Comparative Evaluation of Two Paclitaxel-Coated Stents in an Experimental Setting

Author:

Pouhin Alexandre1ORCID,Coscas Raphaël23,Crespy Valentin1,Poupardin Olivia4,Pais-De-Barros Jean-Paul5,Bouchot Olivier6,Bernard Alain7,Steinmetz Eric1

Affiliation:

1. Department of Vascular Surgery, Dijon University Hospital, Dijon, France

2. Department of Vascular Surgery, Ambroise Paré University Hospital, AP-HP, Boulogne-Billancourt, France

3. UMR 1018, Inserm-Paris11—CESP, Versailles Saint-Quentin-en-Yvelines University, Paris-Saclay University, Paris, France

4. Research Society, Farming Division, Auxois-Sud, Biossan, Créancey, France

5. UMR 1231 Inserm, University of Burgundy, Dijon, France

6. Department of Cardiac Surgery, Dijon University Hospital, Dijon, France

7. Department of Thoracic Surgery, Dijon University Hospital, Dijon, France

Abstract

Introduction: Unlike paclitaxel-coated balloons, pre-clinical data comparing different paclitaxel-coated stents (PCSs) are weak. The study objective was to compare the features of the 2 main PCSs: Eluvia® (Boston Scientific, Marlborough, MA) versus ZilverPTX® (Cook Medical, Bloomington, IN). Method: Analysis was carried out on 12 pigs divided into 2 groups: Eluvia® (n=6) and ZilverPTX® (n=6). The pigs received the PCS corresponding to their group in each external iliac artery and were paired one by one, to examine 6 different post-implantation timepoints: after 30 minutes, 6 hours, 24 hours, 3 days, 7 days, and 14 days. The paclitaxel concentration measurements and the histological analysis were carried out under blind testing on the plasma, arterial, lymph node, and muscle samples. A linear regression model and Wilcoxon Mann-Whitney test were used to study the variables. Results: The plasma paclitaxel rate decrease over 24 hours after PCS implantation was significantly different between the two groups, expressed by the correlation coefficient 0.19 (0.14–0.23; p<0.001) with an undetectable concentration at the 10th hour for Eluvia® versus 3 days for ZilverPTX®. Significantly higher paclitaxel concentrations with ZilverPTX® PCS were observed in muscle samples at each timepoint: extensor digitorum brevis 3.2 (1.17–5.23; p=0.005), biceps femoris 4.27 (2.27–6.26; p<0.001), semi-tendinosus 3.79 (1.85–5.73; p=0.001), tibialis anterior 3.0 (1.37–4.64; p=0.001), and in the femoral nodes 2.27±1.74 ng/g versus 0.14±0.13 ng/g (p<0.001). Histological analysis revealed a trend for more marked intimal inflammation in the arteries stented with ZilverPTX® (p=0.063), especially after the 7th and 14th days. Conclusion: Such a difference in the concentration of paclitaxel in the plasma, muscles, and lymph nodes between the two stents was higher than expected based on differences in device design. The clinical consequences of these results remain to be elucidated, particularly regarding the concerning presence of paclitaxel in muscles and adjacent lymph nodes. Clinical Impact This experimental study compares 2 paclitaxel-coated stents. It demonstrates that differences in stent designs and drug features (coatings and concentrations) translate into differences in terms of concentrations of paclitaxel in the plasma, muscles, and lymph nodes. Our results favor the Eluvia® stent over the ZilverPTX® stent, although more studies are required to confirm this conclusion.

Funder

Association Chirurgicale Pour Le Développement et L’Amélioration des Techniques de Dépistage et de Traitement des Maladies Cardio-vasculaires

Association Bourgogne Coeur

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,Surgery

Reference33 articles.

1. Editor's Choice – 2017 ESC Guidelines on the Diagnosis and Treatment of Peripheral Arterial Diseases, in collaboration with the European Society for Vascular Surgery (ESVS)

2. Microtubule Active Agents: Beyond the Taxane Frontier

3. Food and Drug Administration. Paclitaxel-coated balloons stents for peripheral arterial disease. Date unknown. https://www.fda.gov/medical-devices/cardiovascular-devices/paclitaxel-coated-balloons-and-stents-peripheral-arterial-disease. Accessed August 21, 2023.

4. GOV.UK. Paclitaxel drug-coated balloons (DCBs) or drug-eluting stents (DESs): reconfirmed position on use in patients with intermittent claudication and critical limb ischaemia (DSI/2021/001). Date unknown. https://www.gov.uk/drug-device-alerts/paclitaxel-drug-coated-balloons-dcbs-or-drug-eluting-stents-dess-reconfirmed-position-on-use-in-patients-with-intermittent-claudication-and-critical-limb-ischaemia. Accessed August 21, 2023.

5. Risk of Death Following Application of Paclitaxel‐Coated Balloons and Stents in the Femoropopliteal Artery of the Leg: A Systematic Review and Meta‐Analysis of Randomized Controlled Trials

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