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

Emma H A Stahlie ,
Evalyn E A P Mulder ,
Sophie Reijers ,
Sara Balduzzi ,
Charlotte L Zuur ,
Willem M C Klop ,
Bernies van der Hiel ,
Bart A Van de Wiel ,
Michel W J M Wouters ,
Yvonne M Schrage ,
Winan J van Houdt ,
Dirk J Grunhagen ,
Alexander C J van Akkooi

Abstract

Single-agent Talimogene LaherparepvecĀ (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 rateĀ (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 eventsĀ (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.

More about this publication

Critical reviews in oncology/hematology

Volume 175
Pages 103705
Publication date 01-07-2022

Full text links

Publisher website (DOI) 10.1016/j.critrevonc.2022.103705
Europe PubMed Central 35569723
Pubmed 35569723

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