Total neoadjuvant therapy (TNT)
DrugShort radiotherapy (5X5 Gy) and capecitabine/oxaliplatin
NCT Number: NCT04842006
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.
Interested in participating?
Request Info18 year–100 year
All sexes
Interventional
Not applicable
Helsinki University Central Hospital, Helsinki, Uusimaa, Finland
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Short radiotherapy (5X5 Gy) and capecitabine/oxaliplatin
Postoperative MRD on circulating cell-free DNA
Long-course 50.4 Gy radiation with capecitabine
Time frame: 3 years from surgery
Time frame: 5 years from surgery
Time frame: 3 weeks postoperatively
number of patients with detectable ctDNA at postoperative sample in the conventional treatment arm that are not assigned to chemotherapy
Time frame: 3 years
Time frame: 5 years
Time frame: 3 years
Time frame: 5 years
Time frame: 1 year
Time frame: 1 year
Time frame: 5 years postoperatively
Time frame: 12 weeks after initiation of pretreatment
Time frame: 12 weeks after initiation of pretreatment
Time frame: 1year
Time frame: 3 years
Time frame: 5 years
Time frame: 1 year
Time frame: 1 year
Time frame: 3 years
Time frame: 1 year
population distribution of PDO treatment response is compared to their corresponding clinical response by response MRI and pathological response and compared to organoid in vitro response
Contact information is provided by the study sponsor or research team.
Helsinki University Central Hospital
Other
Systemic Neoadjuvant and Adjuvant Control by Precision Medicine in Rectal Cancer (SYNCOPE) - Approach on High-risk Group to Reduce Metastases
Acronym: SYNCOPE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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