RecruitingPhase 2NCT05378919

Neoadjuvant Therapy vs Standard Therapy in Locally Advanced Rectal Cancer

Evaluation and Comparison of the Efficacy of a New Standard Pre-operative Chemotherapy for Stage II and III Colorectal Cancer According to the FOLFOX4 Regimen With Routine Chemoradiation Therapy


Sponsor

Lithuanian University of Health Sciences

Enrollment

250 participants

Start Date

Jun 1, 2015

Study Type

INTERVENTIONAL

Conditions

Summary

Phase II, Multicenter, Open-label, Randomized Study evaluating neoadjuvant chemotherapy (FOLFOX4) in patients with stage II and III colorectal cancer with standard chemoradiation Defined by Magnetic Resonance Imaging


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing a newer approach to treating rectal cancer — using more intensive pre-surgery treatment (called neoadjuvant therapy) — against the standard treatment approach, to see if it improves outcomes after surgery. **You may be eligible if...** - You have been diagnosed with rectal cancer (adenocarcinoma) - Your cancer is Stage II or III (confirmed by MRI and ultrasound) - Your tumor is located in the rectum (within 15 cm of the anus) - You have no signs of the cancer spreading to distant organs - You are in reasonably good overall health (ECOG 0–2) - Your blood counts and organ function are within acceptable ranges **You may NOT be eligible if...** - Your cancer has already spread to distant organs - Your blood counts (neutrophils, platelets, hemoglobin) are too low - Your liver or kidney function is significantly impaired 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

RADIATIONRadiotherapy 50 Gy

Radiotherapy 50 Gy 5 radiations per week of 2 Gy for 5 weeks

DRUGFluorouracil/folic acid

Fluorouracil 400 mg/m² D1-4 and folic acid 20mg/m2 D1-4 the first and fifth weeks of radiotherapy

DRUGChemotherapy in regimen with Oxaliplatin, fluorouracil, folinic acid (FOLFOX4)

oxaliplatin: 85 mg/m² in 2 hours at D1; folinic acid: 100 mg/m² simultaneously in 2 hours at D1 and D2 during the Oxaliplatin; bolus 5-fluorouracil (5-FU) 400mg/m² D1+D2; infusion 5-fluorouracil (5-FU): 600 mg/m² continuous infusion during 22hours at D1 and D2, every 14 days during 42 months (8 cycles).

RADIATIONRadiotherapy 50 Gy

Chemoradiotherapy 5 weeks (50 Grays (Gy), 2 Gy/session; 25 fractions) + fluorouracil/leucovorin 400 mg/m² 1-4 day the first and fifth weeks of radiotherapy. FOLOFX4 will be administrated for 8 cycles over a 16 week period. Patients will undergo re-staging within 6 weeks of their 8th cycle of FOLFOX. This will include MRI of the pelvis. If the reassessment reveals that there has been no disease progression compared to the pre-treatment evaluation and the patient remains a candidate for an R0 resection, the patient will proceed to definitive rectal cancer surgery within 8 weeks from the last chemotherapy dose. If the surgical oncologist's reassessment reveals that the patient is not a candidate for an R0 resection, the patient will proceed to standard pre-operative radiation with synchronous fluorouracil.


Locations(1)

Rita Ambraziene

Kaunas, Lithuania

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NCT05378919