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对9387例默克尔细胞癌病例的预后因素分析构成了新版美国癌症联合委员会(AJCC)第8版分期系统的基础。

Analysis of Prognostic Factors from 9387 Merkel Cell Carcinoma Cases Forms the Basis for the New 8th Edition AJCC Staging System.

作者信息

Harms Kelly L, Healy Mark A, Nghiem Paul, Sober Arthur J, Johnson Timothy M, Bichakjian Christopher K, Wong Sandra L

机构信息

Department of Dermatology, University of Michigan Health System and Medical School, Ann Arbor, MI, USA.

Department of Surgery, University of Michigan Health System and Medical School, Ann Arbor, MI, USA.

出版信息

Ann Surg Oncol. 2016 Oct;23(11):3564-3571. doi: 10.1245/s10434-016-5266-4. Epub 2016 May 19.

Abstract

BACKGROUND

The first consensus Merkel cell carcinoma (MCC) staging system was published in 2010. New information on the clinical course prompts review of MCC staging.

METHODS

A total of 9387 MCC cases from the National Cancer Data Base Participant User File with follow-up and staging data (1998-2012) were analyzed. Prognostic differences based on clinical and pathological staging were evaluated. Survival estimates were compared by disease extent.

RESULTS

Sixty-five percent of cases presented with local disease, whereas 26 and 8 % presented with nodal and distant disease. Disease extent at presentation was predictive of 5-year overall survival (OS) with estimates of 51, 35, and 14 % for local, nodal, and distant disease. Tumor burden at the regional nodal basin was predictive of 5-year OS with estimates of 40 and 27 % for clinically occult and clinically detected nodal disease. For local disease, we confirm improved prognosis when the regional nodal basin was negative by pathological compared with clinical staging. We identified 336 cases with clinically detected nodal disease and unknown primary tumor and showed improved prognosis over cases presenting with concurrent primary tumor (OS estimates of 42 vs. 27 %).

CONCLUSIONS

Analysis of a national dataset of MCC cases validates the predictive value of disease extent at presentation. Separation of clinical and pathological stage groups and regrouping of unknown primary tumors are supported by the analysis. The revised staging system provides more accurate prognostication and has been formally accepted by the AJCC staging committee for inclusion in the 8th edition.

摘要

背景

首个默克尔细胞癌(MCC)共识分期系统于2010年发布。有关临床病程的新信息促使对MCC分期进行重新审视。

方法

分析了来自国家癌症数据库参与者用户文件的9387例MCC病例,这些病例具有随访和分期数据(1998 - 2012年)。评估了基于临床和病理分期的预后差异。通过疾病范围比较生存估计值。

结果

65%的病例表现为局部疾病,而26%和8%的病例表现为淋巴结和远处疾病。初诊时的疾病范围可预测5年总生存率(OS),局部、淋巴结和远处疾病的估计值分别为51%、35%和14%。区域淋巴结区域的肿瘤负荷可预测5年OS,临床隐匿性和临床检测到的淋巴结疾病的估计值分别为40%和27%。对于局部疾病,我们证实与临床分期相比,当区域淋巴结区域经病理检查为阴性时,预后改善。我们识别出336例临床检测到淋巴结疾病且原发肿瘤不明的病例,并显示其预后优于同时存在原发肿瘤的病例(OS估计值分别为42%和27%)。

结论

对全国MCC病例数据集的分析验证了初诊时疾病范围的预测价值。分析支持将临床和病理分期组分开以及对不明原发肿瘤进行重新分组。修订后的分期系统提供了更准确的预后评估,已被美国癌症联合委员会(AJCC)分期委员会正式接受纳入第8版。

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