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多中心试验中的急性移植物抗宿主病诊断和判定:来自 BMT CTN 1202 生物库研究的报告。

Acute GVHD Diagnosis and Adjudication in a Multicenter Trial: A Report From the BMT CTN 1202 Biorepository Study.

机构信息

Blood and Marrow Transplantation and Cell Therapy Program, Columbia University Irving Medical Center, New York, NY.

Department of Medicine, CIBMTR (Center for International Blood and Marrow Transplant Research), Medical College of Wisconsin, Milwaukee, WI.

出版信息

J Clin Oncol. 2021 Jun 10;39(17):1878-1887. doi: 10.1200/JCO.20.00619. Epub 2021 Jan 28.

Abstract

PURPOSE

Accurate and reproducible methods to diagnose, grade, and report acute graft-versus-host disease (GVHD) are critical for the evaluation of therapies and biomarkers.

PATIENTS AND METHODS

The Blood and Marrow Transplant Clinical Trials Network 1202 study is an observational study of 1,709 allogeneic hematopoietic cell transplantation recipients that implemented weekly data reporting and near real-time data adjudication by an end point review committee (ERC), assigning a confidence level (confirmed, probable, possible, or negative) to the diagnosis of acute GVHD at onset.

RESULTS

During the first 100 days, symptoms consistent with GVHD developed in 90% of cases but were often determined by centers to be due to causes other than GVHD. Indeed, GVHD was under consideration in only 23% of cases at symptom onset. Diagnostic biopsies were obtained in 40% of cases, but treatment often was incongruous with biopsy findings and 10.5% of biopsies were equivocal. Importantly, more than 40% of steroid courses were started for reasons other than GVHD. The ERC modified the determination of GVHD diagnosis and/or grade in 12.3% of onset cases. The cumulative incidence of acute GVHD as reported by the centers was 62%. When the ERC adjudicated GVHD onset to be present only if the confidence level was probable or confirmed, the incidence of GVHD declined to 49%.

CONCLUSION

This study demonstrates that the incidence of GVHD may be overestimated at symptom onset, establishes a contemporary benchmark for acute GVHD, and suggests a structured framework for reporting and adjudication of GVHD that could be used in prospective trials.

摘要

目的

准确且可重现的急性移植物抗宿主病(GVHD)诊断、分级和报告方法对于评估治疗方法和生物标志物至关重要。

患者和方法

血液和骨髓移植临床研究网络 1202 研究是一项针对 1709 例异基因造血细胞移植受者的观察性研究,通过终点审查委员会(ERC)实施每周数据报告和近乎实时的数据裁决,对急性 GVHD 发病时的诊断分配置信水平(确诊、可能、可能或阴性)。

结果

在前 100 天内,90%的病例出现符合 GVHD 的症状,但这些症状通常被中心确定为非 GVHD 原因所致。事实上,在症状出现时,只有 23%的病例考虑 GVHD。40%的病例获得了诊断性活检,但治疗通常与活检结果不一致,10.5%的活检结果模棱两可。重要的是,超过 40%的类固醇疗程是因非 GVHD 原因开始的。ERC 修改了 12.3%发病病例的 GVHD 诊断和/或分级。中心报告的急性 GVHD 的累积发生率为 62%。当 ERC 裁决为只有可能或确诊的置信水平存在时,GVHD 的发生率下降至 49%。

结论

本研究表明,在症状出现时 GVHD 的发生率可能被高估,确立了急性 GVHD 的当代基准,并提出了一种用于报告和裁决 GVHD 的结构化框架,可用于前瞻性试验。

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