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Stereotactic Ablative Radiotherapy for Early-stage Lung Cancer in Patients With Left Ventricular Assist Device: A
Kazuhiko Hayashi1, Hiroshi Ishikawa2, Kei Fujiwara3
1Department of Radiation Oncology, Osaka University Graduate School of Medicine, Osaka, Japan; hayashi@radonc.med.osaka-u.ac.jp.
Anticancer Research
|August 28, 2024
Summary
Stereotactic ablative radiotherapy (SABR) using CyberKnife is safe for early-stage lung cancer patients with implantable left ventricular assist devices (LVADs). This approach minimizes radiation dose to the LVAD, preventing adverse events.
Area of Science:
- Cardiology
- Radiation Oncology
- Medical Physics
Background:
- Radiotherapy can malfunction cardiac devices; guidelines exist for pacemakers and defibrillators.
- Safety of radiotherapy in patients with implantable left ventricular assist devices (LVADs) is not well-established.
- Early-stage lung cancer patients with LVADs often have comorbidities making them inoperable.
Purpose of the Study:
- To evaluate the safety and efficacy of stereotactic ablative radiotherapy (SABR) using CyberKnife in patients with LVADs.
- To report outcomes of early-stage lung cancer treatment in patients with LVADs.
- To assess LVAD function and adverse events following SABR.
Main Methods:
- Three patients with LVADs and early-stage lung cancer underwent SABR with CyberKnife.
- Total radiation dose ranged from 42-52 Gy in four fractions.
- Treatment plans aimed to limit LVAD radiation dose to below 2 Gy.
Main Results:
- SABR was completed in all patients without acute adverse events or LVAD malfunction.
- No disease progression or chronic adverse events were observed during 3-29 months follow-up.
- LVAD radiation dose was successfully kept below 2 Gy in all cases.
Conclusions:
- SABR using CyberKnife is a safe treatment option for early-stage lung cancer in patients with LVADs.
- Minimizing radiation dose to the LVAD is crucial for patient safety.
- This approach offers a viable treatment for inoperable lung cancer patients with LVADs.

