PLASTIC: Evaluation of PET and Laparoscopy in STagIng Advanced Gastric Cancer

Sponsor
UMC Utrecht (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03208621
Collaborator
ZonMw: The Netherlands Organisation for Health Research and Development (Other), Nederlandse Vereniging voor Heelkunde (Other), Federatie Medisch Specialisten (Other), Patientfederatie Nederland (Other), Zorgverzekeraars Nederland (Other)
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Study Details

Study Description

Brief Summary

Objective: To evaluate the impact and cost-effectiveness of FDG-PET/CT (PET) and diagnostic laparoscopy (DLS) in addition to initial staging by CT and gastroscopy in patients with advanced gastric cancer.

Hypothesis: The study hypothesizes that performing DLS and PET for advanced gastric adenocarcinomas results in a reduction in the number of futile gastrectomies performed and a favorable cost-effectiveness. According to the literature, in 27% of patients a futile gastrectomy can be prevented, and the annual cost-reduction is an estimated €916.438.

Study design: The study design is a prospective observational study. Study population: The study population consists of patients with a surgically resectable, advanced gastric adenocarcinoma (cT3-4a,N0-3,M0), that are scheduled for treatment with curative intent after initial staging with gastroscopy and CT.

Usual care / comparison: Both PET and DLS were recently included in the new Dutch guidelines for the treatment of gastric cancer, as staging modalities for advanced (T3-4) tumors after initial staging. The costs of the study population will be compared to retrospective data of patients who underwent curative surgery (gastrectomy) after initial staging with CT alone.

Outcome measures: The primary outcome of this study will be the proportion of patients in whom the PET or DLS lead to a change in treatment strategy. The accuracy of each modality will be analyzed separately. Secondary outcome parameters will be diagnostic performance, morbidity and mortality, quality of life, cost-reduction and cost-effectiveness.

Sample size: Based on the expectation that 22% of patients will have a change in treatment strategy, at least 239 patients will be needed for this study to demonstrate that the diagnostic modalities in the new guideline are break-even. Approximately 543 patients will be eligible for the study in 36 months.

Cost-effectiveness analysis: A state-of-the-art cost-effectiveness analysis and budget impact analysis will be performed on the additive value of PET and DLS by both prospective and retrospective data collection

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    394 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of PET and Laparoscopy in STagIng Advanced Gastric Cancer: a Multicenter Prospective Study
    Actual Study Start Date :
    Aug 1, 2017
    Actual Primary Completion Date :
    Feb 1, 2020
    Anticipated Study Completion Date :
    Aug 1, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    Observational group

    The diagnostic tests to be investigated in this study is the use of PET and DLS in addition to the initial staging with gastroscopy and CT of patients with an advanced tumor (cT3-4)

    Outcome Measures

    Primary Outcome Measures

    1. Change in treatment strategy [6 months after performing staging]

      The primary outcome of this study will be the proportion of patients in whom the PET or DLS lead to a change in treatment strategy.

    Secondary Outcome Measures

    1. Diagnostic performance [6 months after performing staging]

      Sensitivity, specificity, positive predictive value and negative predictive value of FDG/PET-CT and Diagnostic Laparoscopy

    2. Morbidity [3 months after performing staging]

      Complications of staging modalities

    3. Quality of life [Up to 5 years postoperative]

      Quality of life with EORTC questionnaires

    4. Cost-reduction [12 months after performing staging]

      Annual reduction in costs in the Netherlands of FDG-PET/CT and diagnostic laparoscopy, measured by reviewing hospital financial files and comparing with the previous situation without the staging

    5. Cost-effectiveness [12 months after performing staging]

      Cost-effectiveness of FDG-PET/CT and diagnostic laparoscopy, measured by reviewing hospital financial files and comparing with the previous situation without the staging modalities

    6. Mortality [3 months after performing staging]

      90-day mortality of the staging modalities

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Histologically proven adenocarcinoma of the stomach or esophagogastric junction (Siewert II and III), by gastroscopy.

    • Underwent evaluation with computed tomography (CT) of the abdomen and chest.

    • Surgically resectable, advanced tumor (cT3-4a,N0-3,M0), as determined by a multidisciplinary team meeting. An advanced tumor is defined as a transmural tumor with an irregular outer margin, objectified on CT.

    • Intention to perform a curative gastrectomy

    Exclusion Criteria:
    • Siewert type I esophagogastric junction tumor

    • Unfit or unwilling to undergo surgery

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Medical Center Utrecht Utrecht Netherlands 3584 CX

    Sponsors and Collaborators

    • UMC Utrecht
    • ZonMw: The Netherlands Organisation for Health Research and Development
    • Nederlandse Vereniging voor Heelkunde
    • Federatie Medisch Specialisten
    • Patientfederatie Nederland
    • Zorgverzekeraars Nederland

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Jelle P. Ruurda, Doctor, UMC Utrecht
    ClinicalTrials.gov Identifier:
    NCT03208621
    Other Study ID Numbers:
    • 16-1633/C
    First Posted:
    Jul 5, 2017
    Last Update Posted:
    May 5, 2021
    Last Verified:
    Apr 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
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 5, 2021