Molecular targets in diffuse large B cell lymphoma
Molecular targets in diffuse large B cell lymphoma
批准号:
7998215
负责人:
Sandeep Dave
金额:
$25.12万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-02-18 至 2013-11-30
关键词:
AccountingAftercareAnthracyclinesCSF1 geneCategoriesCellsCessation of lifeChemotaxisChemotherapy-Oncologic ProcedureClinicClinicalClinical TrialsCombination Drug TherapyCytogeneticsData SetDependenceDiagnosisDiseaseDrug CombinationsEmployee StrikesExhibitsFailureFollicular LymphomaGene ExpressionGene Expression ProfileGene Expression ProfilingGene TargetingGenesHealthHeterogeneityImmuneImmune responseIn VitroIncidenceLymphomaMethodsMolecularMolecular ProfilingMolecular TargetNatureNon-Hodgkin&aposs LymphomaOncogenicPathway interactionsPatient SelectionPatientsPredispositionRNA InterferenceRegimenRelapseResearchRoleS-NitrosoglutathioneSerum MarkersSubgroupTestingTherapeuticTranslatingTranslationsTumor BiologyUnited StatesValidationWorkanalytical methodbasechemotherapyearly experienceefficacy testingin vitro testingin vivoinsightlarge cell Diffuse non-Hodgkin&aposs lymphomamacrophagemolecular recognitionnew therapeutic targetnovel strategiesoutcome forecastresponserituximabsmall moleculetherapeutic targettumortumor growth
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Diffuse large B cell lymphoma (DLBCL) is the most common form of non Hodgkin lymphoma, with an annual incidence of 25,000 in the United States and nearly 10,000 deaths per year attributable to the disease. Although chemotherapy is the mainstay of therapy, there has been no improvement in the chemotherapy regimens used to treat DLBCL in the past 30 years. The addition of rituximab to standard chemotherapy has been a significant advance in the treatment of the disease. However, only about 50% of patients with this disease are cured after treatment with chemotherapy and rituximab. There have been over 60 clinical trials in patients with DLBCL that have demonstrated no benefit. An important reason for the failure of many clinical trials in DLBCL may be the approach to the disease as a single entity, even though it is known to be molecularly heterogeneous. Gene expression profiling of patients with DLBCL demonstrated that the tumors comprised at least two distinct diseases with different cells of origin, distinct cytogenetic differences and different response rates to anthracycline-based chemotherapy regimens. In this proposal, we demonstrate how the molecular subclassification of DLBCL reveals new tumor-susceptibilities that can be explored in the clinic. PUBLIC HEALTH RELEVANCE: Molecular profiling has provided new opportunities for unraveling tumor biology by the enumeration of differentially expressed genes and oncogenic pathways. In diffuse large B cell lymphoma, the most common form of lymphoma, molecular profiling has demonstrated that the diagnosis comprised at least two molecular subgroups that are dramatically different with regard to their gene expression profile as well as to standard combinations of chemotherapy. We propose a novel approach using the molecular subclassification of diffuse large B cell lymphoma to identify new therapeutic targets that are most likely to be effective in the molecularly defined groups of patients.
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会议论文
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Exome-wide screening for common mutations in lymphoma
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依托单位:
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批准号:10323313
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财政年份:1997
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依托单位:
海外基金