Abstract

BackgroundPrevious studies have demonstrated that no-option angiitis-induced critical limb ischemia (NO-AICLI) could be significantly improved by transplantation of peripheral blood-derived stem cells (PBDSCs). Additionally, a randomized controlled trial (RCT) recently conducted by us suggested that peripheral blood-derived purified CD34+ cells (PCCs) were not inferior to non-purified peripheral blood mononuclear cells (PBMNCs) at limb salvage in treatment of NO-AICLI. However, most of these clinical trials whether RCT or single-arm studies were characterized with a small sample size and absence of long-term outcomes.MethodsTo analyze long-term clinical outcomes of PBDSCs transplantation for NO-AICLI, we reviewed clinical data of patients with NO-AICLI receiving PBDSCs transplantation at our center during the past decade. Meanwhile, we first compared the long-term safety and efficacy of intramuscular transplantation of PCCs versus PBMNCs in a sizable number of patients with NO-AICLI.ResultsFrom May 2009 to December 2019, a total of 160 patients with NO-AICLI patients were treated by PBDSCs transplantation (82 with PCCs, 78 with PBMNCs) at our center. Baseline characteristics between two groups were similar. Up to June 2020, the mean follow-up period was 46.6 ± 35.3 months. No critical adverse events were observed in either group. There was one death during the follow-up period. A total of eight major amputations occurred. The cumulative major amputation-free survival (MAFS) rate at 5 years after PBDSCs transplantation was 94.4%, without difference between two groups (P = .855). Wound healing, rest pain, pain-free walking time, ankle-brachial index, transcutaneous oxygen pressure, and quality of life (QoL) also significantly improved after PBDSCs transplantation.ConclusionsAutologous PBDSCs intramuscular transplantation could significantly decrease the major amputation rates and improve the QoL in patients with NO-AICLI. Long-term observation of a large sample of patients confirmed that the clinical benefits of PBDSCs transplantation were durable, without difference between the PCCs and PBMNCs groups.

Highlights

  • Previous studies have demonstrated that no-option angiitis-induced critical limb ischemia (NO-angiitis-induced Critical limb ischemia (CLI) (AICLI)) could be significantly improved by transplantation of peripheral blood-derived stem cells (PBDSCs)

  • Eightytwo patients received intramuscular transplantation of purified CD34+ cells (PCCs), while 78 patients were treated with peripheral blood mononuclear cells (PBMNCs)

  • PCCs, purified CD34+ cells; PBMNCs, peripheral blood mononuclear cells, PFWT, pain-free walking time; WBFPS, Wong-Baker faces pain rating scale; Ankle-brachial index (ABI), ankle-brachial index; TcPO2, transcutaneous pressure of oxygen. *P < .05 compared with the baseline; **P < .01 compared with the baseline; ‡P < .05 compared between two groups; ‡‡P < .01 compared between two groups the baseline characteristics of patients in PCCs and PBMNCs groups are similar in the current retrospective study, which ensures the comparability of outcomes after transplantation of two types of PBDSCs

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Summary

Introduction

Previous studies have demonstrated that no-option angiitis-induced critical limb ischemia (NO-AICLI) could be significantly improved by transplantation of peripheral blood-derived stem cells (PBDSCs). A randomized controlled trial (RCT) recently conducted by us suggested that peripheral blood-derived purified CD34+ cells (PCCs) were not inferior to non-purified peripheral blood mononuclear cells (PBMNCs) at limb salvage in treatment of NO-AICLI. Most of these clinical trials whether RCT or single-arm studies were characterized with a small sample size and absence of long-term outcomes. Compared with ASO, patients with TAO-induced CLI are remarkably younger and have much higher life expectations, posing a more urgent need for limb salvage and better quality of life (QoL) [6, 7].

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