Systemic therapy for advanced pancreatic cancer

Expert Rev Anticancer Ther. 2002 Aug;2(4):426-36. doi: 10.1586/14737140.2.4.426.

Abstract

Death from pancreatic cancer remains high with few long-term survivors. Systemic chemotherapy with 5-fluorouracil-based combinations had minimal impact on natural history of this disease. Several new agents with activity against pancreatic cancer have been identified over the past decade. Gemcitabine has modest activity in this disease. Combination chemotherapy trials incorporating gemcitabine, cisplatin, 5-fluorouracil, oxaliplatin, docetaxel or irinotecan show improved outcomes in objective response rates and survival that need to be confirmed in prospectively randomized studies. Advancement in the understanding of the biology of pancreatic cancer has helped identify several molecular targets for the development of novel therapies. Ongoing and future treatment regimens for pancreatic cancer will incorporate traditional cytotoxic drugs and novel targeted therapies.

Publication types

  • Review

MeSH terms

  • Angiogenesis Inhibitors / therapeutic use
  • Antimetabolites, Antineoplastic / therapeutic use
  • Antineoplastic Agents / therapeutic use*
  • Cell Cycle / drug effects
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / therapeutic use
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / therapeutic use
  • Drug Therapy, Combination
  • Enzyme Inhibitors / therapeutic use
  • Fluorouracil / therapeutic use
  • Gemcitabine
  • Genes, ras / drug effects
  • Humans
  • Isoenzymes / metabolism
  • Membrane Proteins
  • Pancreatic Neoplasms / drug therapy
  • Pancreatic Neoplasms / therapy*
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Signal Transduction / drug effects
  • Topoisomerase I Inhibitors

Substances

  • Angiogenesis Inhibitors
  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Enzyme Inhibitors
  • Isoenzymes
  • Membrane Proteins
  • Topoisomerase I Inhibitors
  • Deoxycytidine
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Fluorouracil
  • Gemcitabine