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Cancer

Last data update: Sep 24, 2022. (Total: 49607 Documents since 2012)
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Query Trace: all[original query]>>Guidelines Related[Product Type]
Optimising tissue acquisition and the molecular testing pathway for patients with non-small cell lung cancer: A UK expert consensus statement.
Navani Neal et al. Lung cancer (Amsterdam, Netherlands) 2022 172142-153
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Horak Peter et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022 24(9) 1991
Mismatch Repair and Microsatellite Instability Testing for Immune Checkpoint Inhibitor Therapy.
Bartley Angela N et al. Archives of pathology & laboratory medicine 2022
Portuguese Consensus Recommendations for Next-Generation Sequencing of Lung Cancer, Rare Tumors, and Cancers of Unknown Primary Origin in Clinical Practice.
R Teixeira Manuel et al. Acta medica portuguesa 2022
International Consensus Classification of Myeloid Neoplasms and Acute Leukemia: Integrating Morphological, Clinical, and Genomic Data.
Arber Daniel A et al. Blood 2022
Consensus Recommendations of the German Consortium for Hereditary Breast and Ovarian Cancer.
Rhiem Kerstin et al. Breast care (Basel, Switzerland) 2022 17(2) 199-207
Implementation of preventive and predictive BRCA testing in patients with breast, ovarian, pancreatic, and prostate cancer: a position paper of Italian Scientific Societies.
Russo A et al. ESMO open 2022 7(3) 100459
Practice guidelines for BRCA1/2 tumour testing in ovarian cancer.
Grafodatskaya Daria et al. Journal of medical genetics 2022
Expert Consensus on the Use of Prognostic Gene Expression Profiling Tests for the Management of Cutaneous Melanoma: Consensus from the Skin Cancer Prevention Working Group.
Farberg Aaron S et al. Dermatology and therapy 2022
Automated Clinical Practice Guideline Recommendations for Hereditary Cancer Risk Using Chatbots and Ontologies: System Description.
Ritchie Jordon B et al. JMIR cancer 2022 8(1) e29289
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: 2 approved, 2 approved with reservations].
Lewis Celine et al. NIHR open research 2022 123
Overview of the Clinical Features of Li-Fraumeni Syndrome and the Current European ERN GENTURIS Guideline.
Kratz Christian Peter et al. Geburtshilfe und Frauenheilkunde 2022 82(1) 42-49
Practical Consensus Recommendations for Optimizing Risk versus Benefit of Chemotherapy in Patients with HR Positive Her2 Negative Early Breast Cancer in India.
Parikh Purvish M et al. South Asian journal of cancer 2022 10(4) 213-219
Recommendations for the Use of Next-Generation Sequencing and the Molecular Tumor Board for Patients with Advanced Cancer: A Report from KSMO and KCSG Precision Medicine Networking Group.
Yoon Shinkyo et al. Cancer research and treatment 2021
European Experts Consensus: BRCA/Homologous Recombination Deficiency Testing in First-Line Ovarian Cancer.
Vergote I et al. Annals of oncology : official journal of the European Society for Medical Oncology 2021
Management of Immune-Related Adverse Events in Patients Treated With Chimeric Antigen Receptor T-Cell Therapy: ASCO Guideline.
Santomasso Bianca D et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2021 JCO2101992
Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: ASCO Guideline Update.
Schneider Bryan J et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2021 JCO2101440
Medical guidelines for Li-Fraumeni syndrome 2019, version 1.1.
Kumamoto Tadashi et al. International journal of clinical oncology 2021
Clinical Practice Guidelines for Pre-Analytical Procedures of Plasma Epidermal Growth Factor Receptor Variant Testing.
Shin Saeam et al. Annals of laboratory medicine 2021 42(2) 141-149
Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe.
Marmolejo David Humberto et al. European journal of medical genetics 2021 104350
Update Swiss guideline for counselling and testing for predisposition to breast, ovarian, pancreatic and prostate cancer.
Stoll Susanna et al. Swiss medical weekly 2021 151w30038
Exploring Gene-Specific Guidelines for Risk Management of Gynecological Cancer in Lynch Syndrome.
Petelin Lara et al. JAMA network open 2021 4(9) e2124384
Genetic risk assessment for hereditary renal cell carcinoma: Clinical consensus statement.
Bratslavsky Gennady et al. Cancer 2021
Evaluation and comparison of hereditary Cancer guidelines in the population.
Ritchie Jordon B et al. Hereditary cancer in clinical practice 2021 19(1) 31
Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2020 for the Clinical Practice of Hereditary Colorectal Cancer.
Tomita Naohiro et al. International journal of clinical oncology 2021
Uptake and timing of risk-reducing salpingo-oophorectomy among patients with BRCA1/2 mutations.
Smith Maria J et al. American journal of obstetrics and gynecology 2021
Genetic testing for inherited colorectal cancer and polyposis, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Mao Rong et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021
Genetic testing for inherited colorectal cancer and polyposis, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
R Mao et al, Genetics in Medicine, June 17, 2021
Recent Insights on Genetic Testing in Primary Prostate Cancer.
Kafka Mona et al. Molecular diagnosis & therapy 2021
European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender.
Seppälä T T et al. The British journal of surgery 2021 108(5) 484-498
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