Progress and challenges towards targeted delivery of cancer therapeutics

Daniel Rosenblum1, Nitin Joshi2,3, Wei Tao4

  • 1Laboratory of Precision NanoMedicine, School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Sciences, Department of Materials Sciences and Engineering, Iby and Aladar Fleischman Faculty of Engineering; Center for Nanoscience and Nanotechnology, Cancer Biology Research Center, Tel Aviv University, Tel Aviv, 6997801, Israel.

Nature Communications
|April 14, 2018
PubMed

Insights

Targeted cancer nanocarriers show promise but face clinical translation challenges. This review examines reasons for limited success and proposes criteria for developing effective actively targeted nanocarriers for cancer therapy.

Area of Science:

  • Oncology
  • Nanotechnology
  • Drug Delivery

Background:

  • Targeted delivery systems for cancer therapeutics have advanced significantly in preclinical research.
  • Despite numerous successful preclinical studies, clinical translation remains a significant hurdle.
  • Only a limited number of passively targeted nanocarriers (NCs) have gained clinical approval, with no actively targeted NCs progressing beyond clinical trials.

Purpose of the Study:

  • To review the fundamental principles of targeted delivery strategies for cancer therapeutics.
  • To identify potential reasons behind the limited clinical success of targeted nanocarriers.
  • To propose essential criteria for the development of novel actively targeted nanocarriers.

Main Methods:

  • Literature review of targeted delivery approaches in cancer therapy.
  • Analysis of factors limiting clinical translation of nanocarriers.
  • Formulation of criteria for designing effective actively targeted nanocarriers.

Main Results:

  • Preclinical success of targeted nanocarriers does not consistently translate to clinical efficacy.
  • Key challenges include biological barriers, off-target effects, and manufacturing complexities.
  • Lack of standardized criteria for active targeting hinders development.

Conclusions:

  • Actively targeted nanocarriers require rigorous evaluation beyond preclinical models.
  • Development must consider specific tumor microenvironments and patient heterogeneity.
  • Future strategies should focus on robust design principles and clinical validation for successful tumor targeting.

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