Hereditary Cancer in Clinical Practice

Scope & Guideline

Empowering Research to Transform Cancer Treatment

Introduction

Welcome to the Hereditary Cancer in Clinical Practice information hub, where our guidelines provide a wealth of knowledge about the journal’s focus and academic contributions. This page includes an extensive look at the aims and scope of Hereditary Cancer in Clinical Practice, highlighting trending and emerging areas of study. We also examine declining topics to offer insight into academic interest shifts. Our curated list of highly cited topics and recent publications is part of our effort to guide scholars, using these guidelines to stay ahead in their research endeavors.
LanguageEnglish
ISSN1731-2302
PublisherBMC
Support Open AccessYes
CountryUnited Kingdom
TypeJournal
Convergefrom 2004 to 2024
AbbreviationHERED CANCER CLIN PR / Hered. Cancer Clin. Pract.
Frequency1 issue/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
AddressCAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND

Aims and Scopes

The journal 'Hereditary Cancer in Clinical Practice' focuses on the intersection of hereditary cancer syndromes and clinical practice, aiming to enhance the understanding and management of hereditary cancer risks. It serves as a platform for disseminating research findings, clinical experiences, and innovative practices in the field of hereditary cancers.
  1. 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.
  2. 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.
  3. 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.
  4. 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.
  5. 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.
Recent publications in 'Hereditary Cancer in Clinical Practice' indicate emerging themes that are gaining traction, reflecting advancements in genetics, technology, and patient care.
  1. 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.
  2. 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.
  3. 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.
  4. 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.
  5. 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

While the journal covers a broad spectrum of hereditary cancer topics, certain themes appear to be waning in frequency. These declining scopes may reflect shifts in research focus or changing clinical practices.
  1. 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.
  2. 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.
  3. 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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