Department of Surgical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India.
Department of Oncopathology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India.
J Cancer Res Ther. 2021 Jan-Mar;17(1):106-113. doi: 10.4103/jcrt.JCRT_854_19.
Malignant peripheral nerve sheath tumor (MPNST) is a rare and aggressive soft-tissue sarcoma.
The aim of this study was to analyze various prognostic factors and treatment outcome of patients with MPNST.
This was a retrospective study.
Ninety-two patients, who presented with MPNST at a tertiary care cancer center from 2011 to 2018, were included in this study. The median follow-up of all living patients was 33 months. Neurofibromatosis 1 (NF1) was seen in 12 (13%) patients. Sixty (65.2%) patients received curative-intent treatment.
Kaplan-Meier method was used for survival analysis. Log-rank test was used for univariate analysis, and multivariate analysis was done by Cox proportional hazard ratio method.
The 5-year overall survival (OS) of all patients was 47.2% and the 5-year disease-free survival (DFS) of operated patients was 41.5%. On univariate analysis, association with NF1 (P = 0.009), grade (P = 0.017), and margin status (P = 0.002) had a significant effect on DFS, whereas association with NF1 (P = 0.025), metastatic disease on presentation (P < 0.0001), palliative intent of treatment (P < 0.0001), grade (P = 0.049), and margin status (P = 0.036) had a significant effect on OS. On multivariate analysis for patients who were treated with curative-intent treatment, grade (P = 0.015), and margin status (P = 0.028) had a significant effect on DFS, whereas association with NF1 (P = 0.00026) and location of tumor (P = 0.040) had a significant effect on OS.
The presence of distant metastasis, palliative intent of treatment, association with NF1, location of the tumor in the head and neck, high tumor grade, and positive margin status were the risk factors associated with poor survival for the patients with MPNST. Wide local excision with negative resection margin is the highly recommended treatment.
恶性外周神经鞘瘤(MPNST)是一种罕见且侵袭性的软组织肉瘤。
本研究旨在分析 MPNST 患者的各种预后因素和治疗结果。
这是一项回顾性研究。
本研究纳入了 2011 年至 2018 年在一家三级癌症中心就诊的 92 名 MPNST 患者。所有存活患者的中位随访时间为 33 个月。12 例(13%)患者存在神经纤维瘤病 1 型(NF1)。60 例(65.2%)患者接受了根治性治疗。
采用 Kaplan-Meier 法进行生存分析。对数秩检验用于单因素分析,Cox 比例风险比法用于多因素分析。
所有患者的 5 年总生存率(OS)为 47.2%,接受手术治疗的患者的 5 年无病生存率(DFS)为 41.5%。单因素分析显示,与 NF1 相关(P=0.009)、分级(P=0.017)和切缘状态(P=0.002)与 DFS 显著相关,而与 NF1 相关(P=0.025)、初诊时存在转移疾病(P<0.0001)、姑息治疗意图(P<0.0001)、分级(P=0.049)和切缘状态(P=0.036)与 OS 显著相关。多因素分析显示,接受根治性治疗的患者中,分级(P=0.015)和切缘状态(P=0.028)与 DFS 显著相关,而与 NF1 相关(P=0.00026)和肿瘤位置(P=0.040)与 OS 显著相关。
存在远处转移、姑息治疗意图、与 NF1 相关、头颈部肿瘤位置、肿瘤分级高和切缘阳性是 MPNST 患者生存不良的相关危险因素。广泛局部切除并获得阴性切缘是高度推荐的治疗方法。