TrObs: Retrospective Study of Trabectedin in Soft Tissue Sarcomas

Sponsor
Italian Sarcoma Group (Other)
Overall Status
Completed
CT.gov ID
NCT02793050
Collaborator
(none)
510
26
27.6
19.6
0.7

Study Details

Study Description

Brief Summary

This is an independent, observational, retrospective post marketing study on the use of trabectedin in a clinical setting.

A data collection on the clinical use of the drug will help to improve knowledge and might contribute to optimize the clinical use of the drug.

Condition or Disease Intervention/Treatment Phase

Detailed Description

This is a national, multi-centre observational retrospective and prospective chart review study of treatment patterns and clinical outcomes in a subset of patients with Soft Tissue Sarcoma who received trabectedin as per licensed indication.

In the absence of availability of existing databases, a retrospective chart review design was selected.

It is anticipated that the medical charts will contain the information required to answer study objectives. This chart review study will be conducted in 25 sites in Italy An estimated total of 900 charts will be abstracted. This study requires no intervention or interference with standard medical care, and thus it will not affect patient treatment.

The study is sponsored by Italian Sarcoma Group Charts of patients who initiated trabectedin as part of the approved treatment for a Soft Tissue Sarcoma , will be identified by site staff. Each identified chart will be assigned a unique study identification number. Site staff will review the medical charts for all identified patients to determine patient eligibility. Those patients who meet eligibility criteria will be enrolled into the final study cohort as subject.

Data from subject medical charts will be abstracted by local site study staff and entered at the site into an electronic data capture (EDC) system. The system will also facilitate the monitoring of the completeness and quality of study data as the study data accrue.

Study Design

Study Type:
Observational
Actual Enrollment :
510 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Trabectedin in Soft Tissue Sarcomas. A Retrospective Observational Analysis (TrObs)
Actual Study Start Date :
Jun 15, 2016
Actual Primary Completion Date :
Oct 2, 2018
Actual Study Completion Date :
Oct 2, 2018

Arms and Interventions

Arm Intervention/Treatment
Trabectedin

Trabectedin give according the market authorization for advanced soft tissue sarcoma

Drug: Trabectedin
Collection of data on the clinical use of Trabectedin
Other Names:
  • yondelis
  • Outcome Measures

    Primary Outcome Measures

    1. Post-trabectedin received treatment [Through treatment completion, an average of 24 month]

      Number of chemotherapy lines received after trabectedin given according to the approved indication

    Secondary Outcome Measures

    1. Tumor response [after 6 months from trabectedin start date]

      Percent of patients with non progressing disease at 6 months

    2. Trabectedin dose modification [Through treatment completion, an average of 24 month]

      Describe trabectedin treatment experience in term of dose for patients with Soft Tissue Sarcoma treated with trabectedin as per market indication

    3. Progression-free survival [after 5 years and 3 years from trabectedin start date]

      Describe progression-free survival (PFS) for patients with Soft Tissue Sarcoma who received trabectedin.

    4. Trabectedin safety profile [Through treatment completion, an average of 24 month]

      Describe trabectedin safety profile in terms of number of participants with treatment-related adverse events as assessed by CTCAE v4.0 tha caused treatment discontinuation

    5. Overall survival [after 5 years and 3 years from trabectedin start date]

      Describe overall survival (OS) for patients with Soft Tissue Sarcoma who received trabectedin.

    Other Outcome Measures

    1. Histology related treatment response [after 6 months from trabectedin start date]

      Number of patient who did not progress based on the different Soft Tissue Sarcoma histology sub-type

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients who received trabectedin according to the approved indication in the period January 2010 December 2015
    Exclusion Criteria:
    • Trabectedin started before January 2010 and after December 2015

    • Participation into clinical trials with trabectedin

    • Clinical chart missing, empty, or not retrievable.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 A.O. SS Antonio e Biagio e Cesare Arrigo Alessandria AL Italy 15100
    2 Istituto Tumori Giovanni Paolo II Bari BA Italy 70124
    3 Ospedali Riuniti di Bergamo Bergamo BG Italy
    4 Ospedale Oncologico A. Businco Cagliari CA Italy 09122
    5 Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori - IRST Meldola FC Italy
    6 Istituto Europeo di Oncologia Milano MI Italy 20141
    7 Istituto Clinico Humanitas Rozzano MI Italy 20089
    8 Azienda Ospedaliera Universitaria Paolo Giaccone Palermo PA Italy 90127
    9 Centro di Riferimento Oncologico di Aviano Aviano PD Italy 33081
    10 Istituto Oncologico Veneto Padova PD Italy 35128
    11 Azienda Ospedaliera Universitaria Santa Chiara Pisa PI Italy 56124
    12 Policlinico Universitario Campus Biomedico Roma RM Italy 00128
    13 Fondazione del Piemonte per l'Oncologia IRCC Candiolo Candiolo Torino Italy 10060
    14 Istituto Ortopedico Rizzoli Bologna Italy 40136
    15 Policlinico S.Orsola Malpighi - Unit of Medical Oncology Bologna Italy 40138
    16 Pres.Ospedal.Spedali Civili Brescia - Brescia (BS) Italy
    17 Azienda Ospedaliero-Universitaria Careggi Firenze Italy 50134
    18 Irccs Istituto Nazionale Dei Tumori (Int) Milano (MI) Italy 20133
    19 Azienda Ospedaliero-Universitaria di Modena - Policlinico Modena Italy 41124
    20 Irccs Istituto Nazionale Tumori Fondazione Pascale - Napoli (NA) Italy
    21 Ospedale Misericordia e Dolce Ist. Toscano Tumori, Az. USL4 Prato Italy 59100
    22 Arcispedale S. Maria Nuova Azienda Ospedaliera Di Reggio Emilia Reggio EMilia Italy 42123
    23 Fondazione Policlinico Universitario "Agostino Gemelli" Roma Italy 00168
    24 Istituto Regina Elena - IFO Rome Italy 00100
    25 Presidio Sanitario Gradenigo Di Torino Torino (TO) Italy
    26 Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino Torino Italy 10126

    Sponsors and Collaborators

    • Italian Sarcoma Group

    Investigators

    • Principal Investigator: Stefano Ferrari, MD, Italian Sarcoma Group

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Italian Sarcoma Group
    ClinicalTrials.gov Identifier:
    NCT02793050
    Other Study ID Numbers:
    • ISG TrObs
    First Posted:
    Jun 8, 2016
    Last Update Posted:
    May 10, 2019
    Last Verified:
    May 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by Italian Sarcoma Group
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 10, 2019