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Study in Low Risk Gastrointestinal Stromal Tumor (GISTs)

Follow-up in Low Risk Gastrointestinal Stromal Tumors (GISTs) - Retrospective Analysis of Clinical Features and Outcomes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04599660
Acronym
RetroGIST
Enrollment
700
Registered
2020-10-23
Start date
2020-11-25
Completion date
2023-12-20
Last updated
2024-02-01

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

Conditions

GIST

Keywords

GIST, Gastro Intestinal Stromal Tumor

Brief summary

This is a multi-institutional retrospective study in order to identify the most relevant and advisable features of follow-up, and to explore its impact on principal clinical outcomes. Moreover, a dedicated effort will be pursued to identify the peculiar characteristics (if any) of patients that experienced recurrence of the disease. The study will collect data about patients affected by primary GIST at very-low and low risk of recurrence/progression, referred to participating Institutions between January 2000 and February 2020

Detailed description

In the field of soft tissue sarcomas, Gastrointestinal Stromal Tumors (GIST) represents a really peculiar neoplasm for its biological and clinical properties. Surgery (if feasible) is the main therapeutic approach for all the patients with localized disease, while a pharmacological adjuvant treatment is reserved to those with a relevant risk of recurrence/progression. After tumor removal, clinical and radiological follow-up is of central importance to early intercept recurrence and to evaluate the most correct subsequent therapeutic approach. In particular, for the group of patients with GIST at very-low and low risk of recurrence/progression, the evidences to support a specific follow-up program and its features are poor. On the basis of the aforementioned considerations, we propose a multi-institutional retrospective study in order to identify the most relevant and advisable features of follow-up, and to explore its impact on principal clinical outcomes. Moreover, a dedicated effort will be pursued to identify the peculiar characteristics (if any) of patients that experienced recurrence of the disease. The study will collect data about patients affected by primary GIST at very-low and low risk of recurrence/progression, referred to participating Institutions between January 2000 and February 2020

Interventions

OTHERTreatment of Low Risk GISTs according clinical practice (includes drugs, surgery or any other received treatments)

This observational study collects all the treatments received by the patients according clinical practices or experimental trials and therefore includes drug/biological/surgical and any other applicable treatments

Sponsors

Italian Sarcoma Group
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \>18 years at diagnosis * primary GIST removed by surgery or endoscopic procedures * availability of medical data needed for the study * very-low and low risk GIST defined as: * largest size of \< 3 cm (for all sites of origin) * gastric GIST with ≤ 5/50 High Power Fields (HPF) mitoses and ≤ 10 cm in the largest size * gastric GIST with \> 5/50 HPF mitoses and ≤ 5 cm in the largest size * intestinal GIST with ≤ 5/50 HPF mitoses and ≤ 5 cm in the largest size

Exclusion criteria

* Metastases at diagnosis. * Previous treatment with imatinib

Design outcomes

Primary

MeasureTime frameDescription
To describe the most relevant features of follow-up in very-low and low risk GIST patientsChange from diagnosis (baseline)Collection of retrospectively imaging characteristics
To evaluate the onset of other neoplasms in very-low and low risk GIST patientsChage from baseline (time of diagnosis) at 5 yearsOnset of other neoplasm will be recoreded

Secondary

MeasureTime frameDescription
Post-recurrence progression-free survival (PR-PFS)Every 3 months (Month 3, Month 6, Month 9...) up to 5 yearsTime elapsed form the onset of 1st progression to a further progression
To assess baseline clinical and disease-specific factors with possible impact on survival analyses.Every 3 months (Month 3, Month 6, Month 9...) up to 5 yearsCollection of clinical symptoms, pathological and molecular characteristics at disease presentation/diagnosis
Overall survival (OS).at 5 yearsTime elapsed for the diagnosis to the death for any cause
Disease-Specific survival (DSS)at 5 yearsTime elapsed for the diagnosis to the death of disease
Recurrence-free survival (RFS)Every 3 months (Month 3, Month 6, Month 9...) up to 5 yearsTime elapsed form the treatment (any) start and the onset of recurrence

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026