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NCT Number: NCT06200831

Simultaneous vs. Staged Resection of Colorectal Cancer With Synchronous Liver Metastases

The SYLMET Trial is a randomized trial to compare simultaneous and two-staged resection of primary colorectal and synchronous liver metastases. This is an investigator-initiated, multicentre, randomized controlled trial to assess complications (primary endpoint), survival, cost-effectiveness, and quality of life (secondary endpoints).This trial will include patients with resectable primary tumour in the colon or upper rectum with less than five liver metastases that is possible to treat with surgical resection and/or ablation (RFA/MWA) at time of evaluation.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Oslo University Hospital

Oslo, Norway

Location status: Recruiting

Location contact

Frida B Hansen

CONTACT

[email protected]

Sheraz Yaqub, MD, PhD

CONTACT

About this study

Colorectal cancer (CRC) represents the second most common cause of cancer and cancer death in Norway, and the incidence is increasing (Cancer in Norway, 2021, Cancer Registry of Norway). The liver is the most common site of metastasis from CRC. More than 4500 individuals are diagnosed with CRC in Norway each year, and approximately 20% of patients present with liver metastases at time of diagnosis (synchronous metastases). Resection of both the primary tumor and liver metastases is considered the only curative treatment, and has been shown to improve long-term survival, and is considered standard of care. However, the optimal timing of surgical resection of synchronous liver metastases in relation to the primary tumor is not well defined. Traditionally, staged resection has been preferred (i.e., resection of the primary tumour and liver metastases on separate admissions with a period of recovery between the two operations), whereas simultaneous resection is appealing (i.e., resection of both primary and metastases in one operative session). Despite a lack of randomized controlled trials comparing these two surgical approaches, the number of simultaneous resections has increased at several institutions. The evolvement of both liver and colorectal surgery in the last decades has led to reduced complications, making simultaneous resections more feasible. Previous retrospective cohort studies and meta-analyses suggest that simultaneous and staged approach carry similar postoperative complication and perioperative mortality rates as well as long-term survival. A recently published prospective observational study on staged or simultaneous surgery, reported similar outcomes in selected patients. To date, there is only one published randomized controlled trial which was aborted after inclusion of half of the sample size, after an accrual time of 10 years18. Due to lack of evidence, the majority of surgical societies worldwide still treats this patient group with staged resections, resulting in two hospital admissions, two rounds of general anaesthesia and surgery, and finally two episodes of postoperative recovery and rehabilitation. If this trial demonstrates that simultaneous surgery is safe, feasible, and cost-effective, it will potentially have a practice-changing impact worldwide.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18-80 years old.
  • Both CRC and liver metastases in situ at time of evaluation.
  • Resectable primary tumor in the colon or upper rectum.
  • Less than 5 liver metastases, evaluated by the multidisciplinary tumor board meeting as possible to treat with surgical resection and/or ablation (RFA/MWA).

Exclusion criteria

  • Unresectable primary tumor.
  • Locally advanced primary tumor (T4).
  • Primary tumor in the lower rectum with indication for abdominoperineal resection.
  • Acute or imminent bowel obstruction.
  • Perforation or major bleeding from the primary tumor.
  • Pre-treatment of the primary tumor with a colon stent.
  • Liver resection requiring resection of more than 2 adjacent segments (Couinaud).
  • Liver metastases planned treated with irreversible electroporation (IRE).
  • Non-resectable lung metastases.
  • Metastases outside of liver (besides resectable lung metastases).
  • Eastern Cooperative Oncology Group (ECOG) Performance status ≥ 3.

Treatment and study plan

Staged resection

Procedure

Patients randomized to staged resection will be operated according to the decision made by the tumor board meeting (liver or colorectal cancer first, based on tumor burden and symptoms), but both resections have to be done within a time period of 4-12 weeks.

Other names: Two-staged resection, Sequential resection

Simultaneous Resection

Procedure

In cases with simultaneous surgery, the liver resection is performed prior to colon resection in order to keep a low central venous pressure during the first part of the surgical procedure and to avoid congestion of the anastomosis line owing to possible Pringle manoeuvre.

Other names: Combined resection, Synchronous resection

Primary outcomes

  1. Comprehensive Complication Index, CCI

    Time frame: 90 days

    The CCI is calculated as the sum of all complications that are weighted for their severity (multiplication of the median reference values from patients and physicians). The final formula yields a continuous scale to rank the severity of any combination of complications from 0 to 100 in a single patient.

Secondary outcomes

  1. Health Economics

    Time frame: 1 year

    Cost-effectiveness calculated by incremental cost effectiveness ratio (ICER)

  2. Overall survival

    Time frame: 3 and 5 years

    Survival

  3. Clavien Dindo Complications

    Time frame: 90 days

    Scale from 1 to 5. Higher score meaning more severe complication.

  4. Quality of Life: EQ-5D

    Time frame: Pre-operative, 30-days, 90-days, 6 months, 12 months

    EQ-5D is an instrument which evaluates the generic quality of life developed in Europe and widely used. The EQ-5D descriptive system is a preference-based HRQL measure with one question for each of the five dimensions that include mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The scale range from -0.224 to 1; with 0, 1, and negative values corresponding to death, full health, and health states worse than death, respectively.

  5. Quality of Life: EORTC QLQ-30

    Time frame: Pre-operative, 30-days, 90-days, 6 months, 12 months

    The EORTC Core Quality of Life questionnaire (EORTC QLQ-C30) is designed to measure cancer patients' physical, psychological and social functions. The questionnaire is composed of multi-item scales and single items. Score from 1-100.

Study contacts

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

Frida B Hansen

CONTACT

[email protected]

Sheraz Yaqub, MD PhD

CONTACT

[email protected]

+47-23073296

Sponsors and collaborators

Lead sponsor

Oslo University Hospital

Other

Collaborators

  • Haukeland University Hospital
  • Helse Stavanger HF
  • St. Olavs Hospital
  • University Hospital, Akershus
  • University of Oslo

Registry information

Official study title

Simultaneous vs. Staged Resection of Colorectal Cancer With Synchronous Liver Metastases - A Multicentre Randomized Controlled Trial

Acronym: SYLMET

Important dates

Study start
2024
Primary completion
2029
Study completion
2031
First posted
Jan 11, 2024
Registry last updated
Jul 31, 2025

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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