# Bridging via extracorporeal cardiopulmonary resuscitation for hemodynamic collapse in a patient with metastatic lung cancer: a case report

**Authors:** Takayuki Hasegawa, Shoe Kobiyama, Ryosuke Sasaki, Tatsusmi Yakushiji, Keisuke Yoshida, Takahiro Hakozaki, Satoki Inoue

PMC · DOI: 10.1186/s40981-025-00839-z · JA Clinical Reports · 2025-12-05

## TL;DR

A patient with advanced lung cancer and heart failure was successfully treated with VA-ECMO as a bridge to targeted therapy.

## Contribution

This case demonstrates VA-ECMO can be effective in oncology patients with treatment-sensitive disease.

## Key findings

- VA-ECMO stabilized hemodynamics in a patient with metastatic lung cancer and right ventricular failure.
- The patient responded well to osimertinib, allowing VA-ECMO decannulation within 7 days.
- Short-term VA-ECMO may serve as a bridge to targeted therapy in selected oncology patients.

## Abstract

Due to the highly invasive nature of veno-arterial extracorporeal membrane oxygenation (VA-ECMO), advanced malignancy is considered a relative contraindication. We here report a patient with hemodynamic collapse secondary to metastatic lung cancer in whom bridging via VA-ECMO was successful.

A 35-year-old man with metastatic non-small cell lung cancer harboring a deletion in exon 19 of epidermal growth factor receptor developed acute right ventricular failure and hemodynamic collapse due to pulmonary tumor thrombotic microangiopathy. Because treatment with the targeted agent osimertinib had already been initiated and a rapid response was anticipated, VA-ECMO was instituted as a bridge to its therapeutic effect. The patient's hemodynamics stabilized within 7 days, permitting VA-ECMO decannulation. At the time of writing, the patient is continuing to undergo regular outpatient follow-up.

In carefully selected oncology patients with highly treatment-sensitive disease, short-term VA-ECMO may be an effective bridge to systemic therapy.

## Linked entities

- **Chemicals:** osimertinib (PubChem CID 71496458)
- **Diseases:** non-small cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** right ventricular failure (MESH:D051437), lung cancer (MESH:D008175), malignancy (MESH:D009369), hemodynamic collapse (MESH:D001261), thrombotic microangiopathy (MESH:D057049), non-small cell lung cancer (MESH:D002289)
- **Chemicals:** osimertinib (MESH:C000596361), VA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12796032/full.md

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Source: https://tomesphere.com/paper/PMC12796032