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Targeting genomic instability: From chemotherapy to precision medicine in cancer treatment

By

Timothy A. Yap1,6 Send email to [email protected]

2h ago· 42 min readenInsight

Summary

This article examines genomic instability as a hallmark of cancer, explaining how it drives malignant transformation through accumulated genetic and epigenetic alterations. It traces the evolution of treatments targeting this instability, from systemic chemotherapy and radiation to PARP inhibitors for homologous recombination repair-deficient tumors, and more recently to antibody-drug conjugates and radiopharmaceuticals. The piece emphasizes that precision medicine now focuses on patient selection and rational drug combinations to expand the therapeutic index and improve outcomes.

Key quotes

· 4 pulled
Genomic instability is a defining feature of cancer, which arises when the cellular systems that maintain DNA integrity falter
It is both the architect of cancer's evolution and its Achilles' heel
Targeting genomic instability has reshaped oncology: first through systemic chemotherapy and external beam radiation and then with poly(ADP-ribose) polymerase (PARP) inhibitors
Precision medicine targeting genomic instability now emphasizes patient selection and rational drug combinations, expanding the therapeutic index for better outcomes
Snippet from the RSS feed
Genomic instability, a hallmark of cancer, has been targeted by treatments from chemotherapy and radiation to PARP inhibitors for repair-deficient tumors, and more recently to antibody-drug conjugates and radiopharmaceuticals. Precision medicine targeting

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