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Peer-reviewedCC BYCancers

Radioembolization with Intra-Arterial Angiotensin II to Improve Tumor-Absorbed Dose (RADIANT): A Single-Arm Phase II Study Protocol.

  1. 1Department of Radiology and Nuclear Medicine, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

Abstract

Purpose

The effectiveness of transarterial radioembolization (TARE) depends largely on the tumor-to-non-tumor ratio (TNR): the ratio of microsphere concentration between tumor and non-tumorous liver tissue. Angiotensin II (AT-II) may improve TNR by inducing vasoconstriction primarily in arteries supplying healthy liver parenchyma. Tumor-feeding arteries, lacking neurovascular innervation, are largely unresponsive to AT-II, potentially resulting in preferential blood flow redistribution toward tumor tissue. The RADIANT study aims to evaluate whether intra-arterial AT-II infusion prior to yttrium-90 (⁹⁰Y) microsphere injection improves tumor selectivity during TARE in patients with primary or metastatic liver tumors.Materials and methods

This single-center, single-arm phase II study will include 15 patients with primary or metastatic liver tumors (any histological subtype, diameter ≥ 2 cm) referred for ⁹⁰Y glass radioembolization. Each patient serves as their own control: during work-up, technetium-99m macroaggregated albumin (99mTc-MAA) is administered without AT-II and TNR is measured on SPECT/CT. During the therapeutic procedure, AT-II is infused intra-arterially (10 µg/min over 100 s) immediately before ⁹⁰Y microsphere injection, and TNR is measured on post-treatment ⁹⁰Y PET/CT. The primary endpoint is the TNR improvement factor (TNR after ⁹⁰Y + AT-II divided by TNR after 99mTc-MAA). Secondary endpoints include toxicity and technical success of AT-II administration.Discussion

The RADIANT study will provide prospective evidence on the effect of intra-arterial AT-II infusion on tumor selectivity during ⁹⁰Y radioembolization.

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BibTeX
@article{wijnen2026radioembolization,
  title = {{Radioembolization with Intra-Arterial Angiotensin II to Improve Tumor-Absorbed Dose (RADIANT): A Single-Arm Phase II Study Protocol.}},
  author = {Niek Wijnen and Marnix G E H Lam and Khalil Ramdhani and Rutger C G Bruijnen and Martijn M A Dietze and Camiel E M Kerckhaert and Hugo W A M de Jong and Maarten L J Smits},
  journal = {Cancers},
  year = {2026},
  month = sep,
  doi = {10.3390/cancers18193129},
  url = {https://europepmc.org/article/MED/42882823},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Radioembolization with Intra-Arterial Angiotensin II to Improve Tumor-Absorbed Dose (RADIANT): A Single-Arm Phase II Study Protocol.
AU  - Niek Wijnen
AU  - Marnix G E H Lam
AU  - Khalil Ramdhani
AU  - Rutger C G Bruijnen
AU  - Martijn M A Dietze
AU  - Camiel E M Kerckhaert
AU  - Hugo W A M de Jong
AU  - Maarten L J Smits
PY  - 2026
DA  - 2026/09/27
JO  - Cancers
DO  - 10.3390/cancers18193129
UR  - https://europepmc.org/article/MED/42882823
AB  - Purpose  The effectiveness of transarterial radioembolization (TARE) depends largely on the tumor-to-non-tumor ratio (TNR): the ratio of microsphere concentration between tumor and non-tumorous liver tissue. Angiotensin II (AT-II) may improve TNR by inducing vasoconstriction primarily in arteries supplying healthy liver parenchyma. Tumor-feeding arteries, lacking neurovascular innervation, are largely unresponsive to AT-II, potentially resulting in preferential blood flow redistribution toward tumor tissue. The RADIANT study aims to evaluate whether intra-arterial AT-II infusion prior to yttrium-90 (⁹⁰Y) microsphere injection improves tumor selectivity during TARE in patients with primary or metastatic liver tumors.Materials and methods  This single-center, single-arm phase II study will include 15 patients with primary or metastatic liver tumors (any histological subtype, diameter ≥ 2 cm) referred for ⁹⁰Y glass radioembolization. Each patient serves as their own control: during work-up, technetium-99m macroaggregated albumin (99mTc-MAA) is administered without AT-II and TNR is measured on SPECT/CT. During the therapeutic procedure, AT-II is infused intra-arterially (10 µg/min over 100 s) immediately before ⁹⁰Y microsphere injection, and TNR is measured on post-treatment ⁹⁰Y PET/CT. The primary endpoint is the TNR improvement factor (TNR after ⁹⁰Y + AT-II divided by TNR after 99mTc-MAA). Secondary endpoints include toxicity and technical success of AT-II administration.Discussion  The RADIANT study will provide prospective evidence on the effect of intra-arterial AT-II infusion on tumor selectivity during ⁹⁰Y radioembolization.
SN  - 2072-6694
ER  -