CRLX101 nanoparticles localize in human tumors and not in adjacent, nonneoplastic tissue after intravenous dosing.

PubWeight™: 0.82‹?›

🔗 View Article (PMID 27001839)

Published in Proc Natl Acad Sci U S A on March 21, 2016

Authors

Andrew J Clark1, Devin T Wiley1, Jonathan E Zuckerman2, Paul Webster3, Joseph Chao4, James Lin5, Yun Yen6, Mark E Davis7

Author Affiliations

1: Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125;
2: Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125; Department of Pathology and Laboratory Medicine, University of California, Los Angeles, CA 90095;
3: Oak Crest Institute of Science, Pasadena, CA 91107;
4: Department of Medical Oncology, City of Hope Comprehensive Cancer Center, Duarte, CA 91010.
5: Division of Gastroenterology, City of Hope Comprehensive Cancer Center, Duarte, CA 91010;
6: Graduate Institute for Cancer Biology and Drug Discovery, Taipei Medical University, Taipei 11031, Taiwan mdavis@cheme.caltech.edu yyen@tmu.edu.tw.
7: Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125; mdavis@cheme.caltech.edu yyen@tmu.edu.tw.

Associated clinical trials:

Pilot Trial of CRLX101 in Treatment of Patients With Advanced or Metastatic Stomach, Gastroesophageal, or Esophageal Cancer That Cannot be Removed by Surgery | NCT01612546

Alternative Dosing for CRLX101 Alone, With Avastin and With mFOLFOX6 in Advanced Solid Tumors | NCT02648711

Articles cited by this

Nanoparticle therapeutics: an emerging treatment modality for cancer. Nat Rev Drug Discov (2008) 12.72

Evidence of RNAi in humans from systemically administered siRNA via targeted nanoparticles. Nature (2010) 10.09

Effective targeting of solid tumors in patients with locally advanced cancers by radiolabeled pegylated liposomes. Clin Cancer Res (2001) 3.48

Biological and therapeutic impact of intratumor heterogeneity in cancer evolution. Cancer Cell (2015) 2.57

Pharmacokinetics and tumor dynamics of the nanoparticle IT-101 from PET imaging and tumor histological measurements. Proc Natl Acad Sci U S A (2009) 1.63

Ubiquitin-dependent destruction of topoisomerase I is stimulated by the antitumor drug camptothecin. J Biol Chem (1997) 1.56

Transcriptional control of the tumor- and hypoxia-marker carbonic anhydrase 9: A one transcription factor (HIF-1) show? Biochim Biophys Acta (2009) 1.55

Synthesis of linear, beta-cyclodextrin-based polymers and their camptothecin conjugates. Bioconjug Chem (2003) 1.44

Transcription-dependent degradation of topoisomerase I-DNA covalent complexes. Mol Cell Biol (2003) 1.43

Liposomal doxorubicin and conventionally fractionated radiotherapy in the treatment of locally advanced non-small-cell lung cancer and head and neck cancer. J Clin Oncol (1999) 1.33

Toward a full understanding of the EPR effect in primary and metastatic tumors as well as issues related to its heterogeneity. Adv Drug Deliv Rev (2015) 1.32

Cullin 3 promotes proteasomal degradation of the topoisomerase I-DNA covalent complex. Cancer Res (2004) 1.25

Proteasome-dependent processing of topoisomerase I-DNA adducts into DNA double strand breaks at arrested replication forks. J Biol Chem (2009) 1.11

Correlating preclinical animal studies and human clinical trials of a multifunctional, polymeric nanoparticle. Proc Natl Acad Sci U S A (2013) 1.08

First-in-human phase 1/2a trial of CRLX101, a cyclodextrin-containing polymer-camptothecin nanopharmaceutical in patients with advanced solid tumor malignancies. Invest New Drugs (2013) 1.02

Translational impact of nanoparticle-drug conjugate CRLX101 with or without bevacizumab in advanced ovarian cancer. Clin Cancer Res (2014) 0.94

Microvessel count predicts metastasis and prognosis in patients with gastric cancer. J Surg Oncol (1997) 0.88

Pharmacodynamic and pharmacogenomic study of the nanoparticle conjugate of camptothecin CRLX101 for the treatment of cancer. Nanomedicine (2014) 0.86

Degradation of topoisomerase I induced by topoisomerase I inhibitors is dependent on inhibitor structure but independent of cell death. Mol Pharmacol (1999) 0.86

Serial diffusion MRI to monitor and model treatment response of the targeted nanotherapy CRLX101. Clin Cancer Res (2013) 0.85