Pharmacodynamics of Gemcitabine by MRS in Pancreatic CA
Pharmacodynamics of Gemcitabine by MRS in Pancreatic CA
批准号:
7089043
负责人:
HOWARD S HOCHSTER
金额:
$49.98万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-07-01 至 2009-04-30
中文摘要
描述(由申请人提供):去年约有30,000名美国人感染胰腺癌,其中29,900人(99.7%)死于疾病。胰腺癌占所有GI肿瘤的约25%,并且是迄今为止预后最差的肿瘤。事实上,从诊断开始的平均预期寿命只有3个月,这种疾病代表了癌症战争中最严峻的前线之一。目前只有一种FDA批准的药物用于治疗这种疾病,吉西他滨,一种核苷抗代谢药。不幸的是,以FDA批准的剂量和时间表使用单药吉西他滨的多个III期试验已经显示,(i)仅<10%的一致响应率;(ii)约6个月的中位存活率;和(iii)<20%的一年存活率。然而,最近的II期数据表明,吉西他滨的给药速率对中位生存期有有利的影响。因此,我们的总体假设是,肿瘤中吉西他滨摄取和再摄取的量和速率将与特定个体患者的反应相关。验证这一假设是至关重要的,以便能够定制剂量和给药速率和方案,以每一个人的病人。为了验证这一假设,我们建议在7特斯拉的超高磁场下应用局部氟磁共振光谱(19 F-MRS),用于无创体内监测药物及其活性合成代谢副产物二氟脱氧胞苷三磷酸(dFdCTP)。
英文摘要
DESCRIPTION (provided by applicant): Some 30,000 Americans contracted pancreatic cancer last year, and, 29,900 (99.7%) of them succumbed to their disease. Pancreatic cancer accounts for approximately 25% of all Gl neoplasms, and is by far the one with the worst prognosis. Indeed, with a mean life expectancy from diagnosis of only 3 months, this disease represents one of the grimmest fronts of the War on Cancer. Currently there is only one FDA approved drug for the treatment of this disease, Gemcitabine, a nucleoside antimetabolite. Unfortunately, multiple phase III trials using single agent Gemcitabine at the FDA approved dose and schedule have shown, (i) a consistent response rate of only <10%; (ii) median survival of approximately 6 months; and (iii) one year survival rates of <20%. Recent phase II data, however, have suggested that the rate of delivery of gemcitabine can have a favorable impact on the median survival. Consequently, our overarching hypothesis is that the amount and rate of Gemcytabine uptake and anababolism in the tumor will correlate with that particular individual patient response. Validating this assumption is crucial in order to be able to customize dose and administration rate and regimens to each individual patient. To test this hypothesis we propose to apply localized Fluorine Magnetic Resonance Spectroscopy (19F-MRS) at ultra high magnetic field of 7 Tesla, for non invasive, in vivo monitoring the drug and its active anabolic by product di-fluoro, de-oxycytadine tri-phosphate (dFdCTP).
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