Imaging in Risk Assessment of Prostate Cancer Patients
Imaging in Risk Assessment of Prostate Cancer Patients
批准号:
7782704
负责人:
Hedvig Hricak
金额:
$27.27万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-07-07 至 2012-03-31
关键词:
AddressAntigensApoptoticAreaBiochemicalBiologicalBiopsyCancer BiologyCancer EtiologyCancer PatientCell CycleCessation of lifeClinicalClinical DataClinical ManagementClinical assessmentsCyclin-Dependent Kinase InhibitorData SetDatabasesDiagnostic Neoplasm StagingDiseaseDisease ProgressionEvaluationFundingFutureGleason Grade for Prostate CancerGrantGuidelinesHistologicHistologyImageImmunohistochemistryIndolentLiteratureMIB-1 antibodyMagicMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMalignant NeoplasmsMalignant neoplasm of prostateMeasuresMolecularNational Comprehensive Cancer NetworkNatural HistoryOncogenesOperative Surgical ProceduresOrganOutcomePSA screeningPathologyPatient SelectionPatientsPatternPerformancePhysiciansPrognostic MarkerProto-Oncogene Proteins c-aktProtocols documentationPublishing Peer ReviewsRadiation therapyRadical ProstatectomyRandomizedRecurrenceReference StandardsRegulationResearchResolutionRiskRisk AssessmentSamplingSelection for TreatmentsSignal TransductionSpecimenSpectrum AnalysisStagingSurgical PathologyTestingTumor Suppressor GenesTumor VolumeTumor stageVariantWorkbaseclinically significantcohortcyclin-dependent kinase inhibitor 1Bfollow-upimprovedmenmolecular markerspectroscopic imagingtreatment planningtumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Prostate cancer remains the most common cancer overall and the second leading cause of cancer related death in men. In comparison to other cancers, prostate cancer has a long natural history and is frequently indolent (i.e., it does not progress to clinically significant disease before the patient dies of natural causes. In contrast, recurrence is seen in as many as 30% of treated patients. The findings highlight the need to develop prognostic markers beyond PSA and tumor grade in order to better distinguish patients who will most likely benefit from treatment from those for whom treatment should be deferred. We have shown that MRI and MRSI combined with clinical findings of PSA and Gleason score significantly improve the accuracy for predicting tumor stage and aggressiveness. In this competitive renewal, we will build on these findings with the objective of optimizing the use of MRI/MRSI for accurately identifying indolent prostate cancers. Our approach will be to correlate MR findings preoperatively both with patient outcomes and with the expression of key molecular markers known to be important in prostate cancer biology: Ki-67, PTEN, Akt, p27/Kip1, Bax, and Bcl-2. We also intend to use high resolution magic angle spinning spectroscopy on the operative specimen to obtain idealized spectra for non-destructive tumor analysis. The proposed work will test the hypothesis that a low risk localized PCa cohort identified by both clinical parameters and optimized MRI/MRSI will have better long-term outcome than a similar cohort identified by clinical parameters alone. The specific aims of the study are: Specific Aim 1: Evaluate measures of accuracy of MRI/MRSI in the prediction of indolent cancer, using step section pathology as a standard of reference. Specific Aim 2: Correlate the MRI/MRSI features of low-risk localized PCa with the molecular features of the disease assessed in radical prostatectomy specimens and determine whether noninvasive MRI/MRSI can further differentiate between less aggressive variants of Gleason score 6 (pattern 3+3) cancer that are appropriate for a deferred therapy protocol and more aggressive variants of Gleason score 6 cancer that are more appropriate for definitive therapy. Specific Aim 3A: Compare patient outcome (disease progression-rate) between definitive treatment and deferred therapy in low-risk localized PCa patients identified by combined NCCN guidelines and MRI/MRSI Specific Aim 3B: Determine the incremental value of combined NCCN guidelines and MRI/MRSI to a historical literature data set in the selection of patients for deferred therapy.
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DOI:
10.1016/j.juro.2012.07.024
发表时间:
2012-11
期刊:
The Journal of urology
影响因子:
--
作者:
[Vargas HA, Akin O, Afaq A, Goldman D, Zheng J, Moskowitz CS, Shukla-Dave A, Eastham J, Scardino P, Hricak H]
通讯作者:
Hricak H
Incremental value of multiplanar cross-referencing for prostate cancer staging with endorectal MRI.
直肠内 MRI 多平面交叉参考对前列腺癌分期的增量价值。
DOI:
10.2214/ajr.05.1783
发表时间:
2007
期刊:
AJR. American journal of roentgenology
影响因子:
--
作者:
[Wang,Liang, Zhang,Jingbo, Schwartz,LawrenceH, Eisenberg,Halley, Ishill,NicoleM, Moskowitz,ChayaS, Scardino,Peter, Hricak,Hedvig]
通讯作者:
Hricak,Hedvig
DOI:
10.1097/ju.0000000000001474
发表时间:
2021-04
期刊:
The Journal of urology
影响因子:
--
作者:
[Wibmer AG, Chaim J, Lakhman Y, Lefkowitz RA, Nincevic J, Nikolovski I, Sala E, Gonen M, Carlsson SV, Fine SW, Zelefsky MJ, Scardino P, Hricak H, Vargas HA]
通讯作者:
Vargas HA
Retained seminal vesicles after radical prostatectomy: frequency, MRI characteristics, and clinical relevance.
根治性前列腺切除术后保留精囊:频率、MRI 特征和临床相关性。
DOI:
10.2214/ajr.04.1770
发表时间:
2006
期刊:
AJR. American journal of roentgenology
影响因子:
--
作者:
[Sella,Tamar, Schwartz,LawrenceH, Hricak,Hedvig]
通讯作者:
Hricak,Hedvig
MRI-Detectability of Clinically Significant Prostate Cancer Relates to Oncologic Outcomes After Prostatectomy.
临床上显着的前列腺癌的MRI检测性与前列腺切除术后的肿瘤学结局有关。
DOI:
10.1016/j.clgc.2022.04.001
发表时间:
2022-08
期刊:
Clinical genitourinary cancer
影响因子:
3.2
作者:
[]
通讯作者:
共 15 条
Molecular Imaging in Cancer Biology Training Program
-
批准号:10471882
-
项目类别:
-
资助金额:$43.24万
-
财政年份:2021
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging in Cancer Biology Training Program
-
批准号:10673819
-
项目类别:
-
资助金额:$20.39万
-
财政年份:2021
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging in Cancer Biology Training Program
-
批准号:10268545
-
项目类别:
-
资助金额:$41.15万
-
财政年份:2021
-
负责人:Hedvig Hricak
-
依托单位:
Reproducibility of Hyperpolarized Pyruvate Metabolic Imaging in Prostate Cancer
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批准号:9011799
-
项目类别:
-
资助金额:$24.67万
-
财政年份:2015
-
负责人:Hedvig Hricak
-
依托单位:
GE Diamond DNP Polarizer
-
批准号:8640664
-
项目类别:
-
资助金额:$60.0万
-
财政年份:2014
-
负责人:Hedvig Hricak
-
依托单位:
Research Education Core
-
批准号:10477042
-
项目类别:
-
资助金额:$6.37万
-
财政年份:2008
-
负责人:Hedvig Hricak
-
依托单位:
Research Education Core
-
批准号:10250472
-
项目类别:
-
资助金额:$15.12万
-
财政年份:2008
-
负责人:Hedvig Hricak
-
依托单位:
Research Education Core
-
批准号:10021580
-
项目类别:
-
资助金额:$7.61万
-
财政年份:2008
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:6530222
-
项目类别:
-
资助金额:$53.3万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:6647139
-
项目类别:
-
资助金额:$53.44万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:8543545
-
项目类别:
-
资助金额:$49.82万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:7936192
-
项目类别:
-
资助金额:$54.0万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:6933875
-
项目类别:
-
资助金额:$53.96万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:8325932
-
项目类别:
-
资助金额:$48.61万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:6784634
-
项目类别:
-
资助金额:$54.03万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:7124240
-
项目类别:
-
资助金额:$52.73万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
Molecular Imaging: Training for Oncology
-
批准号:8131886
-
项目类别:
-
资助金额:$45.72万
-
财政年份:2002
-
负责人:Hedvig Hricak
-
依托单位:
IMAGING IN RISK ASSESSMENT OF PROSTATE CANCER PATIENTS
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批准号:6173375
-
项目类别:
-
资助金额:$30.59万
-
财政年份:1999
-
负责人:Hedvig Hricak
-
依托单位:
IMAGING IN RISK ASSESSMENT OF PROSTATE CANCER PATIENTS
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批准号:6376593
-
项目类别:
-
资助金额:$27.4万
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财政年份:1999
-
负责人:Hedvig Hricak
-
依托单位:
IMAGING IN RISK ASSESSMENT OF PROSTATE CANCER PATIENTS
-
批准号:6513327
-
项目类别:
-
资助金额:$18.93万
-
财政年份:1999
-
负责人:Hedvig Hricak
-
依托单位:
国内基金
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Neo-antigens暴露对肾移植术后体液性排斥反应的影响及其机制研究
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批准号:2022J011295
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项目类别:省市级项目
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资助金额:10.0万元
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批准年份:2022
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负责人:王亚伟
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依托单位:
结核分枝杆菌持续感染期抗原(latency antigens)的重组BCG疫苗研究
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批准号:30801055
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项目类别:青年科学基金项目
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资助金额:19.0万元
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批准年份:2008
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负责人:王丽梅
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