# Unveiling trends and clinical progress of immunotherapy for endometrial cancer: a scientometric and clinical trial landscape analysis

**Authors:** Ruoyan Liu, Wenhui Shan, Zhuopeng Hu, Hong Wang, Zhening Wang, Lei Yang, Rui Guo

PMC · DOI: 10.3389/fimmu.2026.1668903 · Frontiers in Immunology · 2026-02-09

## TL;DR

This paper analyzes the growth and trends in immunotherapy research and clinical trials for endometrial cancer, showing a shift toward immune checkpoint blockade and combination therapies.

## Contribution

The study provides a comprehensive scientometric and clinical trial landscape analysis of immunotherapy for endometrial cancer.

## Key findings

- Publication output and clinical trials on endometrial cancer immunotherapy have increased steadily over the past two decades.
- The United States and China are leading contributors to both research and clinical trials in this field.
- Recent clinical trials emphasize immune checkpoint blockade and combination therapies as promising approaches.

## Abstract

Endometrial cancer (EC) is a heterogeneous and increasingly prevalent malignancy characterized by distinct molecular subgroups that exhibit fundamentally different immune profiles. These immunologic differences shape tumor–immune interactions, influence responsiveness to immunotherapy, and underscore the importance of biologically informed treatment strategies. As the clinical application of immune checkpoint inhibitors expands, understanding the mechanistic and translational landscape of immunotherapy in EC has become essential for guiding precision oncology.

We systematically retrieved 836 immunotherapy-related publications on EC from the Web of Science Core Collection (1999–2024) and conducted a scientometric analysis using VOSviewer and CiteSpace. Analyses included publication trends, country and institutional collaborations, author networks, and keyword clustering. Furthermore, we screened 391 clinical trials from ClinicalTrials.gov and ICTRP databases to assess the clinical research landscape.

Publication output and clinical trials on EC immunotherapy have shown a continuous upward trend over the past two decades. The United States and China emerged as leading contributors in both publications and pivotal clinical trials. Among the most frequently co-cited references, clinical studies account for a significant proportion, particularly those published in the last five years. The landscape reflects a shift toward immune checkpoint blockade and combination therapy strategies, with some clinical trials demonstrating promising efficacy.

Our integrated scientometric and clinical trial analysis reveals a rapid evolution in EC immunotherapy research, highlighting checkpoint blockade as a central therapeutic approach. The trend toward combination regimens underscores the translational potential of immunotherapy in EC and points toward emerging directions for future research and clinical application.

## Linked entities

- **Diseases:** endometrial cancer (MONDO:0002447)

## Full-text entities

- **Genes:** ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, COL11A2 (collagen type XI alpha 2 chain) [NCBI Gene 1302] {aka DFNA13, DFNB53, FBCG2, HKE5, OSMEDA, OSMEDB}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, MAGEA4 (MAGE family member A4) [NCBI Gene 4103] {aka CT1.4, MAGE-41, MAGE-X2, MAGE4, MAGE4A, MAGE4B}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD274 (CD274 molecule) [NCBI Gene 574058] {aka PDL1}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, AXL (AXL receptor tyrosine kinase) [NCBI Gene 558] {aka ARK, AXL3, JTK11, Tyro7, UFO}
- **Diseases:** oncologic (MESH:D000072716), Lynch syndrome (MESH:D003123), solid (MESH:D018250), obesity (MESH:D009765), ADC (MESH:D009759), Ovarian cancer (MESH:D010051), melanoma and lung cancer (MESH:D008175), TS (MESH:D005879), gynecologic malignancies (MESH:D005833), serous carcinomas (MESH:D018297), Cancer (MESH:D009369), Uterine corpus cancer (MESH:D014594), cytotoxic (MESH:D064420), MSI (MESH:D053842), dMMR disease (MESH:D004194), melanoma (MESH:D008545), hypothyroidism (MESH:D007037), cervical cancer (MESH:D002583), deaths (MESH:D003643), EC (MESH:D016889)
- **Chemicals:** Nivolumab (MESH:D000077594), bevacizumab (MESH:D000068258), talazoparib (MESH:C586365), cyclophosphamide (MESH:D003520), Tislelizumab (MESH:C000707970), SYD985 (MESH:C000656468), Trastuzumab deruxtecan (MESH:C000614160), lenvatinib (MESH:C531958), olaparib (MESH:C531550), atezolizumab (MESH:C000594389), durvalumab (MESH:C000613593), tamoxifen (MESH:D013629), paclitaxel (MESH:D017239), Pembrolizumab (MESH:C582435), trastuzumab (MESH:D000068878), envafolimab (MESH:C000718749), BA (MESH:D018033), ADP (MESH:D000244), tisotumab vedotin (MESH:C000707142), platinum (MESH:D010984), Ivonescimab (-), dostarlimab (MESH:C000719628), axitinib (MESH:D000077784), avelumab (MESH:C000609138), carboplatin (MESH:D016190)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12926481/full.md

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926481/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926481/full.md

---
Source: https://tomesphere.com/paper/PMC12926481