Novel Theranostic Approaches Targeting CCR4-Receptor, Current Status and Translational Prospectives: A Systematic

Joana Gorica1, Maria Silvia De Feo1, Ferdinando Corica1

  • 1Department of Radiological Sciences, Oncology and Anatomo-Pathology, Sapienza, University of Rome, 00161 Rome, Italy.

Abstract

Insights

Novel theranostic approaches targeting chemokine receptor 4 (CCR4) show promise for cancer diagnosis and therapy. Further clinical translation is needed to implement these CCR4-targeting agents widely.

Area of Science:

  • Oncology
  • Radiopharmaceuticals
  • Molecular Imaging

Background:

  • Malignant tumors have high mortality rates, necessitating advanced theranostic strategies for early detection and targeted treatment.
  • Chemokine receptor 4 (CCR4) is frequently overexpressed in various cancers, contributing to tumor development.
  • CCR4 represents a potential target for integrated diagnostic and therapeutic applications in oncology.

Purpose of the Study:

  • To systematically review and synthesize existing clinical and preclinical research on CCR4 as a theranostic target.
  • To classify and analyze studies involving CCR4 in human and animal models across different tumor types and applications.
  • To provide a comprehensive overview of CCR4-based theranostic strategies.

Main Methods:

  • A systematic literature search was performed across major databases (PubMed, Scopus, CENTRAL, Web of Science) from January 2006 to November 2022.
  • Inclusion criteria focused on studies investigating CCR4 expression in tumors in humans, in vivo, or in vitro.
  • Methodological quality of human studies was assessed using the Critical Appraisal Skills Programme (CASP).

Main Results:

  • Out of 17 initially screened articles, 13 were selected for qualitative analysis after excluding 4 ineligible studies.
  • Six studies were further selected for detailed methodological quality assessment using CASP.
  • The review synthesized data on CCR4's role and therapeutic targeting across diverse oncological contexts.

Conclusions:

  • Emerging radionuclides and radiopharmaceuticals targeting CCR4 demonstrate significant potential for theranostics in CCR4-sensitive tumors.
  • Translating preclinical findings into robust clinical data is crucial for broader adoption of CCR4-targeted theranostics.
  • Further research is warranted to optimize and validate CCR4-based theranostic agents for clinical use.