Chintakuntlawar Ashish V, Shon Wonwoo, Erickson-Johnson Michele, Bilodeau Elizabeth, Jenkins Sarah M, Davidson Jennifer A, Keeney Michael G, Rivera Michael, Price Daniel L, Moore Eric J, Olsen Kerry D, Kasperbauer Jan L, Foote Robert L, Price Katharine A, García Joaquín J
Division of Medical Oncology, Department of Oncology, Mayo Clinic Rochester, Rochester, MN, USA.
Department of Pathology, Immunology, and Laboratory Medicine, University of Florida College of Medicine, Gainesville, FL, USA.
Oral Surg Oral Med Oral Pathol Oral Radiol. 2016 May;121(5):542-549.e1. doi: 10.1016/j.oooo.2016.01.011. Epub 2016 Jan 21.
Acinic cell carcinoma (AcCC) is an uncommon salivary gland malignancy. We aim to characterize the clinical and pathologic characteristics of AcCC with and without high-grade transformation (HGT). Importantly, cases of mammary analogue secretory carcinoma, a recently described histologic mimic of AcCC, have been excluded by using cytogenetics and molecular studies.
Archival surgical pathology material was obtained for patients diagnosed with AcCC at Mayo Clinic Rochester between 1990 and 2010. Tumors harboring the ETV6-NTRK3 fusion transcript were excluded from analysis by using cytogenetics and molecular studies. Tumors with HGT were characterized by areas with an infiltrative growth pattern, nuclear anaplasia, prominent nucleoli, brisk mitotic activity, geographic necrosis, and stromal desmoplasia. Demographic and clinical data were extracted from the medical records.
AcCC with HGT was seen in 8 of 48 cases (17%). Patients with AcCC with HGT were significantly older than patients without HGT (median 69 vs 54 years; P = .04). Angiolymphatic invasion was more common in AcCC with HGT (P = .02). Relapse-free survival and overall survival were significantly worse for cases of AcCC with HGT (hazard ratio 10.4 and 9.3, respectively; P < .0001 for both comparisons). Locoregional recurrence-free survival was not significantly different (P = .12), but distant metastases-free survival was significantly worse in patients with HGT compared with non-HGT patients (P < .0001).
Prognosis for overall survival and distant relapse for AcCC patients with HGT is significantly worse than that for patients without HGT.
腺泡细胞癌(AcCC)是一种罕见的涎腺恶性肿瘤。我们旨在描述伴有和不伴有高级别转化(HGT)的AcCC的临床和病理特征。重要的是,通过细胞遗传学和分子研究排除了乳腺样分泌癌(一种最近描述的与AcCC组织学相似的肿瘤)病例。
获取了1990年至2010年间在梅奥诊所罗切斯特被诊断为AcCC的患者的存档手术病理材料。通过细胞遗传学和分子研究将含有ETV6-NTRK3融合转录本的肿瘤排除在分析之外。具有HGT的肿瘤的特征是具有浸润性生长模式、核间变、核仁突出、有丝分裂活跃、地图状坏死和间质纤维组织增生的区域。从病历中提取人口统计学和临床数据。
48例中有8例(17%)出现伴有HGT的AcCC。伴有HGT的AcCC患者明显比不伴有HGT的患者年龄大(中位年龄69岁对54岁;P = .04)。血管淋巴管侵犯在伴有HGT的AcCC中更常见(P = .02)。伴有HGT的AcCC病例的无复发生存率和总生存率明显更差(风险比分别为10.4和9.3;两项比较P均< .0001)。局部区域无复发生存率无显著差异(P = .12),但与非HGT患者相比,HGT患者的无远处转移生存率明显更差(P < .0001)。
伴有HGT的AcCC患者的总生存和远处复发预后明显比不伴有HGT的患者差。