# Efficacy and safety of Cadonilimab plus anlotinib in small cell lung cancer with brain metastases

**Authors:** Hai-Zhen Yi, Wei Lv, Jin-Jing Chen, Zhan Lin

PMC · DOI: 10.3389/fonc.2025.1545101 · Frontiers in Oncology · 2025-07-17

## TL;DR

This study evaluates the effectiveness and safety of combining Cadonilimab and Anlotinib for treating small cell lung cancer with brain metastases.

## Contribution

The study presents a novel combination therapy for SCLC with brain metastases and reports its efficacy and safety profile.

## Key findings

- The combination therapy achieved an objective response rate of 41.3% in intracranial lesions.
- Median overall survival was 19.3 months with certain factors predicting better survival outcomes.
- Most patients experienced treatment-related adverse events, with a notable proportion experiencing severe side effects.

## Abstract

This study aimed to evaluate the efficiency and safety of Cadonilimab and Anlotinib pairing in individuals diagnosed with small cell lung cancer (SCLC) and brain metastases (BMs).

A review was performed on individuals who were diagnosed with small cell lung cancer (SCLC) and had central nervous system (CNS) metastases confirmed via magnetic resonance imaging (MRI) of the brain.We assessed the treatment response of Cadonilimab plus Anlotinib using Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) and Response assessment in neuro-oncology brain metastases (RANO-BM) for evaluating solid tumors and neuro-oncology brain metastases, respectively.The patients’ prognosis was determined using Kaplan-Meier analysis and Cox regression analysis.

The study initially included 46 patients diagnosed with SCLC who presented with brain metastases (BMs). According to the RANO-BM criteria, intracranial lesions showed an objective response rate (ORR) of 41.3%. The median overall survival (OS) was observed to be 19.3 months (95% CI, 17.4-21.1 months). Multivariate Cox regression analysis showed that having a PD1 level below 50% (HR=4.83, P <0.001) or having two or more metastatic organs (HR = 2.71, P = 0.036) were independent factors that positively predicted overall survival of all the patients, 86.9% experienced treatment-related adverse events (TRAEs) associated with the treatment, while 17.4% reported severe TRAEs of grade3-4.

According to our results, the combination of Cadonilimab and Anlotinib appears to be a promising treatment option for SCLC patients with brain metastases.

## Linked entities

- **Chemicals:** Anlotinib (PubChem CID 25017411)
- **Diseases:** small cell lung cancer (MONDO:0008433)

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, PDCD1LG2 (programmed cell death 1 ligand 2) [NCBI Gene 80380] {aka B7DC, Btdc, CD273, PD-L2, PDCD1L2, PDL2}, CD80 (CD80 molecule) [NCBI Gene 941] {aka B7, B7-1, B7.1, BB1, CD28LG, CD28LG1}
- **Diseases:** ES-SCLC (MESH:D055752), melanoma (MESH:D008545), brain disorders (MESH:D001927), death (MESH:D003643), Hepatic dysfunction (MESH:D008107), Leukopenia (MESH:D007970), NSCLC (MESH:D002289), central nervous system (CNS) metastases (MESH:D009362), lesions (MESH:D009059), BMs (MESH:D001932), intracranial lesions (MESH:D020765), Solid Tumors (MESH:D009369), cervical cancer (MESH:D002583), Hypertension (MESH:D006973), leukemia (MESH:D007938), Thyroid dysfunction (MESH:D013959), lung cancer (MESH:D008175), cachexia (MESH:D002100), CNS tumors (MESH:D016543), cognitive decline (MESH:D003072), CDC (MESH:D019966), toxicities (MESH:D064420), kidney, gastric, and lung cancers (MESH:D013274)
- **Chemicals:** pembrolizumab (MESH:C582435), Anlotinib (MESH:C000625192), Nivolumab (MESH:D000077594), atezolizumab (MESH:C000594389), docetaxel (MESH:D000077143), durvalumab (MESH:C000613593), Cadonilimab (-), platinum (MESH:D010984)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12310591/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12310591/full.md

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Source: https://tomesphere.com/paper/PMC12310591