Optimizing the Treatment of Pancreatic Adenocarcinoma
Optimizing the Treatment of Pancreatic Adenocarcinoma
批准号:
10219977
负责人:
Chin Hur
金额:
$39.11万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-08-01 至 2023-07-31
关键词:
Adjuvant TherapyAgeCancer BurdenCancer ControlCaringCharacteristicsChemotherapy-Oncologic ProcedureClinical TrialsDataDatabasesDecision MakingDevelopmentDiagnosisDiseaseDisease modelEarly treatmentEquilibriumEthnic OriginExcisionFutureGenderGoalsKnowledgeMalignant NeoplasmsMalignant neoplasm of pancreasMathematicsMedicareMicrometastasisMicroscopicMissionModelingMorbidity - disease rateNeoadjuvant TherapyNeoplasm MetastasisOperative Surgical ProceduresPancreatic AdenocarcinomaPancreatic Ductal AdenocarcinomaParticipantPatient-Focused OutcomesPatientsPopulationPrimary NeoplasmPrognostic MarkerPublic HealthRaceRadiation therapyRegimenResearchResearch PersonnelResectableResourcesRoleScientistSurvival AnalysisTestingTimeToxic effectUnited States National Institutes of HealthWorkbasechemotherapycomorbiditycurative treatmentsdesignexperienceimprovedindividual patientindividualized medicineinsightmodels and simulationmortalitynovel therapeutic interventionpancreatic cancer modelpancreatic cancer patientspancreatic ductal adenocarcinoma modelpersonalized medicinepredictive markerrandomized trialscreeningsimulationtreatment optimizationtreatment planningtreatment strategytumor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary/Abstract:
The ultimate goal of the proposed research is to improve pancreatic ductal adenocarcinoma (PDAC) patient
survival and population mortality. While survival for many cancers has improved over time, the survival for
PDAC, which constitutes the vast majority (90%) of all cancers of the pancreas, remains poor. This is in part
because the majority of PDACs are detected late in their course when surgical resection is not possible.
However, even in cases with a resectable primary tumor, cure remains elusive because of early metastases,
which are frequently microscopic and undetectable. Early metastasis from very small tumors is a key barrier to
improving pancreatic cancer mortality. Systematic chemotherapy can treat unseen micrometastases in early
PDAC and thus has the potential to improve patient outcomes when used as an adjuvant or neoadjuvant
therapy in conjunction with surgical resection and radiotherapy. At present only about 20% of diagnosed
PDACs are surgically resectable at the time of diagnosis; however, promising newer chemotherapy regimens,
when combined with radiotherapy as neoadjuvant treatment, may enable the definitive resection of many
PDACs (30%) that are now borderline resectable or locally advanced. If proven effective, these new treatment
strategies potentially represent a major step toward improving PDAC survival and may bring a cure within
reach for the majority of patients diagnosed with PDAC. Yet, questions remain about how best to apply
neoadjuvant and adjuvant therapy regimens, which have considerable toxicities. Care must be taken in
applying the results of clinical trials to a significant proportion of patients diagnosed with PDAC, who are older
and less healthy (comorbidities) than trial participants. In scenarios such as these, where there are limitations
to the generalizability of clinical trial data, modeling approaches can serve a complementary role. A disease
simulation model of PDAC can provide a framework to synthesize and incorporate various tumor and patient
factors thereby allowing for a comprehensive balancing of the potential benefits and harms of treatment plans.
The research plan will build upon prior and ongoing work by our diverse team, comprised of mathematical
modelers, population scientists, cancer biologists, and clinicians with experience in all aspects of PDAC
management and treatment. Our plan is to develop a comprehensive PDAC treatment model that will be
analyzed to provide insights to: improve overall survival of patients with early stage PDAC, enhance decision
making regarding personalized treatment plans, optimize resource utilization, and prioritize and inform future
research and trials. The aims of the project will be: Aim 1-Refine and validate a model of PDAC focused on
treatment; Aim 2-Design personalized treatment strategies tailored to individual patient characteristics to
optimize treatment of early PDAC; Aim 3-Determine the impact of the new personalized treatment strategies
on population mortality.
期刊论文(9)
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科研奖励(0)
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Patterns and predictors of end-of-life care in older patients with pancreatic cancer.
老年胰腺癌患者临终关怀的模式和预测因素。
DOI:
10.1002/cam4.1861
发表时间:
2018-12
期刊:
Cancer medicine
影响因子:
4
作者:
[Nipp RD, Tramontano AC, Kong CY, Hur C]
通讯作者:
Hur C
Testing for Verification Bias in Reported Malignancy Risks for Side-Branch Intraductal Papillary Mucinous Neoplasms: A Simulation Modeling Approach.
侧枝导管内乳头状粘液性肿瘤报告的恶性肿瘤风险的验证偏差测试:模拟建模方法。
DOI:
10.2214/ajr.18.20180
发表时间:
2019
期刊:
AJR. American journal of roentgenology
影响因子:
--
作者:
[Weaver,DavisT, Lietz,AnnaP, Mercaldo,SarahF, Peters,MaryLintonB, Hur,Chin, Kong,ChungYin, Wolpin,BrianM, Megibow,AlecJ, Berland,LincolnL, Knudsen,AmyB, Pandharipande,PariV]
通讯作者:
Pandharipande,PariV
Progression to pancreatic ductal adenocarcinoma from pancreatic intraepithelial neoplasia: Results of a simulation model.
从胰腺内肿瘤中向胰腺导管腺癌的进展:模拟模型的结果。
DOI:
10.1016/j.pan.2018.07.009
发表时间:
2018-12
期刊:
PANCREATOLOGY
影响因子:
3.6
作者:
[Peters, Mary Linton B., Eckel, Andrew, Mueller, Peter P., Tramontano, Angela C., Weaver, Davis T., Lietz, Anna, Hur, Chin, Kong, Chung Yin, Pandharipande, Pan, V]
通讯作者:
Pandharipande, Pan, V
DOI:
10.1016/j.amjsurg.2020.03.035
发表时间:
2020-07
期刊:
American journal of surgery
影响因子:
3
作者:
[Fong ZV, Chang DC, Hur C, Jin G, Tramontano A, Sell NM, Warshaw AL, Fernandez-Del Castillo C, Ferrone CR, Lillemoe KD, Qadan M]
通讯作者:
Qadan M
DOI:
10.1186/s12885-021-08306-5
发表时间:
2021-05-24
期刊:
BMC cancer
影响因子:
3.8
作者:
[Rustgi SD, Oh A, Yang JY, Kang D, Wolin E, Kong CY, Hur C, Kim MK]
通讯作者:
Kim MK
共 8 条
Domain-Knowledge Informed Deep Learning for Early Detection of Pancreatic Cancer
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批准号:10458067
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Comparative modeling of gastric cancer disparities and prevention in the US and globally
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Optimal Colorectal Cancer Surveillance Strategy for Lynch Syndrome by Genotype
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Optimal Colorectal Cancer Surveillance Strategy for Lynch Syndrome by Genotype
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财政年份:2021
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依托单位:
Comparative modeling of gastric cancer disparities and prevention in the US and globally
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批准号:10705668
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项目类别:
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资助金额:$81.02万
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依托单位:
Domain-Knowledge Informed Deep Learning for Early Detection of Pancreatic Cancer
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A Personalized Approach to Targeted Esophageal Cancer Screening
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项目类别:
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财政年份:2020
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依托单位:
A Personalized Approach to Targeted Esophageal Cancer Screening
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批准号:10661535
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项目类别:
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资助金额:$50.78万
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财政年份:2020
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依托单位:
A Personalized Approach to Targeted Esophageal Cancer Screening
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批准号:10413908
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项目类别:
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资助金额:$48.92万
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依托单位:
Controlling Esophageal Cancer: A Collaborative Modeling Approach
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批准号:9753971
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项目类别:
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资助金额:$116.31万
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财政年份:2018
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负责人:Chin Hur
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依托单位:
Optimizing the Treatment of Pancreatic Adenocarcinoma
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批准号:9766202
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项目类别:
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资助金额:$38.16万
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财政年份:2017
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依托单位:
Controlling Esophageal Cancer: A Collaborative Modeling Approach
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批准号:9134112
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项目类别:
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资助金额:$117.18万
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财政年份:2015
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依托单位:
Controlling Esophageal Cancer: A Collaborative Modeling Approach
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批准号:8969418
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项目类别:
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资助金额:$118.69万
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财政年份:2015
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Esophageal Cancer from Cells to Population: A Multiscale Approach
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项目类别:
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财政年份:2013
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依托单位:
Esophageal Cancer from Cells to Population: A Multiscale Approach
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批准号:9132706
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项目类别:
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资助金额:$63.03万
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财政年份:2013
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负责人:Chin Hur
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依托单位:
Esophageal Cancer from Cells to Population: A Multiscale Approach
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批准号:8634497
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项目类别:
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资助金额:$72.15万
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财政年份:2013
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负责人:Chin Hur
-
依托单位:
Esophageal Cancer from Cells to Population: A Multiscale Approach
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批准号:8919740
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项目类别:
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资助金额:$66.54万
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财政年份:2013
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负责人:Chin Hur
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依托单位:
Esophageal Adenocarcinoma Policy Model: Trends, Risk Factors and Screening
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批准号:8600151
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项目类别:
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资助金额:$34.56万
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财政年份:2010
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负责人:Chin Hur
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依托单位:
Improving Esophageal Adenocarcinoma Prevention, Screening and Treatment
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批准号:8888319
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项目类别:
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资助金额:$40.03万
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财政年份:2010
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依托单位:
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