Albumin-based cancer therapeutics for intraperitoneal drug delivery: a review

Drug Deliv. 2020 Dec;27(1):40-53. doi: 10.1080/10717544.2019.1704945.

Abstract

Albumin is a remarkable carrier protein with multiple cellular receptor and ligand binding sites, which are able to bind and transport numerous endogenous and exogenous compounds. The development of albumin-bound drugs is gaining increased importance in the targeted delivery of cancer therapy. Intraperitoneal (IP) drug delivery represents an attractive strategy for the local treatment of peritoneal metastasis (PM). PM is characterized by the presence of widespread metastatic tumor nodules on the peritoneum, mostly originating from gastro-intestinal or gynaecological cancers. Albumin as a carrier for chemotherapy holds considerable promise for IP delivery in patients with PM. Data from recent (pre)clinical trials suggest that IP albumin-bound chemotherapy may result in superior efficacy in the treatment of PM compared to standard chemotherapy formulations. Here, we review the evidence on albumin-bound chemotherapy with a focus on IP administration and its efficacy in PM.

Keywords: Albumin; chemotherapy; intraperitoneal delivery; peritoneal metastasis; peritoneum.

Publication types

  • Review

MeSH terms

  • Albumins / administration & dosage*
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / therapeutic use
  • Biological Transport
  • Dose-Response Relationship, Drug
  • Drug Carriers / administration & dosage*
  • Humans
  • Injections, Intraperitoneal
  • Nanoparticles / chemistry
  • Peritoneal Neoplasms / drug therapy*
  • Peritoneal Neoplasms / pathology
  • Peritoneum / anatomy & histology
  • Peritoneum / pathology
  • Protein Binding / physiology

Substances

  • Albumins
  • Antineoplastic Agents
  • Drug Carriers

Grants and funding

This research project was funded by Kom op tegen Kanker (Stand up to Cancer), the Flemish cancer society.