Paclitaxel in the lower limbs: harm outweighs the benefit

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Gepubliceerd in:The Lancet vol. 406, no. 10508 (Sep 13, 2025), p. 1064-1066
Hoofdauteur: Katsanos, Konstantinos
Andere auteurs: Spiliopoulos, Stavros
Gepubliceerd in:
Elsevier Limited
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024 7 |a 10.1016/S0140-6736(25)01684-8  |2 doi 
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100 1 |a Katsanos, Konstantinos  |u Department of Interventional Radiology, Patras University Hospital, Rion 26504, Greece 
245 1 |a Paclitaxel in the lower limbs: harm outweighs the benefit 
260 |b Elsevier Limited  |c Sep 13, 2025 
513 |a Commentary 
520 3 |a Of further significant concern, in the SWEDEPAD 2 trial at 5 years, all-cause mortality was significantly higher in the paclitaxel-coated group than in the uncoated group (HR 1·47 [95% CI 1·09 to 1·98]), echoing our original 2018 meta-analysis. 3 The authors employed a nationwide registry-based randomisation in Sweden and stratified between critical limb-threatening ischaemia and claudication with hard patient-centred endpoints, namely quality of life, major amputations, mortality, and limb re-interventions. 1,2 We applaud the registry-RCT design that leveraged the efficiency and data linkage of the existing Swedish registry infrastructure to produce the two largest randomised studies available to date in the peripheral arterial disease arena. In the BASIL-3 trial, neither paclitaxel-coated balloons (HR 0·84 [95% CI 0·61 to 1·16]), nor paclitaxel-coated stents (HR 0·83 [95% CI 0·60 to 1·15]) conferred any significant clinical benefit in time to major amputation or all-cause death. 4 The SWEDEPAD 2 trial also did not translate the well known anti-restenotic efficacy of paclitaxel into meaningful gains of quality of life. 2 We contend that quality of life is shaped by multiple factors, including, but not limited to, instrument (questionnaire) insensitivities, lifestyle adaptations, socioeconomic environment, psychological wellbeing, systemic progression of atherosclerosis, and other influences often unrelated to the treated limb. Alternative patient-reported functional outcomes, such as pain-free walking distance, have been proposed as more appropriate primary endpoints for claudication trials. 5 The SWEDEPAD 2 trial has once again showed a markedly elevated risk of all-cause mortality—approximately 1·5-fold—in paclitaxel-treated patients at 5 years. 2 Even though this mortality signal appears attenuated in very long-term follow-up, this likely reflects the well recognised statistical properties of hazard functions, in which early differences are progressively diluted over time. 6 Its absence in the SWEDEPAD 1 trial is plausibly explained by the natural history of critical limb-threatening ischaemia, in which multiple systemic comorbidities act as competing risks and might overshadow or mute any potential paclitaxel-related harm. 
653 |a Clinical trials 
653 |a Atherosclerosis 
653 |a Ischemia 
653 |a Mortality 
653 |a Psychological factors 
653 |a Balloon treatment 
653 |a Amputation 
653 |a Implants 
653 |a Medical equipment 
653 |a Intermittent claudication 
653 |a Patients 
653 |a Quality of life 
653 |a Arteriosclerosis 
653 |a Cardiovascular diseases 
653 |a Paclitaxel 
653 |a Coatings 
653 |a Randomization 
653 |a Comorbidity 
653 |a Meta-analysis 
653 |a Social 
700 1 |a Spiliopoulos, Stavros  |u Attikon University Hospital, Athens, Greece 
773 0 |t The Lancet  |g vol. 406, no. 10508 (Sep 13, 2025), p. 1064-1066 
786 0 |d ProQuest  |t Science Database 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/3249560235/abstract/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch 
856 4 0 |3 Full Text  |u https://www.proquest.com/docview/3249560235/fulltext/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch 
856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/3249560235/fulltextPDF/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch