Trial in Patients With Metastatic or Locally Advanced Leiomyosarcoma

Study is aimed at evaluating the activity of Trabectedin (arm A) in advanced leiomyosarcomas, having Gemcitabine (arm B) as the comparator. In addition to the randomized cohort, the study has also an observational prospective cohort which include patients who will refuse the randomization or for whom the investigator will not judge the randomization as an appropriate option. In order to allow the participation of sites only to the prospective-observational (non randomized) cohort, it was introduced the possibility to participate to the study and receive the ethical approval only to the Obser

Trial Details

NCT ID
NCT04383119
Phase
PHASE2
Sponsor
Italian Sarcoma Group
Status
RECRUITING
Cancer Type
Sarcoma
Interventions
  • Trabectedin
  • Gemcitabine
  • No Intervention: Observational Cohort
Locations (sample)
  • Bologna, BO, Italy|44.49381,11.33875
  • Meldola, FC, Italy|44.12775,12.0626
  • Prato, Firenze, Italy|43.8805,11.09699
  • Rozzano, MI, Italy|45.38193,9.1559
  • Aviano, PD, Italy|46.07056,12.59472

Key Eligibility Criteria

  • Patients with histologically documented diagnosis of leiomyosarcoma
  • Patients with diagnosis of unresectable or metastatic leiomyosarcoma
  • Patients who received at least on previous systemic treatment with anthracycline-based chemotherapy.
  • Patients suitable to receive gemcitabine or trabectedin therapy.

For full eligibility, visit ClinicalTrials.gov.

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