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selective estrogen receptor modulators |
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fulvestrant ER (promotes its destruction) |
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aromatase is necessary to produce estrogen are used in menopause because the ovaries of premenopausal women can produce enough aromatase to override the inhibition. |
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Anastrozole Aromatase inhibitors |
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exemestane Aromatase inhibitors |
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letrozole Aromatase inhibitors |
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Imatinib mesylate TKs gastrointestinal stromal tumor, leukemia, dermatofibrosarcoma protuberans, myelodysplastic/myeloproliferative disorders, and systemic mastocytosis. |
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Dasatinib TKs some patients with CML or ALL |
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Trastuzumab HER-2 breast cancer as well as some types of gastric or gastroesophageal junction adenocarcinoma. Trastuzumab may have other effects as well, such as inducing the immune system |
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Pertuzumab HER-2 metastatic breast HER-2+ monoclonal binds region allows HER-2 to interact with other receptors, eg EGFR immune system to attack HER-2-expressing cells. |
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Lapatinib TKs certain types of advanced or metastatic breast cancer. |
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Gefitinib kinase activity of EGFR advanced non-small cell lung cancer. |
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Erlotinib kinase activity of EGFR metastatic non-small cell lung cancer and pancreatic cancer that cannot be removed by surgery or has metastasized |
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Cetuximab monoclonal antibody squamous cell carcinoma of the head and neck or colorectal cancer. The drug binds to the external portion of EGFR |
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Panitumumab EGFR metastatic colon cancer. |
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Temsirolimus mTOR advanced renal cell carcinoma. |
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Everolimus immunophilin FK binding protein-12, forming a complex that binds to and inhibits the mTOR kinase advanced kidney cancer . Subependymal giant cell astrocytoma, advanced breast cancer, or patients with pancreatic neuroendocrine tumors |
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Vandetanib TKs (EGFR, VEGFRs, and RET) metastatic medullary thyroid cancer who are ineligible for surgery. |
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Vemurafenib BRAF V600E inoperable or metastatic melanoma. |
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Crizotinib EML4-ALK metastatic non-small cell lung cancer |
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Vorinostat HDACs cutaneous T-cell lymphoma (CTCL) that has persisted, progressed, or recurred during or after treatment with other medicines. |
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Panretin retinoic acid receptors and retinoid X receptors cutaneous lesions in patients with AIDS-related Kaposi sarcoma. |
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Tretinoin retinoid induction of remission in certain patients with acute promyelocytic leukemia. |
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Bortezomib proteasome multiple myeloma, mantle cell lymphoma. inhibitors. |
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Carfilzomib proteasome multiple myeloma inhibitor. |
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Pralatrexate peripheral anitfolate T-cell lymphoma. Other antifolates, such as methotrexate, are not considered targeted therapies because they interfere all dividing cells. However, pralatrexate appears to selectively accumulate in cells that express RFC-1 |
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Bevacizumab VEGF glioblastoma. also approved non-small cell lung cancer, metastatic colorectal cancer, and metastatic kidney cancer |
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Ziv-aflibercept portions of two different VEGF receptors recombinant fusion protein metastatic colorectal cancer |
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Sorafenib tyrosine kinases, VEGF signaling pathway advanced renal cell carcinoma and some cases of hepatocellular carcinoma. |
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Sunitinib tyrosine kinase VEGF signaling metastatic renal cell carcinoma, gastrointestinal stromal tumor or pancreatic neuroendocrine tumors that cannot be removed by surgery, are locally advanced, or have metastasized. |
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Pazopanib TKs (VEGF receptors, c-KIT, PDGF) advanced renal cell carcinoma and advanced soft tissue sarcoma |
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Regorafenib TKs ( VEGF receptors, the angiopoietin-1 receptor (TIE2), PDGFR, RET, c-KIT, and RAF) metastatic colorectal cancer |
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Cabozantinib TKs (VEGF receptors, RET, MET, TRKB, and TIE2) metastatic medullary thyroid cancer |
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Rituximab mAb CD20 monoclonal antibody B-cell non-Hodgkin lymphoma and, when combined with other drugs, to treat chronic lymphocytic leukemia (CLL). triggers an immune response that results in their destruction. Rituximab may also induce apoptosis. |
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Alemtuzumab B-cell mAb CD52, a protein found on the surface of normal and malignant B and T cells and many other cells of the immune system |
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Ofatumumab CD20 cell surface antigen CLL that does not respond to treatment with fludarabine and alemtuzumab. B-cell |
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Ipilimumab mAb cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) unresectable or metastatic melanoma. By inhibiting CTLA-4, ipilimumab stimulates the immune system to attack melanoma cells. |
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Tositumomab and 131I-tositumomab mixture mAbs CD20 molecule, some hav I131 B-cell non-Hodgkin lymphoma. |
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Ibritumomab tiuxetan CD20 mAb bind radioisotopes such as indium-111 or yttrium-90. B-cell non-Hodgkin lymphoma. |
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Denileukin diftitox IL-2 CTCL protein sequences fused to diphtheria toxin. |
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Brentuximab vedotin CD30 monoclonal antibody linked systemic anaplastic large cell lymphoma and Hodgkin lymphoma that has not responded to prior therapy. Linked to a drug called monomethyl auristatin E (MMAE), which induces cell cycle arrest and apoptosis. |
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