[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07292298":3,"trial-entities:NCT07292298":112,"trial-summary:NCT07292298":116},{"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":24,"primary_purpose":25,"phases":26,"enrollment_info":28,"interventions":31,"primary_outcomes":38,"secondary_outcomes":43,"sex":55,"minimum_age":56,"maximum_age":57,"healthy_volunteers":58,"eligibility_criteria":59,"std_ages":63,"locations":66,"central_contacts":102,"overall_officials":107,"references":110,"see_also_links":111},"NCT07292298","25-1202.cc","Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates","RECRUITING","2031-11","2026-04","2026-04-06","2026-11","University of Colorado, Denver","OTHER",true,"Rectal cancer patients who do not achieve a complete response to standard of care chemotherapy and radiation often require surgical resection as part of curative intent therapy. This study will evaluate whether additional \"focal\" radiation delivered internally (rectal brachytherapy) can provide complete responses and thus spare the requirement for surgery.\n\nThe main questions are whether: 1) rectal brachytherapy is safe in this clinical treatment paradigm and if 2) rectal brachytherapy improves organ preservation (no need for surgery).\n\nThe trial involves an additional MRI pelvis and sigmoidoscopy with marker placement to define high-risk residual disease for radiation planning. Subsequently, 3 outpatient brachytherapy treatments are given on a weekly basis. If a patient achieves a complete response to brachytherapy, standard of care non-operative surveillance visits are conducted with study visits aligned during the first two years following brachytherapy.","Rectal cancer patients with incomplete responses following standard of care chemotherapy and radiation are offered surgery as part of curative intent regimens. Similarly, patients with near-complete responses following initial therapy may require future salvage surgery given high local recurrence risk in the rectum. The goal of this study is to determine whether additional \"internal\" focal radiation delivered by rectal brachytherapy can provide a complete tumor response, such that patients can avoid surgical intervention. While rectal brachytherapy efficacy, technique, and safety has been demonstrated in previous studies conducted in Europe and Canada, it has not been tested to \"boost\" responses following standard of care chemotherapy\u002Fradiation in the United States.\n\nSpecifically, rectal brachytherapy treatment requires placement of a multichannel cylinder into the rectum following local analgesia and oral medication to improve procedure tolerability. A balloon on the cylinder is inflated to displace rectum uninvolved with tumor away from the internal high-dose radiation source that travels through the cylinder channels abutting the tumor. 21 Gy cumulative dose over 3 weekly treatments is administered to the high-risk rectal mucosa at a depth aligning to tumor thickness. The cylinder will be immobilized in the rectum for up to 3 hours during each of the 3 brachytherapy sessions, with radiation treatment being less than 10 minutes following completion of planning.\n\nIf complete response is achieved, surveillance visits will be conducted with an almost identical protocol to patients who achieve complete response following standard of care radiation\u002Fchemotherapy.",[18,19],"Rectal Adenocarcinoma","Rectal Cancer",[21,22,23],"Locally Advanced Rectal Cancer","Non-metastatic Rectal Cancer","Rectal Neoplasms","INTERVENTIONAL","TREATMENT",[27],"PHASE2",{"count":29,"type":30},44,"ESTIMATED",[32],{"type":33,"name":34,"description":35,"armGroupLabels":36},"RADIATION","High Rare Dose Rectal Brachytherapy Boost","HDR rectal brachytherapy boost using Iridium-192 delivered via an intracavitary applicator in three weekly fractions (total dose: 21 Gy) for patients with low-lying residual rectal adenocarcinoma following total neoadjuvant therapy.",[37],"HDR Rectal Brachytherapy Boost",[39],{"measure":40,"description":41,"timeFrame":42},"Organ preservation (no surgical requirement) of the rectum associated with complete clinical response","As evaluated by standard of care sigmoidoscopy and MRI","2 years following study treatment",[44,47,50,52],{"measure":45,"description":46,"timeFrame":42},"Locoregional recurrence free survival","As defined by CT and MRI pelvis",{"measure":48,"description":49,"timeFrame":42},"Distant metastatic free survivial","As assessed by CT c\u002Fa\u002Fp",{"measure":51,"description":51,"timeFrame":42},"Overall survival",{"measure":53,"description":54,"timeFrame":42},"Bowel function","As assessed by LARS (low anterior resection syndrome) questionnaire","ALL","18 Years","100 Years",false,{"inclusion":60,"exclusion":61,"raw_text":62},[],[],"Inclusion Criteria:\n\n1. Provision to sign and date the consent form.\n2. Stated willingness to comply with all study procedures and be available for the duration of the study.\n3. Adults (18-100 years old)\n4. ECOG 0-3\n5. Patients with MMR-proficient low-mid rectal adenocarcinoma cT1-4 N0-2 M0 who underwent total neoadjuvant therapy who have not achieved complete response (i.e. incomplete or near-complete) in the rectal primary tumor such that surgical resection, if offered presently or in the future, would be an APR or low LAR per colorectal surgeon expert opinion and central review at University of Colorado rectal tumor board. Tumor restaging will be 4-16 weeks following completion of total neoadjuvant therapy, and no sooner than 8 weeks if patients received chemotherapy followed by chemoradiation\u002Fshort course radiation.\n6. Residual rectal disease must have its craniocaudal extent \\\u003C4 cm with thickness \\\u003C1.2 cm. Tumor must have \\\u003C50% circumferential involvement. Residual disease must be above the dentate line and not involving the anal canal.\n7. In patients with original cN1-2 disease, restaging CT and MRI after total neoadjuvant therapy must demonstrate at least near-complete response of the pelvic lymph nodes per NCCN criteria as evaluated by central review at University of Colorado rectal tumor board.\n8. Interval of time between completion of TNT and initiation of rectal brachytherapy must be between 4-16 weeks.\n9. Patients must be recovered from total neoadjuvant therapy and must not have significant rectal incontinence at time of screening.\n10. Received conventionally fractionated external beam chemoradiation between 45-56 Gy or short-course external beam radiation prescription of 25 Gy to rectal mucosa, in addition to systemic chemotherapy before or after radiation per National Comprehensive Cancer Network (NCCN) guidelines.\n11. Women of child-bearing potential must have a negative urine or serum pregnancy test within 14 days of HDR treatment.\n12. Men and women of reproductive potential who are sexually active must agree to follow instructions of contraception for the duration of the study and 6 months post-rectal brachytherapy completion.\n13. CBC at the time of screening must have platelets\\>50 10\\^9\u002FL, Hemoglobin\\>8 g\u002FdL and Absolute Neutrophil Count \\> 500 10\\^9\u002FL\n\nExclusion Criteria:\n\n1. History of ulcerative colitis or Crohn's disease.\n2. Pelvic radiotherapy given prior to rectal cancer external beam radiation.\n3. Prior colorectal surgery in which anastomotic site is at or near HDR brachytherapy target.\n\n   o Prior local excision is not an exclusion criterion.\n4. Uncontrolled intercurrent severe illness, including but not limited to, ongoing or active infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia, interstitial lung disease, serious chronic gastrointestinal conditions associated with diarrhea, or psychiatric illness\u002Fsocial situations that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent.\n5. Life expectancy \\\u003C3 years per provider discretion.\n6. Concurrent administration of any cytotoxic chemotherapy, immunotherapy, or other any targeted oncologic agent that would impact rectal cancer is not allowed during study protocol.\n7. If rectal cancer has been treated outside of standard total neoadjuvant therapy per NCCN guidelines, patients are ineligible for the trial. This includes if patients received external beam chemoradiation dose with prescription \\>56 Gy or short-course radiation to rectal mucosa prescription \\>30 Gy.\n8. Pregnant women.",[64,65],"ADULT","OLDER_ADULT",[67,85,94],{"facility":68,"status":7,"city":69,"state":70,"zip":71,"country":72,"contacts":73,"geoPoint":82},"University of Colorado Cancer Center","Aurora","Colorado","80045","United States",[74,79],{"name":75,"role":76,"phone":77,"email":78},"Radiation Therapy Group","CONTACT","303-724-8822","RTClinicalResearch@olucdenver.onmicrosoft.com",{"name":80,"role":81},"David Binder, MD, PhD","PRINCIPAL_INVESTIGATOR",{"lat":83,"lon":84},39.72943,-104.83192,{"facility":86,"status":87,"city":88,"state":89,"zip":90,"country":72,"geoPoint":91},"University of Rochester Medical Center","NOT_YET_RECRUITING","Rochester","New York","14642",{"lat":92,"lon":93},43.15478,-77.61556,{"facility":95,"status":87,"city":96,"state":97,"zip":98,"country":72,"geoPoint":99},"Oregon Health and Sciences University","Portland","Oregon","97239",{"lat":100,"lon":101},45.52345,-122.67621,[103,104],{"name":75,"role":76,"phone":77,"email":78},{"name":105,"role":76,"email":106},"Alex Fonder","alex.fonder@cuanschutz.edu",[108],{"name":109,"affiliation":12,"role":81},"David Binder",[],[],{"nct_id":4,"conditions":113,"biomarkers":114},[18],[115],"MRC1 wt Allele",{"nct_id":4,"found":14,"summary":117,"prompt_version":127},{"design":118,"status":119,"heading":120,"summary":121,"follow_up":122,"word_count":123,"commitments":124,"compensation":125,"drugs_mentioned":126},"This is a Phase 2, single-arm study, meaning all 44 participants will receive the High Rare Dose Rectal Brachytherapy Boost. The study is interventional.","completed","Phase 2 Rectal Cancer Brachytherapy for Organ Preservation","This study is for people with rectal adenocarcinoma (a type of rectal cancer) that hasn't completely gone away after standard chemotherapy and radiation. Instead of surgery, this trial tests if an additional treatment called High Rare Dose Rectal Brachytherapy Boost (a type of internal radiation using Iridium-192) can help you avoid surgery. This brachytherapy is given in three weekly treatments. The main goal is to see if this treatment can lead to a complete response, meaning you wouldn't need surgery to remove the rectum. To join, you must be 18-100 years old, have a good performance status (ECOG 0-3), and have MMR-proficient low-mid rectal adenocarcinoma. The study aims to enroll 44 participants.","The main goal of the study, organ preservation, will be measured at 2 years following study treatment.",112,"You would have an additional MRI pelvis and sigmoidoscopy with marker placement. Then, you would receive three outpatient brachytherapy treatments on a weekly basis.","Not stated in the trial record.",[34],"v2"]