# Sequential tyrosine kinase inhibitor therapy for EGFR L747P-mutated lung adenocarcinoma in a renal transplant recipient: a 24-month case report

**Authors:** Wenxiu Xie, Feng Chen, Lei Zhang, Baoquan Lin, Jia Ye, Zongyang Yu, Lei Gu, Wei Liu

PMC · DOI: 10.3389/fmed.2025.1651584 · Frontiers in Medicine · 2025-10-08

## TL;DR

A kidney transplant recipient with a rare lung cancer mutation lived 24 months using a sequence of targeted therapies, showing potential for personalized treatment in transplant patients.

## Contribution

First reported case of sequential tyrosine kinase inhibitor therapy for EGFR L747P-mutated lung cancer in a renal transplant recipient.

## Key findings

- Sequential use of gefitinib, osimertinib, and dacomitinib achieved 24 months of overall survival in a renal transplant recipient.
- Treatment was well tolerated with manageable adverse events and no significant graft dysfunction.
- The case highlights the potential for individualized TKI therapy in rare EGFR-mutated cancers among transplant patients.

## Abstract

Kidney transplant recipients (KTRs) are at increased risk of malignancies, including lung adenocarcinoma (LUAD). The therapeutic efficacy of tyrosine kinase inhibitors (TKIs) against the rare EGFR L747P mutation remains controversial.

We report a 60-years-old female renal transplant recipient who developed advanced lung adenocarcinoma harboring the EGFR L747P mutation.

The patient was treated sequentially with three generations of EGFR TKIs–gefitinib, osimertinib, and dacomitinib–while continuing immunosuppressive therapy for graft function. Gefitinib achieved a progression-free survival (PFS) of 9 months, osimertinib 4.5 months, and dacomitinib 2.5 months, resulting in a total overall survival (OS) of 24 months. Treatment was generally well tolerated, with only mild adverse events and manageable renal function changes.

To our knowledge, this is the first reported case of an EGFR L747P-mutated lung adenocarcinoma in a renal transplant recipient benefiting from sequential multi-TKI therapy. This case underscores the importance of vigilant cancer surveillance in transplant recipients and suggests that individualized TKI sequencing may offer clinical benefit, although further evidence is required.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956]
- **Chemicals:** gefitinib (PubChem CID 123631), osimertinib (PubChem CID 71496458), dacomitinib (PubChem CID 11511120)
- **Diseases:** lung adenocarcinoma (MONDO:0005061)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** cancer (MESH:D009369), LUAD (MESH:D000077192)
- **Chemicals:** osimertinib (MESH:C000596361), dacomitinib (MESH:C525726), Gefitinib (MESH:D000077156)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** L747P

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12540125/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12540125/full.md

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Source: https://tomesphere.com/paper/PMC12540125