News

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  • Database release

    In this release, we add two recent precision oncology approvals from the FDA.

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  • Database release

    In this release, we have removed neoantigen burden as a cataloged feature type and combined Silencing with Knockdown feature types. We additionally expanded upon fields required for each feature type within our S.O.P.

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  • Database release

    Added entries:

    • (FDA) FGFR2 rearrangements and sensitivity to futibatinib in intrahepatic cholangiocarcinoma.
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  • Database release

    Added entries:

    • (FDA) FGFR1 rearrangements and sensitivity to pemigatinib in myeloid/lymphoid neoplasms.
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  • Database release

    Added entries:

    • (FDA) ALK-EML4 and sensitivity to crizotinib in inflammatory myofibroblastic tumors.
    • (Clinical trial) BRCA1 and BRCA2 germline variants and sensitivity to olaparib.
    • (Clinical evidence) BRCA2 copy number deletion and loss-of-function somatic variants and sensitivity to olaparib in uterine leiomyosarcoma.
    • (Clinical evidence) CDKN2A deletion and sensitivity to palbociclib in uterine leiomyosarcoma.
    • (Clinical evidence) MYOCD amplification as a diagnostic for strong smooth muscle differentiation in leiomyosarcoma.
    • (Preclinical) RB1 copy number deletion and somatic variants and sensitivity to olaparib and talazoparib in prostate cancer.
    • (Preclinical) RB1 knockout and resistance to palbociclib in prostate cancer.
    • (Preclinical) USP11 silencing and sensitivity to olaparib in osteosarcoma.
    • (Inferential) ATRX copy number deletions and poor prognosis in leiomyosarcoma.
    • (Inferential) BRCA1 and BRCA2 copy number deletion and loss-of-function somatic variants and sensitivity to PARP inhibition (KU0058684, KU0058948).
    • (Inferential) CDKN2C deletion may confer sensitivity to CDK4/6 inhibitors.
    • (Inferential) MAP2K4 and MAPK7 copy number amplification and not sensitive to chemotherapy as well as poor prognosis in osteosarcoma.
    • (Inferential) PDGFRA copy number amplification and poor prognosis in breast cancer.
    • (Inferential) PTEN copy number deletion and poor prognosis in uterine leiomyosarcoma.
    • (Inferential) PTEN copy number deletion and sensitivity to sapanisertib in combination with alpelisib in uterine leiomyosarcoma.
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