Limerick: Liver Magnetic Resonance Imaging Before Treatment for Rectal Cancer. A Randomised Controlled Trial.

Sponsor
Vastra Gotaland Region (Other)
Overall Status
Recruiting
CT.gov ID
NCT05215535
Collaborator
(none)
400
1
2
79.7
5

Study Details

Study Description

Brief Summary

This multicentre randomized controlled trial aims to investigate whether an abbreviated MRI is comparable to a combined single venous phase CT with an additional 3 min equilibrium phase of the liver, in the pretreatment radiological workup in patients with rectal cancer.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Abbreviated MRI of the liver/abdomen
  • Radiation: Combined single venous and 3 min equilibrium phase CT of the abdomen/liver
N/A

Detailed Description

The incidence of rectal cancer in the European Union is approximately 125 000 per year, constituting a third of the total colorectal cancer incidence(1). In Sweden approximately 2000 individuals are diagnosed with rectal cancer each year. Evaluation of patients and possible treatment strategies (including neo-adjuvant chemo/radiotherapy, choice of surgical technique and adjuvant chemotherapy) are based on tumor specific characteristics together with patient factors such as general condition and comorbidity. These characteristics include tumor, lymph node and metastasis classification (cTNM), height of tumor (distance from anal verge), engagement of circumferential margin or mesorectal fascia, signs of extramural invasion and the presence of distant metastases. Clinical examination and endoscopy together with magnetic resonance imaging (MRI) of the pelvic region are essential in the local staging process, where MRI provides the most accurate radiological assessment, especially for rectal tumors in stage T3 and T4. The recommended methods regarding evaluation of metastases (M stage) include contrast enhanced computed tomography (CT) or MRI of the liver/abdomen, CT of the thorax, and in selected cases positron emission tomography (PET)- CT, if extensive extramural vascular invasion is present.

Previous studies have investigated the efficiency of MRI compared to other radiological methods and found that MRI of the liver is superior to contrast enhanced CT, in terms of specificity and sensitivity for diagnosis of liver metastasis (both per patient and per lesion).

Even though MRI has been recommended as the first line modality for evaluating colorectal cancer liver metastases in patients who have not previously undergone therapy the Swedish national guidelines, as well as the European Society for Medical Oncology (ESMO), include recommendations of single venous phased contrast enhanced CT of the liver/abdomen in the pre-treatment radiological workup. Progress within diagnostics has led to development of CT examination with an additional 3 min equilibrium phase of the liver that may be added to the single venous phase in order to increase the sensitivity and specificity of the diagnosis of liver metastases. However, this has not yet been included in guidelines nor implemented on a national basis in the pre-treatment radiological workup in patients with colorectal cancer.

Objective The primary objective of the present study is to compare percentage of patients requiring further radiological examinations after index examination (due to inconclusive results) between patients randomized to an abbreviated MRI liver protocol and patients randomized to a combined single venous phase CT with an additional 3 min equilibrium phase of the liver. A secondary aim is to compare time to treatment initiation, survival and development of liver metatstases between patients randomized to either an abbreviated MRI or a combined single-venous phase CT with an additional 3 min equilibrium phase of the liver.

The study is a multicentre randomized controlled trial where the hypothesis is that there is no clinical difference between the two groups, and the study is designed as a non inferiority trial.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Consenting patients with newly diagnosed rectal cancer who fulfil the inclusion criteria and no exclusion criteria will be randomized into two groups with regard to radiological investigation of the liver; Intervention: An abbreviated MRI of the liver/abdomen Control: A combined single venous and 3 min equilibrium phase CT of the abdomen/liver Randomization will be conducted in blocks of 6, and stratified for sex and hospital.Consenting patients with newly diagnosed rectal cancer who fulfil the inclusion criteria and no exclusion criteria will be randomized into two groups with regard to radiological investigation of the liver; Intervention: An abbreviated MRI of the liver/abdomen Control: A combined single venous and 3 min equilibrium phase CT of the abdomen/liver Randomization will be conducted in blocks of 6, and stratified for sex and hospital.
Masking:
Single (Outcomes Assessor)
Masking Description:
It will not be possible to mask for either patients nor participating health care professionals if patients are enrolled in the control- or intervention group. Hence, the study will not be blinded. When the final data analysis is performed for the primary outcome measure the person performing the analysis will not be aware of which group each patient was a part of.
Primary Purpose:
Diagnostic
Official Title:
Limerick - Liver Magnetic Resonance Imaging Before Treatment for Rectal Cancer. A Randomised Controlled Trial.
Actual Study Start Date :
Apr 12, 2022
Anticipated Primary Completion Date :
Dec 1, 2025
Anticipated Study Completion Date :
Dec 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: MRI group

An abbreviated MRI of the liver/abdomen

Radiation: Abbreviated MRI of the liver/abdomen
The MRI examinations of the liver/abdomen will be performed at the same time as the pelvic MRI. A 1,5 T scanner will be used together with a dedicated torso/abdominal coil. An abbreviated MRI liver protocol includes 3 different sequences as follows: Axial T2-weighted respiratory triggered sequence with 5 mm slice thickness. Axial diffusion weighted spin echo respiratory triggered sequence with fatsat with b-factors 50/800 s/mm2 and ADC calculation maps, 5 mm slice thickness An axial breath-hold 3D T1-weighted gradient echo with fatsat with 4 mm slice thickness, gap 2 mm, contrast enhanced venous phase and in a 3 min equilibrium phase, using regular i.v bolus injection of gadolinium contrast medium with standard clinical dose.

Active Comparator: CT group

A combined single venous and 3 min equilibrium phase CT of the abdomen/liver

Radiation: Combined single venous and 3 min equilibrium phase CT of the abdomen/liver
The CT examination of the liver will be performed as a combined examination in a single venous phase starting with the thoracic region directly followed by the abdomen down to the pelvis. An additional 3 min equilibrium phase of the liver only will end the examination. Regular iodinated low-osmolar non-ionic contrast media will be used of 350 mg I/ml using a power injector, 2-4 ml/s, 100-150 ml dependent on patient weight and kidney function. Reconstructed images in axial, coronal and sagittal plane will be performed.

Outcome Measures

Primary Outcome Measures

  1. Need for supplementary radiologic liver examination [3 months]

    Number of patients in need for supplementary radiologic liver examination/s before treatment decision, after index examination (CT or MRI) of the abdominal organs, due to inconclusive results.

  2. Cost effectiveness [12 months]

    Costs related to all index radiological examinations will be included. Costs will be collected from national sources such as the Swedish association of local authorities and regions (SKR - Sveriges kommuner och regioner) whenever possible and alternatively from Sahlgrenska university hospital cost-per-patient files. Possibly a more complex model will be relevant depending on outcome, where total health care costs are compared between the two radiological work-up routines. Such an analysis will take survival into account.

Secondary Outcome Measures

  1. Time to start of treatment [12 months]

    Time from index radiological workup to start of treatment

  2. Recurrence of rectal cancer [12 months]

    Number of patients with recurrence of rectal cancer (local or metastatic disease)

  3. Liver metastasis [36 months]

    Number of patients diagnosed with liver metastasis

  4. Survival [36 months]

    Overall survival

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults >18 years of age

  • Endoscopically or clinically diagnosed with (suspected) rectal cancer and considered for further radiological investigation

  • Are able to understand trial information and provide oral and written consent

Exclusion Criteria:
  • Patients unable to undergo MRI (causes may include claustrophobia, presence of pacemaker or certain metal components in their body).

  • Patients diagnosed with benign disease of the rectum or squamous cell carcinoma

  • Patients diagnosed with recurrent rectal cancer

  • Patients unable to understand the trial information

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sahlgrenska University Hospital/Östra Gothenburg Sweden

Sponsors and Collaborators

  • Vastra Gotaland Region

Investigators

  • Principal Investigator: Jennifer Park, MD, PhD, Sahlgrenska University Hospital, Sahlgrenska Academy, Gothenburg Sweden

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Vastra Gotaland Region
ClinicalTrials.gov Identifier:
NCT05215535
Other Study ID Numbers:
  • Limerick
First Posted:
Jan 31, 2022
Last Update Posted:
Apr 27, 2022
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Vastra Gotaland Region
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 27, 2022