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Related Concept Videos

Treatment Resistant Cancers02:56

Treatment Resistant Cancers

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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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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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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.
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Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
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Hybridoma technology is used for the large-scale production of monoclonal antibodies. Monoclonal antibodies bind to only a single antigenic determinant or epitope. Such antibodies are used in research, diagnostics, and disease therapy. The hybridoma technology established in 1975 by Georges Köhler and Cesar Milstein was awarded the Nobel Prize in Medicine in 1984 for revolutionizing research and therapy.
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Related Experiment Video

Updated: Mar 12, 2026

Multimodal Bioluminescent and Positronic-emission Tomography/Computational Tomography Imaging of Multiple Myeloma Bone Marrow Xenografts in NOG Mice
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Toward a cure for multiple myeloma within a decade.

Mohamad Mohty1, Florent Malard2, Thierry Facon3

  • 1Sorbonne Université, Centre de Recherche Saint-Antoine INSERM UMRs938, Service d'Hématologie Clinique et de Thérapie Cellulaire, Hôpital Saint Antoine, AP-HP, Paris, France. mohamad.mohty@inserm.fr.

Blood Cancer Journal
|March 11, 2026
PubMed
Summary

Multiple myeloma (MM) is nearing a cure era with deeper remissions and longer survival. Early, risk-adapted treatment targeting minimal residual disease (MRD) is key to achieving long-term outcomes.

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Area of Science:

  • Hematology
  • Oncology
  • Immunotherapy

Background:

  • Multiple myeloma (MM) was historically considered incurable.
  • Recent advances offer deeper remissions and prolonged survival, with a realistic prospect of cure.

Purpose of the Study:

  • To outline a transformative strategy for achieving cure in multiple myeloma.
  • To define optimal treatment paradigms focusing on early intervention and sustained minimal residual disease (MRD) negativity.

Main Methods:

  • Integrating genomics, microenvironmental, and immune profiling with artificial intelligence for risk stratification.
  • Utilizing targeted antibodies and combination therapies for early intervention.
  • Achieving sustained MRD negativity (10⁻⁶ sensitivity) validated by functional imaging.

Main Results:

  • Early intervention in high-risk smoldering MM can delay progression and improve survival.
  • Sustained MRD negativity for 2 years (standard-risk) or 3+ years (high-risk) predicts long-term progression-free survival.
  • Five years off therapy may approximate operational cure for MM.

Conclusions:

  • A cure for MM is increasingly attainable within the next decade through decisive, risk-adapted strategies.
  • Key priorities include standardized MRD assays, MRD-adapted trials, balancing toxicity, and ensuring global access.
  • Achieving sustained MRD negativity is central to realizing the goal of MM cure.