Evidence map›Paper›PMID 41438485›Full record

ArticleAdvances in radiation oncology2026

Radioenhancing Hafnium Oxide Nanoparticles (NBTXR3) Followed by Stereotactic Body Radiation Therapy in Patients With Hepatocellular Carcinoma and Liver Metastases (NBTXR3-103): Phase 1 Dose-Escalation Trial.

Enrique Chajon, Marc Pracht, Yan Rolland, France Nguyen, Jean-Pierre Bronowicki, Jérôme Durand-Labrunie, Véronique Vendrely, Antonio Sa Cunha, Valérie Laurent, Emmanuel Rio and 9 more

Abstract read
In one paragraph

Article in Advances in radiation oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Enrique ChajonDepartment of Radiation Oncology, Centre Eugène Marquis, Rennes, France.
Marc PrachtDepartment of Medical Oncology, Centre Eugène Marquis, Rennes, France.
Yan RollandInterventional Radiology, Centre Eugène Marquis, Rennes, France.
France NguyenRadiotherapy Institut Gustave Roussy, Villejuif, France.
Jean-Pierre BronowickiDepartment of Hepato-gastroenterology, University Hospital, Nancy, France.
Jérôme Durand-LabrunieRadiotherapy Institut Gustave Roussy, Villejuif, France.
Véronique VendrelyRadiotherapy Department, Hôpital Haut-Lévêque, Universitary Hospital of Bordeaux, University of Bordeaux, Bordeaux, France.
Antonio Sa CunhaCentre Hépato-Biliaire Hôpital Paul Brousse, Villejuif, France.
Valérie LaurentDepartment of Radiology, University Hospital, Nancy, France.
Emmanuel RioRadiotherapy, Institut de cancérologie de l'Ouest, Nantes, France.
Samuel Le SourdDepartment of Medical Oncology, Centre Eugène Marquis, Rennes, France.
Pierre GustinRadiotherapy Institut Gustave Roussy, Villejuif, France.
Patricia C SaidNanobiotix SA, Paris, France.
Mikaela DimitriuNanobiotix SA, Paris, France.
Benjin D FacerNanobiotix SA, Paris, France.
Omar I VivarNanobiotix SA, Paris, France.
Didier PeiffertRadiotherapy, Institut de Cancérologie de Lorraine, Nancy, France.
Eric DeutschDepartment of Radiation Oncology, Gustave Roussy, Paris-Saclay University, INSERM1030, France.
Thierry de BaèreInterventional Radiology, Institut Gustave Roussy, Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Stereotactic body radiation therapy (SBRT) is a common treatment for unresectable liver cancers; however, delivering ablative doses while minimizing normal tissue toxicity is challenging. NBTXR3, a novel radioenhancer, demonstrated enhanced radiation therapy (RT) efficacy with minimal toxicity in healthy tissue. We evaluated NBTXR3 intratumoral injection followed by SBRT for hepatocellular carcinoma (HCC) or liver metastases. Methods and Materials: This phase 1, multicenter, dose-escalation trial enrolled adults with unresectable HCC or liver metastases. Five dose levels of NBTXR3 were evaluated (3 + 3 design): 10%, 15%, 22%, 33% and 42% of gross tumor volume (GTV) determined by magnetic resonance imaging. Patients received RT (15 Gy × 3 or 10 Gy × 5 over 5-15 days) starting 1 to 5 days after NBTXR3 injection. Primary endpoints included: incidence of early dose-limiting toxicities (DLTs) and determination of the recommended phase 2 dose (RP2D) of NBTXR3. Results: Between December 2015 and May 2020, 26 liver lesions in 23 patients with HCC (17 lesions in 15 patients) or liver metastases (9 lesions in 8 patients) were treated. No early DLTs were reported, and the maximum tolerated dose was not reached. The RP2D of NBTXR3 was 42% of GTV. During the treatment period, 6 patients experienced grade ≥3 toxicities; none were NBTXR3-related, one was RT-related (grade 3 fatigue), and 2 were injection procedure-related (grade 3 abdominal pain). During the follow-up period, 2 patients experienced treatment-related grade ≥3 AEs (grade 3 bile duct stenosis related to cancer/RT/NBTXR3, and grade 3 anemia related to cancer/RT/underlying liver disease). No treatment-related deaths were reported. The 12-week objective response rate in treated lesions was 58.3% (7/12) in patients with HCC, and 50.0% (4/8) in patients with liver metastases. Conclusions: NBTXR3 + RT has a manageable safety profile with no DLTs identified during dose escalation. The RP2D for treatment of HCC or liver metastases is 42% of GTV. Future studies will further evaluate efficacy.

Identifiers

PMID41438485
PMCPMC12721159

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.