Liver Tumor Procedure Approved by FDA in 2023 Shows Promise in First Three Years

There are questions about which patients would benefit most from the procedure, though.

Key Highlights

  • Histotripsy demonstrated low rates of laboratory toxicity and procedural complications in a large patient cohort.
  • Nearly 70% of treatments were performed on patients with metastatic liver cancer, raising questions about patient selection criteria.
  • Researchers emphasize the importance of defining which patients are most likely to benefit from histotripsy to optimize outcomes.
  • The study provides real-world evidence supporting the safety of histotripsy following its FDA approval in 2023.
  • Further research is needed to understand long-term benefits and identify ideal candidates for this noninvasive liver tumor treatment.

Researchers at UVA Health have reviewed outcomes from a new, noninvasive way to treat liver tumors called histotripsy and concluded the procedure was associated with low rates of laboratory toxicity and procedural complications.

The findings also highlight the need to better define which patients are most likely to benefit from the procedure. 

The FDA cleared the procedure in 2023, but researchers wanted to see how results played out in the real world. They examined outcomes from 972 patients who underwent the procedure between 2023 and 2026. They looked at factors such as patient survival, liver function before and after histotripsy, and the chances of kidney injury.

Nearly 70% of treatments were performed in patients with metastatic cancer involving the liver. This raises questions about which patients with metastatic disease are most likely to benefit from a treatment directed specifically at liver tumors.

About the Author

Matt MacKenzie

Matt MacKenzie

Associate Editor

Matt is Associate Editor for Healthcare Purchasing News.

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