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供体心脏的体外灌流用于人体心脏移植(PROCEED II):一项前瞻性、开放标签、多中心、随机、非劣效性试验。

Ex-vivo perfusion of donor hearts for human heart transplantation (PROCEED II): a prospective, open-label, multicentre, randomised non-inferiority trial.

机构信息

UCLA Medical Center, Los Angeles, CA, USA.

The Cedars-Sinai Heart Institute, Los Angeles, CA, USA.

出版信息

Lancet. 2015 Jun 27;385(9987):2577-84. doi: 10.1016/S0140-6736(15)60261-6. Epub 2015 Apr 14.

Abstract

BACKGROUND

The Organ Care System is the only clinical platform for ex-vivo perfusion of human donor hearts. The system preserves the donor heart in a warm beating state during transport from the donor hospital to the recipient hospital. We aimed to assess the clinical outcomes of the Organ Care System compared with standard cold storage of human donor hearts for transplantation.

METHODS

We did this prospective, open-label, multicentre, randomised non-inferiority trial at ten heart-transplant centres in the USA and Europe. Eligible heart-transplant candidates (aged >18 years) were randomly assigned (1:1) to receive donor hearts preserved with either the Organ Care System or standard cold storage. Participants, investigators, and medical staff were not masked to group assignment. The primary endpoint was 30 day patient and graft survival, with a 10% non-inferiority margin. We did analyses in the intention-to-treat, as-treated, and per-protocol populations. This trial is registered with ClinicalTrials.gov, number NCT00855712.

FINDINGS

Between June 29, 2010, and Sept 16, 2013, we randomly assigned 130 patients to the Organ Care System group (n=67) or the standard cold storage group (n=63). 30 day patient and graft survival rates were 94% (n=63) in the Organ Care System group and 97% (n=61) in the standard cold storage group (difference 2·8%, one-sided 95% upper confidence bound 8·8; p=0·45). Eight (13%) patients in the Organ Care System group and nine (14%) patients in the standard cold storage group had cardiac-related serious adverse events.

INTERPRETATION

Heart transplantation using donor hearts adequately preserved with the Organ Care System or with standard cold storage yield similar short-term clinical outcomes. The metabolic assessment capability of the Organ Care System needs further study.

FUNDING

TransMedics.

摘要

背景

器官保存系统是唯一用于体外灌注人类供体心脏的临床平台。该系统可使供体心脏在从供体医院运输到受体医院的过程中保持温暖跳动状态。我们旨在评估器官保存系统与用于移植的人类供体心脏标准冷藏相比的临床结果。

方法

我们在美国和欧洲的 10 个心脏移植中心进行了这项前瞻性、开放标签、多中心、随机非劣效性试验。符合条件的心脏移植候选者(年龄>18 岁)被随机分配(1:1)接受使用器官保存系统或标准冷藏保存的供体心脏。参与者、研究者和医务人员对分组分配不知情。主要终点是 30 天患者和移植物存活率,非劣效性边界为 10%。我们在意向治疗、实际治疗和方案人群中进行了分析。该试验在 ClinicalTrials.gov 注册,编号为 NCT00855712。

结果

在 2010 年 6 月 29 日至 2013 年 9 月 16 日期间,我们随机将 130 名患者分配至器官保存系统组(n=67)或标准冷藏组(n=63)。器官保存系统组 30 天患者和移植物存活率为 94%(n=63),标准冷藏组为 97%(n=61)(差异 2.8%,单侧 95%置信上限 8.8;p=0.45)。器官保存系统组有 8 名(13%)患者和标准冷藏组有 9 名(14%)患者发生与心脏相关的严重不良事件。

解释

使用适当保存的器官保存系统或标准冷藏保存的供体心脏进行心脏移植可产生相似的短期临床结果。器官保存系统的代谢评估能力需要进一步研究。

资金来源

TransMedics。

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