Fibroblast Activation Protein Inhibitor (FAPI)-Based Theranostics-Where We Are at and Where We Are Heading: A

Marko Magdi Abdou Sidrak1, Maria Silvia De Feo1, Ferdinando Corica1

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

Insights

Fibroblast activation protein (FAP) imaging tracers show promise for cancer theranostics. Current research indicates FAP tracers are well-tolerated and may aid in assessing cancer progression.

Area of Science:

  • Oncology
  • Nuclear Medicine
  • Radiochemistry

Background:

  • Cancer remains a leading global cause of mortality.
  • Precision medicine tailors diagnostics and therapeutics to individual patients.
  • Fibroblast activation protein (FAP) imaging tracers are emerging tools for cancer assessment and treatment.

Approach:

  • A systematic literature review was conducted using MEDLINE, PubMed, Cochrane, Scopus, and Web of Science.
  • Eight studies from 2018 to November 2022, focusing on FAP theranostics, were critically appraised using the CASP checklist.
  • The review assessed study objectives, diagnostic/reference tests, results, patient samples, and future applications.

Key Points:

  • Studies included heterogeneous sample sizes and tumor types; only one focused on a single cancer type.
  • Disease progression was the most frequently reported outcome.
  • No significant adverse effects were observed, and FAP tracers demonstrated good tolerability.

Conclusions:

  • FAPI theranostics is an emerging field with potential in oncology.
  • While still in early development, FAP tracers exhibit a favorable safety profile for patient administration.
  • Further research is needed to establish FAP theranostics in clinical practice.

Related Concept Videos

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.8K
Introduction to Fibroblasts01:09

Introduction to Fibroblasts

Rudolph Virchow discovered spindle-shaped cells called fibroblasts in 1858. Inactive fibroblasts, called fibrocytes, become activated by various stimuli, such as growth factors and inflammatory cytokines. Activated fibroblasts play a crucial role in wound healing, inflammation, formation of new blood vessels, and cancer progression. Uncontrolled activation of fibroblasts results in fibrosis, the excess deposition of fibrous tissue, which can lead to scarring and affect normal organs. This...
3.2K
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.4K
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
5.0K