# Pulmonary Cryptococcosis During Osimertinib Treatment for Epidermal Growth Factor Receptor (EGFR) L858R-Mutant Lung Adenocarcinoma: A Case Report

**Authors:** Yuki Hamada, Toshiaki Motegi, Kenya Kuramoto, Tatsuya Akiyama, Shigen Hayashi

PMC · DOI: 10.7759/cureus.83929 · 2025-05-11

## TL;DR

A patient with lung cancer on osimertinib developed a rare fungal infection, highlighting the need for early diagnosis in immunocompromised individuals.

## Contribution

This case report presents a rare instance of pulmonary cryptococcosis during osimertinib treatment and discusses diagnostic challenges.

## Key findings

- Pulmonary cryptococcosis was confirmed via biopsy despite negative serum cryptococcal antigen results.
- Elevated serum β-D-glucan levels were observed, an atypical finding in cryptococcal infections.
- The patient responded well to antifungal therapy with amphotericin B, flucytosine, and fluconazole.

## Abstract

Pulmonary cryptococcosis is a rare but important opportunistic fungal infection that may occur during epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) therapy for lung cancer. We describe the case of a woman in her 60s receiving osimertinib for EGFR L858R-mutant lung adenocarcinoma who developed new pulmonary lesions. A CT-guided biopsy confirmed pulmonary cryptococcosis despite negative serum cryptococcal antigen results, with markedly elevated serum β-D-glucan levels, an atypical finding in cryptococcal infections. The patient was also receiving dexamethasone for brain metastases. Although her lymphocyte count was within the normal range, functional immunosuppression was suspected due to the combined effects of EGFR-TKItherapy and corticosteroid use. This case highlights the limitations of serological testing in immunocompromised patients undergoing molecular-targeted therapy and underscores the importance of early pathological evaluation. The patient responded well to induction therapy with amphotericin B and flucytosine, followed by fluconazole consolidation. While causality cannot be definitively established, this case suggests the need for vigilance for opportunistic infections in similar clinical settings.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956]
- **Chemicals:** osimertinib (PubChem CID 71496458), dexamethasone (PubChem CID 5743), amphotericin B (PubChem CID 1972), flucytosine (PubChem CID 3366), fluconazole (PubChem CID 3365)
- **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:** metastases (MESH:D009362), lung cancer (MESH:D008175), pulmonary lesions (MESH:D008171), Lung Adenocarcinoma (MESH:D000077192), Pulmonary Cryptococcosis (MESH:D003453), fungal infection (MESH:D009181), cryptococcal (MESH:D016919), opportunistic infections (MESH:D009894)
- **Chemicals:** fluconazole (MESH:D015725), flucytosine (MESH:D005437), amphotericin B (MESH:D000666), Osimertinib (MESH:C000596361), beta-D-glucan (-), dexamethasone (MESH:D003907)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** L858R

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12152402/full.md

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Source: https://tomesphere.com/paper/PMC12152402