Alexandre Ingels

Dr. Alexandre Ingels

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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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JCJean Courcier
Jean Courcier
ATAlexandre de la Taille
Alexandre de la Taille
MNMaya Nourieh
Maya Nourieh
ILIngrid Leguerney
Ingrid Leguerney
NLNathalie Lassau
Nathalie Lassau
AIAlexandre Ingels
Alexandre Ingels
Carbonic Anhydrase IX (CAIX) is a well-described enzyme in renal cell carcinoma, with its expression being regulated by the hypoxia-inducible factor 1 alpha, it is known for interfering with hypoxia processes. Renal carcinoma encompasses a broad spectrum of histological entities and is also described as a heterogeneous malignant tumor. Recently, various combinations of checkpoint inhibitors and targeted therapies have been validated to manage this disease. Reliable markers to confirm the diagnosis, estimate the prognosis, predict or monitor the treatment response are required. Molecular imaging developments allow a comprehensive analysis of the tumor, overcoming the spatial heterogeneity issue. CAIX, being highly expressed at the tumor cell surfaces of clear cell renal carcinoma, also represents a potential treatment target. In this manuscript we reviewed the current knowledge from the literature on the pathophysiological interactions between renal cell carcinoma and CAIX, the role of CAIX as a marker for diagnosis, prognosis, treatment monitoring and molecular imaging, and the potential target for therapeutic strategies.

16 June 2023 in Nature Reviews Urology
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RCRiccardo Campi
Riccardo Campi
GRGiacomo Rebez
Giacomo Rebez
Tobias KlatteTobias Klatte
Tobias Klatte
EREduard Roussel
Eduard Roussel
IOIdir Ouizad
Idir Ouizad
MMMaria Carmen Mir
Maria Carmen Mir

11 May 2022 in Nature Reviews Urology
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AIAlexandre Ingels
Alexandre Ingels
RCRiccardo Campi
Riccardo Campi
UCUmberto Capitanio
Umberto Capitanio
DADaniele Amparore
Daniele Amparore
Riccardo BertoloRiccardo Bertolo
Riccardo Bertolo
ATAlexandre de la Taille
Alexandre de la Taille

5 November 2021 in Journal of Cachexia, Sarcopenia and Muscle
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AMAntoine Morel
Antoine Morel
YOYaniss Ouamri
Yaniss Ouamri
FCFlorence Canouï‐Poitrine
Florence Canouï‐Poitrine
SMSébastien Mulé
Sébastien Mulé
CCCécile Maud Champy
Cécile Maud Champy
TSThomas Stehlé
Thomas Stehlé
Background: Patients with end‐stage renal disease may display both a loss of skeletal muscle mass and an increase in muscle fat deposits. We aimed to analyse the impact of low skeletal muscle mass index (SMI, surrogate marker of sarcopenia) and low muscle density (MD, surrogate marker of myosteatosis) on patient survival after kidney transplantation (KT).Methods: In a retrospective cohort of 200 kidney transplant recipients (KTr), we measured on an unenhanced cross‐sectional computed tomography scan taken at the level of the third lumbar vertebra within the previous year or at the time of KT, both SMI (muscle cross‐sectional area normalized for height2, reported in cm2/m2) and MD (mean attenuation of muscle cross‐sectional area, expressed in Hounsfield units). We determined age‐specific and sex‐specific normality thresholds on 130 healthy subjects. The baseline factors associated with low MD were assessed by logistic regression analysis. Cox proportional hazard univariable and multivariable models were constructed to identify predictive factors of patient survival.Results: Among the 200 patients of the cohort, 123 were male (62%), and mean age was 54.8 ± 13.8 years. A total of 181 KTr required renal replacement therapy before KT (91%), and 36 KTr (18%) received repeat kidney transplant after previous failed KT. Mean MD was 30.6 ± 9 HU in men and 29.7 ± 8.3 HU in women, whereas SMI was 49.7 ± 8.6 cm2/m2 in men and 42.3 ± 7.3 cm2/m2 in women. MD was below the 2.5th percentile for the healthy population in 49 KTr (25%), defining the myosteatosis group, while SMI was below the 2.5th percentile for the reference population in 10 KTr (5%). Independent risk factors for myosteatosis were two or more KT [adjusted odds ratio (aOR) 5.2, 95% confidence interval (95% CI): 2.22–12.4, P = 0.0001], a history of stroke (aOR 3.7, 95% CI: 1.30–10.7, P = 0.015), and body mass index > 25 kg/m2 (aOR 2.94, 95% CI: 1.4–6.18, P = 0.004). Myosteatosis was independently associated with mortality [adjusted hazard ratio (aHR) 2.12, 95% CI: 1.06–4.24, P = 0.033], as were cardiovascular disease (HR 2.06, 95% CI: 1.02–4.15, P = 0.043) and age (aHR 1.06, 95% CI: 1.03–1.09, P = 0.0003). Low SMI was not associated with mortality.Conclusions: Myosteatosis, which was more prevalent than low skeletal muscle mass, might be an important prognostic marker in patients undergoing KT.

25 March 2022 in Journal of Clinical Medicine
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CMConstantijn Hendrikus Jacobus Muselaers
Constantijn Hendrikus Jacobus Muselaers
SESelcuk Erdem
Selcuk Erdem
Riccardo BertoloRiccardo Bertolo
Riccardo Bertolo
AIAlexandre Ingels
Alexandre Ingels
ÖKÖnder Kara
Önder Kara
OGon behalf of the European Association of Urology (EAU) Young Academic Urologists (YAU) Renal Cancer Working Group
on behalf of the European Association of Urology (EAU) Young Academic Urologists (YAU) Renal Cancer Working Group
Although the vast majority of prostate-specific membrane antigen (PSMA) positron emission tomography (PET) imaging occurs in the field of prostate cancer, PSMA is also highly expressed on the cell surface of the microvasculature of several other solid tumors, including renal cell carcinoma (RCC). This makes it a potentially interesting imaging target for the staging and monitoring of RCC. The objective of this review is to provide an overview of the current evidence regarding the use of PSMA PET/Computed Tomography in RCC patients.

8 November 2022 in Scientific Reports
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AIAlexandre Ingels
Alexandre Ingels
KBK. Bensalah
K. Bensalah
JBJ. B. Beauval
J. B. Beauval
PPP. Paparel
P. Paparel
MRM. Rouprêt
M. Rouprêt
LAL. Albiges
L. Albiges
We compared the outcomes of robotic-assisted partial nephrectomy (RPN) and open partial nephrectomy (OPN) using contemporary data to respond to unmet clinical needs. Data from patients included in the registry who underwent partial nephrectomy between January 01, 2014 and June 30, 2017 within 20 centres of the French Network for Research on Kidney Cancer UroCCR were collected (NCT03293563). Statistical methods included adjusted multivariable analyses. Rates of peri- and post-operative transfusion, and of surgical revision, were lower in the RPN (n = 1434) than the OPN (n = 571) group (2.9% vs. 6.0%, p = 0.0012; 3.8% vs. 11.5%, p < 0.0001; 2.4% vs. 6.7%, p < 0.0001, respectively). In multivariable analyses, RPN was independently associated with fewer early post-operative complications than OPN (overall: odds-ratio [95% confidence interval, CI] = 0.48 [0.35–0.66]; severe: 0.29 [0.16–0.54], p < 0.0001 for both) and shorter hospital stays (34% [30%; 37%], p < 0.0001). RPN was also a significantly associated with a decresedrisk of post-operative acute renal failure, and new-onset chronic kidney disease at 3 and 12 months post-surgery. There were no between-group differences in oncological outcomes. In comparison with OPN, RPN was associated with improved peri- and post-operative morbidity, better functional outcomes, and shorter hospital stays. Our results support the use of RPN, even for large and complex tumours.