[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100085658":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":34,"centralContacts":7,"locations":38,"responsibleParty":51,"collaborators":53,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":7,"eligibilityCriteria":63,"healthyVolunteers":59,"sex":64,"minAge":65,"maxAge":7,"enrollmentInfo":66,"targetDuration":7,"studyType":69,"phases":7,"briefSummary":70,"conditions":71,"keywords":73,"overallStatus":80,"whyStopped":7,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"fullName":5,"class":6},"Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins","OTHER",null,[9,13,15,19,21,23,26,29,31],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":7},"DRUG","chemotherapy","N\u002FA- not dictated by study",{"type":10,"name":14,"description":12,"armGroupLabels":7,"otherNames":7},"endocrine therapy",{"type":16,"name":17,"description":18,"armGroupLabels":7,"otherNames":7},"GENETIC","DNA methylation analysis","laboratory analysis",{"type":16,"name":20,"description":18,"armGroupLabels":7,"otherNames":7},"protein analysis",{"type":6,"name":22,"description":18,"armGroupLabels":7,"otherNames":7},"laboratory biomarker analysis",{"type":6,"name":24,"description":25,"armGroupLabels":7,"otherNames":7},"questionnaire administration","questionnaire",{"type":27,"name":28,"description":12,"armGroupLabels":7,"otherNames":7},"PROCEDURE","adjuvant therapy",{"type":27,"name":30,"description":12,"armGroupLabels":7,"otherNames":7},"conventional surgery",{"type":32,"name":33,"description":12,"armGroupLabels":7,"otherNames":7},"RADIATION","radiation therapy",[35],{"name":36,"affiliation":5,"role":37},"Vered Stearns, MD","PRINCIPAL_INVESTIGATOR",[39],{"facility":5,"status":7,"city":40,"state":41,"zip":42,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":7},"Baltimore","Maryland","21231-2410","United States","US",{"type":46,"coordinates":47},"Point",[48,49],-76.61219,39.29038,{"lat":49,"lon":48},{"type":52,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR",[54],{"name":55,"class":56},"National Cancer Institute (NCI)","NIH","100085658","effect-of-surgery-radiation-therapy-chemotherapy-and-hormone-therapy-on-biomarkers-in-women-with-stage-i-stage-ii-stage-iii-breast-cancer-or-ductal-carcinoma-in-situ-that-can-be-removed-by-surgery-100085658",false,"NCT00373191","Effect of Surgery, Radiation Therapy, Chemotherapy, and Hormone Therapy on Biomarkers in Women With Stage I, Stage II, Stage III Breast Cancer, or Ductal Carcinoma In Situ That Can Be Removed By Surgery","Effects of Surgery, Radiation Therapy, Chemotherapy, and Endocrine Therapy on High-Sensitivity C-Reactive Protein in Women With Operable Breast Cancer","DISEASE CHARACTERISTICS:\n\n* Histologically and\u002For cytologically confirmed stage I-III invasive breast carcinoma or ductal carcinoma in situ\n\n  * Newly diagnosed disease\n* Patient must be initiating a new course of treatment for breast carcinoma, including surgery (mastectomy or lumpectomy with or without nodal evaluation) with or without any of the following:\n\n  * Radiation therapy\n  * Chemotherapy\n  * Endocrine therapy\n* No known or suspected metastatic disease\n* Hormone receptor status:\n\n  * Not specified\n\nPATIENT CHARACTERISTICS:\n\n* Female\n* Menopausal status not specified\n* No infectious or inflammatory condition, at the discretion of the principal investigator\n* No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer\n\nPRIOR CONCURRENT THERAPY:\n\n* More than 6 months since prior surgery\n\n  * Fine-needle aspirate or biopsy allowed\n* More than 6 months since prior radiotherapy\n* More than 6 months since prior chemotherapy\n* More than 6 months since prior endocrine therapy\n* No neoadjuvant endocrine therapy or chemotherapy\n* More than 2 weeks since prior and no concurrent regular use of any of the following:\n\n  * Hydroxymethyl glutaryl coenzyme A reductase inhibitor (statin)\n  * Nonsteroidal anti-inflammatory drug (NSAID)\\*\n  * Cyclooxygenase-2 (COX-2) inhibitor\n  * Aspirin\\*\n* Acetaminophen and opioid use is permitted as needed NOTE: \\*Use of these products ≤ 2 times per week at standard over-the-counter doses allowed","FEMALE","18 Years",{"count":67,"type":68},35,"ACTUAL","OBSERVATIONAL","RATIONALE: Collecting and storing samples of blood from patients with cancer to study in the laboratory may help doctors learn more about changes that may occur in DNA and identify biomarkers related to cancer.\n\nPURPOSE: This laboratory study is looking at the effects of surgery, radiation therapy, chemotherapy, and hormone therapy on biomarkers in women with stage I, stage II, stage III breast cancer, or ductal carcinoma in situ that can be removed by surgery.",[72],"Breast Cancer",[74,75,76,77,78,79],"stage I breast cancer","stage II breast cancer","stage IIIA breast cancer","stage IIIB breast cancer","stage IIIC breast cancer","ductal breast carcinoma in situ","COMPLETED","2015-10-09",{"date":83,"type":84},"2015-10-12","ESTIMATED",{"date":86,"type":7},"2006-05",{"date":88,"type":68},"2013-12",{"name":5,"class":6},1]