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比较两种基因表达谱检测与识别前哨淋巴结阳性低风险皮肤黑色素瘤患者的标准治疗方法。

Comparing Two Gene Expression Profile Tests to Standard of Care for Identifying Patients With Cutaneous Melanoma at Low Risk of Sentinel Lymph Node Positivity.

作者信息

Prieto Peter A, Ferris Laura K, Guenther Michael J

机构信息

University of Rochester Medical Center, Rochester, NY, U.S.A.

Department of Dermatology, University of North Carolina School of Medicine, Chapel Hill, NC, U.S.A.

出版信息

Cancer Diagn Progn. 2025 May 3;5(3):261-267. doi: 10.21873/cdp.10438. eCollection 2025 May-Jun.

DOI:10.21873/cdp.10438
PMID:40322208
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12046662/
Abstract

BACKGROUND/AIM: The National Comprehensive Cancer Network (NCCN) Guidelines for cutaneous melanoma (CM) recommend avoiding sentinel lymph node biopsy (SLNB) when the positivity risk is <5%, considering SLNB when the risk is 5-10%, or offering SLNB when the risk is >10%. Most patients undergoing SLNB have a negative result, showing that reliance upon the American Joint Committee on Cancer (AJCC) T-stage alone results in most patients undergoing an unnecessary, negative, unreliable, invasive procedure.

MATERIALS AND METHODS

Two gene expression profile (GEP) tests, the CP-GEP and the 31-GEP, have been developed to identify patients at low risk of SLN positivity who may consider avoiding SLNB. We analyzed the accuracy of the CP-GEP and 31-GEP in identifying patients with <5% risk of SLN positivity across the five validation studies of the CP-GEP and four validation studies of the 31-GEP in T1-T2 tumors.

RESULTS

Patients considered low risk by the CP-GEP had an SLN positivity rate of 6.2%, higher than the risk threshold of 5% used by the NCCN to guide SLNB decisions. In contrast, patients considered low risk by the 31-GEP or i31-SLNB had a 2.8% SLN positivity rate, a substantial improvement over AJCC-staging guidance.

CONCLUSION

Overall, the CP-GEP did not perform as well as AJCC, while the 31-GEP performed better than AJCC.

摘要

背景/目的:美国国立综合癌症网络(NCCN)皮肤黑色素瘤(CM)指南建议,当前哨淋巴结活检(SLNB)阳性风险<5%时避免进行该检查;风险为5 - 10%时考虑进行SLNB;风险>10%时则进行SLNB。大多数接受SLNB的患者结果为阴性,这表明仅依靠美国癌症联合委员会(AJCC)的T分期会导致大多数患者接受不必要、阴性、不可靠的侵入性检查。

材料与方法

已开发出两种基因表达谱(GEP)检测方法,即CP-GEP和31-GEP,用于识别前哨淋巴结阳性风险较低、可能考虑避免进行SLNB的患者。我们在CP-GEP的五项验证研究以及31-GEP针对T1 - T2肿瘤的四项验证研究中,分析了CP-GEP和31-GEP在识别前哨淋巴结阳性风险<5%患者方面的准确性。

结果

CP-GEP判定为低风险的患者前哨淋巴结阳性率为6.2%,高于NCCN用于指导SLNB决策的5%风险阈值。相比之下,31-GEP或i31-SLNB判定为低风险的患者前哨淋巴结阳性率为2.8%,相较于AJCC分期指导有显著改善。

结论

总体而言,CP-GEP的表现不如AJCC,而31-GEP的表现优于AJCC。

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本文引用的文献

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World J Surg Oncol. 2025 Jan 3;23(1):5. doi: 10.1186/s12957-024-03640-x.
2
The Prognostic Value of the 31-Gene Expression Profile Test in Cutaneous Melanoma: A Systematic Review and Meta-Analysis.31基因表达谱检测在皮肤黑色素瘤中的预后价值:一项系统评价与Meta分析
Cancers (Basel). 2024 Nov 4;16(21):3714. doi: 10.3390/cancers16213714.
3
Integrating the melanoma 31-gene expression profile test with clinical and pathologic features can provide personalized precision estimates for sentinel lymph node positivity: an independent performance cohort.将黑色素瘤 31 基因表达谱检测与临床和病理特征相结合,可为前哨淋巴结阳性提供个体化的精确估计:一项独立的性能队列研究。
World J Surg Oncol. 2024 Aug 30;22(1):228. doi: 10.1186/s12957-024-03512-4.
4
The 31-Gene Expression Profile Test Outperforms AJCC in Stratifying Risk of Recurrence in Patients with Stage I Cutaneous Melanoma.31基因表达谱检测在I期皮肤黑色素瘤患者复发风险分层方面优于美国癌症联合委员会(AJCC)的评估。
Cancers (Basel). 2024 Jan 9;16(2):287. doi: 10.3390/cancers16020287.
5
Validation of the Melanoma Institute of Australia's Sentinel Lymph Node Biopsy Risk Prediction Tool for Cutaneous Melanoma.澳大利亚黑色素瘤研究所前哨淋巴结活检风险预测工具对皮肤黑色素瘤的验证。
Ann Surg Oncol. 2024 Apr;31(4):2737-2746. doi: 10.1245/s10434-023-14862-w. Epub 2024 Jan 12.
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Clinical evaluation of the clinicopathologic and gene expression profile (CP-GEP) in patients with melanoma eligible for sentinel lymph node biopsy: A multicenter prospective Dutch study.临床评估黑色素瘤患者的临床病理和基因表达谱(CP-GEP)在适合前哨淋巴结活检中的表现:一项多中心前瞻性荷兰研究。
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Routine imaging guided by a 31-gene expression profile assay results in earlier detection of melanoma with decreased metastatic tumor burden compared to patients without surveillance imaging studies.常规影像学检查结合 31 基因表达谱检测可较无监测影像学研究的患者更早地检测到黑色素瘤,且转移瘤负荷降低。
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