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Lenvatinib plus Pembrolizumab Combination Therapy for Advanced or Recurrent Endometrial Cancer: A Single-Center,
Mikako Tochigi1, Shogo Shigeta1, Muneaki Shimada1,2
1Department of Obstetrics and Gynecology, Tohoku University School of Medicine.
Abstract:
A multi-kinase inhibitor, lenvatinib, plus an immune checkpoint inhibitor, pembrolizumab, became a viable therapeutic option for advanced or recurrent endometrial cancer in Japan by the end of 2021. The Japanese population has a relatively unique genetic background. Hence, the safety profile and effectiveness of lenvatinib plus pembrolizumab may differ between the Japanese and other populations. This single-center, retrospective study aimed to evaluate the treatment efficacy of lenvatinib plus pembrolizumab and the safety profile of the associated adverse events. The clinical records of 15 patients, who received lenvatinib plus pembrolizumab for advanced or recurrent endometrial cancer at the Tohoku University Hospital, were reviewed. Best overall response and disease control rates were 40.0% and 73.3%, respectively. Treatment was discontinued owing to disease progression and adverse events in six patients, respectively. As of the end of July 2023, treatment was ongoing in the remaining three patients. The median treatment and progression-free survival durations were 118 and 258 days, respectively. Relative dose intensity of lenvatinib was not positively associated with progression-free survival, neither during the first 4 weeks after treatment initiation nor during the entire treatment period. All patients experienced one or more adverse events, the most common of which were hypothyroidism (90%) and hypertension (83.3%). Among the 15 patients, 13 required lenvatinib dose reduction owing to adverse events. One patient developed grade 4 interstitial pneumonia requiring intensive care. Our results validate the short-term efficacy of lenvatinib plus pembrolizumab, and indicate that dose optimization of lenvatinib could be individualized without impairing efficacy.
Insights
Lenvatinib plus pembrolizumab shows efficacy for advanced endometrial cancer in Japan. However, careful management of adverse events like hypothyroidism and hypertension is crucial, with dose adjustments often needed.
Area of Science:
- Oncology
- Pharmacology
Background:
- Lenvatinib plus pembrolizumab is a therapeutic option for advanced or recurrent endometrial cancer.
- The Japanese population's unique genetic background may influence treatment outcomes.
- This study evaluates the efficacy and safety of this combination in a Japanese cohort.
Purpose of the Study:
- To assess the treatment efficacy of lenvatinib plus pembrolizumab in Japanese patients with advanced or recurrent endometrial cancer.
- To evaluate the safety profile and adverse events associated with this combination therapy.
- To explore the relationship between lenvatinib dose intensity and progression-free survival.
Main Methods:
- Retrospective analysis of clinical records from 15 patients at Tohoku University Hospital.
- Evaluation of best overall response, disease control rate, and survival durations.
- Analysis of adverse events, dose reductions, and treatment discontinuation reasons.
Main Results:
- Best overall response rate was 40.0%, and disease control rate was 73.3%.
- Median progression-free survival was 258 days; treatment was ongoing for 3 patients.
- Common adverse events included hypothyroidism (90%) and hypertension (83.3%); 13 patients required dose reduction.
Conclusions:
- Lenvatinib plus pembrolizumab demonstrates short-term efficacy in this Japanese cohort.
- Individualized lenvatinib dose optimization may be possible without compromising efficacy.
- Close monitoring and management of adverse events are essential for successful treatment.
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