Han Albert Y, Patel Pratik B, Anderson Mitchell, Diaz Miguel F P, Chin Robert, St John Maie A
Department of Head and Neck Surgery, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, California.
Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, California.
Laryngoscope. 2018 Aug;128(8):1862-1866. doi: 10.1002/lary.27031. Epub 2018 Jan 4.
OBJECTIVES/HYPOTHESIS: Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine neoplasm of the skin. Growing evidence supports the benefit of postoperative adjuvant radiation therapy (RT) for locoregional control, but whether it improves overall survival (OS) has been debated. Our objective was to compare the OS of MCC patients who received postoperative RT with those who received surgery alone.
Retrospective case series.
Cases of MCC between 2001 and 2016 at the University of California, Los Angeles Health System were reviewed. We identified 87 unique cases of MCC. Among the patients, 74% were identified as male and 26% as female. The average age at diagnosis was 71.2 years. The median survival was 48.0 months. The OS of all the patients at 2 years, 5 years, and 10 years was 54%, 46%, and 26%, respectively. Univariate analysis showed that stage, T stage, N stage, and M stage were significant determinants of OS. The inclusion of RT was not found to be a determinant; however, when restricting the analysis to early-stage MCC (stages I and II), postoperative adjuvant RT was associated with significantly improved OS. A Cox regression model confirmed that inclusion of RT was an independent prognosticator of OS even when controlled for overall stage and negative margin status. The small sample size and retrospective nature of this study limit its statistical power.
MCC is an aggressive tumor with a poor prognosis for survival especially in elderly patients. In this study, we found that RT during early-stage MCC improves OS. Prospective randomized control trials are necessary to validate the observed benefit for MCC patients.
4 Laryngoscope, 1862-1866, 2018.
目的/假设:默克尔细胞癌(MCC)是一种罕见的侵袭性皮肤神经内分泌肿瘤。越来越多的证据支持术后辅助放疗(RT)对局部区域控制有益,但它是否能改善总生存期(OS)一直存在争议。我们的目的是比较接受术后放疗的MCC患者与仅接受手术的患者的总生存期。
回顾性病例系列研究。
回顾了2001年至2016年加利福尼亚大学洛杉矶分校医疗系统的MCC病例。我们确定了87例独特的MCC病例。在这些患者中,74%为男性,26%为女性。诊断时的平均年龄为71.2岁。中位生存期为48.0个月。所有患者在2年、5年和10年时的总生存率分别为54%、46%和26%。单因素分析表明,分期、T分期、N分期和M分期是总生存期的重要决定因素。未发现放疗的纳入是一个决定因素;然而,当将分析局限于早期MCC(I期和II期)时,术后辅助放疗与总生存期显著改善相关。Cox回归模型证实,即使在控制了总体分期和切缘阴性状态后,放疗的纳入仍是总生存期的独立预后因素。本研究样本量小且具有回顾性,限制了其统计效力。
MCC是一种侵袭性肿瘤,生存预后较差,尤其是在老年患者中。在本研究中,我们发现早期MCC放疗可改善总生存期。需要进行前瞻性随机对照试验来验证对MCC患者观察到的益处。
4《喉镜》,2018年,第1862 - 1866页。