Single agent Talimogene Laherparepvec for stage IIIB-IVM1c melanoma patients: A systematic review and meta-analysis

Crit Rev Oncol Hematol. 2022 Jul:175:103705. doi: 10.1016/j.critrevonc.2022.103705. Epub 2022 May 13.

Abstract

Single-agent Talimogene Laherparepvec (T-VEC) was developed for treatment of unresectable and injectable stage III-IV melanoma. Since its approval and reimbursement, studies have reported varying response rates. The purpose of this systematic review and meta-analysis was to investigate the efficacy and safety of T-VEC. Of 341 publications that were identified, eight studies with a total of 642 patients were included. In patients with stage IIIB-IVM1a, the pooled complete- and overall response rate (CRR and ORR) were 41% and 64%, respectively. In patients with stage IIIB-IVM1c, the pooled CRR and ORR were 30% and 44%, respectively. In patients with stage IVM1b and IVM1c, the pooled CRR and ORR were 4% and 9%, respectively. Adverse events (AEs) were seen in 41-100% of all patients and 0-11% of AEs were severe. In conclusion, single agent T-VEC achieves the highest response rates in patients with early metastatic melanoma and is well-tolerated with generally only mild toxicities.

Keywords: Immunotherapy; Melanoma; Metastatic; T-VEC.

Publication types

  • Meta-Analysis
  • Review
  • Systematic Review

MeSH terms

  • Biological Products* / therapeutic use
  • Herpesvirus 1, Human
  • Humans
  • Immunotherapy
  • Melanoma* / drug therapy
  • Melanoma* / etiology
  • Melanoma, Cutaneous Malignant
  • Oncolytic Virotherapy* / adverse effects
  • Skin Neoplasms* / pathology

Substances

  • Biological Products
  • talimogene laherparepvec