Clinical added value of MRI to CT in patients scheduled for local therapy of colorectal liver metastases (CAMINO): study protocol for an international multicentre prospective diagnostic accuracy study.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
18 Oct 2021
Historique:
received: 15 07 2021
accepted: 04 10 2021
entrez: 19 10 2021
pubmed: 20 10 2021
medline: 29 1 2022
Statut: epublish

Résumé

Abdominal computed tomography (CT) is the standard imaging method for patients with suspected colorectal liver metastases (CRLM) in the diagnostic workup for surgery or thermal ablation. Diffusion-weighted and gadoxetic-acid-enhanced magnetic resonance imaging (MRI) of the liver is increasingly used to improve the detection rate and characterization of liver lesions. MRI is superior in detection and characterization of CRLM as compared to CT. However, it is unknown how MRI actually impacts patient management. The primary aim of the CAMINO study is to evaluate whether MRI has sufficient clinical added value to be routinely added to CT in the staging of CRLM. The secondary objective is to identify subgroups who benefit the most from additional MRI. In this international multicentre prospective incremental diagnostic accuracy study, 298 patients with primary or recurrent CRLM scheduled for curative liver resection or thermal ablation based on CT staging will be enrolled from 17 centres across the Netherlands, Belgium, Norway, and Italy. All study participants will undergo CT and diffusion-weighted and gadoxetic-acid enhanced MRI prior to local therapy. The local multidisciplinary team will provide two local therapy plans: first, based on CT-staging and second, based on both CT and MRI. The primary outcome measure is the proportion of clinically significant CRLM (CS-CRLM) detected by MRI not visible on CT. CS-CRLM are defined as liver lesions leading to a change in local therapeutical management. If MRI detects new CRLM in segments which would have been resected in the original operative plan, these are not considered CS-CRLM. It is hypothesized that MRI will lead to the detection of CS-CRLM in ≥10% of patients which is considered the minimal clinically important difference. Furthermore, a prediction model will be developed using multivariable logistic regression modelling to evaluate the predictive value of patient, tumor and procedural variables on finding CS-CRLM on MRI. The CAMINO study will clarify the clinical added value of MRI to CT in patients with CRLM scheduled for local therapy. This study will provide the evidence required for the implementation of additional MRI in the routine work-up of patients with primary and recurrent CRLM for local therapy. The CAMINO study was registered in the Netherlands National Trial Register under number NL8039 on September 20th 2019.

Sections du résumé

BACKGROUND BACKGROUND
Abdominal computed tomography (CT) is the standard imaging method for patients with suspected colorectal liver metastases (CRLM) in the diagnostic workup for surgery or thermal ablation. Diffusion-weighted and gadoxetic-acid-enhanced magnetic resonance imaging (MRI) of the liver is increasingly used to improve the detection rate and characterization of liver lesions. MRI is superior in detection and characterization of CRLM as compared to CT. However, it is unknown how MRI actually impacts patient management. The primary aim of the CAMINO study is to evaluate whether MRI has sufficient clinical added value to be routinely added to CT in the staging of CRLM. The secondary objective is to identify subgroups who benefit the most from additional MRI.
METHODS METHODS
In this international multicentre prospective incremental diagnostic accuracy study, 298 patients with primary or recurrent CRLM scheduled for curative liver resection or thermal ablation based on CT staging will be enrolled from 17 centres across the Netherlands, Belgium, Norway, and Italy. All study participants will undergo CT and diffusion-weighted and gadoxetic-acid enhanced MRI prior to local therapy. The local multidisciplinary team will provide two local therapy plans: first, based on CT-staging and second, based on both CT and MRI. The primary outcome measure is the proportion of clinically significant CRLM (CS-CRLM) detected by MRI not visible on CT. CS-CRLM are defined as liver lesions leading to a change in local therapeutical management. If MRI detects new CRLM in segments which would have been resected in the original operative plan, these are not considered CS-CRLM. It is hypothesized that MRI will lead to the detection of CS-CRLM in ≥10% of patients which is considered the minimal clinically important difference. Furthermore, a prediction model will be developed using multivariable logistic regression modelling to evaluate the predictive value of patient, tumor and procedural variables on finding CS-CRLM on MRI.
DISCUSSION CONCLUSIONS
The CAMINO study will clarify the clinical added value of MRI to CT in patients with CRLM scheduled for local therapy. This study will provide the evidence required for the implementation of additional MRI in the routine work-up of patients with primary and recurrent CRLM for local therapy.
TRIAL REGISTRATION BACKGROUND
The CAMINO study was registered in the Netherlands National Trial Register under number NL8039 on September 20th 2019.

Identifiants

pubmed: 34663243
doi: 10.1186/s12885-021-08833-1
pii: 10.1186/s12885-021-08833-1
pmc: PMC8524830
doi:

Substances chimiques

Contrast Media 0
gadolinium ethoxybenzyl DTPA 0
Gadolinium DTPA K2I13DR72L

Types de publication

Clinical Trial Protocol Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1116

Subventions

Organisme : kwf kankerbestrijding
ID : 11916 / 2018-2

Investigateurs

C Bnà (C)
C De Meyere (C)
W A Draaisma (WA)
M F Gerhards (MF)
F Imani (F)
K F D Kuhlmann (KFD)
M S L Liem (MSL)
Y Meyer (Y)
J S D Mieog (JSD)
G P Serafino (GP)
H C Van Beek (HC)
J A B Van der Hoeven (JAB)
C J Veeken (CJ)

Informations de copyright

© 2021. The Author(s).

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Auteurs

B Görgec (B)

Department of Surgery, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Department of Radiology and Nuclear Medicine, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.

I Hansen (I)

Department of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Oslo, Norway.
The Intervention Centre, Oslo University Hospital - Rikshospitalet, Oslo, Norway.

G Kemmerich (G)

Department of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.

T Syversveen (T)

Department of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.

M Abu Hilal (M)

Department of Surgery, Poliambulanza Foundation Hospital, Brescia, Italy.

E J T Belt (EJT)

Department of Surgery, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

R H C Bisschops (RHC)

Department of Radiology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

T L Bollen (TL)

Department of Radiology, St. Antonius Hospital, Nieuwegein, The Netherlands.

K Bosscha (K)

Department of Surgery, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.

M C Burgmans (MC)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

V Cappendijk (V)

Department of Radiology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.

M T De Boer (MT)

Department of Surgery, University Medical Centre Groningen, Groningen, The Netherlands.

M D'Hondt (M)

Department of Digestive and Hepatobiliary/Pancreatic Surgery, Groeninge Hospital, Kortrijk, Belgium.

B Edwin (B)

Department of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Oslo, Norway.
The Intervention Centre, Oslo University Hospital - Rikshospitalet, Oslo, Norway.

H Gielkens (H)

Department of Radiology, Medical Spectrum Twente, Enschede, The Netherlands.

D J Grünhagen (DJ)

Department of Surgical Oncology, Erasmus Medical Center, Rotterdam, The Netherlands.
Erasmus MC Cancer Institute, Erasmus Medical Center, Rotterdam, The Netherlands.

P Gillardin (P)

Department of Radiology, Hospital Oost-Limburg, Genk, Belgium.

P D Gobardhan (PD)

Department of Surgery, Amphia Hospital, Breda, The Netherlands.

H H Hartgrink (HH)

Department of Surgery, Leiden University Medical Centre, Leiden, The Netherlands.

K Horsthuis (K)

Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.

N F M Kok (NFM)

Department of Surgery, Netherlands Cancer Institute, Amsterdam, The Netherlands.

P A M Kint (PAM)

Department of Radiology, Amphia Hospital, Breda, The Netherlands.

J W H Kruimer (JWH)

Department of Radiology, Máxima Medical Centre, Veldhoven, The Netherlands.

W K G Leclercq (WKG)

Department of Surgery, Máxima Medical Centre, Veldhoven, The Netherlands.

D J Lips (DJ)

Department of Surgery, Medical Spectrum Twente, Enschede, The Netherlands.

B Lutin (B)

Department of Radiology, Groeninge Hospital, Kortrijk, Belgium.

M Maas (M)

Department of Radiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

H A Marsman (HA)

Department of Surgery, OLVG, Amsterdam, The Netherlands.

M Morone (M)

Department of Radiology, Poliambulanza Foundation Hospital, Brescia, Italy.

J P Pennings (JP)

Department of Radiology, University Medical Centre Groningen, Groningen, The Netherlands.

J Peringa (J)

Department of Radiology, OLVG, Amsterdam, The Netherlands.

W W Te Riele (WW)

Department of Surgery, St. Antonius Hospital, Nieuwegein, The Netherlands.

M Vermaas (M)

Department of Surgery, IJsselland Hospital, Capelle aan den IJssel, The Netherlands.

D Wicherts (D)

Department of Surgery, Hospital Oost-Limburg, Genk, Belgium.

F E J A Willemssen (FEJA)

Department of Radiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

B M Zonderhuis (BM)

Department of Surgery, Amsterdam UMC, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.

P M M Bossuyt (PMM)

Department of Epidemiology and Data Science, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

R J Swijnenburg (RJ)

Department of Surgery, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Department of Surgery, Amsterdam UMC, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Å A Fretland (ÅA)

Department of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Oslo, Norway.
The Intervention Centre, Oslo University Hospital - Rikshospitalet, Oslo, Norway.

C Verhoef (C)

Department of Surgical Oncology, Erasmus Medical Center, Rotterdam, The Netherlands.
Erasmus MC Cancer Institute, Erasmus Medical Center, Rotterdam, The Netherlands.

M G Besselink (MG)

Department of Surgery, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.

J Stoker (J)

Department of Radiology and Nuclear Medicine, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands. j.stoker@amsterdamumc.nl.

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