Anatomical Targeting of Anticancer Drugs to Solid Tumors Using Specific Administration Routes: Review.

Pharmaceutics

Division of Translational Research, Clinical Research Center, Jichi Medical University Hospital, Tochigi, Tochigi 329-0498, Japan.

Published: June 2023

AI Article Synopsis

  • Despite advances in anti-cancer drug development, patients with solid tumors still face poor outcomes due to ineffective drug delivery to tumor sites.
  • Systemic chemotherapy, involving IV administration, often leads to low concentrations of drugs in tumors and can harm healthy organs, despite efforts to increase doses.
  • Local administration of anti-cancer agents may provide higher drug concentrations with less toxicity, particularly for specific tumors, yet the resulting improvements in survival rates remain limited.

Article Abstract

Despite remarkable recent progress in developing anti-cancer agents, outcomes of patients with solid tumors remain unsatisfactory. In general, anti-cancer drugs are systemically administered through peripheral veins and delivered throughout the body. The major problem with systemic chemotherapy is insufficient uptake of intravenous (IV) drugs by targeted tumor tissue. Although dose escalation and treatment intensification have been attempted in order to increase regional concentrations of anti-tumor drugs, these approaches have produced only marginal benefits in terms of patient outcomes, while often damaging healthy organs. To overcome this problem, local administration of anti-cancer agents can yield markedly higher drug concentrations in tumor tissue with less systemic toxicity. This strategy is most commonly used for liver and brain tumors, as well as pleural or peritoneal malignancies. Although the concept is theoretically reasonable, survival benefits are still limited. This review summarizes clinical results and problems and discusses future directions of regional cancer therapy with local administration of chemotherapeutants.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301590PMC
http://dx.doi.org/10.3390/pharmaceutics15061664DOI Listing

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