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Rationale for the use of metronomic chemotherapy in gastrointestinal cancer.

AbstractINTRODUCTION:
Metronomic chemotherapy (mCT) is endowed with various properties, ranging from antiangiogenic to immunomodulation, and may revert tumor resistance to conventional drug administration. A variety of antineoplastic agents displayed activity when administered with metronomic schedules in preclinical models of gastrointestinal cancers. However, most of the field is still unexplored.
AREAS COVERED:
Herein, the authors review the existing literature from PubMed, concerning the use of mCT in gastrointestinal oncology.
EXPERT OPINION:
A mounting body of evidence is emerging in support of mCT as a treatment option for gastrointestinal tumors, but the frequent signs of clinical activity inconsistently translate into a benefit for survival. Research in this field should focus on providing high-quality evidence on the safety and efficacy of mCT, with more prospective, comparative trials; identifying the subgroups of patients for whom mCT would be the best approach; establishing standardized protocols based on mCT pharmacokinetics and pharmacodynamics; developing drug activity biomarkers. mCT is also potentially suitable for combinations with targeted antiangiogenic drugs and may be incorporated with conventional administration into dual regimens.
AuthorsRoberto Filippi, Pasquale Lombardi, Ilaria Depetris, Elisabetta Fenocchio, Virginia Quarà, Giovanna Chilà, Massimo Aglietta, Francesco Leone
JournalExpert opinion on pharmacotherapy (Expert Opin Pharmacother) Vol. 19 Issue 13 Pg. 1451-1463 (09 2018) ISSN: 1744-7666 [Electronic] England
PMID30161003 (Publication Type: Journal Article, Review)
Chemical References
  • Angiogenesis Inhibitors
  • Antineoplastic Agents
Topics
  • Angiogenesis Inhibitors (administration & dosage, therapeutic use)
  • Animals
  • Antineoplastic Agents (administration & dosage, therapeutic use)
  • Antineoplastic Combined Chemotherapy Protocols (administration & dosage, therapeutic use)
  • Gastrointestinal Neoplasms (drug therapy)
  • Humans

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