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NCT Number: NCT04842006

Systemic Neoadjuvant and Adjuvant Control by Precision Medicine in Rectal Cancer

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.

Recruiting

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Helsinki University Central Hospital, Helsinki, Uusimaa, Finland

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • rectal adenocarcinoma,
  • World Health Organization (WHO) performance status 0-1, assessed by the MDT to be able to undergo capecitabine and oxaliplatin (CAPOX) treatment, 3) extramural vein invasion by magnetic resonance imaging (mrEMVI+) and
  • assessed by the multi-disciplinary team (MDT) to require either radiotherapy (RT) or long chemoradiotherapy (CRT) by the current standards.

Exclusion criteria

  • deficient mismatch repair (MMR) status,
  • non-dihydropyrimidine dehydrogenase (DPYD) genotype,
  • a contraindication to capecitabine, oxaliplatin or RT, or
  • failing in blood tests that describe the adequate circulatory, liver and kidney function for chemotherapy.

Treatment and study plan

Total neoadjuvant therapy (TNT)

Drug

Short radiotherapy (5X5 Gy) and capecitabine/oxaliplatin

Minimal residual disease (MRD)

Diagnostic Test

Postoperative MRD on circulating cell-free DNA

Long radiation therapy

Radiation

Long-course 50.4 Gy radiation with capecitabine

Primary outcomes

  1. Recurrence-free survival

    Time frame: 3 years from surgery

  2. Recurrence-free survival

    Time frame: 5 years from surgery

  3. Postoperative ctDNA

    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

Secondary outcomes

  1. CRC-specific survival

    Time frame: 3 years

  2. CRC-specific survival

    Time frame: 5 years

  3. overall survival

    Time frame: 3 years

  4. overall survival

    Time frame: 5 years

  5. number of surgically resected patients resected patients

    Time frame: 1 year

  6. R0-resection rate

    Time frame: 1 year

  7. local recurrence rate

    Time frame: 5 years postoperatively

  8. complete pathological response response rate

    Time frame: 12 weeks after initiation of pretreatment

  9. complete clinical response rate

    Time frame: 12 weeks after initiation of pretreatment

  10. total uptake of chemotherapy

    Time frame: 1year

  11. total uptake of chemotherapy

    Time frame: 3 years

  12. total uptake of chemotherapy

    Time frame: 5 years

  13. adverse effects of surgery effects of surgery

    Time frame: 1 year

  14. adverse effects of chemotherapy

    Time frame: 1 year

  15. adverse effects of chemotherapy

    Time frame: 3 years

  16. Treatment response by patient-derived organoid (PDO) therapy response

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Toni T Seppala, MD, PhD

CONTACT

[email protected]

+358444722846

Sponsors and collaborators

Lead sponsor

Helsinki University Central Hospital

Other

Registry information

Official study title

Systemic Neoadjuvant and Adjuvant Control by Precision Medicine in Rectal Cancer (SYNCOPE) - Approach on High-risk Group to Reduce Metastases

Acronym: SYNCOPE

Important dates

Study start
2021
Primary completion
2028
Study completion
2031
First posted
Apr 12, 2021
Registry last updated
Mar 6, 2023

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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