Molecular and Clinical Approach to Intra-abdominal Adverse Effects of Targeted Cancer Therapies

Stephanie T Chang1, Christine O Menias1, Meghan G Lubner1

  • 1From the Department of Radiology, VA Palo Alto Health Care System, Palo Alto, Calif (S.T.C.); Department of Radiology, Stanford University School of Medicine, 300 Pasteur Dr, H1307 MC 5621, Stanford, CA 94305 (S.T.C., T.S.D.); Department of Radiology, Mayo Clinic, Scottsdale, Ariz (C.O.M., A.K.H.); Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison, Wis (M.G.L.); and Mallinckrodt Institute of Radiology, Washington University School of Medicine, St Louis, Mo (V.M.M.).

Insights

Radiologists need a molecular framework to understand targeted cancer therapy side effects. This approach helps differentiate toxic effects from tumor progression, improving patient management.

Area of Science:

  • Radiology
  • Oncology
  • Molecular Biology

Background:

  • Targeted cancer therapies are rapidly evolving, involving complex molecular pathways.
  • Traditional organ system-based adverse effect cataloging is insufficient for modern oncology.
  • Radiologists require a new framework integrating molecular mechanisms and clinical outcomes.

Purpose of the Study:

  • To present a conceptual framework for understanding adverse effects of targeted cancer therapies.
  • To classify these adverse effects based on molecular mechanisms.
  • To aid radiologists in differentiating treatment toxicities from tumor progression.

Main Methods:

  • Review of established and hypothesized molecular mechanisms of targeted therapy adverse effects.
  • Classification of adverse effects into four categories based on molecular targets and treatment response.
  • Illustration of key imaging findings for abdominal and pelvic toxicities.

Main Results:

  • Adverse effects can be categorized as on-target with or without response, off-target, or tumor necrosis-related.
  • Understanding molecular underpinnings aids in recognizing and managing toxicities.
  • Imaging manifestations of adverse effects are linked to specific molecular pathways.

Conclusions:

  • A molecular-based approach is essential for radiologists in the era of targeted cancer therapies.
  • This framework enhances the ability to differentiate adverse effects from tumor progression.
  • Radiologists can better guide oncologic treatment decisions by understanding these mechanisms.

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...
9.0K
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...
6.2K
Cancer Therapies02:49

Cancer Therapies

Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
10.3K
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase01:11

Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase

Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
51