Supersonic Shear Wave Elastography of Response to Anti-cancer Therapy in a Xenograft Tumor Model

Foucauld Chamming's1, Marie-Aude Le-Frère-Belda2, Heldmuth Latorre-Ossa3

  • 1Cardiovascular Research Center-PARCC, Université Paris Descartes Sorbonne Paris Cité, UMR-S970, Paris, France; Radiology Department, Université Paris Descartes Sorbonne Paris Cité, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France.

Insights

Supersonic shear wave elastography (SSWE) can detect breast cancer tumor stiffness changes during anti-angiogenic therapy. Early softening indicates treatment response, but later stiffening may also reflect efficacy.

Area of Science:

  • Biomedical Engineering
  • Oncology
  • Medical Imaging

Background:

  • Assessing anti-cancer treatment efficacy non-invasively is crucial.
  • Tumor stiffness changes can indicate therapeutic response.
  • Supersonic shear wave elastography (SSWE) measures tissue stiffness.

Purpose of the Study:

  • To evaluate if SSWE can detect stiffness changes in a breast cancer model during anti-angiogenic therapy.
  • To correlate stiffness changes with treatment response and pathological findings.

Main Methods:

  • A human invasive carcinoma model was established in 22 mice.
  • Mice received either anti-angiogenic therapy or glucose for 24 days.
  • Tumor volume and stiffness were monitored using SSWE before and after treatment initiation.
  • Pathology was assessed at 12 and 24 days.

Main Results:

  • Treated tumors showed early softening, significantly differing from controls after 12 days (p=0.03).
  • Pathology revealed necrosis in treated tumors at 12 days.
  • Tumors later stiffened between days 12-24, despite continued efficacy, with minimal necrosis at day 24.

Conclusions:

  • SSWE effectively measures tumor stiffness changes in response to anti-cancer treatment.
  • Early softening correlates with treatment response, while later stiffening may also indicate efficacy.
  • Stiffness dynamics provide valuable insights into tumor response over time.

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