Efficacy of pembrolizumab in advanced cancer of the vulva : a systematic review and single-arm meta-analysis

dc.contributor.authorSchwab, Roxana
dc.contributor.authorSchiestl, Lina Judit
dc.contributor.authorCascant Ortolano, Lorena
dc.contributor.authorKlecker, Philipp Herbert
dc.contributor.authorSchmidt, Mona Wanda
dc.contributor.authorAlmstedt, Katrin
dc.contributor.authorHeimes, Anne-Sophie
dc.contributor.authorBrenner, Waburgis
dc.contributor.authorStewen, Kathrin
dc.contributor.authorSchmidt, Marcus
dc.contributor.authorHasenburg, Annette
dc.date.accessioned2024-11-11T10:55:17Z
dc.date.available2024-11-11T10:55:17Z
dc.date.issued2024
dc.description.abstractIntroduction: Vulvar cancer carries a favourable prognosis in early stages. However, therapeutic options for advanced or recurrent cases are limited despite a variety of therapeutic modalities, such as extensive surgical resection, chemotherapy, and radiotherapy. The most important emerging treatment modalities are immune checkpoint inhibitors. This systematic review and meta-analysis aims to assess the efficacy and safety of pembrolizumab, an immune checkpoint inhibitor, in women with advanced vulvar cancer. Materials and methods: Following a comprehensive search, review, and appraisal, two relevant single-arm studies were included. Meta-analysis was conducted using R4.3.0 software and RStudio 2023.03.0, presenting the overall effect size with a 95% confidence interval. Heterogeneity was assessed using I2 and the Cochrane Q χ2 statistics. Results: Out of 154 studies screened for eligibility, two single-arm studies involving 119 patients receiving pembrolizumab for advanced vulvar cancer were included. The pooled objective response rate (ORR) was overall 10% (95% CI: 0.00-0.84) and 9% (95% CI: 0.00-0.89) in the PD-L1 positive subgroup. In the intention-to-treat (ITT) population, 31% (95% CI: 0.04-0.85) exhibited any clinical benefit (complete response, partial response, or stable disease). In the ITT population at six months, progression-free survival (PFS) was 19% (95% CI: 0.01-0.82), and overall survival (OS) was 48% (95% CI: 0.08-0.90). At 12 months, PFS decreased to 9% (95% CI: 0.00-0.85), and OS was 33% (95% CI: 0.04-0.85). No statistically significant heterogeneity was observed in PFS and OS analyses. Discussion and conclusion: This study suggests that one-third of women with advanced or recurrent vulvar cancer may, without the influence of PD-L1 status, benefit from pembrolizumab treatment despite a decline in both PFS and OS at 12 months. These findings provide support for considering pembrolizumab in the treatment paradigm for this specific subset of cancer patients.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-10861
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/10880
dc.language.isoengde
dc.rightsCC-BY-4.0*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleEfficacy of pembrolizumab in advanced cancer of the vulva : a systematic review and single-arm meta-analysisen_GB
dc.typeZeitschriftenaufsatzde
jgu.journal.titleFrontiers in oncologyde
jgu.journal.volume14de
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternative1352975de
jgu.publisher.doi10.3389/fonc.2024.1352975de
jgu.publisher.issn2234-943Xde
jgu.publisher.nameFrontiers Mediade
jgu.publisher.placeLausannede
jgu.publisher.year2024
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610de
jgu.subject.dfgLebenswissenschaftende
jgu.type.contenttypeScientific articlede
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde

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