Pace: randomized, controlled, multicentre, multinational, phase III study of PLX-PAD for critical limb ischaemia in patients unsuitable for revascularization: randomized clinical trial

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Lars Norgren - , Örebro University Hospital (Author)
  • Norbert Weiss - , Department of Internal Medicine III, University Vascular Centre (Author)
  • Sigrid Nikol - , Asklepios Klinik St. Georg (Author)
  • John C Lantis - , Mount Sinai Hospital NY (Author)
  • Manesh R Patel - , Duke University (Author)
  • Robert J Hinchliffe - , University of Bristol (Author)
  • Holger Reinecke - , University Hospital Münster (Author)
  • Hans Dieter Volk - , Charité – Universitätsmedizin Berlin (Author)
  • Petra Reinke - , Charité – Universitätsmedizin Berlin (Author)
  • Gian Paolo Fadini - , University of Padua, Veneto Institute of Molecular Medicine (Author)
  • Racheli Ofir - , Betalin Therapeutics (Author)
  • Daniel Rothenstein - , Pluri-Biotech (Author)
  • Nitsan Halevy - , Pluri-Biotech (Author)
  • Mitko Karagjozov - , Hospital Acibadem Sistina (Author)
  • John H Rundback - , Advanced Interventional and Vascular Services (AIVS) (Author)

Abstract

BACKGROUND: Revascularization is the primary treatment modality for chronic limb-threatening ischaemia (CLTI), but is not feasible in all patients. PLX-PAD is an off-the-shelf, placental-derived, mesenchymal stromal cell-like cell therapy. This study aimed to evaluate whether PLX-PAD would increase amputation-free survival in people with CLTI who were not candidates for revascularization.

METHODS: People with CLTI and minor tissue loss (Rutherford 5) who were unsuitable for revascularization were entered into a randomized, parallel-group, placebo-controlled, multinational, blinded, trial, in which PLX-PAD was compared with placebo (2 : 1 randomization), with 30 intramuscular injections (0.5 ml each) into the index leg on days 0 and 60. Planned follow-up was 12-36 months, and included vital status, amputations, lesion size, pain and quality-of-life assessments, haemodynamic parameters, and adverse events.

RESULTS: Of 213 patients enrolled, 143 were randomized to PLX-PAD and 70 to placebo. Demographics and baseline characteristics were balanced. Most patients were Caucasian (96.2%), male (76.1%), and ambulatory (85.9%). Most patients (76.6%) reported at least one adverse event, which were mostly expected events in CLTI, such as skin ulcer or gangrene. The probability of major amputation or death was similar for placebo and PLX-PAD (33 and 28.6% respectively; HR 0.93, 95% c.i. 0.53 to 1.63; P = 0.788). Revascularization and complete wound healing rates were similar in the two groups. A post hoc analysis of a subpopulation of 121 patients with a baseline haemoglobin A1c level below 6.5% showed improved 12-month amputation-free survival (HR 0.46, 0.21 to 0.99; P = 0.048).

CONCLUSION: Although there was no evidence that PLX-PAD reduced amputation-free survival in the entire study population, benefit was observed in patients without diabetes mellitus or whose diabetes was well controlled; this requires confirmation in further studies. Trial registration: NCT03006770 (http://www.clinicaltrials.gov); 2015-005532-18 (EudraCT Clinical Trials register - Search for 2015-005532-18).

Details

Original languageEnglish
Article numberznad437
JournalBritish Journal of Surgery
Volume111
Issue number2
Publication statusPublished - 1 Feb 2024
Peer-reviewedYes

External IDs

PubMedCentral PMC10828925
Scopus 85183696603

Keywords

Sustainable Development Goals

Keywords

  • Humans, Male, Female, Pregnancy, Chronic Limb-Threatening Ischemia, Peripheral Arterial Disease/therapy, Ischemia, Placenta/metabolism, Vascular Surgical Procedures, Treatment Outcome