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二十多年来淋巴结阳性皮肤黑色素瘤的结果。

Outcomes for lymph node-positive cutaneous melanoma over two decades.

机构信息

Department of Surgery, Division of Surgical Oncology Sacramento, University of California at Davis, 4501 X Street, Suite 3010, Sacramento, CA 95817, USA.

出版信息

World J Surg. 2011 Jul;35(7):1567-72. doi: 10.1007/s00268-010-0903-8.

Abstract

BACKGROUND

Our aim was to demonstrate that, despite advances in treatment and surveillance of node-positive cutaneous melanoma, rates of overall survival (OS) and melanoma-specific survival (MSS) have not changed over the last two decades.

METHODS

We used the Surveillance, Epidemiology, and End Results (SEER) database of the National Cancer Institute to identify patients with node-positive cutaneous melanoma. Patients were categorized by treatment era; the first era encompassed patients diagnosed from 1988 to 1999 and the second era 2000 to 2006. Multivariate Cox proportional hazards models compared rates of OS and MSS between treatment eras while controlling for known prognostic factors. We reported risks of death as hazard ratios (HR) with 95% confidence intervals (CI) and set significance at P≤0.05.

RESULTS

Entrance criteria were met by 6,868 patients, 1,631 (23.8%) treated in era I and 5,237 (76.3%) treated in era II. On multivariate analysis, era II patients did not demonstrate a significantly different risk of death from any cause (HR 0.89, CI 0.79-1.01; P<0.08), but they did have a lower risk of melanoma-specific mortality (HR 0.81, CI 0.71-0.93; P=0.003) relative to their era I counterparts.

CONCLUSIONS

Over nearly two decades, MSS but not OS has improved for AJCC stage III melanoma patients. Stage migration is likely responsible for any improvement in MSS among patients in the most recently diagnosed era.

摘要

背景

我们的目的是证明,尽管在治疗和监测阳性淋巴结皮肤黑色素瘤方面取得了进展,但在过去二十年中,总生存率(OS)和黑色素瘤特异性生存率(MSS)并未改变。

方法

我们使用美国国立癌症研究所的监测、流行病学和最终结果(SEER)数据库来确定阳性淋巴结皮肤黑色素瘤患者。患者按治疗时代进行分类;第一个时代包括 1988 年至 1999 年诊断的患者,第二个时代包括 2000 年至 2006 年诊断的患者。多变量 Cox 比例风险模型比较了治疗时代之间 OS 和 MSS 的比率,同时控制了已知的预后因素。我们报告了死亡风险作为风险比(HR)和 95%置信区间(CI),并设定 P≤0.05 为显著性水平。

结果

符合入选标准的患者有 6868 例,其中 1631 例(23.8%)在时代 I 治疗,5237 例(76.3%)在时代 II 治疗。多变量分析显示,时代 II 患者的任何原因死亡风险无显著差异(HR 0.89,CI 0.79-1.01;P<0.08),但黑色素瘤特异性死亡率较低(HR 0.81,CI 0.71-0.93;P=0.003)与时代 I 患者相比。

结论

在近二十年中,AJCC 分期 III 黑色素瘤患者的 MSS 但不是 OS 有所改善。分期迁移可能是最近诊断的时代患者中 MSS 任何改善的原因。

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