VOLUNET: Volumetric Imaging Follow up of Patients With Liver Metastases of Small Intestinal Neuroendocrine Tumors (NETs).

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Unknown status
CT.gov ID
NCT03689231
Collaborator
(none)
80
1
10
8

Study Details

Study Description

Brief Summary

More than 50% of intestinal NETs are metastatic at the time of diagnosis, the liver being the main affected organ in 50-90% of cases.

Initial liver tumor burden and slope of the tumor growth rate are two major prognostic factors in patients with intestinal NETs, followed by tumor grade at pathology. They are used in routine practice by oncologists to adapt patient treatment.

Unlike other tumors, most NETs metastases are slow-growing tumors. Previous studies have shown that approximately half of the patients diagnosed with liver metastases showed no progression over a period of 3 to 6 months.

The aim of this non randomised retrospective cohort study is to investigate whether the volumetric monitoring of the total tumor burden compared to the RECIST 1.1 criteria (used in routine practice by radiologists) at baseline and early follow-up (3 to 6 months) is more suitable for NETs, making possible to predict the prognosis at the onset of the disease, and also allowing a better adaptation of the treatment.

The secondary objectives are to evaluate if the initial volume of the liver tumor is a prognostic factor of time to progression, to correlate the initial liver tumor volume and the number of liver lesions to the blood concentration of Chromogranin A (CgA), the presence of extra-abdominal disease and to correlate the tumor growth rate (TGR) and KI 67 (%) at base-line.

Condition or Disease Intervention/Treatment Phase
  • Other: Volumetric measurements of liver metastases

Study Design

Study Type:
Observational
Actual Enrollment :
80 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Volumetric Imaging Follow up of Patients With Liver Metastases of Small Intestinal Neuroendocrine Tumors (NETs).
Actual Study Start Date :
Mar 1, 2018
Actual Primary Completion Date :
Aug 30, 2018
Anticipated Study Completion Date :
Dec 30, 2018

Outcome Measures

Primary Outcome Measures

  1. Could the evolution of the initial liver tumor volume (on two follow-up CT scans / MRI over a period of 3 to 6 months) be predictive of progression-free survival according to the RECIST criteria? [6 months]

    To assess if the evolution of the initial liver tumor volume compared to a follow-up CT scans / MRI over a period of 3 to 6 months is predictive of progression-free survival according to the RECIST criteria

Secondary Outcome Measures

  1. Could the evolution of the initial liver tumor volume (on two follow-up CT scans / MRI over a period of 3 to 6 months) be predictive of progression-free survival according to the RECIST criteria? [6 months]

    To evaluate whether the initial volume of the liver tumor is a prognostic factor of time to progression

  2. Could the evolution of the initial liver tumor volume (on two follow-up CT scans / MRI over a period of 3 to 6 months) be predictive of progression-free survival according to the RECIST criteria? [6 months]

    To determine the tumor growth rate

  3. Could the evolution of the initial liver tumor volume (on two follow-up CT scans / MRI over a period of 3 to 6 months) be predictive of progression-free survival according to the RECIST criteria? [6 months]

    To estimate the evolution of tumor volume as a function of time that may anticipate earlier than RECIST the tumor growth

  4. Could the evolution of the initial liver tumor volume (on two follow-up CT scans / MRI over a period of 3 to 6 months) be predictive of progression-free survival according to the RECIST criteria? [6 months]

    To correlate the initial liver tumor volume and the number of liver lesions to the blood concentration of Chromogranin A (CgA) and the presence of extra-abdominal disease.

  5. Could the evolution of the initial liver tumor volume (on two follow-up CT scans / MRI over a period of 3 to 6 months) be predictive of progression-free survival according to the RECIST criteria? [6 months]

    To correlate the tumor growth rate (TGR) and KI 67 (%) at base-line (on liver metastasis if available or on primary tumor)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Well differentiated intestinal neuroendocrine tumor with at least one liver metastasis

  • The liver metastasis must be visible and measurable on CT scans or MRI

  • Patients monitored without invasive liver treatment : surgery, RF ablation / Trans-arterial chemoembolization

  • Patients monitored without systemic treatment such as: Chemotherapy, Everolimus, Sunitinib (Somatostatin analogues allowed)

  • Surgery of the primary tumor allowed

Exclusion Criteria:
  • Other type of NETs

  • Absence of liver metastases

  • Liver metastases not visible on CT scans/MRI, poorly limited lesions and small target lesions ( less than 10mm) that are difficult to measure

  • Lesions visible only on diffusion-weighted imaging -MRI acquisitions, thus presenting poorly limited contours

  • Invasive liver treatment : surgery, Radio frequency / Trans-arterial chemoembolization

  • Systemic treatments: Chemotherapy / Everolimus / Sunitinib

  • Insufficient follow-up data

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service de radiologie-Pavillon B-Cellule Recherche imagerie - Hôpital Edouard Herriot Lyon France 69003

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT03689231
Other Study ID Numbers:
  • VOLUNET
First Posted:
Sep 28, 2018
Last Update Posted:
Sep 28, 2018
Last Verified:
Sep 1, 2018
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 28, 2018