prediction-corrected visual predictive checks for diagnosing nonlinear mixed-effects models. AAPS J 13:143–151CrossRefPubMedPubMedCentral Bergstrand M, Hooker AC, Wallin JE, Karlsson MO (2011) Prediction-corrected visual predictive checks for diagnosing nonlinear mixed-effects models. AAPS J 13:143–151CrossRefPubMedPubMedCentral
21.
go back to reference Mould DR, Upton RN (2013) Basic concepts in population modeling, simulation, and model-based drug development—Part 2: introduction to pharmacokinetic modeling methods. Pharmacometrics & Systems Pharmacology, CPT, p e38. doi:10.1038/psp.2013.14 Mould DR, Upton RN (2013) Basic concepts in population modeling, simulation, and model-based drug development—Part 2: introduction to pharmacokinetic modeling methods. Pharmacometrics & Systems Pharmacology, CPT, p e38. doi:10.​1038/​psp.​2013.​14
22.
go back to reference Mould D, Green B (2010) Pharmacokinetics and pharmacodynamics of monoclonal antibodies. Concepts and lessons for drug development. Biodrugs 24:23–39CrossRefPubMed Mould D, Green B (2010) Pharmacokinetics and pharmacodynamics of monoclonal antibodies. Concepts and lessons for drug development. Biodrugs 24:23–39CrossRefPubMed
Metadata
Title
Population pharmacokinetics and exposure–response relationship of amatuximab, an anti-mesothelin monoclonal antibody, in patients with malignant pleural mesothelioma and its application in dose selection
Authors
Anubha Gupta
Ziad Hussein
Raffit Hassan
Jason Wustner
Julia D. Maltzman
Bruce A. Wallin
Publication date
01-04-2016
Publisher
Springer Berlin Heidelberg
Published in
Cancer Chemotherapy and Pharmacology / Issue 4/2016
Print ISSN: 0344-5704
Electronic ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-016-2984-z

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