# Case Report: Omalizumab combined with voriconazole for the treatment of ABPA complicating IPA: a case report

**Authors:** Tingrui Zhao, Yukai Chen, He Sun

PMC · DOI: 10.3389/fphar.2025.1588182 · Frontiers in Pharmacology · 2025-07-02

## TL;DR

This case report describes a new treatment approach combining omalizumab and voriconazole for a patient with both ABPA and IPA, highlighting a switch to dupilumab for better management.

## Contribution

The paper introduces a novel treatment strategy and mechanism-driven transition from omalizumab to dupilumab for managing coexisting ABPA and IPA.

## Key findings

- Combining omalizumab with voriconazole achieved clinical stabilization in a patient with ABPA and IPA.
- Switching to dupilumab was more effective in managing persistently elevated serum IgE levels.
- The treatment approach followed ISHAM guidelines and provided guidance for ABPA-IPA management.

## Abstract

Aspergillus invading hosts may manifest as Allergic bronchopulmonary aspergillosis (ABPA) or invasive pulmonary aspergillosis (IPA) in individuals with varying immune statuses. ABPA predominantly occurs in severe asthma patients, whereas IPA is typically observed in immunocompromised individuals. ABPA management centers on glucocorticoids to mitigate hypersensitivity-driven inflammation, while IPA requires aggressive antifungal therapy. Concurrent ABPA and IPA presents a therapeutic dilemma, as glucocorticoids use may exacerbate fungal dissemination, while antifungal agents alone inadequately address the allergic component. Adjusting treatment strategies to balance immunosuppression to control ABPA with sufficient antifungal coverage for IPA is critical step. The case report presents an innovative therapeutic strategy for a 73-year-old female with co-existing ABPA and IPA. After suboptimal clinical response to conventional glucocorticoid-antifungal therapy, we implemented a guideline-aligned, evidence-based regimen combining omalizumab with voriconazole. While this dual therapy achieved clinical stabilization, persistently elevated serum IgE (>5000 IU/mL). By reviewing the literature and comparing the differences between the mechanisms of omalizumab and dupilumab, the treatment was finally changed from omalizumab to dupilumab and followed up. This case is also a practice guided by ISHAM guidelines while pioneering a mechanism-driven transition from omalizumab to dupilumab in ABPA-IPA co-management. In order to provide guidance for the treatment of ABPA-IPA disease.

## Linked entities

- **Chemicals:** voriconazole (PubChem CID 71616)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** inflammation (MESH:D007249), ABPA (MESH:D001229), allergic (MESH:D004342), asthma (MESH:D001249), fungal dissemination (MESH:D000072742), IPA (MESH:D055744)
- **Chemicals:** Omalizumab (MESH:D000069444), voriconazole (MESH:D065819), dupilumab (MESH:C582203)
- **Species:** Aspergillus (genus) [taxon 5052], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12263934/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12263934/full.md

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Source: https://tomesphere.com/paper/PMC12263934