Targeted therapy in patients with genetic tumor syndromes

Significant progress in comprehensive molecular diagnostics and targeted therapies for advanced malignancies has, in part, led to substantial improvements in patient outcomes. Nevertheless, comprehensive genomic profiling necessitates interdisciplinary discussion of potential clinical recommendations within interdisciplinary molecular tumor boards. (Likely) pathogenic germline variants (PGVs) typically warrant genetic counseling for patients and, where appropriate, their relatives. Concurrently, the rapidly expanding availability of targeted therapies introduces new therapeutic implications based on germline alterations that must be integrated into clinical decision-making. Moreover, the identification of PGVs may not only inform therapy in patients with manifest malignancy but also offer opportunities for targeted chemoprevention.

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Publication Details

Journal
Medizinische Genetik
Published
2025-11-06
DOI
https://doi.org/10.1515/medgen-2025-2045
Primary Topic
Genomics and Rare Diseases
Type
article
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article

Targeted therapy in patients with genetic tumor syndromes

Stefan Fröhling, Arne Jahn, Evelin Schröck, Christoph Heining et al.
Medizinische Genetik
Genomics and Rare Diseases
article

Targeted therapy in patients with genetic tumor syndromes

Stefan Fröhling, Arne Jahn, Evelin Schröck, Christoph Heining, Hanno Glimm
article en

Abstract

Significant progress in comprehensive molecular diagnostics and targeted therapies for advanced malignancies has, in part, led to substantial improvements in patient outcomes. Nevertheless, comprehensive genomic profiling necessitates interdisciplinary discussion of potential clinical recommendations within interdisciplinary molecular tumor boards. (Likely) pathogenic germline variants (PGVs) typically warrant genetic counseling for patients and, where appropriate, their relatives. Concurrently, the rapidly expanding availability of targeted therapies introduces new therapeutic implications based on germline alterations that must be integrated into clinical decision-making. Moreover, the identification of PGVs may not only inform therapy in patients with manifest malignancy but also offer opportunities for targeted chemoprevention.

Medizinische GenetikVol. 37(4)
German Cancer Research Center (DE), Heidelberg University (DE), University Hospital Carl Gustav Carus (DE)
Openalex Percentile: Top 65%
Genomics and Rare Diseases
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Targeted therapy in patients with genetic tumor syndromes — Stefan Fröhling, Arne Jahn, et al. · Medizinische Genetik (2025) | TGRS Research Map | TGRS