RecruitingPhase 2Phase 3NCT06758830

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

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


Sponsor

National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos

Enrollment

400 participants

Start Date

Jan 7, 2025

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two approaches for rectal cancer: (1) using intensive pre-surgery treatment (total neoadjuvant therapy, or TNT) to potentially avoid surgery altogether and preserve the rectum, versus (2) standard surgery. It is also collecting observational data from patients who have already received or are planning neoadjuvant treatment. **You may be eligible if...** - You are over 18 years old - You have been diagnosed with rectal cancer (adenocarcinoma) confirmed by biopsy - Your tumor is located within 10–12 cm of the anus without distant spread - You are in reasonably good health (ECOG 0–2) with adequate blood, kidney, and liver function **You may NOT be eligible if...** - You have already received radiation or chemotherapy for this cancer - You have cancer that has spread to other organs - You have had another cancer in the past 5 years (except certain skin or cervical cancers) - You have severe uncontrolled health or psychiatric conditions - You have an active infection requiring antibiotics Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONRadiation Therapy

Radiation 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.

DRUGChemoradiotherapy

Capecitabine: 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 Chemotherapy

XELOX: 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.

PROCEDURESurgery

Transabdominal Resection: Abdominoperineal resection, low anterior resection, or coloanal anastomosis using total mesorectal excision.

OTHERPart two

Standard treatment protocols and follow-up procedures are implemented in clinical practice.

OTHERAdjuvant treatment

If indicated, adjuvant therapy will be administered as usual in clinical practice.


Locations(1)

Nacional Cancer Institute

Vilnius, Lithuania

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NCT06758830


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