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多中心、前瞻性队列评估用于预测皮肤黑色素瘤的 31 个基因表达谱的长期结果。

Long-Term Outcomes in a Multicenter, Prospective Cohort Evaluating the Prognostic 31-Gene Expression Profile for Cutaneous Melanoma.

机构信息

Department of Surgery, St Louis University, St Louis, MO.

South Carolina Skin Cancer Center, Greenville, SC.

出版信息

JCO Precis Oncol. 2021 Apr 6;5. doi: 10.1200/PO.20.00119. eCollection 2021.

Abstract

PURPOSE

Current guidelines for postoperative management of patients with stage I-IIA cutaneous melanoma (CM) do not recommend routine cross-sectional imaging, yet many of these patients develop metastases. Methods that complement American Joint Committee on Cancer (AJCC) staging are needed to improve identification and treatment of these patients. A 31-gene expression profile (31-GEP) test predicts metastatic risk as low (class 1) or high (class 2). Prospective analysis of CM outcomes was performed to test the hypotheses that the 31-GEP provides prognostic value for patients with stage I-III CM, and that patients with stage I-IIA melanoma and class 2 31-GEP results have metastatic risk similar to patients for whom surveillance is recommended.

MATERIALS AND METHODS

Two multicenter registry studies, INTEGRATE (ClinicalTrials.gov identifier:NCT02355574) and EXPAND (ClinicalTrials.gov identifier:NCT02355587), were initiated under institutional review board approval, and 323 patients with stage I-III CM and median follow-up time of 3.2 years met inclusion criteria. Primary end points were 3-year recurrence-free survival (RFS), distant metastasis-free survival (DMFS), and overall survival (OS).

RESULTS

The 31-GEP was significant for RFS, DMFS, and OS in a univariate analysis and was a significant, independent predictor of RFS, DMFS, and OS in a multivariable analysis. GEP class 2 results were significantly associated with lower 3-year RFS, DMFS, and OS in all patients and those with stage I-IIA disease. Patients with stage I-IIA CM and a class 2 result had recurrence, distant metastasis, and death rates similar to patients with stage IIB-III CM. Combining 31-GEP results and AJCC staging enhanced sensitivity over each approach alone.

CONCLUSION

These data provide a rationale for using the 31-GEP along with AJCC staging, and suggest that patients with stage I-IIA CM and a class 2 31-GEP signature may be candidates for more intense follow-up.

摘要

目的

目前,对于 I 期-IIA 期皮肤黑色素瘤(CM)患者的术后管理,指南不建议常规进行横断面成像,但这些患者中有许多会发生转移。需要补充美国癌症联合委员会(AJCC)分期的方法来提高对这些患者的识别和治疗能力。31 基因表达谱(31-GEP)检测预测低风险(I 类)或高风险(II 类)转移风险。对 CM 结果进行了前瞻性分析,以检验以下假设:31-GEP 为 I-III 期 CM 患者提供预后价值,以及 I-IIA 期黑色素瘤且 31-GEP 结果为 II 类的患者具有与建议进行监测的患者相似的转移风险。

材料和方法

两项多中心注册研究 INTEGRATE(ClinicalTrials.gov 标识符:NCT02355574)和 EXPAND(ClinicalTrials.gov 标识符:NCT02355587)在机构审查委员会批准下启动,323 名 I-III 期 CM 患者符合纳入标准,中位随访时间为 3.2 年。主要终点是 3 年无复发生存率(RFS)、无远处转移生存(DMFS)和总生存(OS)。

结果

31-GEP 在单因素分析中对 RFS、DMFS 和 OS 具有显著意义,在多变量分析中是 RFS、DMFS 和 OS 的显著独立预测因子。GEP 类 2 结果与所有患者和 I-IIA 期疾病患者的 3 年 RFS、DMFS 和 OS 显著相关。I-IIA 期 CM 患者和类 2 结果患者的复发、远处转移和死亡率与 IIB-III 期 CM 患者相似。31-GEP 结果与 AJCC 分期相结合比单独使用任何一种方法的敏感性都更高。

结论

这些数据为使用 31-GEP 联合 AJCC 分期提供了依据,并表明 I-IIA 期 CM 患者和 31-GEP 类 2 特征患者可能是更密切随访的候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdb/8140806/badc7f20bbd7/po-5-po.20.00119-g001.jpg

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