Prognostic Implication of Histopathologic Indicators in Salivary Duct Carcinoma: Proposal of a Novel Histologic Risk Stratification Model. (April 2020)

• Record Type: Journal Article
• Authors: Nakaguro, Masato; Sato, Yukiko; Tada, Yuichiro; Kawakita, Daisuke; Hirai, Hideaki; Urano, Makoto; Shimura, Tomotaka; Tsukahara, Kiyoaki; Kano, Satoshi; Ozawa, Hiroyuki; Okami, Kenji; Sato, Yuichiro; Fushimi, Chihiro; Shimizu, Akira; Takase, Soichiro; Okada, Takuro; Sato, Hiroki; Imanishi, Yorihisa; Otsuka, Kuninori; Watanabe, Yoshihiro; Sakai, Akihiro; Ebisumoto, Koji; Togashi, Takafumi; Ueki, Yushi; Ota, Hisayuki; Saigusa, Natsuki; Takahashi, Hideaki; Ando, Mizuo; Hanazawa, Toyoyuki; Nagao, Toshitaka
• Is Part Of: American journal of surgical pathology. Volume 44:Number 4(2020)
• Publication Date: 2020-04
• Subjects: histologic risk stratification model -- poorly differentiated clusters -- prognosis -- salivary duct carcinoma -- tumor budding; Pathology, Surgical -- Periodicals; 617.0705
• DOI: 10.1097/PAS.0000000000001413
• Languages: English
• ISSNs: 0147-5185

Abstract

Abstract : 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; P trend <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. Abstract : Supplemental Digital Content is available in the text.