MagicTouch PTA Sirolimus Coated Balloon for Femoropopliteal and Below the Knee Disease: Results From XTOSI Pilot Study Up To 12 Months

被引:22
作者
Choke, Edward [1 ]
Tang, Tjun Yip [1 ,2 ]
Peh, Eilane [1 ]
Damodharan, Karthikeyan [1 ]
Cheng, Shin Chuen [1 ]
Tay, Jia Sheng [1 ]
Finn, Aloke, V [3 ,4 ]
机构
[1] Sengkang Gen Hosp, Singapore, Singapore
[2] Singapore Gen Hosp, Singapore, Singapore
[3] CVPath Inst Inc, Gaithersburg, MD USA
[4] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
关键词
sirolimus; drug coated balloons; peripheral arterial occlusive disease; femoropopliteal; below the knee; INFRAPOPLITEAL ARTERIES; ELUTING STENTS; PACLITAXEL; METAANALYSIS; ANGIOPLASTY;
D O I
10.1177/15266028211064816
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction: Sirolimus coated balloon (SCB) is a promising treatment option to prevent restenosis for peripheral arterial occlusive disease (PAOD). This is a pilot first-in-human study of MagicTouch percutaneous transluminal angioplasty (PTA) SCB for treatment of PAOD for both femoropopliteal and below the knee arteries (BTK). Material and Methods: Xtreme Touch-Neo [MagicTouch PTA] Sirolimus Coated Balloon (XTOSI) pilot study is a prospective, single-arm, open-label, single-center trial evaluating MagicTouch PTA SCB for symptomatic PAOD. Primary endpoint was defined as primary patency at 6 months (duplex ultrasound peak systolic velocity ratio <= 2.4). Secondary endpoints included clinically driven target lesion revascularization (CD-TLR), amputation free survival (AFS), all-cause mortality, and limb salvage success. Results: Fifty patients were recruited. The mean age was 67 (n=31 [62%] males). SCB was applied to femoropopliteal in 20 patients (40%) and BTK in 30 patients (60%). Majority of treatments (94%) were performed for limb salvage indications (Rutherford scores 5 or 6). This was a high risk cohort, in which 90% had diabetes, 36% had coronary artery disease, 20% had end stage renal failure, and American Society of Anaesthesiologists (ASA) score was 3 or more in 80%. Mean lesion length treated was 227 +/- 81 mm, of which 36% were total occlusions. Technical and device success were both 100%. At 30 days, mortality was 2% and major limb amputation was also 2%. Six-month primary patency was 80% (88.2% for femoropopliteal; 74% for BTK). At 12 months, freedom from CD-TLR was 89.7% (94.1% for femoropopliteal; 86.3% for BTK), AFS was 81.6% (90.0% for femoropopliteal; 75.9% for BTK), all-cause mortality was 14.3% (10.0% for femoropopliteal; 17.2% for BTK), and limb salvage success was 92.9% (94.4% for femoropopliteal; 91.7% for BTK). There was a statistically significant increase between baseline and 6-month toe pressures for both femoropopliteal (57.3 +/- 23.3 mm Hg vs 82.5 +/- 37.8 mm Hg; p<.001) and BTK lesions (52.8 +/- 19.2 mm Hg vs 70.7 +/- 37 mm Hg; p<.037). At 12 months, wound healing rate was 33/39 (84.6%). Conclusions: MagicTouch PTA SCB in the XTOSI study showed promising 6-month primary patency and encouraging 12-month freedom from CD-TLR, AFS, and limb salvage rates. No early safety concerns were raised. Randomized trials are needed to investigate the safety and efficacy of SCB for treatment of PAOD.
引用
收藏
页码:780 / 789
页数:10
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