Study in Low Risk Gastrointestinal Stromal Tumor (GISTs)

NCT04599660 — Completed, 700 participants, Italian Sarcoma Group

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

RegistryNCT04599660, acronym RetroGIST
StatusCompleted
Study typeObservational
Enrollment700 (Actual)
SponsorItalian Sarcoma Group (Network)
ConditionsGIST
InterventionsTreatment of Low Risk GISTs according clinical practice (includes drugs, surgery or any other received treatments) (Other)
Datesstart 2020-11-25, primary completion 2021-12-30, completion 2023-12-20, first posted 2020-10-23, last updated 2024-02-01
Locations13 sites in Italy

Related Papers Related Patents Related Grants Related Experts
All trials for GIST All trials of Treatment of Low Risk GISTs according clinical practice (includes drugs, surgery or any other received treatments)

-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

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+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

+Arms and interventions

ArmTypeInterventionsDescription
Low Risk GISTsOther: Treatment of Low Risk GISTs according clinical practice (includes drugs, surgery or any other received treatments)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.
  • Treatment of Low Risk GISTs according clinical practice (includes drugs, surgery or any other received treatments) (Other): 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 outcomes

  • 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
  • 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.
  • 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.
  • 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.
  • 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.
  • 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 outcomes

  • 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
  • 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
  • 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
  • Disease-Specific survival (DSS) [at 5 years]: Time elapsed for the diagnosis to the death of disease
  • Overall survival (OS). [at 5 years]: Time elapsed for the diagnosis to the death for any cause

+Eligibility

Sex: All, ages: 19 Years to any

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

+Locations (13)

FacilityCityCountryStatus
Azienda Ospedaliero-Universitaria Di BolognaBologna, BOItaly
Nuovo Ospedale di PratoPrato, FirenzeItaly
Istituto Europeo di OncologiaMilan, MIItaly
Istituto Clinico HumanitasRozzano, MIItaly
Azienda Ospedaliera Universitaria Paolo GiacconePalermo, PAItaly
Centro di Riferimento Oncologico - Unit of Medical OncologyAviano, PordenoneItaly
Policlinico Universitario Campus BiomedicoRoma, RMItaly
Fondazione del Piemonte per l'Oncologia IRCC CandioloCandiolo, TorinoItaly
Ospedale San Giovanni BoscoTorino, TOItaly
Policlinico S.Orsola Malpighi - Unit of Medical OncologyBolognaItaly
Azienda Ospedaliera Universitaria CareggiFlorenceItaly
Fondazione IRCCS INT MilanoMilanItaly
Istituto Nazionale Tumori Regina Elena - Unit of Medical Oncology IRomaItaly

+Publications

  • Joensuu H, Hohenberger P, Corless CL. Gastrointestinal stromal tumour. Lancet. 2013 Sep 14;382(9896):973-83. doi: 10.1016/S0140-6736(13)60106-3. Epub 2013 Apr 24. PMID 23623056
  • Gold JS, Gonen M, Gutierrez A, Broto JM, Garcia-del-Muro X, Smyrk TC, Maki RG, Singer S, Brennan MF, Antonescu CR, Donohue JH, DeMatteo RP. Development and validation of a prognostic nomogram for recurrence-free survival after complete surgical resection of localised primary gastrointestinal stromal tumour: a retrospective analysis. Lancet Oncol. 2009 Nov;10(11):1045-52. doi: 10.1016/S1470-2045(09)70242-6. Epub 2009 Sep 28. PMID 19793678
  • D'Ambrosio L, Palesandro E, Boccone P, Tolomeo F, Miano S, Galizia D, Manca A, Chiara G, Bertotto I, Russo F, Campanella D, Venesio T, Sangiolo D, Pignochino Y, Siatis D, De Simone M, Ferrero A, Pisacane A, Dei Tos AP, Aliberti S, Aglietta M, Grignani G. Impact of a risk-based follow-up in patients affected by gastrointestinal stromal tumour. Eur J Cancer. 2017 Jun;78:122-132. doi: 10.1016/j.ejca.2017.03.025. Epub 2017 Apr 24. PMID 28448856
  • Joensuu H, Reichardt P, Eriksson M, Sundby Hall K, Vehtari A. Gastrointestinal stromal tumor: a method for optimizing the timing of CT scans in the follow-up of cancer patients. Radiology. 2014 Apr;271(1):96-103. doi: 10.1148/radiol.13131040. Epub 2013 Nov 18. PMID 24475826
  • Rossi S, Miceli R, Messerini L, Bearzi I, Mazzoleni G, Capella C, Arrigoni G, Sonzogni A, Sidoni A, Toffolatti L, Laurino L, Mariani L, Vinaccia V, Gnocchi C, Gronchi A, Casali PG, Dei Tos AP. Natural history of imatinib-naive GISTs: a retrospective analysis of 929 cases with long-term follow-up and development of a survival nomogram based on mitotic index and size as continuous variables. Am J Surg Pathol. 2011 Nov;35(11):1646-56. doi: 10.1097/PAS.0b013e31822d63a7. PMID 21997685
  • Casali PG, Abecassis N, Aro HT, Bauer S, Biagini R, Bielack S, Bonvalot S, Boukovinas I, Bovee JVMG, Brodowicz T, Broto JM, Buonadonna A, De Alava E, Dei Tos AP, Del Muro XG, Dileo P, Eriksson M, Fedenko A, Ferraresi V, Ferrari A, Ferrari S, Frezza AM, Gasperoni S, Gelderblom H, Gil T, Grignani G, Gronchi A, Haas RL, Hassan B, Hohenberger P, Issels R, Joensuu H, Jones RL, Judson I, Jutte P, Kaal S, Kasper B, Kopeckova K, Krakorova DA, Le Cesne A, Lugowska I, Merimsky O, Montemurro M, Pantaleo MA, Piana R, Picci P, Piperno-Neumann S, Pousa AL, Reichardt P, Robinson MH, Rutkowski P, Safwat AA, Schoffski P, Sleijfer S, Stacchiotti S, Sundby Hall K, Unk M, Van Coevorden F, van der Graaf WTA, Whelan J, Wardelmann E, Zaikova O, Blay JY; ESMO Guidelines Committee and EURACAN. Gastrointestinal stromal tumours: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2018 Oct 1;29(Suppl 4):iv267. doi: 10.1093/annonc/mdy320. No abstract available. PMID 30188977

+Investigators