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恶性周围神经鞘膜瘤病理分级的临床相关性:日本北部56例病例的多机构TMTS研究

Clinical relevance of pathological grades of malignant peripheral nerve sheath tumor: a multi-institution TMTS study of 56 cases in Northern Japan.

作者信息

Okada Kyoji, Hasegawa Tadashi, Tajino Takahiro, Hotta Tetsuo, Yanagisawa Michiro, Osanai Toshihisa, Nishida Jun, Seki Kunihiko, Itoi Eiji

机构信息

Tohoku Musculoskeletal Tumor Society, Yamagata, Japan.

出版信息

Ann Surg Oncol. 2007 Feb;14(2):597-604. doi: 10.1245/s10434-006-9053-5.

Abstract

BACKGROUND

Malignant peripheral nerve sheath tumor (MPNST) is a relatively rare soft tissue tumor, and its clinical relevance of pathological grades remains obscure.

METHODS

Fifty-six cases of MPNST identified from the files of seven oncology centers of the Tohoku Musculoskeletal Tumor Society (TMTS) and National Cancer Center were analyzed for histologic grades, demographics, treatments, and prognostic factors. The average follow-up period was 41 months.

RESULTS

Twenty-two men and 34 women with a mean age of 45 years were involved. Forty-four (78.6%) of 56 tumors were in the lower extremity or trunk. Fifty tumors (89%) were classified as high grade, and the remaining six as low grade. Twenty-one (39.6%) of 53 patients who underwent tumor excision developed local recurrences. An axial site and inadequate surgical margin were defined as risk factors for local recurrence. The overall survival rates of the 56 patients were 55.1% at 3 years and 43.3% at 5 years. Univariate analysis of the 56 patients revealed large-sized tumors, metastasis at presentation, and histologically high grade were significantly associated with poor prognosis. Multivariate analysis revealed a large tumor and metastasis at presentation to be independent prognostic factors.

CONCLUSIONS

The current study involving 56 patients with MPNST showed the aggressive clinical behavior of the tumor. Large-sized tumors, metastasis at presentation, and high histological grade were related to poor prognosis on univariate analysis, but independency of histological grade was still obscure. In the treatment for a large and high-grade MPNST, an alternative strategy should be further considered.

摘要

背景

恶性外周神经鞘瘤(MPNST)是一种相对罕见的软组织肿瘤,其病理分级的临床相关性仍不明确。

方法

对从东北肌肉骨骼肿瘤学会(TMTS)和国家癌症中心的七个肿瘤中心档案中识别出的56例MPNST病例进行组织学分级、人口统计学、治疗方法和预后因素分析。平均随访期为41个月。

结果

纳入22名男性和34名女性,平均年龄45岁。56个肿瘤中有44个(78.6%)位于下肢或躯干。50个肿瘤(89%)被分类为高级别,其余6个为低级别。53例行肿瘤切除的患者中有21例(39.6%)出现局部复发。轴向部位和手术切缘不充分被确定为局部复发的危险因素。56例患者的3年总生存率为55.1%,5年总生存率为43.3%。对56例患者的单因素分析显示,肿瘤体积大、初诊时转移和组织学高级别与预后不良显著相关。多因素分析显示肿瘤体积大和初诊时转移是独立的预后因素。

结论

目前这项涉及56例MPNST患者的研究显示了该肿瘤具有侵袭性的临床行为。单因素分析显示,肿瘤体积大、初诊时转移和组织学高级别与预后不良有关,但组织学分级的独立性仍不明确。在治疗体积大且高级别的MPNST时,应进一步考虑替代策略。

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