[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100505086":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":26,"centralContacts":25,"locations":30,"responsibleParty":154,"collaborators":25,"id":156,"slug":157,"hasResults":158,"nctId":159,"briefTitle":160,"officialTitle":161,"acronym":162,"eligibilityCriteria":163,"healthyVolunteers":158,"sex":164,"minAge":165,"maxAge":25,"enrollmentInfo":166,"targetDuration":25,"studyType":169,"phases":170,"briefSummary":172,"conditions":173,"keywords":175,"overallStatus":33,"whyStopped":25,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":181,"completionDateStruct":183,"leadSponsor":185,"locationsCount":186},{"fullName":5,"class":6},"Proton Collaborative Group","NETWORK",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm A - Standard Fractionation","ACTIVE_COMPARATOR","50-50.4 Gy (RBE) in 25-28 daily fractions of 1.8-2.0 Gy (RBE) plus a Tumor Bed Boost (for intact breast) of 10 Gy (RBE) in 4-5 daily fractions of 2-2.5 Gy (RBE)\n\n\\*\\*Additional boost of 10-20 Gy (RBE) in 2-2.5 Gy (RBE) fractions to clinically involved lymph nodes or chest wall\u002Fscar allowed at the treating physician's discretion\\*\\*",[13],"Radiation: Proton Therapy",{"label":15,"type":16,"description":17,"interventionNames":18},"Arm B - Hypofractionation","OTHER","40.05 Gy (RBE) in 15 daily fractions of 2.67 Gy (RBE) plus a Tumor Bed Boost (for intact breast) of 10 Gy (RBE) in 4-5 daily fractions of 2-2.5 Gy (RBE)\n\n\\*\\*Additional boost of 10-20 Gy (RBE) in 2-2.5 Gy (RBE) fractions to clinically involved lymph nodes or chest wall\u002Fscar allowed at the treating physician's discretion\\*\\*",[13],[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"RADIATION","Proton Therapy","Pencil Beam Scanning (PBS)",[9,15],null,[27],{"name":28,"affiliation":5,"role":29},"Isabelle Choi, MD","STUDY_CHAIR",[31,54,71,88,104,121,137],{"facility":32,"status":33,"city":34,"state":35,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Mayo Clinic","RECRUITING","Scottsdale","Arizona","85259","United States","US",{"type":40,"coordinates":41},"Point",[42,43],-111.89903,33.50921,{"lat":43,"lon":42},[46,51],{"name":47,"role":48,"phone":49,"phoneExt":25,"email":50},"June Leonard","CONTACT","855-776-0015 (toll free)","leonard.june@mayo.edu",{"name":52,"role":53,"phone":25,"phoneExt":25,"email":25},"Carlos Vargas, MD","PRINCIPAL_INVESTIGATOR",{"facility":55,"status":33,"city":56,"state":57,"zip":58,"country":37,"countryCode":38,"cosmosGeoPoint":59,"geoPoint":63,"contacts":64},"California Protons Cancer Therapy Center","San Diego","California","92121",{"type":40,"coordinates":60},[61,62],-117.16472,32.71571,{"lat":62,"lon":61},[65,69],{"name":66,"role":48,"phone":67,"phoneExt":25,"email":68},"Alexandra Crawford, MPH","858-549-7431","alexandra.crawford@californiaprotons.com",{"name":70,"role":53,"phone":25,"phoneExt":25,"email":25},"Iain MacEwan, MD",{"facility":72,"status":33,"city":73,"state":74,"zip":75,"country":37,"countryCode":38,"cosmosGeoPoint":76,"geoPoint":80,"contacts":81},"University of Florida Proton Therapy Institute","Jacksonville","Florida","32206",{"type":40,"coordinates":77},[78,79],-81.65565,30.33218,{"lat":79,"lon":78},[82,86],{"name":83,"role":48,"phone":84,"phoneExt":25,"email":85},"Robin Cacchio","904-588-1460","rcacchio@floridaproton.org",{"name":87,"role":53,"phone":25,"phoneExt":25,"email":25},"Julie Bradley, MD",{"facility":89,"status":33,"city":90,"state":74,"zip":91,"country":37,"countryCode":38,"cosmosGeoPoint":92,"geoPoint":96,"contacts":97},"Miami Cancer Institute","Miami","33176",{"type":40,"coordinates":93},[94,95],-80.19366,25.77427,{"lat":95,"lon":94},[98,102],{"name":99,"role":48,"phone":100,"phoneExt":25,"email":101},"Alex Kudryashev","786-596-2000","alexku@baptisthealth.net",{"name":103,"role":53,"phone":25,"phoneExt":25,"email":25},"Joseph Panoff, MD",{"facility":105,"status":33,"city":106,"state":107,"zip":108,"country":37,"countryCode":38,"cosmosGeoPoint":109,"geoPoint":113,"contacts":114},"Emory Proton Therapy Center","Atlanta","Georgia","30308",{"type":40,"coordinates":110},[111,112],-84.38798,33.749,{"lat":112,"lon":111},[115,119],{"name":116,"role":48,"phone":117,"phoneExt":25,"email":118},"Leann Schilling, MPH, CCRP","404-686-0286","leann.schilling@emory.edu",{"name":120,"role":53,"phone":25,"phoneExt":25,"email":25},"Sunil Dutta, MD",{"facility":122,"status":33,"city":123,"state":123,"zip":124,"country":37,"countryCode":38,"cosmosGeoPoint":125,"geoPoint":129,"contacts":130},"New York Proton Center","New York","10035",{"type":40,"coordinates":126},[127,128],-74.00597,40.71427,{"lat":128,"lon":127},[131,136],{"name":132,"role":48,"phone":133,"phoneExt":134,"email":135},"Ryan Holder","646-968-9055","387","rholder@nyproton.com",{"name":28,"role":53,"phone":25,"phoneExt":25,"email":25},{"facility":138,"status":33,"city":139,"state":140,"zip":141,"country":37,"countryCode":38,"cosmosGeoPoint":142,"geoPoint":146,"contacts":147},"Inova Schar Cancer Institute","Fairfax","Virginia","22031",{"type":40,"coordinates":143},[144,145],-77.30637,38.84622,{"lat":145,"lon":144},[148,152],{"name":149,"role":48,"phone":150,"phoneExt":25,"email":151},"Sangeetha Moturi","571-472-0343","sangeetha.moturi@inova.org",{"name":153,"role":53,"phone":25,"phoneExt":25,"email":25},"Ashish Chawla, MD",{"type":155,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR","100505086","phase-3-conventionally-fractionated-vs-hypofractionated-comprehensive-nodal-irradiation-for-breast-cancer-using-pencil-beam-scanning-proton-therapy-100505086",false,"NCT05856773","Conventionally Fractionated vs. Hypofractionated Comprehensive Nodal Irradiation for Breast Cancer Using Pencil Beam Scanning Proton Therapy","Phase III Randomized Trial of Conventionally Fractionated vs. Hypofractionated COMprehensive Nodal Irradiation for Breast Cancer Using Pencil Beam Scanning PROton Therapy (COMPRO)","COMPRO","Inclusion Criteria:\n\n* Patients with Stage I-III breast cancer who have undergone breast conserving surgery or mastectomy and have been recommended to receive postoperative radiation therapy to the breast or chest wall and regional draining lymph nodes (axilla levels I-III, SCV, IMN)\n* Histologically documented breast cancer (invasive mammary, ductal, medullary, tubular, mucinous, lobular, or ductal carcinoma in situ) for which treatment with radiation therapy to the breast\u002Fchest wall and comprehensive regional lymph nodes including the internal mammary chain is recommended\n* Documentation of negative metastatic workup by whole body Positron Emission Tomography - Computed Tomography (PET\u002FCT) or by combined CT of the chest, abdomen, pelvis and Bone scan\n* History and physical exam within 90 days prior to study registration\n* Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, or 2\n* Negative pregnancy test for women of child-bearing potential\n* Able to begin radiation treatment within 12 weeks of last surgery or last day of chemotherapy\n* Presence of breast implants, breast expanders, tissue flap, or other breast reconstruction are allowed\n* Bilateral breast cancer is allowed if at least one side will be treated with comprehensive nodal irradiation per protocol treatment and will be recorded as the laterality receiving comprehensive nodal irradiation. If both sides will be treated comprehensively, it will be documented as such\n\nExclusion Criteria:\n\n* Presence of skin ulceration and \u002F or ipsilateral satellite nodules and\u002For edema (including peau d'orange) (T4b or T4c disease) or diagnosis of inflammatory breast cancer (T4d disease)\n* Residual gross disease detected by imaging or clinical exam with the exception of \\\u003C2cm internal mammary lymph node or supraclavicular lymph node amenable to sequential boost\n* Prior history of radiation therapy overlapping with current target volume (including intraoperative brachytherapy, interstitial catheter brachytherapy, balloon brachytherapy, external beam radiation therapy)\n* Prior history of explant surgery or implant removal due to infection or wound healing issues without subsequent implant or flap reconstruction\n* Presence of double\u002Fdual port tissue expander\n* Clinical or radiographic evidence of distant metastatic disease\n* Pregnant or breast-feeding females\n* Non-malignant systemic disease that would preclude the patient from receiving study treatment or would prevent required follow-up\n* History of connective tissue disorder (i.e., systemic lupus erythematosus, scleroderma), dermatomyositis, xeroderma pigmentosum\n* Known BRCA 1 or BRCA 2 mutation\n* Presence of an active skin rash\n* Prior invasive non-study malignancy unless disease free for ≥ 3 years. Non-melanoma skin cancer, well-differentiated thyroid cancers, in situ carcinomas of the oral cavity, cervix, and other organs, and tumors that are not thought to impact the life expectancy of the patient are permissible.","FEMALE","19 Years",{"count":167,"type":168},276,"ESTIMATED","INTERVENTIONAL",[171],"PHASE3","The purpose of this research study is to learn more about the effects of using proton radiation therapy delivered over a shorter course of treatment (3 weeks) compared with a longer, standard course of treatment (5 weeks) for women with breast cancer who require radiotherapy to the breast\u002Fchest wall and regional lymph nodes.",[174],"Breast Cancer",[176],"Proton Radiation","2025-09-02",{"date":179,"type":180},"2025-09-09","ACTUAL",{"date":182,"type":180},"2024-03-21",{"date":184,"type":168},"2041-02",{"name":5,"class":6},7]