Actively Recruiting
Systemic Neoadjuvant and Adjuvant Control by Precision Medicine in Rectal Cancer
Led by Helsinki University Central Hospital · Updated on 2023-03-06
93
Participants Needed
2
Research Sites
523 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Rectal cancer represents the most complex area of multidisciplinary treatment in bowel surgery. In 2017, there were 1221 new rectal cancers in Finland. The prognosis of colorectal cancer (CRC) patients these days is almost exclusively driven by the occurrence of the metastatic form of the disease. The treatment of rectal cancer often includes a long delay between diagnosis and the initiation of systemic chemotherapy, increasing risk for systemic metastases for those at high risk. On the other hand, the waiting time during pretreatment before surgery enables comprehensive systematic characterization of the primary tumor status before the decisions on adjuvant chemotherapy, opening a window to the use of precision in decision-making. In this randomized controlled treatment trial, outcomes of novel precision methods to select right rectal cancer patients for treatment that they need will be compared to conventional treatment. The study aims to reduce over-treatment of those that most likely do not benefit from additional treatments. With the overall aim to reduce metastatic form of the disease, patients with high-risk features will be randomized to a treatment strategy with early systemic control by chemotherapy followed by circulating tumor DNA (ctDNA) and organoid-guided adjuvant therapy, or to conventional treatment strategy. Both state-of-the-art laboratory practice and routine diagnostic clinical pipelines are introduced to bring future diagnostic models of minimal residual disease and chemoresistance closer to current practice. The outcomes will reveal the clinical benefit of such strategy by recurrence-free survival at highest level of evidence, and produce important clinical outcome data on the application of ctDNA in everyday cancer treatment practice. The translational data on the use of ctDNA organoids to inform treatment decision and regimen selection will build knowledge of the use of such biomarkers as tools for clinical practice and clinical research. The results will be scalable worldwide in the practice of rectal cancer treatment.
CONDITIONS
Official Title
Systemic Neoadjuvant and Adjuvant Control by Precision Medicine in Rectal Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with rectal adenocarcinoma
- World Health Organization (WHO) performance status 0-1, suitable for capecitabine and oxaliplatin (CAPOX) chemotherapy
- Presence of extramural vein invasion detected by magnetic resonance imaging (mrEMVI+)
- Multi-disciplinary team assessment requiring radiotherapy or long chemoradiotherapy based on current standards
You will not qualify if you...
- Deficient mismatch repair (MMR) status
- Non-dihydropyrimidine dehydrogenase (DPYD) genotype
- Contraindications to capecitabine, oxaliplatin, or radiotherapy
- Blood test results showing inadequate circulatory, liver, or kidney function for chemotherapy
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Helsinki University Central Hospital
Helsinki, Uusimaa, Finland, 00029
Actively Recruiting
2
Tampere University Hospital
Tampere, Finland, 33520
Actively Recruiting
Research Team
T
Toni T Seppala, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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