Hereditary Cancer in Clinical Practice
Scope & Guideline
Empowering Research to Transform Cancer Treatment
Introduction
Aims and Scopes
- Hereditary Cancer Syndromes Research:
The journal emphasizes research on various hereditary cancer syndromes, such as Lynch syndrome, BRCA1/2 mutations, and Li-Fraumeni syndrome, providing insights into genetic predispositions and their implications for cancer risk. - Clinical Management Strategies:
It covers methodologies for the clinical management of hereditary cancers, including risk assessment, screening protocols, and treatment options tailored to genetic profiles. - Patient Experiences and Psychosocial Aspects:
The journal explores the psychosocial impacts of hereditary cancer diagnoses on patients and families, focusing on their experiences, emotional responses, and the decision-making processes regarding genetic testing and preventive measures. - Genetic Testing and Screening Innovations:
A significant focus is on advancements in genetic testing techniques, including next-generation sequencing and population-based screening strategies, to better identify individuals at risk. - International Perspectives and Guidelines:
The journal includes contributions on international guidelines and practices in hereditary cancer management, fostering a global dialogue on best practices and emerging trends.
Trending and Emerging
- Multimodal Approaches to Treatment:
There is a growing trend towards exploring multimodal treatment strategies that combine genetic insights with advanced therapeutic options, such as targeted therapies and immunotherapy for hereditary cancers. - Patient-Centric Research:
An increase in studies focusing on patient experiences, preferences, and psychosocial factors related to genetic testing and cancer prevention strategies highlights a shift towards more patient-centered research. - Integration of Telemedicine in Genetic Services:
The incorporation of telemedicine for genetic counseling and follow-up care has emerged as a significant theme, especially in the context of the COVID-19 pandemic, indicating a shift towards accessible healthcare solutions. - Emerging Genetic Testing Technologies:
Innovations in genetic testing technologies, such as liquid biopsies and expanded gene panels, are increasingly featured, reflecting the rapid evolution of genetic diagnostics and their application in clinical practice. - Focus on Minority and Diverse Populations:
There is a notable rise in research addressing hereditary cancer risks in diverse populations, emphasizing the importance of understanding genetic variations and cancer risks across different ethnic groups.
Declining or Waning
- General Cancer Epidemiology Studies:
The journal has seen a decrease in publications that focus solely on general cancer epidemiology without a hereditary context, as the emphasis shifts towards hereditary-specific research. - Traditional Risk Factor Assessments:
There has been a decline in studies that focus on traditional lifestyle-related risk factors (like diet and exercise) in the context of hereditary cancers, as the field moves towards more genetic and molecular insights. - Single Pathogenetic Variant Studies:
Research centered on the implications of single genetic variants without broader context or comprehensive genetic testing approaches is becoming less common, with a preference for studies that consider multiple genetic factors.
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