Search Results - "Drilon, A."

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    TRK inhibitors in TRK fusion-positive cancers by Drilon, A

    Published in Annals of oncology (01-11-2019)
    “…TRK fusions are oncogenic drivers of various adult and paediatric cancers. The first-generation TRK inhibitors, larotrectinib and entrectinib, were granted…”
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    Journal Article
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    Selective RET kinase inhibition for patients with RET-altered cancers by Subbiah, V., Velcheti, V., Tuch, B.B., Ebata, K., Busaidy, N.L., Cabanillas, M.E., Wirth, L.J., Stock, S., Smith, S., Lauriault, V., Corsi-Travali, S., Henry, D., Burkard, M., Hamor, R., Bouhana, K., Winski, S., Wallace, R.D., Hartley, D., Rhodes, S., Reddy, M., Brandhuber, B.J., Andrews, S., Rothenberg, S.M., Drilon, A.

    Published in Annals of oncology (01-08-2018)
    “…Alterations involving the RET kinase are implicated in the pathogenesis of lung, thyroid and other cancers. However, the clinical activity of multikinase…”
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    NRG1 fusion-driven tumors: biology, detection, and the therapeutic role of afatinib and other ErbB-targeting agents by Laskin, J., Liu, S.V., Tolba, K., Heining, C., Schlenk, R.F., Cheema, P., Cadranel, J., Jones, M.R., Drilon, A., Cseh, A., Gyorffy, S., Solca, F., Duruisseaux, M.

    Published in Annals of oncology (01-12-2020)
    “…Oncogenic gene fusions are hybrid genes that result from structural DNA rearrangements, leading to deregulated activity. Fusions involving the neuregulin-1…”
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    Characterization of on-target adverse events caused by TRK inhibitor therapy by Liu, D., Flory, J., Lin, A., Offin, M., Falcon, C.J., Murciano-Goroff, Y.R., Rosen, E., Guo, R., Basu, E., Li, B.T., Harding, J.J., Iyer, G., Jhaveri, K., Gounder, M.M., Shukla, N.N., Roberts, S.S., Glade-Bender, J., Kaplanis, L., Schram, A., Hyman, D.M., Drilon, A.

    Published in Annals of oncology (01-09-2020)
    “…The tropomyosin receptor kinase (TRK) pathway controls appetite, balance, and pain sensitivity. While these functions are reflected in the on-target adverse…”
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    ESMO recommendations on the standard methods to detect RET fusions and mutations in daily practice and clinical research by Belli, C., Penault-Llorca, F., Ladanyi, M., Normanno, N., Scoazec, J.-Y., Lacroix, L., Reis-Filho, J.S., Subbiah, V., Gainor, J.F., Endris, V., Repetto, M., Drilon, A., Scarpa, A., André, F., Douillard, J.-Y., Curigliano, G.

    Published in Annals of oncology (01-03-2021)
    “…Aberrant activation of RET is a critical driver of growth and proliferation in diverse solid tumours. Multikinase inhibitors (MKIs) showing anti-RET activities…”
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    Clinical outcomes with pemetrexed-based systemic therapies in RET-rearranged lung cancers by Drilon, A., Bergagnini, I., Delasos, L., Sabari, J., Woo, K.M., Plodkowski, A., Wang, L., Hellmann, M.D., Joubert, P., Sima, C.S., Smith, R., Somwar, R., Rekhtman, N., Ladanyi, M., Riely, G.J., Kris, M.G.

    Published in Annals of oncology (01-07-2016)
    “…RET rearrangements are targetable, oncogenic lung cancer drivers. While previous series have shown durable clinical benefit with pemetrexed-based therapies in…”
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    A prospective study of total plasma cell-free DNA as a predictive biomarker for response to systemic therapy in patients with advanced non-small-cell lung cancers by Li, B.T., Drilon, A., Johnson, M.L., Hsu, M., Sima, C.S., McGinn, C., Sugita, H., Kris, M.G., Azzoli, C.G.

    Published in Annals of oncology (01-01-2016)
    “…While previous studies have reported on the prognostic value of total plasma cell-free deoxyribonucleic acid (cfDNA) in lung cancers, few have prospectively…”
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    Enrichment of kinase fusions in ESR1 wild-type, metastatic breast cancer revealed by a systematic analysis of 4854 patients by Ross, D.S., Liu, B., Schram, A.M., Razavi, P., Lagana, S.M., Zhang, Y., Scaltriti, M., Bromberg, J.F., Ladanyi, M., Hyman, D.M., Drilon, A., Zehir, A., Benayed, R., Chandarlapaty, S., Hechtman, J.F.

    Published in Annals of oncology (01-08-2020)
    “…Kinase fusions are rare and poorly characterized in breast cancer (BC). We aimed to characterize kinase fusions within a large cohort of advanced BC. A total…”
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    The type II switch control kinase inhibitor, DCC-2701 (altiratinib) effectively inhibits resistant NTRK kinase domain mutants by Drilon, A, Hofmann, N, Flynn, D, Smith, B, Davare, M

    Published in European journal of cancer (1990) (01-12-2016)
    “…Background: Oncoproteins resulting from NTRK family gene rearrangements function as dominant drivers in multiple malignancies. Ongoing clinical trials…”
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