Study of biomarkers in ovarian cancer: modulation by activity & diet intervention

卵巢癌生物标志物的研究：活性调节

• 批准号: 8991675
• 负责人: KAREN M BASEN-ENGQUIST
• 金额: $ 61.55万
• 依托单位: UNIVERSITY OF ARIZONA
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-01-01 至 2019-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8991675
• 关键词: Accounting; Adopted; Aftercare; Attention; Behavior Therapy; Behavioral; Biological; Biological Markers; Blood specimen; Cancer Advocacy; Cancer Survivor; Cancer Survivorship; Cessation of life; Clinical; Community Clinical Oncology Program; Control Groups; Controlled Study; Data; Diet; Dietary Intervention; Disease; Disease Progression; Enrollment; Funding; Goals; Health; High Density Lipoproteins; Inflammation; Inflammatory; Inflammatory Response; Insulin; Insulin Resistance; Interleukin-6; Intervention; Knowledge; LDL Cholesterol Lipoproteins; Life Style; Lipids; Malignant Female Reproductive System Neoplasm; Malignant Neoplasms; Malignant neoplasm of ovary; Mediating; Mesothelium; Metabolic; Monitor; Obesity; Oncology Group; Outcome; Participant; Patient-Focused Outcomes; Patients; Physical activity; Play; Postdoctoral Fellow; Progression-Free Survivals; Protocols documentation; Randomized; Recurrence; Recurrent disease; Regulation; Research; Research Infrastructure; Resources; Risk; Risk Factors; Role; Sampling; Scanning; Schedule; Staging; Survivors; Testing; Time; Translating; Visceral; Vulnerable Populations; Woman; Work; X-Ray Computed Tomography; arm; base; cancer diagnosis; cancer survival; design; energy balance; evidence base; follow-up; group intervention; high risk; improved; indexing; intervention effect; lifestyle intervention; lipid metabolism; mortality; novel; outcome forecast; programs; tumor progression

DESCRIPTION (provided by applicant): Ovarian cancer accounts for over 18,000 deaths each year in the U.S. with disease progression rates estimated at 60-70% after 4 years. The efficacy of a physical activity + dietary intervention to increase progression-free survival (PFS) in this vulnerable population is currently being tested in a hypothesis-driven, randomized, attention-control study of 1070 women with prior invasive disease [(Gynecological Oncology Group (GOG) 0225 study (Lifestyle Intervention for oVarian cancer Enhanced Survival- (LIVES) Trial]. Here, we propose to take advantage of the trial infrastructure and capacity to collect repeat blood samples to evaluate the mechanistic underpinnings that might explain any changes in health indices by treatment arm over time. The overarching hypothesis is that change in metabolic and inflammatory status of participants, that is expected to demonstrate a reduction in inflammation and metabolic deregulation in the intervention group participants more so than the attention-control group, will be associated with increased PFS. A secondary focus of the proposed work will be the interaction with central adiposity. The Specific Aims include: To determine if the LIVES intervention alters biomarkers of metabolic deregulation in women previously treated for stage II-IV ovarian cancer; Aim 2: To determine if any effect of the intervention on biomarkers is mediated by change in central adiposity; and Aim 3: To determine if any effect of the intervention on biomarkers is modified by baseline central adiposity including exploration of central adiposity using Computerized Tomography (CT) scans. Our longer term goal is to determine whether change in central adiposity, insulin/lipid metabolism or inflammation is associated with progression free survival.

描述（由申请人提供）：卵巢癌在美国每年导致超过18,000人死亡，4年后疾病进展率估计为60-70%。目前，在一项假设驱动、随机、注意力控制的研究中，1070名既往患有侵袭性疾病的女性正在进行一项身体活动+饮食干预提高这一弱势人群无进展生存期（PFS）的有效性测试[妇科肿瘤组（GOG） 0225研究(生活方式干预卵巢癌提高生存期- (LIVES)试验]。在这里，我们建议利用试验基础设施和收集重复血液样本的能力来评估可能解释治疗组随时间变化的健康指数的机制基础。最重要的假设是，参与者代谢和炎症状态的变化，预计会证明干预组参与者炎症和代谢放松的减少比注意控制组参与者更明显，这将与PFS的增加有关。提出的工作的第二个重点将是与中心性肥胖的相互作用。具体目的包括：确定LIVES干预是否会改变先前接受过II-IV期卵巢癌治疗的女性代谢失调的生物标志物；目的2：确定干预对生物标志物的任何影响是否由中枢性肥胖的变化介导；目的3：确定干预对生物标志物的任何影响是否会因基线中心性肥胖而改变，包括