Real-world utilization of lenvatinib and pembrolizumab combination therapy for the treatment of endometrial cancer in the USA

Author:

Wada Keiko1,Zhang Jingchuan2,Lee Inyoung1ORCID,Wang Yi1,Near Aimee1ORCID,Prabhu Vimalanand S3ORCID

Affiliation:

1. Real World Solutions, IQVIA Inc., Durham, NC 27703, USA

2. Worldwide Real World Evidence (WW RWE), Eisai Inc., Nutley, NJ 07110, USA

3. Center for Observational and Real World Evidence(CORE), MRL, Merck & Co., Inc., Rahway, NJ 07065, USA

Abstract

Aim: Describe treatment and dosing patterns of lenvatinib and pembrolizumab combination therapy (lenva+pembro) among endometrial cancer (EC) patients in US clinical practice. Materials & methods: Retrospective cohort study among adults with EC initiating lenva+pembro in second line (2L) or third line and later [≥3L] between 17 September 2019 and 30 June 2021. Results: 110 patients initiated lenva+pembro in 2L and 135 patients in ≥3L. Majority of patients initiated lenva+pembro at label-recommended starting doses/interval. Less than half changed lenvatinib dose over time. At median follow-up of 7.3 and 8.7 months, median (95% CI) duration of therapy was 5.1 (4.7–6.1) and 5.8 (4.2–7.3) months for patients in 2L and ≥3L, respectively. Conclusion: Lenva+pembro was mostly initiated at label-recommended dose.

Funder

Merck Sharp and Dohme

Eisai Inc.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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