Skip to main content
OpenTrials
Completed

NCT Number: NCT03818386

Radiotherapy of Multiple Brain Metastases Using AGuIX®

This is a Prospective Randomized Open Blinded Endpoint phase II clinical trial. The study will be adaptive: an interim analysis is planned after enrolment of 20 patients in each arm of treatment (WBRT and AGuIX® + WBRT), to select and continue the study with group(s) that present the best response rate to the experimental treatment (AGuIX® + WBRT).

The main endpoint will be evaluated by a blinded endpoint committee.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hospices Civils de Lyon-Hôpital Lyon Sud, Lyon, France

Loading trial locations.

About this study

The occurrence of brain metastases is a common event in the history of cancer and negatively affects the life expectancy of patients. Their incidence varies between 15 and 50% according to the histologic types. Surgery, stereotactic radiosurgery, radiotherapy and chemotherapy are the main treatments currently proposed.

For patients with multiple brain metastases, whole brain radiation therapy (WBRT) remains the standard of care. However, the median overall survival is less than 6 months and new approaches need to be developed to improve treatment of these patients.

In this context, the weak control of the disease comes from three main factors: the multiplicity of the brain lesions, the radioresistance of certain histologies and the poor distribution of cytotoxic agents in brain metastases.

The use of radiosensitizing agents is here of great interest. The radiosensitizing agent chosen in this study is AGuIX®. It is a Gadolinium-chelated polysiloxane based nanoparticle developed by NH TherAguix company for its theranostic properties (radiosensitization and diagnosis by multimodal imaging). Preclinical studies have demonstrated the radiosensitizing effect of AGuIX® in vivo in 8 tumor models xenografted in rodents, and particularly in brain tumors.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with brain metastases, from a histologically confirmed solid tumor, eligible for WBRT
  • At least 18 years old
  • Signed informed consent after informing the patient
  • ECOG (Eastern Cooperative Oncology Group) performance status 0-2
  • Extracranial disease:
  • Complete or partial response or stability under systemic treatment
  • No extracranial disease
  • Or first line of treatment
  • Life expectancy greater than 6 weeks
  • Effective contraceptive method for all patient of childbearing potential
  • Affiliated to a social security regimen

Exclusion criteria

  • Leptomeningeal metastasis
  • Evidence of metastasis with recent large hemorrhage
  • Progressive and threatening extracranial disease under systemic treatment
  • Previous cranial irradiation (except stereotactic irradiation)
  • Known contra-indication, sensitivity or allergy to gadolinium
  • Known contra-indication for Magnetic Resonance Imaging
  • Renal insufficiency (glomerular filtration rate ≤ 50 mL/min/1.73m²)
  • Pregnancy or breastfeeding
  • Subject under administrative or judicial control

Treatment and study plan

AGuIX®

Drug

3 intravenous injection at 100mg/kg

  • D0: AGuIX® injection followed by MRI (within 7 days before commencement of WBRT)
  • Fr1: AGuIX® injection before the first radiation session
  • Fr6: AGuIX® injection before the sixth radiation session

Other names: Gadolinium-chelated polysiloxane based nanoparticles

Whole brain radiation therapy

Radiation

30 Gy in 10 fractions of 3 Gy over 2-3 weeks

Other names: WBRT

Primary outcomes

  1. Best objective intracranial response rate - intent-to-treat

    Time frame: at 6 weeks

    Evaluation of brain metastases response, according to RECIST v1.1 criteria (or modified RECIST) by MRI, with MRI centralized reading

  2. Best objective intracranial response rate - intent-to-treat

    Time frame: at 3 months

    Evaluation of brain metastases response, according to RECIST v1.1 criteria (or modified RECIST) by MRI, with MRI centralized reading

Secondary outcomes

  1. Evaluation of the quality of life

    Time frame: at D0, 6 weeks, 3, 6, 9, 12 months

    Quality of life test score EORTC QLQ C30

  2. Evaluation of the quality of life

    Time frame: at day 0, 6 weeks, 3, 6, 9, 12 months

    Quality of life test score EORTC QLQ BN20

  3. Neurocognitive evaluation

    Time frame: at Day 0, 6 weeks, 3, 6, 9, 12 months

    Neurocognitive test (MoCA)

  4. Best objective intracranial response rate - per-protocol

    Time frame: at 6 weeks and 3 months

    Evaluation of brain metastases response on per-protocol population, according to RECIST v1.1 criteria (or modified RECIST), by MRI with centralized reading

  5. Evaluation of the intracranial response rate

    Time frame: for 12 months

    Evaluation of brain metastases response, according to RANO, to RECIST v1.1 criteria, and as the evolution of the sum of longest diameters (for all metastases with a sum of diameters > 1cm), by MRI, at 6 weeks and 3, 6, 9 and 12 months

  6. Evaluation of individual metastasis response

    Time frame: at 6 weeks and 3, 6, 9 and 12 months

    Evaluation of individual brain metastasis response, for all metastases with the sum of diameters > 1cm, by MRI rate

  7. Intracranial progression-free survival

    Time frame: at 12 months

    Evaluation of the time between the start of the treatment and the occurence of intracranial progression or neuriologic death

  8. Intracranial progression-free survival, brain survival

    Time frame: at 12 months

    Death related to brain metastases progression

  9. Overall survival

    Time frame: at 12 months

    Death

  10. Change in steroid dependence

    Time frame: at 6 weeks and 3, 6, 9 and 12 months

    Reporting of daily steroid dose

  11. Incidence of adverse events

    Time frame: at 6 weeks and 3, 6, 9 and 12 months

    Reporting of adverse events by type, frequency and severity for both treatments (WBRT and AGuIX® + WBRT)

  12. MRI study of the distribution of the product in brain metastases

    Time frame: Day 0

    MRI evaluation of contrast enhancement at D0 after AGuIX® injection

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Collaborators

  • NH TherAguix SAS

Registry information

Official study title

Radiotherapy of Multiple Brain Metastases Using AGuIX® Gadolinium-chelated Polysiloxane Based Nanoparticles: a Prospective Randomized Phase II Clinical Trial.

Acronym: NANORAD2

Important dates

Study start
2019
Primary completion
2024
Study completion
2025
First posted
Jan 28, 2019
Registry last updated
Sep 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.