Population pharmacokinetic analysis of nanoparticle-bound and free camptothecin after administration of NLG207 in adults with advanced solid tumors

Cancer Chemother Pharmacol. 2020 Oct;86(4):475-486. doi: 10.1007/s00280-020-04134-9. Epub 2020 Sep 8.

Abstract

Purpose: NLG207 (formerly CRLX101) is a nanoparticle-drug conjugate (NDC) of the potent topoisomerase I inhibitor, camptothecin (CPT). The present study sought to characterize the complex pharmacokinetics (PK) of NLG207 and better describe CPT release from nanoparticles using a population PK (popPK) model.

Methods: From 27 patients enrolled on two phase II clinical trials (NCT02769962 and NCT03531827), dense sampling was performed up to 48 h post-administration of NLG207 during cycle one and six of treatment; samples were also collected at ~ 360 h post-dose. Conjugated and free CPT concentrations were quantified from each sample, resulting in 477 observations to build a popPK model using non-linear mixed-effects modeling.

Results: The PK of NLG207 was characterized by combining two linear two-compartment models with first-order kinetics each to describe nanoparticle-bound (conjugated) and free CPT. Allometric scaling based on body weight provided the best body-size descriptor for all PK parameters. The typical volumes of distribution of the conjugated CPT central and free CPT central compartments were 3.16 L (BSV CV%; 18.1%) and 21.1 L (CV%; 79.8%), respectively. CPT release from the nanoparticle formulation was characterized via an initial rapid clearance of 5.71 L/h (CV%; 62.6%), which decreased via first-order decay (estimated half-life of 0.307 h) to the steady-state value of 0.0988 L/h (CV%; 33.5%) by ~ 4 h after end of infusion. Renal clearance of free CPT was 0.874 L/h (CV%; 42.2%).

Conclusion: The popPK model confirmed nanoparticle behavior of conjugated CPT and mechanistically characterized CPT release from NLG207. The current analysis provides a strong foundation for future study as a potential predictive tool in ongoing NLG207 clinical trials.

Keywords: Drug release; NLMEM; Nanoparticle; Population pharmacokinetics; Topoisomerase I.

Publication types

  • Clinical Trial, Phase I
  • Clinical Trial, Phase II
  • Research Support, N.I.H., Intramural

MeSH terms

  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / pharmacokinetics*
  • Benzamides / administration & dosage
  • Benzamides / pharmacokinetics
  • Camptothecin / administration & dosage
  • Camptothecin / pharmacokinetics*
  • Cyclodextrins / administration & dosage
  • Cyclodextrins / pharmacokinetics*
  • Drug Liberation
  • Female
  • Half-Life
  • Humans
  • Male
  • Middle Aged
  • Models, Biological*
  • Neoplasm Staging
  • Neoplasms / blood
  • Neoplasms / diagnosis
  • Neoplasms / drug therapy*
  • Neoplasms / pathology
  • Nitriles / administration & dosage
  • Nitriles / pharmacokinetics
  • Phenylthiohydantoin / administration & dosage
  • Phenylthiohydantoin / pharmacokinetics
  • Phthalazines / administration & dosage
  • Phthalazines / pharmacokinetics
  • Piperazines / administration & dosage
  • Piperazines / pharmacokinetics
  • Topoisomerase I Inhibitors / administration & dosage
  • Topoisomerase I Inhibitors / pharmacokinetics*

Substances

  • Benzamides
  • Cyclodextrins
  • IT-101
  • Nitriles
  • Phthalazines
  • Piperazines
  • Topoisomerase I Inhibitors
  • Phenylthiohydantoin
  • enzalutamide
  • olaparib
  • Camptothecin

Associated data

  • ClinicalTrials.gov/NCT02769962
  • ClinicalTrials.gov/NCT03531827