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SnapShot: The hallmarks of cancer treatment
Pietro Paolo Vitiello1, Vito Amodio1, Alberto Bardelli2
1IFOM ETS - The AIRC Institute of Molecular Oncology, 20139 Milan, Italy.
Abstract:
Cancer therapy evolved from cytotoxic chemotherapy to targeted and immune treatments guided by molecular profiling. Early cytotoxic drugs, rooted in mustard-gas observations, remain effective but toxic. Targeted agents exploit oncogenic vulnerabilities yet commonly select resistant clones. Checkpoint inhibitors and engineered modalities (ADCs, BiTEs, CAR-T) yield responses but are limited by toxicity and adaptive antigen loss. Future treatment combinations will require targeting the evolution of resistance. To view this SnapShot, open or download the PDF.
Insights
Cancer treatment has advanced from cytotoxic chemotherapy to targeted and immune therapies. Future strategies must address treatment resistance by targeting its evolution.
Area of Science:
- Oncology
- Cancer Therapeutics
- Molecular Biology
Background:
- Cancer therapy has evolved significantly, moving from traditional cytotoxic chemotherapy to more precise targeted and immune-based treatments.
- Early cytotoxic drugs, while effective, are associated with significant toxicity.
- Molecular profiling guides modern cancer treatments, but challenges like drug resistance persist.
Purpose of the Study:
- To review the evolution of cancer therapeutics.
- To highlight the limitations of current targeted and immune treatments.
- To emphasize the need for strategies that overcome treatment resistance.
Main Methods:
- Literature review of cancer therapy evolution.
- Analysis of cytotoxic, targeted, and immune treatment modalities.
- Discussion of resistance mechanisms and future directions.
Main Results:
- Cytotoxic chemotherapy, though toxic, remains a cornerstone.
- Targeted therapies and immune checkpoint inhibitors show promise but face resistance.
- Engineered modalities like Antibody-Drug Conjugates (ADCs), Bispecific T-cell Engagers (BiTEs), and Chimeric Antigen Receptor T-cell (CAR-T) therapies offer new avenues but have toxicity and antigen loss limitations.
Conclusions:
- Current cancer treatments, including targeted and immune therapies, are limited by toxicity and the emergence of resistance.
- Future cancer treatment combinations must proactively target the evolution of resistance to improve patient outcomes.
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