# Pathological complete response to conversion therapy for lung adenocarcinoma with brain metastasis: a case report

**Authors:** Xingqiang Ran, Tao Luo, Jie Xiong, Maoyong Fu

PMC · DOI: 10.3389/fonc.2025.1625918 · 2025-10-14

## TL;DR

A patient with advanced lung cancer and brain metastases achieved complete response after combined therapy, allowing for successful surgery.

## Contribution

Demonstrates successful conversion therapy and surgery in a patient with brain metastases from lung cancer.

## Key findings

- Combined targeted, immunotherapy, and chemotherapy led to complete response in brain metastases.
- Patient became eligible for surgery after 11 months of treatment.
- Postoperative pathology confirmed complete response.

## Abstract

Lung cancer is the leading cause of cancer mortality worldwide. Fortunately, the advent of precision medicine, which includes targeted therapy and immunotherapy, has significantly improved the survival rates of patients with locally advanced lung cancer. This article reports on a case of stage IVB (cT2bN1M1c1) non-small cell lung cancer (NSCLC) with brain metastases harboring compound mutations in epidermal growth factor receptor (EGFR) exon 21 Leu858Arg and mitogen-activated protein kinase 1 (MEK1) exon 3 lle112Thr and with a high program death ligand 1 (PD-L1) expression that successfully underwent radical lung cancer surgery following combined therapy. We report on a case of a 60-year-old man diagnosed preoperatively with stage IVB adenocarcinoma of the left upper lung (cT2bN1M1c1) who was diagnosed with multiple brain metastases. After multidisciplinary discussion, it was decided to administer targeted therapy with furmonertinib, chemotherapy with pemetrexed and lobaplatin, and immunotherapy with tislelizumab. Following 2 months of treatment, tumor assessment showed partial response (PR). After 11 months, assessment showed a PR of all lung lesions and complete response of the brain lesions, making the patient eligible for surgery. Finally, the patient underwent video-assisted thoracoscopic left upper lobectomy + mediastinal lymphadenectomy. Postoperative pathology confirmed complete response, and the patient continued adjuvant therapy with furmonertinib. For patients with metastatic advanced NSCLC, systemic treatment involving chemotherapy plus immunotherapy and targeted therapy is expected to become one of the options. Moreover, it is likely to achieve successful conversion surgery and further efficacy after combined therapy.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956], MAP2K1 (mitogen-activated protein kinase kinase 1) [NCBI Gene 5604]
- **Chemicals:** furmonertinib (PubChem CID 118861389), pemetrexed (PubChem CID 135410875), lobaplatin (PubChem CID 10000860)
- **Diseases:** lung cancer (MONDO:0005138), adenocarcinoma (MONDO:0004970)

## Full-text entities

- **Genes:** 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}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}
- **Diseases:** stage IVB adenocarcinoma of the left (MESH:D000230), brain metastases (MESH:D001932), Lung cancer (MESH:D008175), brain lesions (MESH:D001927), cancer (MESH:D009369), brain metastasis (MESH:D009362), lung adenocarcinoma (MESH:D000077192), lung (MESH:D008171), NSCLC (MESH:D002289)
- **Chemicals:** tislelizumab (MESH:C000707970), lobaplatin (MESH:C066228), furmonertinib (MESH:C000705711), pemetrexed (MESH:D000068437)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Leu858Arg

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12558825/full.md

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Source: https://tomesphere.com/paper/PMC12558825