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An Orthotopic Endometrial Cancer Model with Retroperitoneal Lymphadenopathy Made From In Vivo Propagated and Cultured VX2 Cells
Published on: September 12, 2019
Promising response to neoadjuvant pembrolizumab and low-dose chemotherapy in advanced endometrial cancer: A
Angel Chao1, Chien-Chi Lu2, Yen-Ling Huang3
1Department of Obstetrics and Gynecology, Linkou Chang Gung Memorial Hospital, Taoyuan, Taiwan; Chang Gung University College of Medicine, Taoyuan, Taiwan; Gynecologic Cancer Research Center, Linkou Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Objective:
Recent trials demonstrated improved outcomes with immunotherapy-chemotherapy combinations in advanced endometrial cancer (EC) with mismatch repair deficiency (dMMR). We evaluated clinical characteristics, treatment responses, and safety of patients with advanced EC receiving neoadjuvant immunotherapy with low-dose chemotherapy (NIC).
Study Design:
Eight patients received treatment between January 2024 and August 2025. The NIC regimen comprised pembrolizumab (100 mg) on day 1 followed by paclitaxel (80 mg/m2) and carboplatin (AUC 2) on days 8 and 15 every 21 days, for one to four cycles prior to surgery.
Results:
The median age was 64.5 years (range: 45-78). Molecular studies revealed dMMR tumors in four patients, including two also with p53-abnormal features (p53abn); missmatch repair proficient (pMMR) and p53abn in three patients; and nonspecific molecular profile in one patient. Four patients achieved complete radiologic response by RECIST v1.1 criteria, whereas four demonstrated partial responses with tumor regression ranging from 41% to 92%. Pathological evaluation documented complete response in four patients with diverse histologic subtypes: undifferentiated/dedifferentiated (n = 1), serous (n = 1), grade 3 endometrioid (n = 1), and clear cell carcinoma (n = 1). Complete responses occurred in both serous and clear cell carcinomas despite typically unfavorable p53abn molecular profiles. At median follow-up of 3.6 months after complete therapy, one patient progressed. All patients completed treatment without grade ≥3 adverse events per CTCAE criteria.
Conclusion:
Neoadjuvant pembrolizumab with low-dose chemotherapy demonstrated promising efficacy and acceptable safety in advanced EC, with favorable outcomes in high-grade malignancies regardless of molecular subtype. These findings warrant further investigation in selected patients.
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