Development of regional chemotherapies: feasibility, safety and efficacy in clinical use and preclinical studies

Ther Deliv. 2011 Nov;2(11):1467-84. doi: 10.4155/tde.11.112.

Abstract

Conventional oral and intravenous chemotherapies permeate throughout the body, exposing healthy tissues to similar cytotoxic drug levels as tumors. This leads to significant dose-limiting toxicities that may prevent patients from receiving sufficient treatment to overcome cancers. Therefore, a number of locoregional drug-delivery strategies have been evaluated and implemented in preclinical studies, clinical trials and in practice, in the past decades to minimize systemic toxicities from chemotherapeutic agents and to improve treatment outcomes. Localized treatment is beneficial because many cancers, such as melanoma, peritoneal cancer and breast cancer, advance locally adjacent to the site of the primary tumors prior to their circulatory invasion. In this article, we will review the feasibility, safety and efficacy of multiple localized chemotherapies in clinical use and preclinical development.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacokinetics
  • Clinical Trials as Topic
  • Dose-Response Relationship, Drug
  • Drug Delivery Systems
  • Drug Evaluation, Preclinical
  • Feasibility Studies
  • Humans
  • Neoplasms / drug therapy*
  • Neoplasms / pathology
  • Tissue Distribution

Substances

  • Antineoplastic Agents