The Fibrosis-Lymphedema Continuum in Head and Neck Cancer
头颈癌的纤维化-淋巴水肿连续体
基本信息
- 批准号:8098131
- 负责人:
- 金额:$ 60.81万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-07-01 至 2014-04-30
- 项目状态:已结题
- 来源:
- 关键词:Activities of Daily LivingAcuteAddressAdverse effectsAdvocateAffectAftercareAgeAlcoholsAnti-Inflammatory AgentsAreaBiologic CharacteristicBiologicalBreastCancer PatientCancer SurvivorCharacteristicsChronicClinicalCodon NucleotidesCollectionCombined Modality TherapyConsensusDataData CollectionDeglutitionDevelopmentDiagnosisDiseaseDoseEconomic BurdenEdemaElectromagnetic EnergyEvaluationFibrosisFutureGelatinase AGelatinase BGenderGenetic PolymorphismGoalsHardnessHead and Neck CancerHead and neck structureHealth PersonnelHealth ProfessionalHealthcare SystemsImpairmentIncidenceInflammationInflammatoryInflammatory ResponseInterventionLate EffectsLifeLiquid substanceLong-Term SurvivorsLymphedemaMalignant NeoplasmsMalignant neoplasm of prostateMeasuresMental DepressionMethodsModelingNational Cancer InstituteNatureNeckOperative Surgical ProceduresOvarianPathway interactionsPatientsPatternPhysiciansPhysiologicalPlaguePlayPopulationPredictive FactorPrevalencePreventiveProcessProteinsQuality of lifeRadiationRadiosurgeryRecommendationRecording of previous eventsRecoveryResearchResearch PersonnelResearch SupportRiskRisk FactorsRoleSecondary toSeveritiesShoulderSiteSpeechStrategic PlanningStructureSurvival RateSwellingSymptomsTNF geneTimeTissuesTobacco useToxic effectTreatment EfficacyTreatment FactorTreatment ProtocolsTreatment outcomeWithdrawalbasecancer therapychemotherapycytokineexperiencefunctional outcomeshead and neck cancer patienthigh riskimprovedinterstitialmelanomapsychologicpsychosocialpublic health relevanceresponsesocialstressorsurvivorshiptherapy designtumor
项目摘要
DESCRIPTION (provided by applicant): Aggressive treatment for head and neck cancer (HNC) has improved survival rates. This improvement comes with a marked increase in acute and late-effects of treatment. [Late-effects may be secondary to treatment] (surgery, radiation, and chemotherapy) or effects of the tumor itself. They have a profound impact on [survivor's long-term symptom burden, functionality, and overall quality of life (QOL). Under- standing the mechanisms and manifestations of late-effects is critical to the design of interventions for improvement of quality of survivorship in HNC patients.] Fibrosis and lymphedema secondary to the stromal response to [tissue damage from tumor or treatment are understudied and poorly understood mechanisms that contribute to late-effects of therapy.] We hypothesize [that late-effect fibrosis and lymphedema represent inter-related processes that exist on biological and clinical continuums. Further- more, recent data indicates that both] fibrosis and lymphedema may be associated [with chronic] inflammation resulting in [an active, ongoing process. Thus, lymphedema and fibrosis may: develop after treatment is completed; progress over time; and be self perpetuating]. The National Cancer Institute's strategic plan addresses the need to "expand efforts to understand biologic, physical, psychological, and social mechanisms and their interactions that affect a cancer patient's response to disease, treatment, and recovery," and to "support research on the biologic and physiological mechanisms involved in adverse chronic and late-effects of both current and new cancer treatment." The objective of this longitudinal, descriptive study is to investigate the fibrosis/ lymphedema continuum [in HNC patients]. Specific Aims are to: 1) determine prevalence and nature of late-effect (e 3 months post-treatment) fibrosis and/or lymphe- dema in HNC patients; 2) explore relationships among biological mechanisms of inflammatory response, genetic polymorphisms, [treatment factors], and late-effect fibrosis and/or lymphedema in HNC patients; and 3) [explore relationships among late-effect fibrosis and/or lymphedema and psychosocial stressors (depression and social withdrawal) in HNC patients. Data collection, using select repeated measures, will take place at end of treatment, six week intervals after treatment through 48 weeks post-treatment, and 15 and 18 month intervals post-treatment.] Nagin's group-based trajectory modeling will be used to evaluate our findings. If the aims are achieved and information is disseminated, important new information will be available to: 1) [serve as underpinnings for future studies in other cancer populations at high risk for development of fibrosis and/or lymphedema, such as those with breast, ovarian, prostate cancers, and melanoma; 2) aid in development of predictive risk models; 3) stimulate new avenues of preventive. interventional research (e.g. anti-inflammatory agents);] and 4) assist physicians and other healthcare professionals to better diagnose, reduce risk for, and treat late-effect fibrosis and/or lymphedema.
PUBLIC HEALTH RELEVANCE: Head and neck cancer patients are living longer, and many suffer hardness and swelling in the head and neck post-treatment. We do not know why some experience these problems and others do not. This study will provide information so healthcare providers can better treat these patients.
描述(由申请人提供):针对头颈癌(HNC)的积极治疗提高了存活率。这种改进是急性和晚期治疗的明显增加。 [晚期作用可能是治疗的继发性](手术,放射和化学疗法)或肿瘤本身的作用。他们对[幸存者的长期症状负担,功能和整体生活质量(QOL)产生了深远的影响。未经理解晚期作用的机制和表现对于改善HNC患者的生存质量的设计至关重要。在生物和临床连续体上存在的相关过程。更重要的是,最近的数据表明,纤维化和淋巴水肿可能与[慢性]炎症相关,从而导致[一个积极的,正在进行的过程。因此,淋巴水肿和纤维化可能:治疗完成后发展;随着时间的推移;并保持持久性]。国家癌症研究所的战略计划解决了“扩大努力,了解生物学,身体,心理和社会机制及其相互作用,影响癌症患者对疾病,治疗和康复的反应”,并“支持对涉及生物学和生理机制的研究,涉及涉及的生物学和生理机制,这些机制涉及当前和新癌症治疗的不良慢性和晚期治疗。”这项纵向,描述性研究的目的是研究纤维化/淋巴水肿连续体[HNC患者]。具体目的是:1)确定HNC患者的纤维化(治疗后3个月)纤维化和/或淋巴DEMA的患病率和性质; 2)探索HNC患者的炎症反应,遗传多态性,治疗因子]和晚期纤维化和/或淋巴水肿的生物学机制之间的关系;和3)[探索HNC患者的晚期效应纤维化和/或淋巴水肿和社会心理压力源(抑郁和社交戒断)之间的关系。数据收集(使用精选的重复措施)将在治疗结束时进行,治疗后48周后进行六周的间隔以及治疗后的15和18个月间隔。] Nagin的基于组的轨迹建模将用于评估我们的发现。如果实现了目标并传播信息,则可以使用重要的新信息:1)[作为对其他癌症人群的未来研究的基础,该研究具有纤维化和/或淋巴水肿的高风险,例如患有乳腺癌,卵巢癌,前列腺癌和黑色素瘤的基础; 2)帮助开发预测风险模型; 3)刺激预防性的新途径。介入研究(例如,抗炎药);]和4)协助医师和其他医疗保健专业人员更好地诊断,降低患有晚期效应纤维化的风险和/或淋巴水肿。
公共卫生相关性:头颈癌患者的寿命更长,许多人在治疗后头和颈部遭受硬度和肿胀。我们不知道为什么有些人遇到这些问题,而另一些则没有。这项研究将提供信息,以便医疗保健提供者可以更好地治疗这些患者。
项目成果
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Barbara A. Murphy其他文献
Development of a model for inducing transient insulin resistance in the mare: preliminary implications regarding the estrous cycle.
开发用于诱导母马短暂胰岛素抵抗的模型:对发情周期的初步影响。
- DOI:
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2004 - 期刊:
- 影响因子:3.3
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D. R. Sessions;Stephanie E. Reedy;M. M. Vick;Barbara A. Murphy;B. Fitzgerald - 通讯作者:
B. Fitzgerald
Longitudinal oncology registry of head and neck carcinoma (LORHAN®): initial supportive care findings
头颈癌纵向肿瘤学登记 (LORHAN®):初步支持治疗结果
- DOI:
- 发表时间:
2009 - 期刊:
- 影响因子:3.1
- 作者:
Barbara A. Murphy;Amy Y. Chen;Walter J. Curran;A. Garden;P. Harari;Stuart J. Wong;K. Ang - 通讯作者:
K. Ang
Interferon regulatory factor‐1 is a major regulator of epidermal growth factor receptor gene expression
干扰素调节因子-1是表皮生长因子受体基因表达的主要调节因子
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- 发表时间:
1998 - 期刊:
- 影响因子:3.5
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Y. Rubinstein;Kimberle N Proctor;M. Bergel;Barbara A. Murphy;A. Johnson - 通讯作者:
A. Johnson
Mobile blue light therapy is as effective as stable lighting at advancing seasonal reproductive activity in mares
- DOI:
10.1016/j.jevs.2013.10.070 - 发表时间:
2014-01-01 - 期刊:
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Caroline M. Walsh;Elizabeth M. Woodward;Ralph L. Prendergast;James P. Rylei;Luke H. Fallon;Mats H.T. Troedsson;Barbara A. Murphy - 通讯作者:
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Parental Grief Responses and Personals Growth Following the Death of a Child
孩子去世后父母的悲伤反应和个人成长
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- 发表时间:
2007 - 期刊:
- 影响因子:3.8
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Barbara A. Murphy的其他文献
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{{ truncateString('Barbara A. Murphy', 18)}}的其他基金
The Fibrosis-Lymphedema Continuum in Head and Neck Cancer
头颈癌的纤维化-淋巴水肿连续体
- 批准号:
8541621 - 财政年份:2010
- 资助金额:
$ 60.81万 - 项目类别:
The Fibrosis-Lymphedema Continuum in Head and Neck Cancer
头颈癌的纤维化-淋巴水肿连续体
- 批准号:
8255582 - 财政年份:2010
- 资助金额:
$ 60.81万 - 项目类别:
Hospice Pain Control: Developing an Opioid Order Sheet
临终关怀疼痛控制:制定阿片类药物订单表
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7121936 - 财政年份:2005
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Hospice Pain Control: Developing an Opioid Order Sheet
临终关怀疼痛控制:制定阿片类药物订单表
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5219416 - 财政年份:
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