Lurbinectedin

(Zepzelca®)

Lurbinectedin

Drug updated on 9/4/2024

Dosage FormInjection (intravenous; 4 mg)
Drug ClassAlkylating agents
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of adult patients with metastatic small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy.

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Summary
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  • Zepzelca (lurbinectedin) is indicated for the treatment of adult patients with metastatic small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy.
  • This summary is based on the review of two systematic review(s)/meta-analysis(es). [1-2]
  • Lurbinectedin demonstrated a survival benefit in platinum-sensitive small-cell lung cancer (SCLC) patients compared to oral topotecan (HR 0.43, 95% CrI: 0.27, 0.67), intravenous topotecan (HR 0.43, 95% CrI: 0.26, 0.70), and platinum re-challenge (HR 0.42, 95% CrI: 0.30, 0.58).
  • The effectiveness outcomes highlighted the superior overall survival of lurbinectedin compared to oral and intravenous topotecan and platinum re-challenge in platinum-sensitive SCLC patients.
  • Lurbinectedin demonstrated a favorable safety profile compared to oral and IV topotecan, and platinum re-challenge in platinum-sensitive SCLC patients, with no detailed adverse effects provided in the studies.
  • There were no specific safety concerns or adverse effects highlighted in the reviewed studies.
  • There is no population types or subgroups information available in the reviewed studies.

Product Monograph / Prescribing Information

Document TitleYearSource
Zepzelca (lurbinectedin) Prescribing Information.2023Jazz Pharmaceuticals, Inc., Palo Alto, CA

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines

Document TitleYearSource
SEOM clinical guidelines for the treatment of small‑cell lung cancer (SCLC) (2019).2020Clinical and Translational Oncology