# A study on the effectiveness and safety of interventional embolization using drug-loaded microspheres in combination with sorafenib and envafolimab for intermediate and advanced renal cell carcinoma

**Authors:** Cheng Chen, Yanfeng Shen, Yanhong Ma, Yingying Zhang, Shuyan Zhang, Na Su, Hefei Guo, Yapeng Guo, Xuehui Zhang, Xianming Liu, Suhua Zhang, Shuai Li, Xin You, Zhiwei Zhang, Xiaoting Duan, Guiying Li

PMC · DOI: 10.3389/fonc.2025.1558410 · Frontiers in Oncology · 2025-05-29

## TL;DR

This study examines combining drug-loaded microsphere embolization with sorafenib and envafolimab to treat advanced kidney cancer, finding it more effective and safer than embolization alone.

## Contribution

The study introduces a novel combination therapy for renal cell carcinoma using D-TAE with sorafenib and envafolimab.

## Key findings

- The combination group showed significantly higher objective tumor response and tumor control rates compared to the D-TAE-only group.
- The combination therapy resulted in lower serum VEGF, CEA, and CA125 levels, improved progression-free survival, and reduced mortality.
- Adverse reactions were less frequent in the combination group compared to the D-TAE-only group.

## Abstract

To investigate the effectiveness and safety of drug-loaded microsphere interventional embolization (D-TAE) in conjunction with sorafenib and envafolimab in the management of intermediate and advanced renal carcinoma.

120 cases of intermediate and advanced renal cell carcinoma cured in the Oncology Department of our hospital from January 2022 to December 2023 were selected. Individuals in the combination group received D-TAE paired with sorafenib and envafolimab. Individuals in the D-TAE group received only D-TAE. The clinical data, clinical efficacy, vascular endothelial growth factor (VEGF), carcinoembryonic antigen (CEA), carbohydrate antigen 125 (CA125), mortality, progression-free survival time (PFS), objective tumor response rate (ORR) and tumor control rate (DCR) and adverse reactions were compared in both groups.

The proportion of individuals with ORR and DCR in the combination group was greatly increased compared to that in the D-TAE group (P <0.05). After 1 week and 1 month of treatment, the serum VEGF levels in both groups showed a great decrease compared to pre-treatment levels (P<0.05), with the combination group demonstrating notably lower serum VEGF levels than the D-TAE group (P<0.05). Following treatment, serum CA125 and CEA levels in both groups experienced a great decrease compared to pre-treatment levels, with the combination group showing notably lower levels than the D-TAE group (P<0.05). Additionally, the mortality rate in the combination group was greatly lower than that in the D-TAE group, and the PFS was greatly increased in the combination group compared to the D-TAE group (P<0.05). In addition, the observed adverse reactions included gastrointestinal reactions, liver and kidney damage, myelosuppression and rash. Overall, the incidence of adverse reactions in the combination group was greatly decreased than that in the D-TAE group (P<0.05).

Drug-loaded microsphere interventional embolization combined with sorafenib and envafolimab has certain efficacy and acceptable safety in treating intermediate and late-stage renal tumor, providing a new treatment option for patients with renal cell carcinoma.

## Linked entities

- **Proteins:** VEGFA (vascular endothelial growth factor A)
- **Chemicals:** sorafenib (PubChem CID 216239)
- **Diseases:** renal cell carcinoma (MONDO:0005086)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}
- **Diseases:** gastrointestinal reactions (MESH:D005767), rash (MESH:D005076), liver and kidney damage (MESH:D056486), renal tumor (MESH:D007680), tumor (MESH:D009369), renal carcinoma (MESH:D002292)
- **Chemicals:** envafolimab (MESH:C000718749), D (MESH:D003903), sorafenib (MESH:D000077157), TAE (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12158990/full.md

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Source: https://tomesphere.com/paper/PMC12158990