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Published on: September 3, 2013
[Molecular Targeted Therapies for Hereditary Cancer Syndrome]
1Division of Medical Oncology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University.
Abstract:
Development of molecular targeted drugs has achieved remarkable improvement of systemic cancer therapy. Recently, the several molecular targeted drugs have become available which associated with the status of responsible genes for hereditary cancer syndrome. These drugs would allow to establish specific strategy for hereditary cancer syndrome or sporadic cancers with similar biological phenotype with hereditary cancer. Genetic tests for the diagnosis of hereditary cancer syndrome will have the meaning of biomarker for predicting the efficacy of these molecular targeted drugs. This review summarized the molecular targeted drugs including immune checkpoint inhibitors with potential effects for hereditary cancer syndrome, such as anti-PD-1 antibody for Lynch syndrome, PARP inhibitor for hereditary breast and ovarian cancer syndrome, multi-kinase inhibitor for multiple endocrine neoplasia type 2.
Insights
Molecular targeted drugs offer new strategies for hereditary cancer syndromes. Genetic testing can predict treatment response to these novel therapies, including immune checkpoint inhibitors and PARP inhibitors.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- Molecular targeted drugs have significantly advanced cancer therapy.
- New drugs are emerging that target genes responsible for hereditary cancer syndromes.
- These targeted therapies offer personalized treatment strategies for hereditary and sporadic cancers with similar biological profiles.
Purpose of the Study:
- To review molecular targeted drugs with potential efficacy in hereditary cancer syndromes.
- To highlight the role of genetic testing as a biomarker for predicting drug response.
Main Methods:
- Literature review of molecular targeted drugs.
- Focus on drugs associated with hereditary cancer syndrome genes.
- Inclusion of immune checkpoint inhibitors and other targeted agents.
Main Results:
- Anti-PD-1 antibodies show potential for Lynch syndrome.
- PARP inhibitors are effective for hereditary breast and ovarian cancer syndromes.
- Multi-kinase inhibitors are relevant for multiple endocrine neoplasia type 2.
Conclusions:
- Genetic testing for hereditary cancer syndromes serves as a biomarker for predicting molecular targeted drug efficacy.
- Targeted therapies, including immune checkpoint inhibitors and PARP inhibitors, represent a significant advancement in managing hereditary cancers.
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