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Titlebook: Novel Therapeutics for Rare Lymphomas; Christopher Dittus Book 2020 Springer Nature Switzerland AG 2020 lymphoma.novel therapeutics for ra

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發(fā)表于 2025-3-21 16:50:19 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Novel Therapeutics for Rare Lymphomas
編輯Christopher Dittus
視頻videohttp://file.papertrans.cn/669/668467/668467.mp4
概述Discusses the clinical presentation, diagnosis, and treatment approach to rare lymphomas.Focuses on new diagnostic approaches, novel chemotherapy combinations, and new treatment modalities with novel
圖書封面Titlebook: Novel Therapeutics for Rare Lymphomas;  Christopher Dittus Book 2020 Springer Nature Switzerland AG 2020 lymphoma.novel therapeutics for ra
描述.This comprehensive volume reviews the clinical presentation, diagnosis, and treatment approach to rare lymphomas. There is particular emphasis placed on new diagnostic approaches, novel chemotherapy combinations, and treatment modalities with novel therapeutics. It highlights research advances in a group of diseases that are often overlooked, and serves as a single repository of information on the most recent advances in targeted small molecule inhibitors, monoclonal antibodies, immunotherapy, and CAR-T therapy as they pertain to rare types of lymphoma. Written for practicing oncologists, hematologists, fellows, and residents,?.Novel Therapeutics for Rare Lymphomas.?covers rare subtypes of lymphoma, including indolent and aggressive T-cell lymphomas and B-cell lymphomas..
出版日期Book 2020
關(guān)鍵詞lymphoma; novel therapeutics for rare lymphomas; rare lymphomas; novel therapeutics; t-cell lymphomas; ag
版次1
doihttps://doi.org/10.1007/978-3-030-25610-4
isbn_softcover978-3-030-25612-8
isbn_ebook978-3-030-25610-4
copyrightSpringer Nature Switzerland AG 2020
The information of publication is updating

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Immunotherapy in Hodgkin Lymphoma and Other CD30+ Lymphomas,e Ki-1 antibody binding to Reed-Sternberg cells in Hodgkin lymphoma (Stein et al., Blood 66(4):848–858, 1985). Since it has high expression within Hodgkin lymphoma (HL) and anaplastic large cell lymphoma (ALCL), variable expression in other non-Hodgkin lymphoma subgroups, and limited expression in n
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Novel Agents in Primary Central Nervous System Lymphoma,te-based therapies has improved patient outcomes in the first-line setting, the prognosis of relapsed and refractory disease is poor. PCNSL has a unique pathophysiology and gene expression profile, making it more amenable to novel targeted and immunotherapeutic agents. Therapies such as ibrutinib, n
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Extranodal NK/T-Cell Lymphoma,and is characterized by localized lesions involving the nose, nasopharynx, or oropharynx. Extra-nasal disease is less common and generally more aggressive. The immunophenotype of ENKTCL is unique, with most cases expressing NK-cell markers (CD2+, cytoplasmic CD3+, and CD56+). Treatment options for l
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