[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07221825":3,"trial-entities:NCT07221825":145,"trial-summary:NCT07221825":149},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":6,"overall_status":7,"completion_date":8,"status_verified_date":9,"last_update_date":10,"start_date":11,"sponsor_name":12,"lead_sponsor_class":13,"has_dmc":14,"brief_summary":15,"detailed_description":16,"conditions":17,"keywords":20,"study_type":28,"primary_purpose":29,"phases":30,"enrollment_info":32,"interventions":35,"primary_outcomes":43,"secondary_outcomes":48,"sex":82,"minimum_age":83,"maximum_age":16,"healthy_volunteers":84,"eligibility_criteria":85,"std_ages":103,"locations":106,"central_contacts":136,"overall_officials":138,"references":140,"see_also_links":141},"NCT07221825","202506234","Low-Count Quantitative SPECT for Men Treated With Radium-223","RECRUITING","2028-07-31","2026-07","2026-07-21","2026-09-01","Washington University School of Medicine","OTHER",true,"Internal radiotherapies (radiolabeled molecules that are systemically administered and localize to sites of disease) provide cancer-ablating doses to diseased cells while sparing adjacent normal tissues. \\[223Ra\\]RaCl2 (Xofigo) is the first FDA-approved alpha-particle emitting radiopharmaceutical therapy (αRPT), providing a survival benefit for men with bone metastatic castration-resistant prostate cancer. Systemically administered radiotherapies distribute throughout the patient, accumulating to unknown levels at sites of disease and in radiosensitive vital organs. The whole-body distribution means that absorbed doses in the patient extend far beyond a pre-defined treatment field. There is a lack of information about αRPT distribution and localization, and this confounds treatment monitoring, complicates dose and schedule personalization, and impedes drug development.\n\nSingle-photon emission computed tomography (SPECT) imaging offers a mechanism to quantify uptake; however, αRPT administered activities are significantly lower than those used with diagnostic procedures, which presents a challenge for quantitation with conventional methods. Preliminary research shows that low-count quantitative SPECT (LC-QSPECT) imaging demonstrates reliable quantitation of regional uptake for αRPTs. The purpose of this study is to demonstrate the feasibility, tolerability and performance of LC-QSPECT imaging.",null,[18,19],"Prostate Cancer","Cancer of the Prostate",[21,22,23,24,25,26,27],"Prostate cancer","Bone metastasis","SPECT","Radiopharmaceutical therapies","Theranostics","Alpha-particle","Xofigo","INTERVENTIONAL","DIAGNOSTIC",[31],"NA",{"count":33,"type":34},38,"ESTIMATED",[36],{"type":37,"name":38,"description":39,"armGroupLabels":40,"otherNames":42},"DEVICE","Low-count quantitative single-photon emission computed tomography imaging","LC-QSPECT scans will be performed between 6 and 36 hours after administration of Xofigo during Cycles 1 and 3.",[41],"LC-QSPECT",[41],[44],{"measure":45,"description":46,"timeFrame":47},"Spearman's correlation coefficient between the LC-QSPECT estimated uptake in the lesions and intestine with ex vivo activity sampling","The investigators will assess if the correlation (in absolute magnitude) ≥ 0.60 between the tissue and SPECT data against a low correlation of \\\u003C 0.2 based on 1-sided normal test at a 5% level.","Through collection of ex vivo sample (estimated to be 3 months)",[49,52,54,58,62,64,66,69,72,75,77,79],{"measure":50,"timeFrame":51},"LC-QSPECT related adverse events","From start of LC-QSPECT imaging through 12 hours following LC-QSPECT imaging",{"measure":53,"timeFrame":51},"Percentage of enrolled patients who withdraw from the study due to adverse events at least possibly related to LC-QSPECT (as chosen by patients or treating physician team)",{"measure":55,"description":56,"timeFrame":57},"Feasibility of conducting LC-QSPECT will be determined by percentage of SPECT scans that can be processed using the investigators' computational method","Feasibility is defined as at least 80% of scans able to be processed.","Through completion of LC-QSPECT imaging (estimated to be 3 months)",{"measure":59,"description":60,"timeFrame":61},"Correlation between the LC-QSPECT measurements and PSA (Spearman Correlation Coefficient)","Spearman correlation coefficient measures the strength and direction of the linear correlation (dependence) between 2 variables after converting the raw data to ranks, giving a value between +1 and -1 inclusive, where 1 indicates perfect positive correlation, 0 indicates no correlation, and -1 indicates perfect negative correlation.","Through completion of Xofigo treatment (estimated to be 6 months)",{"measure":63,"description":60,"timeFrame":61},"Correlation between the LC-QSPECT measurements and PSA doubling time (Spearman Correlation Coefficient)",{"measure":65,"description":60,"timeFrame":61},"Correlation between the LC-QSPECT measurements and bone-turnover markers (Spearman Correlation Coefficient)",{"measure":67,"description":68,"timeFrame":61},"Correlation between the LC-QSPECT measurements and Functional Assessment of Cancer Therapy-Prostate (FACT-P) questionnaire (Spearman Correlation Coefficient)","* Spearman correlation coefficient measures the strength and direction of the linear correlation (dependence) between 2 variables after converting the raw data to ranks, giving a value between +1 and -1 inclusive, where 1 indicates perfect positive correlation, 0 indicates no correlation, and -1 indicates perfect negative correlation.\n* The FACT-P scale is a tool used for assessing the health-related quality of life (QoL) in men with prostate cancer. It consists of 27 core items which assess patient function in four domains (Physical, Social\u002FFamily, Emotional, and Functional well-being), and it is further supplemented by 12 site specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert type scale, and then combined to produce a global QoL score, with a range of scores of 0 to 156. Higher scores represent better QoL.",{"measure":70,"description":71,"timeFrame":61},"Correlation between the LC-QSPECT measurements and EuroQol-5 (EQ-5D-5L) questionnaire (Spearman Correlation Coefficient)","* Spearman correlation coefficient measures the strength and direction of the linear correlation (dependence) between 2 variables after converting the raw data to ranks, giving a value between +1 and -1 inclusive, where 1 indicates perfect positive correlation, 0 indicates no correlation, and -1 indicates perfect negative correlation.\n* EQ-5D-5L is a descriptive system for health-related quality of life states in adults, consisting of five dimensions (Mobility, Self-care, Usual activities, Pain \\& discomfort, Anxiety \\& depression), each of which has five severity levels that are described by statements appropriate to that dimension. Scale Minimum: 0. Scale Maximum: 100. Higher score indicates better outcome.",{"measure":73,"description":74,"timeFrame":61},"Correlation between the LC-QSPECT measurements and Brief Pain Inventory (BPI) questionnaire (Spearman Correlation Coefficient)","* Spearman correlation coefficient measures the strength and direction of the linear correlation (dependence) between 2 variables after converting the raw data to ranks, giving a value between +1 and -1 inclusive, where 1 indicates perfect positive correlation, 0 indicates no correlation, and -1 indicates perfect negative correlation.\n* BPI score ranges from 0 to 10 with a higher score denoting a higher pain severity.",{"measure":76,"description":60,"timeFrame":61},"Correlation between the LC-QSPECT measurements and bone turnover (Spearman Correlation Coefficient)",{"measure":78,"timeFrame":61},"Percentage of times that the use of the LC-QSPECT procedure resulted in any changes in treatment plans of the patients",{"measure":80,"description":81,"timeFrame":57},"Performance of the LC-QSPECT procedure using a no-gold-standard evaluation technique.","* The investigators will use the no-gold-standard technique to assess whether the LC-QSPECT technique yields precise performance on the task of isotope uptake quantification, where slope and noise will be estimated and the noise-to-slope ratio (NSR) will be calculated.\n* The no-gold-standard technique can be found here: Jha AK, Caffo B, Frey EC. A no-gold-standard technique for objective assessment of quantitative nuclear-medicine imaging methods. Phys Med Biol. 2016 Apr 7;61(7):2780-800. doi: 10.1088\u002F0031-9155\u002F61\u002F7\u002F2780. Epub 2016 Mar 16. PMID: 26982626; PMCID: PMC4921224 and here: Yan Liu, Ziping Liu, Zekun Li, Daniel Thorek, Barry Siegel, Abhinav Jha, \"No-gold-standard evaluation of quantitative SPECT methods for alpha-particle radiopharmaceutical therapy\", Journal of Nuclear Medicine Jun 2023, 64 (supplement 1) P1331","MALE","18 Years",false,{"inclusion":86,"exclusion":93,"raw_text":102},[87,88,89,90,91,92],"Histologically or cytologically confirmed castration-resistant prostate cancer with symptomatic bone metastases.","Minimum detectable skeletal lesion count of 3.","Eligible to receive Xofigo.","At least 18 years of age.","ECOG performance status ≤ 3.","Ability to understand and willingness to sign an IRB-approved written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of study participants.",[94,95,96,97,98,99,100,101],"Predominant visceral metastatic disease.","Prior or concurrent malignancy whose natural history has the potential to interfere with the safety or efficacy assessment of the investigational regimen. Patients with prior or concurrent malignancy that does NOT meet that definition are eligible for this trial","Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.","Concurrent alternative radiopharmaceuticals","Inability to maintain stationary supine pose for 45-60 minutes","Medical Oncologist or Radiation Oncologist at Siteman Cancer Center.","Treating patients with prostate cancer.","Willing to complete Physician Questionnaire during participation.","Inclusion Criteria - Patients:\n\n* Histologically or cytologically confirmed castration-resistant prostate cancer with symptomatic bone metastases.\n* Minimum detectable skeletal lesion count of 3.\n* Eligible to receive Xofigo.\n* At least 18 years of age.\n* ECOG performance status ≤ 3.\n* Ability to understand and willingness to sign an IRB-approved written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of study participants.\n\nExclusion Criteria - Patients:\n\n* Predominant visceral metastatic disease.\n* Prior or concurrent malignancy whose natural history has the potential to interfere with the safety or efficacy assessment of the investigational regimen. Patients with prior or concurrent malignancy that does NOT meet that definition are eligible for this trial\n* Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.\n* Concurrent alternative radiopharmaceuticals\n* Inability to maintain stationary supine pose for 45-60 minutes\n\nEligibility Criteria - Physicians:\n\n* Medical Oncologist or Radiation Oncologist at Siteman Cancer Center.\n* Treating patients with prostate cancer.\n* Willing to complete Physician Questionnaire during participation.",[104,105],"ADULT","OLDER_ADULT",[107],{"facility":12,"status":7,"city":108,"state":109,"zip":110,"country":111,"contacts":112,"geoPoint":133},"St Louis","Missouri","63110","United States",[113,118,120,123,125,127,129,131],{"name":114,"role":115,"phone":116,"email":117},"Abhinav K Jha, Ph.D.","CONTACT","314-273-2655","a.jha@wustl.edu",{"name":114,"role":119},"PRINCIPAL_INVESTIGATOR",{"name":121,"role":122},"Daniel Thorek, Ph.D.","SUB_INVESTIGATOR",{"name":124,"role":122},"Tyler J Fraum, M.D.",{"name":126,"role":122},"Richard L Wahl, M.D.",{"name":128,"role":122},"Jingqin (Rosy) Luo, Ph.D.",{"name":130,"role":122},"Richard Laforest, Ph.D.",{"name":132,"role":122},"Hiram Gay, M.D.",{"lat":134,"lon":135},38.62727,-90.19789,[137],{"name":114,"role":115,"phone":116,"email":117},[139],{"name":114,"affiliation":12,"role":119},[],[142],{"label":143,"url":144},"Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine","http:\u002F\u002Fwww.siteman.wustl.edu",{"nct_id":4,"conditions":146,"biomarkers":148},[147],"Prostate Carcinoma",[],{"nct_id":4,"found":14,"summary":150,"prompt_version":159},{"design":151,"status":152,"heading":6,"summary":153,"follow_up":154,"word_count":155,"commitments":156,"compensation":157,"drugs_mentioned":158},"This is an interventional study, meaning participants will receive a specific intervention (LC-QSPECT scans). It is planned to include 38 participants.","completed","This study is looking at a new way to measure how much of the cancer medicine Xofigo (Radium-223) goes to bone tumors and other areas in the body. Xofigo is an approved treatment for men with prostate cancer that has spread to the bones and is no longer responding to hormone therapy (castration-resistant prostate cancer). Researchers will use a special imaging scan called LC-QSPECT (low-count quantitative single-photon emission computed tomography) to see how Xofigo is distributed. The main goal is to see if these scans accurately show how much Xofigo is in the tumors and intestine by comparing it to samples taken later. This study is for men aged 18 or older with prostate cancer that has spread to the bones and who are eligible to receive Xofigo. The study plans to enroll 38 participants, but its current status is unclear.","The primary endpoint involves measurements taken through ex vivo sample collection, estimated to be 3 months after the start of the study.",141,"You would have LC-QSPECT scans performed between 6 and 36 hours after receiving Xofigo during Cycles 1 and 3. Ex vivo samples will be collected, estimated to be 3 months after the start of the study.","Not stated in the trial record.",[],"v2"]