# An Advanced IVB Lung Adenocarcinoma Patient With KRAS Mutations, Benefited From Camrelizumab Combined With Anti‐Angiogenic Agents for Therapy: A Case Report

**Authors:** Li Wang, Jiaqi Wu, Ping Shao, Wuping Bao, Lin Mao, Zhendong Pan, Aihua Bao, Min Zhang, Zhenghua Wu, Guorong Fan

PMC · DOI: 10.1002/cnr2.70186 · Cancer Reports · 2025-06-09

## TL;DR

A patient with advanced lung cancer and KRAS mutations experienced long-term benefits from immunotherapy combined with anti-angiogenic drugs.

## Contribution

This is the first reported case of long-term success with camrelizumab and anti-angiogenic agents in KRAS-mutated NSCLC.

## Key findings

- The patient survived 27 months with no significant discomfort after treatment.
- Combination therapy showed good persistence and clinical efficacy in a KRAS-mutated NSCLC case.
- Pharmaceutical care improved treatment outcomes through drug adjustment and safety evaluation.

## Abstract

Although the presence of Kirsten murine sarcoma virus (KRAS) mutations predicts a failure of non‐small cell carcinoma (NSCLC) patients to benefit from epidermal growth factor receptor (EGFR)—tyrosine kinase inhibitor (TKI) therapy it may be more sensitive to programmed combination therapy of programmed death 1 (PD‐1)/programmed death ligand 1 (PD‐L1) inhibitors + anti‐angiogenesis. Recent treatment guidelines and clinical studies related to adenocarcinoma in NSCLC have indicated that in patients with inoperable stage IV lung adenocarcinoma, immune checkpoint inhibitors in combination with anti‐angiogenic drugs may exert a synergistic effect and significantly improve the efficacy of near‐term treatment, but quantification and long‐term follow‐up of specific clinical indicators are still lacking. No previous cases of long‐term good results with camrelizumab combined with anti‐angiogenic agents for KRAS‐mutated NSCLC have been described.

This manuscript reports a case of a patient with advanced NSCLC with pleural effusion and KRAS mutations treated poorly with conventional chemotherapy who had long‐term (more than 18 months) benefit with immunotherapy combined with an anti‐angiogenic inhibitor in Shanghai General Hospital. In this case, pharmaceutical care of the patient was carried out through therapeutic drug adjustment, compliance, efficacy assessment, and safety evaluation to provide a reference for improving the efficacy and safety of drug therapy in clinical practice. As of the last follow‐up date (December 2023), overall survival was 27 months, and the patient is currently in good general condition with no significant complaints of discomfort.

ICLs in combination with antiangiogenic therapy may be a therapeutic option for patients with KRAS mutations in advanced non‐small cell lung cancer with good persistence.

## Linked entities

- **Genes:** KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845]
- **Diseases:** lung adenocarcinoma (MONDO:0005061)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** Lung Adenocarcinoma (MESH:D000077192), adenocarcinoma (MESH:D000230), NSCLC (MESH:D002289), pleural effusion (MESH:D010996)
- **Chemicals:** Camrelizumab (MESH:C000631724)
- **Species:** Kirsten murine sarcoma virus (no rank) [taxon 11808], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12147042/full.md

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Source: https://tomesphere.com/paper/PMC12147042