Pembrolizumab plus lenvatinib in advanced endometrial cancer: case report and systematic review of lung toxicity

The optimal strategy for the treatment of recurrent and/or advanced endometrial cancer is still undefined. Recently, despite the lack of any predictive biomarker, the combination of pembrolizumab with lenvatinib has improved survival outcomes. We here report the long-term management of lung toxicity...

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Veröffentlicht in:Frontiers in oncology 2023-07, Vol.13, p.1145986
Hauptverfasser: Staropoli, Nicoletta, Salvino, Angela, Falcone, Federica, Farenza, Valentina, Costa, Martina, Rossini, Giacomo, Manti, Francesco, Crispino, Antonella, Riillo, Caterina, Ciliberto, Domenico, Arbitrio, Mariamena, Tassone, Pierfrancesco, Tagliaferri, Pierosandro
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Sprache:eng
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Zusammenfassung:The optimal strategy for the treatment of recurrent and/or advanced endometrial cancer is still undefined. Recently, despite the lack of any predictive biomarker, the combination of pembrolizumab with lenvatinib has improved survival outcomes. We here report the long-term management of lung toxicity in a patient with endometrial cancer, and we critically review the current therapeutic options for this disease. A patient with heavily pretreated endometrial cancer took pembrolizumab plus lenvatinib for 1 year, achieving a persistent partial response with a time to treatment failure of 18 months, despite relevant lung toxicity that did not affect the remarkable overall clinical benefit. A systematic review of this combination underlines the efficacy outcome despite toxicity. Interestingly, the literature review on lung toxicity suggested the role of anti-angiogenetic agents in the pathogenesis of lung cavitation, probably related to direct treatment activity, and disclosed a potential radiological sign predictive of the activity of anti-angiogenetic agents. We underline the efficacy of pembrolizumab plus lenvatinib in the current treatment landscape of endometrial cancer, underscoring the relevance of a correct management of toxicity.
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2023.1145986