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

advanced endometrial cancer immunotherapy lenvatinib lung toxicity pembrolizumab targeted therapy

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2023
Historique:
received: 15 03 2023
accepted: 07 06 2023
medline: 26 7 2023
pubmed: 26 7 2023
entrez: 26 7 2023
Statut: epublish

Résumé

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.

Sections du résumé

Background UNASSIGNED
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.
Results UNASSIGNED
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.
Conclusion UNASSIGNED
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.

Identifiants

pubmed: 37492471
doi: 10.3389/fonc.2023.1145986
pmc: PMC10363977
doi:

Types de publication

Case Reports

Langues

eng

Pagination

1145986

Informations de copyright

Copyright © 2023 Staropoli, Salvino, Falcone, Farenza, Costa, Rossini, Manti, Crispino, Riillo, Ciliberto, Arbitrio, Tassone and Tagliaferri.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Nicoletta Staropoli (N)

Medical and Translational Oncology Unit, AOU Renato Dulbecco, Catanzaro, Italy.
Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Angela Salvino (A)

Medical and Translational Oncology Unit, AOU Renato Dulbecco, Catanzaro, Italy.

Federica Falcone (F)

Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Valentina Farenza (V)

Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Martina Costa (M)

Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Giacomo Rossini (G)

Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Francesco Manti (F)

Radiology Unit, AOU Renato Dulbecco, Catanzaro, Italy.

Antonella Crispino (A)

Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Caterina Riillo (C)

Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Domenico Ciliberto (D)

Medical and Translational Oncology Unit, AOU Renato Dulbecco, Catanzaro, Italy.

Mariamena Arbitrio (M)

Institute for Biomedical Research and Innovation (IRIB), National Research Council of Italy (CNR), Catanzaro, Italy.

Pierfrancesco Tassone (P)

Medical and Translational Oncology Unit, AOU Renato Dulbecco, Catanzaro, Italy.
Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Pierosandro Tagliaferri (P)

Medical and Translational Oncology Unit, AOU Renato Dulbecco, Catanzaro, Italy.
Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Classifications MeSH