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唾液腺分泌性癌的临床行为与分子见解:单中心经验

Clinical Behavior and Molecular Insights of Secretory Carcinoma of Salivary Glands, a Single Center Experience.

作者信息

Bassani Sara, Fiorini Denise, Destefanis Miriam Sara, Arsie Athena Eliana, Mulone Davide, Eccher Albino, Brunelli Matteo, Marani Filippo, Monzani Daniele, Molteni Gabriele

机构信息

Otolaryngology-Head and Neck Surgery Department, University of Verona, Verona, Italy.

Department of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Verona, Italy.

出版信息

Indian J Otolaryngol Head Neck Surg. 2024 Oct;76(5):4153-4162. doi: 10.1007/s12070-024-04807-4. Epub 2024 Jun 20.

Abstract

OBJECTIVE

the study aimed to characterize the novel entity referred to as secretory carcinoma of the salivary glands.

METHODS

we comprehensively evaluated 150 patients afflicted by malignant salivary gland tumors who had been under treatment at the University of Verona. Inclusion criteria primarily focused on the availability of paraffin block materials and adequate follow-up data. Subsequently, we conducted a comprehensive Fluorescent In Situ Hybridization (FISH) analysis, utilizing probes targeting NTRK-3, MALM-2, EWRS-1, HER-2, MDM-2, and NTRK1-2.

RESULTS

out of the initial cohort, 37 patients met the eligibility criteria for our study. We identified NTRK3 gene rearrangements in four patients (11%), two of whom had mucoepidermoid carcinoma, and the remaining two had acinic cell carcinoma. Notably, none of these patients had initially received a secretory carcinoma diagnosis. The primary treatment approach for all patients entailed surgical parotid gland resection. The overall survival (OS) for patients with NTRK3 rearrangements amounted to 78 months, with a corresponding progression-free survival (PFS) of 73 months.

CONCLUSION

in summary, our case series suggests that secretory carcinomas exhibit a favorable clinical course and underscores the pivotal importance of distinguishing secretory carcinomas from other histological subtypes.

摘要

目的

本研究旨在对被称为唾液腺分泌性癌的新实体进行特征描述。

方法

我们全面评估了150例在维罗纳大学接受治疗的罹患恶性唾液腺肿瘤的患者。纳入标准主要集中在石蜡块材料的可用性和充分的随访数据。随后,我们进行了全面的荧光原位杂交(FISH)分析,使用针对NTRK - 3、MALM - 2、EWRS - 1、HER - 2、MDM - 2和NTRK1 - 2的探针。

结果

在最初的队列中,37例患者符合我们研究的入选标准。我们在4例患者(11%)中发现了NTRK3基因重排,其中2例患有黏液表皮样癌,其余2例患有腺泡细胞癌。值得注意的是,这些患者最初均未被诊断为分泌性癌。所有患者的主要治疗方法是腮腺手术切除。NTRK3重排患者的总生存期(OS)为78个月,相应的无进展生存期(PFS)为73个月。

结论

总之,我们的病例系列表明分泌性癌呈现出良好的临床病程,并强调了将分泌性癌与其他组织学亚型区分开来的关键重要性。

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