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RecruitingNCT06758830

Total Neoadjuvant Therapy and Organ Preservation Versus Surgery for Rectal Cancer.

Total Neoadjuvant Therapy for Rectal Cancer - a New Standard of Care?

Status
Recruiting
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study hypothesizes that approximately 50% of rectal cancer patients can preserve their rectum using a watch-and-wait strategy if they achieve a complete or near-complete clinical response to total neoadjuvant therapy (TNT). The objective is to determine whether the complications, quality of life, and survival rates of rectal cancer patients who have achieved a complete or near-complete clinical response to TNT, followed by a watch-and-wait approach, are comparable to those of patients who undergo surgery first. Additionally, the study aims to identify potential prognostic and predictive markers for rectal cancer and examine survival rates and factors influencing responses to chemoradiotherapy (CRT) or TNT. The study is divided into two parts: \*\*Part One:\*\* Participants with cT1N1, T2-T3 N0-1 rectal cancer, MRF-, and EMVI-, with surgery as one of the possible first-line treatment options, will be randomized into two groups. The experimental group will consist of participants receiving TNT, including CRT and consolidation chemotherapy (Ch). If these participants achieve a complete or near-complete clinical response, they will be observed using a watch-and-wait strategy, which is a non-operative approach. The control group will consist of participants who undergo surgical treatment initially. \*\*Part Two:\*\* All participants with rectal cancer who have received CRT or TNT will be included. Additionally, participants diagnosed with rectal cancer who are scheduled for CRT or TNT but declined to participate in Part One or do not meet the inclusion criteria will also be included.

Conditions

Interventions

TypeNameDescription
RADIATIONRadiation TherapyRadiation therapy (RT) is administered at a dose of 2 Gy per day for a total dose of 50 Gy delivered to the pelvis. This is done throughout 5 to 6 weeks.
DRUGChemoradiotherapyCapecitabine: 825 mg/m² twice daily, prescribed 1-5 days per week, for 5 weeks during RT. Or Bolus 5-FU regimen: 5-fluorouracil (5-FU) 400 mg/m2/day intravenously, administered on days 1-4 and 33-35. Calcium folinate (folinic acid) 20 mg/m2/day intravenously on days 1-4 and 33-35.
DRUGConsolidation ChemotherapyXELOX: Oxaliplatin 130 mg/m² (day 1) + capecitabine 1000 mg/m² (days 1-14), every 3 weeks for 4 cycles. Or FOLFOX: Oxaliplatin - 85 mg/m2 intravenously (2-hour infusion), drip for 1 day. Calcium folinate (folinic acid) - 400 mg/m2/d. intravenously (2-hour infusion), started on day 1. F(5-fluorouracil) - 400 mg/m2/d. intravenously (bolus), started on day 1. Repeat every 2 weeks for 6 times.
PROCEDURESurgeryTransabdominal Resection: Abdominoperineal resection, low anterior resection, or coloanal anastomosis using total mesorectal excision.
OTHERPart twoStandard treatment protocols and follow-up procedures are implemented in clinical practice.
OTHERAdjuvant treatmentIf indicated, adjuvant therapy will be administered as usual in clinical practice.

Timeline

Start date
2025-01-07
Primary completion
2029-12-27
Completion
2029-12-27
First posted
2025-01-06
Last updated
2025-01-09

Locations

1 site across 1 country: Lithuania

Source: ClinicalTrials.gov record NCT06758830. Inclusion in this directory is not an endorsement.

Total Neoadjuvant Therapy and Organ Preservation Versus Surgery for Rectal Cancer. (NCT06758830) · Clinical Trials Directory