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    Purpose At the molecular level, myeloma is characterized by copy number abnormalities and recurrent translocations into the immunoglobulin heavy chain locus. Novel methods, such as massively parallel sequencing, have begun to describe the pattern of tumor-acquired mutations, but their clinical relevance has yet to be established. Methods We performed whole-exome sequencing for 463 patients who presented with myeloma and were enrolled onto the National Cancer Research Institute Myeloma XI trial, for whom complete molecular cytogenetic and clinical outcome data were available. Results We identified 15 significantly mutated genes: IRF4, KRAS, NRAS, MAX, HIST1H1E, RB1, EGR1, TP53, TRAF3, FAM46C, DIS3, BRAF, LTB, CYLD, and FGFR3. The mutational spectrum is dominated by mutations in the RAS (43%) and nuclear factor-κB (17%) pathways, but although they are prognostically neutral, they could be targeted therapeutically. Mutations in CCND1 and DNA repair pathway alterations (TP53, ATM, ATR, and

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    • Mutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma [Aug 17, 2015] Walker et al. @JCO_ASCO https://t.co/kjH9EunwM1 #mmsm #camoldx #PrecisionMedicine Table 2. Actionable Mutations https://t.co/Y8WG1LcSNO

    • Mutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma [Aug 17, 2015] Walker et al. @JCO_ASCO https://t.co/kjH9EunwM1 #mmsm #camoldx #PrecisionMedicine

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    • The Longitudinal Dynamics and Natural History of Clonal Hematopoiesis [Dec 14, 2021] Margarete A Fabre et al. LBA-2 #ASH21 https://t.co/UZJgM7JOVm #leusm #mdssm #camoldx

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    Clonal hematopoiesis can be identified by the presence of somatic mutations in blood or bone marrow even in individuals without a myeloid malignancy. Advances in DNA sequencing have led to the discovery that clonal hematopoiesis is remarkably common and occurs in a wide variety of settings, each often described by unique acronym. These distinctions can be useful as the implications of clonal…

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    • CHIP, ICUS, CCUS and other four-letter words [Jun 8, 2017] Bejar @LeukemiaJnl https://t.co/KIC78XHsHd #leusm #mdssm #camoldx https://t.co/3go8Cy0qav

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    Liquid biopsy is a valuable precision oncology tool that is increasingly used as a non-invasive approach to identify biomarkers, detect resistance mutations, monitor disease burden, and identify early recurrence. The Tempus xF liquid biopsy assay is a 105-gene, hybrid-capture, next-generation sequencing (NGS) assay that detects single-nucleotide variants, insertions/deletions, copy number…

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    • Validation of a liquid biopsy assay (@TempusLabs xF) with molecular and clinical profiling of circulating tumor DNA [Jul 2, 2021] Finkle et al. npj Precision Oncology https://t.co/xFjMey93PM #PrecisionMedicine #LiquidBiopsy #camoldx #openaccess

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    Liquid biopsy is a valuable precision oncology tool that is increasingly used as a non-invasive approach to identify biomarkers, detect resistance mutations, monitor disease burden, and identify early recurrence. The Tempus xF liquid biopsy assay is a 105-gene, hybrid-capture, next-generation sequencing (NGS) assay that detects single-nucleotide variants, insertions/deletions, copy number…

    Tweet Tweets with this article
    • Validation of a liquid biopsy assay (@TempusLabs xF) with molecular and clinical profiling of circulating tumor DNA [Jul 2, 2021] Finkle et al. npj Precision Oncology https://t.co/xFjMey93PM #PrecisionMedicine #LiquidBiopsy #camoldx #openaccess

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    Liquid biopsy is a valuable precision oncology tool that is increasingly used as a non-invasive approach to identify biomarkers, detect resistance mutations, monitor disease burden, and identify early recurrence. The Tempus xF liquid biopsy assay is a 105-gene, hybrid-capture, next-generation sequencing (NGS) assay that detects single-nucleotide variants, insertions/deletions, copy number…

    Tweet Tweets with this article
    • Validation of a liquid biopsy assay (@TempusLabs xF) with molecular and clinical profiling of circulating tumor DNA [Jul 2, 2021] Finkle et al. npj Precision Oncology https://t.co/xFjMey93PM #PrecisionMedicine #LiquidBiopsy #camoldx #openaccess

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    Access educational materials, eLearning activities, accredited Live webinar sessions with polls and chat on this fast Digital Library and Hybrid Virtual Event Platform powered by MULTILEARNING LMS.

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    • Molecular Genetic Testing Patterns in Newly Dx AML: CONNECT® Registry [May 18, 2017] @DanPollyea et al. Abstract: E923 #EHA22 https://t.co/NOvxkVe5nr #NCT01688011 #AMLsm #leusm #oncopath #camoldx #PrecisionMedicine https://t.co/WY1p7tOThu