RetroGIST: Study in Low Risk Gastrointestinal Stromal Tumor (GISTs)

Sponsor
Italian Sarcoma Group (Other)
Overall Status
Recruiting
CT.gov ID
NCT04599660
Collaborator
(none)
700
13
13.1
53.8
4.1

Study Details

Study Description

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

Condition or Disease Intervention/Treatment Phase
  • Other: Treatment of Low Risk GISTs according clinical practice (includes drugs, surgery or any other received treatments)

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

Study Design

Study Type:
Observational
Anticipated Enrollment :
700 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Follow-up in Low Risk Gastrointestinal Stromal Tumors (GISTs) - Retrospective Analysis of Clinical Features and Outcomes
Actual Study Start Date :
Nov 25, 2020
Anticipated Primary Completion Date :
Dec 30, 2021
Anticipated Study Completion Date :
Dec 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Low Risk GISTs

This cohort include patients affected by primary GIST at very-low and low risk of recurrence/progression, referred to participating Institutions between January 2000 and February 2020.

Other: Treatment 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

Outcome Measures

Primary Outcome Measures

  1. To describe the most relevant features of follow-up in very-low and low risk GIST patients [Change from diagnosis (baseline)]

    Collection of retrospectively imaging characteristics

  2. To describe the most relevant features of follow-up in very-low and low risk GIST patients [At 1 year]

    Collection of retrospectively imaging characteristics.

  3. To describe the most relevant features of follow-up in very-low and low risk GIST patients [At 2 years]

    Collection of retrospectively imaging characteristics.

  4. To describe the most relevant features of follow-up in very-low and low risk GIST patients [At 3 years]

    Collection of retrospectively imaging characteristics.

  5. To describe the most relevant features of follow-up in very-low and low risk GIST patients [At 5 years]

    Collection of retrospectively imaging characteristics.

  6. To evaluate the onset of other neoplasms in very-low and low risk GIST patients [Chage from baseline (time of diagnosis) at 5 years]

    Onset of other neoplasm will be recoreded

Secondary Outcome Measures

  1. 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 years]

    Collection of clinical symptoms, pathological and molecular characteristics at disease presentation/diagnosis

  2. Recurrence-free survival (RFS) [Every 3 months (Month 3, Month 6, Month 9...) up to 5 years]

    Time elapsed form the treatment (any) start and the onset of recurrence

  3. Post-recurrence progression-free survival (PR-PFS) [Every 3 months (Month 3, Month 6, Month 9...) up to 5 years]

    Time elapsed form the onset of 1st progression to a further progression

  4. Disease-Specific survival (DSS) [at 5 years]

    Time elapsed for the diagnosis to the death of disease

  5. Overall survival (OS). [at 5 years]

    Time elapsed for the diagnosis to the death for any cause

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Azienda Ospedaliero-Universitaria Di Bologna Bologna BO Italy 40139
2 Nuovo Ospedale di Prato Prato Firenze Italy 59100
3 Istituto Europeo di Oncologia Milano MI Italy 20141
4 Istituto Clinico Humanitas Rozzano MI Italy 20089
5 Azienda Ospedaliera Universitaria Paolo Giaccone Palermo PA Italy 90127
6 Centro di Riferimento Oncologico - Unit of Medical Oncology Aviano Pordenone Italy 33081
7 Policlinico Universitario Campus Biomedico Roma RM Italy 00128
8 Fondazione del Piemonte per l'Oncologia IRCC Candiolo Candiolo Torino Italy 10060
9 Ospedale San Giovanni Bosco Torino TO Italy
10 Policlinico S.Orsola Malpighi - Unit of Medical Oncology Bologna Italy 40138
11 Azienda Ospedaliera Universitaria Careggi Firenze Italy 50100
12 Fondazione IRCCS INT Milano Milano Italy 20133
13 Istituto Nazionale Tumori Regina Elena - Unit of Medical Oncology I Roma Italy 00144

Sponsors and Collaborators

  • Italian Sarcoma Group

Investigators

  • Study Chair: Giovanni Grignani, giovanni.grignani@ircc.it

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Italian Sarcoma Group
ClinicalTrials.gov Identifier:
NCT04599660
Other Study ID Numbers:
  • ISG-RetroGIST LR
First Posted:
Oct 23, 2020
Last Update Posted:
Nov 1, 2021
Last Verified:
Oct 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
Keywords provided by Italian Sarcoma Group
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 1, 2021