Bertrand MATHON

Dr. Bertrand MATHON

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2019 in Clinical Cancer Research
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AIAhmed Idbaih
Ahmed Idbaih
MCMichael Canney
Michael Canney
LBLisa Belin
Lisa Belin
CDCarole Desseaux
Carole Desseaux
AVAlexandre Vignot
Alexandre Vignot
ACAlexandre Carpentier
Alexandre Carpentier
Purpose: The blood-brain barrier (BBB) limits the efficacy of drug therapies for glioblastoma (GBM). Pre-clinical data indicate that low-intensity pulsed ultrasound (LIPU) can transiently disrupt the BBB and increase intracerebral drug concentrations. Experimental Design: A first-in-man, single-arm, single-center trial (NCT02253212) was initiated to investigate the transient disruption of the BBB in patients with recurrent glioblastoma (rGBM). Patients were implanted with a 1 MHz, 11.5-mm diameter cranial ultrasound device (SonoCloud-1, CarThera, Paris, France). The device was activated monthly to transiently disrupt the BBB before intravenous (IV) carboplatin chemotherapy. Results: Between 2014 and 2016, 21 patients were registered for the study and implanted with the SonoCloud-1; 19 patients received at least one sonication. In 65 US sessions, BBB disruption was visible on T1w MRI for 52 sonications. Treatment-related adverse events observed were transient and manageable: a transient edema at H1 and at D15. No carboplatin-related neurotoxicity was observed. Patients with no or poor BBB disruption (n=8) visible on MRI had a median progression-free survival (PFS) of 2.73 months, and a median overall survival (OS) of 8.64 months. Patients with clear BBB disruption (n=11) had a median PFS of 4.11 months, and a median OS of 12.94 months. Conclusions:SonoCloud-1 treatments were well tolerated and may increase the effectiveness of systemic drug therapies, such as carboplatin, in the brain without inducing neurotoxicity.

6 January 2020 in Neurology
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CHCaroline Houillier
Caroline Houillier
CSCarole Soussain
Carole Soussain
HGHervé Ghesquières
Hervé Ghesquières
PSPierre Soubeyran
Pierre Soubeyran
OCOlivier Chinot
Olivier Chinot
EGEmmanuel Gyan
Emmanuel Gyan
Objective Real-life studies on patients with primary CNS lymphoma (PCNSL) are scarce. Our objective was to analyze, in a nationwide population-based study, the current medical practice in the management of PCNSL. Methods The French oculo-cerebral lymphoma network (LOC) database prospectively records all newly diagnosed PCNSL cases from 32 French centers. Data of patients diagnosed between 2011 and 2016 were retrospectively analyzed. Results We identified 1,002 immunocompetent patients (43% aged >70 years, median Karnofsky Performance Status [KPS] 60). First-line treatment was high-dose methotrexate-based chemotherapy in 92% of cases, with an increasing use of rituximab over time (66%). Patients 60 years of age, WBRT and HCT-ASCT consolidation were administered in only 9% and 2%, respectively. The complete response rate to initial chemotherapy was 50%. Median progression-free survival was 10.5 months. For relapse, second-line chemotherapy, HCT-ASCT, WBRT, and palliative care were offered to 55%, 17%, 10%, and 18% of patients, respectively. The median, 2-year, and 5-year overall survival was 25.3 months, 51%, and 38%, respectively (60 years: 15.4 months, 44%, and 28%). Age, KPS, sex, and response to induction CT were independent prognostic factors in multivariate analysis. Conclusions Our study confirms the increasing proportion of elderly within the PCNSL population and shows comparable outcome in this population-based study with those reported by clinical trials, reflecting a notable application of recent PCNSL advances in treatment.

23 February 2024 in Nature Communications
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ACAlexandre Carpentier
Alexandre Carpentier
RSRoger Stupp
Roger Stupp
ASAdam M. Sonabend
Adam M. Sonabend
HDHenry Dufour
Henry Dufour
OCOlivier Chinot
Olivier Chinot
AIAhmed Idbaih
Ahmed Idbaih
Here, the results of a phase 1/2 single-arm trial (NCT03744026) assessing the safety and efficacy of blood-brain barrier (BBB) disruption with an implantable ultrasound system in recurrent glioblastoma patients receiving carboplatin are reported. A nine-emitter ultrasound implant was placed at the end of tumor resection replacing the bone flap. After surgery, activation to disrupt the BBB was performed every four weeks either before or after carboplatin infusion. The primary objective of the Phase 1 was to evaluate the safety of escalating numbers of ultrasound emitters using a standard 3 + 3 dose escalation. The primary objective of the Phase 2 was to evaluate the efficacy of BBB opening using magnetic resonance imaging (MRI). The secondary objectives included safety and clinical efficacy. Thirty-three patients received a total of 90 monthly sonications with carboplatin administration and up to nine emitters activated without observed DLT. Grade 3 procedure-related adverse events consisted of pre syncope (n = 3), fatigue (n = 1), wound infection (n = 2), and pain at time of device connection (n = 7). BBB opening endpoint was met with 90% of emitters showing BBB disruption on MRI after sonication. In the 12 patients who received carboplatin just prior to sonication, the progression-free survival was 3.1 months, the 1-year overall survival rate was 58% and median overall survival was 14.0 months from surgery.

9 May 2025 in Nature Genetics
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MNMasashi Nomura
Masashi Nomura
ASAvishay Spitzer
Avishay Spitzer
KJKevin C. Johnson
Kevin C. Johnson
LGLuciano Garofano
Luciano Garofano
DNDjamel Nehar-Belaid
Djamel Nehar-Belaid
ITItay Tirosh
Itay Tirosh
In isocitrate dehydrogenase wildtype glioblastoma (GBM), cellular heterogeneity across and within tumors may drive therapeutic resistance. Here we analyzed 121 primary and recurrent GBM samples from 59 patients using single-nucleus RNA sequencing and bulk tumor DNA sequencing to characterize GBM transcriptional heterogeneity. First, GBMs can be classified by their broad cellular composition, encompassing malignant and nonmalignant cell types. Second, in each cell type we describe the diversity of cellular states and their pathway activation, particularly an expanded set of malignant cell states, including glial progenitor cell-like, neuronal-like and cilia-like. Third, the remaining variation between GBMs highlights three baseline gene expression programs. These three layers of heterogeneity are interrelated and partially associated with specific genetic aberrations, thereby defining three stereotypic GBM ecosystems. This work provides an unparalleled view of the multilayered transcriptional architecture of GBM. How this architecture evolves during disease progression is addressed in the companion manuscript by Spitzer et al.

1 December 2020 in Radiology
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LCLydia Chougar
Lydia Chougar
NSNatalia Shor
Natalia Shor
NWNicolas Weiss
Nicolas Weiss
DGDamien Galanaud
Damien Galanaud
DLDelphine Leclercq
Delphine Leclercq
FGFor the CoCo Neurosciences Study Group
For the CoCo Neurosciences Study Group
Background This study provides a detailed imaging assessment in a large series of COVID-19 patients with neurological manifestations. Purpose To review the MRI findings associated with acute neurol...

4 January 2020 in Neurosurgical Review
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MRMaximilien Riche
Maximilien Riche
AAAymeric Amelot
Aymeric Amelot
MPMatthieu Peyre
Matthieu Peyre
LCLaurent Capelle
Laurent Capelle
ACAlexandre Carpentier
Alexandre Carpentier
BMBertrand MATHON
Bertrand MATHON