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基线和治疗期间的血清 S100B 和 LDH 可预测接受 BRAF 抑制剂治疗的转移性黑色素瘤患者的结局。

Serum S100B and LDH at Baseline and During Therapy Predict the Outcome of Metastatic Melanoma Patients Treated with BRAF Inhibitors.

机构信息

Department of Dermatology, University Hospital Tübingen, Tübingen, Germany.

Department of Dermatology and Allergology, Kantonsspital St. Gallen, Rorschacherstrasse 95, 9007, St. Gallen, Switzerland.

出版信息

Target Oncol. 2021 Mar;16(2):197-205. doi: 10.1007/s11523-021-00792-8. Epub 2021 Feb 8.

Abstract

BACKGROUND

Despite impressive response rates, most patients with advanced melanoma ultimately progress following therapy with B-Raf proto-oncogene (BRAF) inhibitors (BRAFi). Therefore, frequent radiologic assessments are necessary, and reliable serum biomarkers would be beneficial for disease monitoring.

OBJECTIVE

This study investigated the ability of lactate dehydrogenase (LDH) and S100 calcium-binding protein B (S100B) to detect response and disease progression during treatment with BRAFi.

PATIENTS AND METHODS

Baseline levels of LDH and S100B and repeated measurements during therapy were recorded retrospectively in 191 patients with metastatic melanoma. LDH and S100B levels were compared between distinct time points (baseline, first follow-up visit [FV], best objective response [BR], and progressive disease [PD]). The prognostic ability of the serum biomarkers in relation to disease-specific survival (DSS) was assessed with univariable and multivariable Cox regression analysis.

RESULTS

Elevated baseline LDH and S100B correlated with impaired DSS. In contrast with LDH (P = 0.12), S100B levels at FV correlated with response (P = 0.0030). Both markers significantly decreased during the first weeks of BRAFi treatment (LDH, P = 0.00034; S100B, P < 0.0001) and increased between BR and PD (LDH, P = 0.016; S100B, P < 0.0001). Patients with elevated S100B (P = 0.00062) but not with elevated LDH (P = 0.067) at the time point of radiologically confirmed PD showed significantly impaired DSS after PD. Interestingly, DSS after PD differed significantly according to S100B levels determined as early as 8 weeks (median) before PD (P = 0.0024).

CONCLUSIONS

LDH and S100B are suitable serum biomarkers during therapy with BRAFi. S100B shows stronger correlation with response and exhibits more accuracy in predicting PD. Close biomarker monitoring with S100B is recommended during treatment with BRAFi to detect PD early.

摘要

背景

尽管接受 B-Raf 原癌基因(BRAF)抑制剂(BRAFi)治疗的晚期黑色素瘤患者的缓解率令人印象深刻,但大多数患者最终仍会出现疾病进展。因此,需要频繁进行影像学评估,而可靠的血清生物标志物将有助于疾病监测。

目的

本研究旨在探讨乳酸脱氢酶(LDH)和 S100 钙结合蛋白 B(S100B)在 BRAFi 治疗期间检测应答和疾病进展的能力。

患者和方法

回顾性记录了 191 例转移性黑色素瘤患者的基线 LDH 和 S100B 水平以及治疗过程中的重复测量值。在不同时间点(基线、首次随访、最佳客观缓解和疾病进展)比较了 LDH 和 S100B 水平。采用单变量和多变量 Cox 回归分析评估血清生物标志物与疾病特异性生存(DSS)的相关性。

结果

基线时 LDH 和 S100B 升高与 DSS 受损相关。与 LDH 相比(P = 0.12),首次随访时 S100B 水平与疗效相关(P = 0.0030)。在 BRAFi 治疗的最初几周内,两种标志物均显著降低(LDH,P = 0.00034;S100B,P < 0.0001),在 BR 与 PD 之间增加(LDH,P = 0.016;S100B,P < 0.0001)。在影像学证实 PD 时,LDH 升高(P = 0.067)而 S100B 升高(P = 0.00062)的患者,PD 后 DSS 显著受损。有趣的是,PD 前 8 周(中位数)即可确定的 S100B 水平与 PD 后 DSS 差异有统计学意义(P = 0.0024)。

结论

LDH 和 S100B 是 BRAFi 治疗期间合适的血清生物标志物。S100B 与疗效的相关性更强,在预测 PD 方面更准确。建议在 BRAFi 治疗期间密切监测 S100B 标志物,以早期发现 PD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ff/7935737/8ffcbb1693c6/11523_2021_792_Fig1_HTML.jpg

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