Administrative Core

行政核心

基本信息

项目摘要

PROJECT SUMMARY (ADMINISTRATIVE CORE) The Administrative Core provides essential support to the MD Anderson Cancer Center and Temple/Fox Chase Cancer Center Leukemia SPORE PIs and investigators to maximize success. It is co-directed by Drs. Hagop Kantarjian and Jean-Pierre Issa, who co-chair the Executive Committee and provide overall supervision of five Projects, two additional Cores, Developmental Research (DRP) and Career Enhancement (CEP) Programs, and scientific direction of the SPORE. The Core co-Directors rely on the extensive broad-based scientific, research, and SPORE experience of the Internal and External Advisory Boards in critical decision- making. Success of the complex interdisciplinary research in the SPORE depends on integration of diverse leukemia research approaches. The Core will overcome barriers to interdisciplinary collaboration and data sharing and will ensure a unified translational research effort. The SPORE is founded on planning, integration, and translational research efforts supported by this Core. Its leadership and staff will be responsible for monitoring/planning scientific activities; providing scientific direction; ensuring emphasis on translational research; ensuring interdisciplinary and inter-SPORE integration with major leukemia programs within/outside MD Anderson and other broad translational research activities; and providing optimal administrative and fiscal management. Specific responsibilities of the Administrative Core are: Oversee and monitor all SPORE activities; promote integration and communication among the SPORE-related clinical programs; monitor the scientific integrity of all research projects, and grant awards; assure compliance with institutional, governmental, and National Cancer Institute regulations; oversee the fiscal and budgetary activities of the SPORE; coordinate data control quality assurance issues in conjunction with the Internal Advisory Board and the Biostatistics, Data Management, and Bioinformatics Core (Core 3); coordinate activities associated with clinical trials, including design of protocols, approval by regulatory bodies, implementation, and eligibility screening and assignment of patients to different studies; provide oversight and support for Core 3 and the Pathology and Tissue Core (Core 2); coordinate and manage meetings of the SPORE Executive Committee, the Internal and External Advisory Boards, monthly investigator meetings, quarterly research meetings, lectures, and symposia; administer the DRP and the CEP; coordinate interdisciplinary and inter-SPORE interactions and exchanges/meetings with other Leukemia SPORE programs and investigators, and other organ-site SPORE programs; administer the activities of the Patient Advocates; comply with, and improve policies addressing recruitment and retention of women and minorities; organize seminars to bring to MD Anderson consultants and speakers with expertise in various clinical and laboratory aspects of leukemia research; maintain a Leukemia SPORE website focused on issues in leukemia translational research.
项目摘要(行政核心) 行政核心为 MD 安德森癌症中心和 Temple/Fox 提供必要的支持 大通癌症中心白血病 SPORE PI 和研究人员最大限度地取得成功。它是由博士共同导演。 Hagop Kantarjian 和 Jean-Pierre Issa,担任执行委员会联合主席并提供全面监督 五个项目,两个额外的核心,发展研究(DRP)和职业提升(CEP) SPORE 的计划和科学方向。核心联合董事依靠广泛的基础 内部和外部顾问委员会在关键决策方面的科学、研究和 SPORE 经验 制作。 SPORE 复杂的跨学科研究的成功取决于不同学科的整合 白血病研究方法。核心将克服跨学科协作和数据的障碍 共享并将确保统一的转化研究工作。 SPORE 建立在规划、整合、 以及该核心支持的转化研究工作。其领导层和工作人员将负责 监测/规划科学活动;提供科学指导;确保强调翻译 研究;确保跨学科和跨 SPORE 与内部/外部主要白血病项目的整合 MD 安德森癌症中心和其他广泛的转化研究活动;并提供最佳的行政和财政 管理。行政核心的具体职责是: 监督和监控所有 SPORE 活动;促进SPORE相关临床项目之间的整合和交流;监控 所有研究项目的科学诚信,并授予奖励;确保遵守制度, 政府和国家癌症研究所法规;监督财政和预算活动 孢子;与内部顾问委员会协调数据控制质量保证问题,并 生物统计学、数据管理和生物信息学核心(核心 3);协调相关活动 临床试验,包括方案设计、监管机构批准、实施和资格 筛选患者并将其分配至不同的研究;为核心 3 和 病理学和组织核心(核心2);协调和管理 SPORE 执行委员会的会议, 内部和外部顾问委员会、每月研究者会议、每季度研究会议、 讲座和研讨会;管理 DRP 和 CEP;协调跨学科和跨 SPORE 与其他白血病孢子项目和研究人员的互动和交流/会议,以及其他 器官部位 SPORE 程序;管理患者权益倡导者的活动;遵守并改进 关于招聘和保留妇女和少数群体的政策;组织研讨会以带给MD 安德森顾问和演讲者在白血病的各个临床和实验室方面拥有专业知识 研究;维护一个专注于白血病转化研究问题的白血病孢子网站。

项目成果

期刊论文数量(0)
专著数量(0)
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Marina Y Konopleva其他文献

Azacitidine, Venetoclax, and Gilteritinib in Newly Diagnosed and Relapsed or Refractory FLT3-Mutated AML
阿扎胞苷、维奈托克和 Gilteritinib 治疗新诊断和复发或难治性 FLT3 突变 AML
  • DOI:
  • 发表时间:
    2024
  • 期刊:
  • 影响因子:
    45.3
  • 作者:
    N. Short;N. Daver;C. Dinardo;T. Kadia;L. Nasr;W. Macaron;M. Yilmaz;G. Borthakur;G. Montalban;G. Garcia;G. Issa;K. Chien;E. Jabbour;Cedric Nasnas;Xuelin Huang;W. Qiao;J. Matthews;Christopher J Stojanik;K. Patel;R. Abramova;J. Thankachan;Marina Y Konopleva;H. Kantarjian;F. Ravandi
  • 通讯作者:
    F. Ravandi

Marina Y Konopleva的其他文献

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{{ truncateString('Marina Y Konopleva', 18)}}的其他基金

Defining the novel cancer testis antigen HSPA1L as immunotherapeutic target in AML
将新型癌症睾丸抗原 HSPA1L 定义为 AML 的免疫治疗靶点
  • 批准号:
    10625516
  • 财政年份:
    2022
  • 资助金额:
    $ 17.74万
  • 项目类别:
Defining the novel cancer testis antigen HSPA1L as immunotherapeutic target in AML
将新型癌症睾丸抗原 HSPA1L 定义为 AML 的免疫治疗靶点
  • 批准号:
    10433726
  • 财政年份:
    2022
  • 资助金额:
    $ 17.74万
  • 项目类别:
Inhibition of Bcl-xL by Targeted Degradation
通过靶向降解抑制 Bcl-xL
  • 批准号:
    10737840
  • 财政年份:
    2020
  • 资助金额:
    $ 17.74万
  • 项目类别:
Chaperone-Mediated Protein Degradation of Bcl-xL and Bcl-2
分子伴侣介导的 Bcl-xL 和 Bcl-2 蛋白质降解
  • 批准号:
    10599452
  • 财政年份:
    2020
  • 资助金额:
    $ 17.74万
  • 项目类别:
Inhibition of Bcl-xL by Targeted Degradation
通过靶向降解抑制 Bcl-xL
  • 批准号:
    10378075
  • 财政年份:
    2020
  • 资助金额:
    $ 17.74万
  • 项目类别:
Inhibition of Bcl-xL by Targeted Degradation
通过靶向降解抑制 Bcl-xL
  • 批准号:
    10133018
  • 财政年份:
    2020
  • 资助金额:
    $ 17.74万
  • 项目类别:
Inhibition of Bcl-xL by Targeted Degradation
通过靶向降解抑制 Bcl-xL
  • 批准号:
    10644990
  • 财政年份:
    2020
  • 资助金额:
    $ 17.74万
  • 项目类别:
Targeting apoptosis in high-risk AML and MDS with BCL-2 inhibitor Venetoclax and optimized 10-day Decitabine regimen
使用 BCL-2 抑制剂 Venetoclax 和优化的 10 天地西他滨方案靶向高危 AML 和 MDS 中的细胞凋亡
  • 批准号:
    10415997
  • 财政年份:
    2019
  • 资助金额:
    $ 17.74万
  • 项目类别:
Targeting apoptosis in high-risk AML and MDS with BCL-2 inhibitor Venetoclax and optimized 10-day Decitabine regimen
使用 BCL-2 抑制剂 Venetoclax 和优化的 10 天地西他滨方案靶向高危 AML 和 MDS 中的细胞凋亡
  • 批准号:
    10654631
  • 财政年份:
    2019
  • 资助金额:
    $ 17.74万
  • 项目类别:
Targeting mitochondrial complex I in acute lymphoblastic leukemia
靶向急性淋巴细胞白血病中的线粒体复合物 I
  • 批准号:
    9815737
  • 财政年份:
    2019
  • 资助金额:
    $ 17.74万
  • 项目类别:

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