Prognostic Implication of Histopathologic Indicators in Salivary Duct Carcinoma

M. Nakaguro, Yukiko Sato, Y. Tada, D. Kawakita, H. Hirai, M. Urano, Tomotaka Shimura, K. Tsukahara, S. Kano, Hiroyuki Ozawa, K. Okami, Yuichiro Sato, C. Fushimi, A. Shimizu, Soichiro Takase, Takuro Okada, Hiroki Sato, Y. Imanishi, Kuninori Otsuka, Yoshihiro Watanabe, A. Sakai, K. Ebisumoto, Takafumi Togashi, Yushi Ueki, Hisayuki Ota, Natsuki Saigusa, Hideaki Takahashi, M. Ando, T. Hanazawa, T. Nagao
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引用次数: 9

Abstract

Supplemental Digital Content is available in the text. Salivary duct carcinoma (SDC) is a rare, aggressive malignancy that histologically resembles high-grade mammary duct carcinoma. Because of the rarity of this entity, data verifying the association between histologic features and patient survival are limited. We conducted a comprehensive histologic review of 151 SDC cases and performed an analysis of the association between various histomorphologic parameters and the clinical outcome with the aim of developing a histologic risk stratification model that predicts the prognosis of SDC patients. A multivariate analysis revealed that prominent nuclear pleomorphism (overall survival [OS]: P=0.013; progression-free survival [PFS]: P=0.019), ≥30 mitoses/10 HPF (PFS: P=0.013), high tumor budding (OS: P=0.011; PFS: P<0.001), and high poorly differentiated clusters (OS: P<0.001; PFS: P<0.001) were independent prognostic factors. Patients with vascular invasion demonstrated a marginally significant association with shorter PFS (P=0.064) in a multivariate analysis. We proposed a 3-tier histologic risk stratification model based on the total number of positive factors among 4 prognostically relevant parameters (prominent nuclear pleomorphism, ≥30 mitoses/10 HPF, vascular invasion, and high poorly differentiated clusters). The OS and PFS of patients with low-risk (0 to 1 point) (23% of cases), intermediate-risk (2 to 3 points) (54% of cases), and high-risk (4 points) (23% of cases) tumors progressively deteriorated in this order (hazard ratio, 2.13 and 2.28, and 4.99 and 4.50, respectively; Ptrend<0.001). Our histologic risk stratification model could effectively predict patient survival and may be a useful aid to guide clinical decision-making in relation to the management of patients with SDC.
涎腺导管癌组织病理学指标的预后意义
补充数字内容可在文本中找到。涎腺导管癌是一种罕见的侵袭性恶性肿瘤,组织学上类似于高级别乳腺导管癌。由于这种疾病的罕见性,证实组织学特征与患者生存之间关系的数据有限。我们对151例SDC病例进行了全面的组织学回顾,并分析了各种组织学参数与临床结果之间的关系,目的是建立一个预测SDC患者预后的组织学风险分层模型。多变量分析显示,核多形性显著(总生存率[OS]: P=0.013;无进展生存期[PFS]: P=0.019),≥30个有丝分裂/10个HPF (PFS: P=0.013),高肿瘤出芽(OS: P=0.011;PFS: P<0.001)和高低分化群集(OS: P<0.001;PFS: P<0.001)是独立的预后因素。在多变量分析中,血管侵犯患者与较短的PFS有轻微的显著相关(P=0.064)。我们提出了一个3层的组织学风险分层模型,该模型基于4个预后相关参数(突出的核多形性、≥30个有丝分裂/10个HPF、血管侵犯和高低分化簇)中阳性因素的总数。低危(0 ~ 1分)(23%)、中危(2 ~ 3分)(54%)、高危(4分)(23%)肿瘤患者的OS和PFS依次进行性恶化(风险比分别为2.13和2.28,4.99和4.50;Ptrend < 0.001)。我们的组织学风险分层模型可以有效地预测患者的生存,并可能有助于指导与SDC患者管理相关的临床决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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