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Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

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Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
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Cytotoxic T Cells-mediated Immune Response01:27

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Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
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Predictive Immune Modeling of Solid Tumors
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Artificial Intelligence Algorithm Predicts Response to Immune Checkpoint Inhibitors.

Faisal Fa'ak1,2, Nicolas Coudray3,4, George Jour5

  • 1Division of Medical Oncology, Washington University School of Medicine, St. Louis, Missouri.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|June 24, 2025
PubMed
Summary
This summary is machine-generated.

Machine learning models predict response to immune checkpoint inhibitors (ICI) in melanoma patients. Novel tumor features like epithelioid histology and low tumor-stroma ratio are linked to improved survival outcomes with ICI therapy.

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Area of Science:

  • Oncology
  • Computational Pathology
  • Immunotherapy

Background:

  • Immune checkpoint inhibitors (ICIs) have transformed cancer care, but patient response varies significantly.
  • Predicting ICI response and adverse events remains challenging due to a lack of generalizable biomarkers.
  • Previous work established a supervised machine learning (ML) model for ICI response in metastatic melanoma.

Purpose of the Study:

  • To validate and expand the generalizability of a supervised ML algorithm for predicting ICI response in larger melanoma cohorts.
  • To develop a self-supervised ML model to identify histologic features associated with patient survival after ICI treatment.
  • To investigate ICI response and survival in both adjuvant and metastatic melanoma settings.

Main Methods:

  • Analysis of pretreatment hematoxylin and eosin slides from 639 stage III/IV melanoma patients treated with ICIs (anti-CTLA-4, anti-PD-1, or combination).
  • Testing the generalizability of a supervised ML algorithm on a metastatic melanoma cohort.
  • Developing a self-supervised ML model to correlate histologic morphologies with progression-free and overall survival.

Main Results:

  • The supervised ML algorithm achieved an AUC of 0.72 in predicting ICI treatment response.
  • A deep convolutional neural network classified patients into high and low risk groups for progression-free survival (P < 0.0001).
  • Novel associations were found between epithelioid histology, low tumor-stroma ratio, and improved survival following ICI treatment.

Conclusions:

  • The developed ML algorithm demonstrates generalizability in predicting ICI treatment response for metastatic melanoma.
  • This study provides the first identification of specific tumor histologic features associated with overall survival in patients receiving ICIs.
  • These findings pave the way for integrating ML-based biomarkers into clinical practice for personalized melanoma treatment.