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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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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.
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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...
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Stem cell therapy is a method used in regenerative medicine to repair and restore function to damaged tissues and organs. Stem cells have the potential to proliferate and differentiate into various tissue types, making them ideal candidates for tissue regeneration. For example, hematopoietic stem cell transplants are commonly used in blood cancer treatment to replenish damaged bone marrow and restore healthy blood cells.
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Related Experiment Video

Updated: Sep 11, 2025

Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
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Adoptive T-Cell Therapy in Sarcomas.

Monika Kucharczyk1, Emine Hatipoglu1, Robin L Jones1,2

  • 1The Royal Marsden NHS Foundation Trust, London, UK.

Current Oncology Reports
|August 14, 2025
PubMed
Summary
This summary is machine-generated.

Adoptive T-cell therapies show promise for sarcomas, with engineered T-cell receptors (TCR-T) targeting NY-ESO-1 and MAGE-A4 leading the way. Innovations in CAR-T and TIL therapies aim to overcome challenges like tumor heterogeneity and improve patient outcomes.

Keywords:
Adoptive T-cell TherapyCancer-testis AntigenChimeric Antigen Receptor TEngineered T-cell ReceptorNY-ESO-1Sarcoma ImmunotherapyTumour Infiltrating Lymphocyte

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Area of Science:

  • Oncology
  • Immunotherapy
  • Cellular Therapy

Background:

  • Sarcomas are a heterogeneous group of rare cancers.
  • Adoptive T-cell therapy represents a novel approach to cancer treatment.

Purpose of the Study:

  • To review and assess recent advancements in adoptive T-cell therapies for sarcomas.
  • Focus on therapeutic targets, efficacy, safety, and limitations of these treatments.

Main Methods:

  • Review of current clinical trials and FDA approvals for adoptive T-cell therapies in sarcomas.
  • Analysis of T-cell receptor (TCR-T) therapies targeting NY-ESO-1 and MAGE-A4.
  • Evaluation of Chimeric Antigen Receptor (CAR-T) strategies targeting B7H3, GD2, FGFR4, and HER2.
  • Assessment of Tumour Infiltrating Lymphocyte (TIL) therapy in combination with other agents.

Main Results:

  • FDA approval of afamitresgene autoleucel and breakthrough designation for letetresgene autoleucel highlight progress in TCR-T therapy.
  • CAR-T strategies are exploring dual antigen targeting and safety switches.
  • TIL therapy is being investigated with checkpoint inhibitors and oncolytic agents.
  • Early promise shown by TCR-T therapy, but challenges like HLA restriction and tumor heterogeneity persist.

Conclusions:

  • Adoptive T-cell therapy, especially TCR-T, offers significant potential for sarcoma treatment.
  • Overcoming challenges in HLA restriction, tumor heterogeneity, and manufacturing is crucial.
  • Future directions include novel antigens, multi-targeting, and combination regimens to expand eligibility and enhance outcomes.