Journal of Clinical Oncology, 2005 ASCO Annual Meeting Proceedings.
Vol 23, No 16S (June 1 Supplement), 2005: 2118
© 2005 American Society of Clinical Oncology

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Abstract

Two-dimensional chemotherapy simulations demonstrate fundamental transport and tumor response limitations involving nanoparticles

Univ of CA, Irvine, Irvine, CA

2118

Zheng et al. (Bull. Math. Biol. 2004) developed a multiscale, two-dimensional simulator with the capability of showing tumoral lesion progression through the stages of diffusion-limited dormancy, neo-vascularization (angiogenesis) and consequent rapid growth and tissue invasion. In this paper (Sinek et al., Biomed. Microdev. 2004) we extend their simulator to describe delivery of chemotherapeutic drugs to a highly perfused tumoral lesion and the tumor’s response to the therapy. 2-D simulations based on a self-consistent parameter estimation demonstrate fundamental convective and diffusive transport limitations in delivering anticancer drug into tumors, whether this delivery is viafree drug administration (e.g., intravenous drip), or via100 nm nanoparticles injected into the bloodstream, extravasating and releasing the drug that then diffuses into the tumoral tissue, or viasmaller 1–10 nm nanoparticles that are capable of diffusing directly and targeting the individual tumor cell. Even in a best-case scenario involving: constant drug release from the nanoparticles; a homogenous tumor of one cell type, which is drug-sensitive and does not develop resistance; targeted nanoparticle delivery, with resulting low host tissue toxicity; and for model parameters calibrated to ensure sufficient drug or nanoparticle blood concentration to rapidly kill all cells in vitro; our analysis shows that fundamental transport limitations are severe in vivo and that drug levels inside the tumor are far less than in vitro, leaving large parts of the tumor with inadequate drug concentration. A comparison of cell death rates predicted by our simulations reveals that the in vivorate of tumor shrinkage is several orders of magnitude less than in vitrofor equal chemotherapeutic carrier concentrations in the blood serum and in vitro, and after some shrinkage the tumor may achieve a new mass equilibrium far above detectable levels. We also demonstrate that adjuvant anti-angiogenic therapy "normalizing" the vasculature may ameliorate transport limitations, although leading to unwanted tumor fragmentation.

No significant financial relationships to disclose.