Combination of pembrolizumab and lenvatinib in second-line therapy for MSS/pMMR advanced endometrial cancer: literature review and a case report
- Authors: Darenskaya A.D.1, Medvedeva B.M.1, Rumyantsev A.A.1
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Affiliations:
- N.N. Blokhin Russian Cancer Research Center, Ministry of Health of Russia
- Issue: Vol 19, No 4 (2023)
- Pages: 132-139
- Section: GYNECOLOGY. CLINICAL CASE
- Published: 20.12.2023
- URL: https://ojrs.abvpress.ru/ojrs/article/view/1172
- DOI: https://doi.org/10.17650/1994-4098-2023-19-4-132-139
- ID: 1172
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Abstract
Despite the existing standard treatments for endometrial cancer, the prognosis for these patients remained poor until recently. None of currently available cytostatics ensured long-term disease control and long-term survival of patients receiving standard platinum-based therapy. Poor treatment outcomes in patients with advanced endometrial cancer necessitated changes in therapeutic approaches and development of more effective treatment regimens. Better understanding of carcinogenesis mechanisms, emergence of a new molecular classification of endometrial cancer, and implementation of tailored treatment approaches based on tumor types led to a significant breakthrough in the treatment of advanced endometrial cancer. Currently, the most effective second-line therapy for endometrial cancer with high level microsatellite instability (MSI-h) or deficient mismatch repair system (dMMR) (25 % of cases), and no indications for surgery is pembrolizumab monotherapy. Most of cancers (about 75 %) are represented by microsatellite-stable and mismatch repair proficient tumors (MSS/рMMR). Patients with such tumors demonstrating disease progression after systemic therapy should receive a combinations of the immune checkpoint inhibitor pembrolizumab and the multi-targeted tyrosine kinase inhibitor lenvatinib. In this article, we review relevant literature and report a case of successful treatment of MSS/pMMR advanced endometrial cancer with a combination of pembrolizumab and lenvatinib as a second-line therapy (after disease progression in response to platinum-containing first-line chemotherapy), which ensured long-term disease control.
About the authors
A. D. Darenskaya
N.N. Blokhin Russian Cancer Research Center, Ministry of Health of Russia
Author for correspondence.
Email: darenskaya@bk.ru
ORCID iD: 0000-0002-6505-2202
Anna Dmitrievna Darenskaya
24 Kashirskoe Shosse, Moscow 115522
Russian FederationB. M. Medvedeva
N.N. Blokhin Russian Cancer Research Center, Ministry of Health of Russia
ORCID iD: 0000-0003-1779-003X
24 Kashirskoe Shosse, Moscow 115522
Russian FederationA. A. Rumyantsev
N.N. Blokhin Russian Cancer Research Center, Ministry of Health of Russia
ORCID iD: 0000-0003-4443-9974
24 Kashirskoe Shosse, Moscow 115522
Russian FederationReferences
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