Trabectedin

(Yondelis®)

Yondelis®

Drug updated on 3/28/2024

Dosage FormInjection (intravenous; 1 mg)
Drug ClassAlkylating agents
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • For the treatment of patients with unresectable or metastatic liposarcoma or leiomyosarcoma who received a prior anthracycline-containing regimen.

Summary
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  • Trabectedin (Yondelis) is indicated for the treatment of patients with unresectable or metastatic liposarcoma or leiomyosarcoma who received a prior anthracycline-containing regimen.
  • Two systematic reviews/meta-analyses were reviewed to gather information about this drug.
  • A study examining the efficacy/effectiveness of trabectedin in previously treated metastatic synovial sarcoma reported poor outcomes across agents and settings, highlighting a need for novel treatments with improved efficacy.
  • The pooled median overall survival was 10.4 months and overall response rate was 14.7% in studies involving trabectedin; these results were consistent across real-world and clinical trial settings.
  • Another review focusing on cardiac safety found an estimated incidence of cardiac toxicity at 3,4% among patients receiving trabectedin, suggesting a higher rate of heart failure than previously recognized especially among those exposed to previous or concomitant anthracyclines therapy.
  • This same review suggested that assaying for NT-pro-BNP may be useful for early detection of individuals experiencing heart failure induced by Trabectedin (Yondelis).

Product Monograph / Prescribing Information

Document TitleYearSource
Yondelis (trabectedin) Prescribing Information.2020Janssen Products, LP, Horsham, PA

Systematic Reviews / Meta-Analyses