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Pembrolizumab combined with lenvatinib and metronomic cyclophosphamide in platinum-resistant ovarian cancer: a case report of durable clinical response.

作者信息

Dai Guanlin, Tang Furong, Wang Ping, Wang Danqing

机构信息

Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.

Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, Sichuan, China.

出版信息

Front Oncol. 2025 Aug 20;15:1582701. doi: 10.3389/fonc.2025.1582701. eCollection 2025.


DOI:10.3389/fonc.2025.1582701
PMID:40909975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12404960/
Abstract

Most patients with ovarian cancer experience disease recurrence or progression, and ultimately progress to platinum resistance. Standard treatments for platinum-resistant ovarian cancer (PROC) include non-platinum chemotherapy, targeted agents, and immunotherapy. Despite recent advances in individualized management of PROC, median progression-free survival remains limited. Effective treatments are still lacking for PROC treatment. Given the current landscape of immunotherapy in ovarian cancer, research is ongoing to investigate immune modulators to counteract immune escape and enhance the efficacy of immune checkpoint inhibitors. Here, we reported a successful administration of a triple regimen comprising pembrolizumab, lenvatinib and metronomic cyclophosphamide, as the third-line treatment in a patient with PROC. This combination resulted in a durable response, with a PFS of 52 months as of the last follow up. This is the first report on this triple regimen in PROC and its promising outcome suggested that this regimen deserves further investigation as a potential therapeutic option for PROC.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/48f4ebac6f51/fonc-15-1582701-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/0f6cac189dbc/fonc-15-1582701-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/418fe4db0828/fonc-15-1582701-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/a015980c30bc/fonc-15-1582701-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/48f4ebac6f51/fonc-15-1582701-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/0f6cac189dbc/fonc-15-1582701-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/418fe4db0828/fonc-15-1582701-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/a015980c30bc/fonc-15-1582701-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/12404960/48f4ebac6f51/fonc-15-1582701-g004.jpg

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[1]
Pembrolizumab combined with lenvatinib and metronomic cyclophosphamide in platinum-resistant ovarian cancer: a case report of durable clinical response.

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本文引用的文献

[1]
Vascular Endothelial Growth Factor (VEGF) Family and the Immune System: Activators or Inhibitors?

Biomedicines. 2024-12-24

[2]
Current trends in sensitizing immune checkpoint inhibitors for cancer treatment.

Mol Cancer. 2024-12-26

[3]
Lenvatinib plus pembrolizumab for patients with previously treated advanced ovarian cancer: Results from the phase 2 multicohort LEAP-005 study.

Gynecol Oncol. 2024-7

[4]
Evaluation of potential biomarkers for lenvatinib plus pembrolizumab among patients with advanced endometrial cancer: results from Study 111/KEYNOTE-146.

J Immunother Cancer. 2024-1-19

[5]
Mirvetuximab Soravtansine in FRα-Positive, Platinum-Resistant Ovarian Cancer.

N Engl J Med. 2023-12-7

[6]
National and subnational trends in cancer burden in China, 2005-20: an analysis of national mortality surveillance data.

Lancet Public Health. 2023-12

[7]
Treatment Approaches for Platinum-Resistant Ovarian Cancer.

J Clin Oncol. 2024-1-10

[8]
Current progress in cancer treatment by targeting FGFR signaling.

Cancer Biol Med. 2023-7-24

[9]
Lenvatinib Plus Pembrolizumab in Previously Treated Advanced Endometrial Cancer: Updated Efficacy and Safety From the Randomized Phase III Study 309/KEYNOTE-775.

J Clin Oncol. 2023-6-1

[10]
Unleashing the potential of combining FGFR inhibitor and immune checkpoint blockade for FGF/FGFR signaling in tumor microenvironment.

Mol Cancer. 2023-3-25

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