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Evaluation of PET and Laparoscopy in STagIng Advanced Gastric Cancer

Evaluation of PET and Laparoscopy in STagIng Advanced Gastric Cancer: a Multicenter Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03208621
Acronym
PLASTIC
Enrollment
394
Registered
2017-07-05
Start date
2017-08-01
Completion date
2025-08-01
Last updated
2021-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diagnostic Laparoscopy, FDG-PET/CT, Gastric Cancer, Staging

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

Interventions

None listed

Sponsors

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

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
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

Design outcomes

Primary

MeasureTime frameDescription
Change in treatment strategy6 months after performing stagingThe 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

MeasureTime frameDescription
Morbidity3 months after performing stagingComplications of staging modalities
Quality of lifeUp to 5 years postoperativeQuality of life with EORTC questionnaires
Diagnostic performance6 months after performing stagingSensitivity, specificity, positive predictive value and negative predictive value of FDG/PET-CT and Diagnostic Laparoscopy
Cost-effectiveness12 months after performing stagingCost-effectiveness of FDG-PET/CT and diagnostic laparoscopy, measured by reviewing hospital financial files and comparing with the previous situation without the staging modalities
Mortality3 months after performing staging90-day mortality of the staging modalities
Cost-reduction12 months after performing stagingAnnual 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

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026