Suppr超能文献

分子检测技术在诊断甲状腺结节中的有效性:一项随机临床试验。

Effectiveness of Molecular Testing Techniques for Diagnosis of Indeterminate Thyroid Nodules: A Randomized Clinical Trial.

机构信息

Section of Endocrine Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California.

Department of Biostatistics, Fielding School of Public Health, University of California, Los Angeles.

出版信息

JAMA Oncol. 2021 Jan 1;7(1):70-77. doi: 10.1001/jamaoncol.2020.5935.

Abstract

IMPORTANCE

Approximately 20% of thyroid nodules display indeterminate cytology. Molecular testing can refine the risk of malignancy and reduce the need for diagnostic hemithyroidectomy.

OBJECTIVE

To compare the diagnostic performance between an RNA test (Afirma genomic sequencing classifier) and DNA-RNA test (ThyroSeq v3 multigene genomic classifier).

DESIGN, SETTING, AND PARTICIPANTS: This parallel randomized clinical trial of monthly block randomization included patients in the UCLA Health system who underwent thyroid biopsy from August 2017 to January 2020 with indeterminate cytology (Bethesda System for Reporting Thyroid Cytopathology category III or IV).

INTERVENTIONS

Molecular testing with the RNA test or DNA-RNA test.

MAIN OUTCOMES AND MEASURES

Diagnostic test performance of the RNA test compared with the DNA-RNA test. The secondary outcome was comparison of test performance with prior versions of the molecular tests.

RESULTS

Of 2368 patients, 397 were eligible for inclusion based on indeterminate cytology, and 346 (median [interquartile range] age, 55 [44-67] years; 266 [76.9%] women) were randomized to 1 of the 2 tests. In the total cohort assessed for eligibility, 3140 thyroid nodules were assessed, and 427 (13.6%) nodules were cytologically indeterminate. The prevalence of malignancy was 20% among indeterminate nodules. The benign call rate was 53% (95% CI, 47%-61%) for the RNA test and 61% (95% CI, 53%-68%) for the DNA-RNA test. The specificities of the RNA test and DNA-RNA test were 80% (95% CI, 72%-86%) and 85% (95% CI, 77%-91%), respectively (P = .33); the positive predictive values (PPV) of the RNA test and DNA-RNA test were 53% (95% CI, 40%-67%) and 63% (95% CI, 48%-77%), respectively (P = .33). The RNA test exhibited a higher PPV compared with the prior test version (Afirma gene expression classifier) (54% [95% CI, 40%-67%] vs 38% [95% CI, 27%-48%]; P = .01). The DNA-RNA test had no statistically significant difference in PPV compared with its prior version (ThyroSeq v2 next-generation sequencing) (63% [95% CI, 48%-77%] vs 58% [95% CI, 43%-73%]; P = .75). Diagnostic thyroidectomy was avoided in 87 (51%) patients tested with the RNA test and 83 (49%) patients tested with the DNA-RNA test. Surveillance ultrasonography was available for 90 nodules, of which 85 (94%) remained stable over a median of 12 months follow-up.

CONCLUSIONS AND RELEVANCE

Both the RNA test and DNA-RNA test displayed high specificity and allowed 49% of patients with indeterminate nodules to avoid diagnostic surgery. Although previous trials demonstrated that the prior version of the DNA-RNA test was more specific than the prior version of the RNA test, the current molecular test techniques have no statistically significant difference in performance.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT02681328.

摘要

重要性

约 20%的甲状腺结节显示出不确定的细胞学特征。分子检测可以细化恶性肿瘤的风险,并减少对诊断性甲状腺叶切除术的需求。

目的

比较 RNA 检测(Afirma 基因测序分类器)和 DNA-RNA 检测(ThyroSeq v3 多基因基因组分类器)的诊断性能。

设计、设置和参与者:这项每月进行的随机分组平行临床试验包括来自 UCLA 健康系统的患者,他们在 2017 年 8 月至 2020 年 1 月期间因不确定的细胞学(美国甲状腺协会甲状腺细胞病理学报告系统分类为 III 或 IV 类)接受了甲状腺活检。

干预措施

进行 RNA 检测或 DNA-RNA 检测的分子检测。

主要结果和测量指标

与 DNA-RNA 检测相比,RNA 检测的诊断检测性能。次要结果是比较与之前版本的分子检测的性能。

结果

在 2368 名患者中,根据不确定的细胞学特征,有 397 名符合纳入标准,346 名(中位数[四分位距]年龄 55[44-67]岁;266[76.9%]名女性)随机分配到 2 种检测方法中的 1 种。在总评估合格的队列中,评估了 3140 个甲状腺结节,其中 427 个(13.6%)结节细胞学不确定。不确定结节的恶性肿瘤患病率为 20%。RNA 检测的良性检出率为 53%(95%CI,47%-61%),DNA-RNA 检测为 61%(95%CI,53%-68%)。RNA 检测和 DNA-RNA 检测的特异性分别为 80%(95%CI,72%-86%)和 85%(95%CI,77%-91%)(P=0.33);RNA 检测和 DNA-RNA 检测的阳性预测值(PPV)分别为 53%(95%CI,40%-67%)和 63%(95%CI,48%-77%)(P=0.33)。与之前的检测版本(Afirma 基因表达分类器)相比,RNA 检测的 PPV 更高(54%[95%CI,40%-67%]比 38%[95%CI,27%-48%];P=0.01)。与之前的版本(ThyroSeq v2 下一代测序)相比,DNA-RNA 检测的 PPV 没有统计学上的显著差异(63%[95%CI,48%-77%]比 58%[95%CI,43%-73%];P=0.75)。在接受 RNA 检测的 87 名(51%)患者和接受 DNA-RNA 检测的 83 名(49%)患者中避免了诊断性甲状腺切除术。对 90 个结节进行了监测超声检查,其中 85 个(94%)在中位 12 个月的随访期间保持稳定。

结论和相关性

RNA 检测和 DNA-RNA 检测均显示出较高的特异性,可使 49%的不确定结节患者避免诊断性手术。尽管之前的试验表明,DNA-RNA 检测的前一个版本比 RNA 检测的前一个版本更特异,但目前的分子检测技术在性能上没有统计学上的显著差异。

试验注册

ClinicalTrials.gov 标识符:NCT02681328。

相似文献

引用本文的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验