Țăpoi Dana Antonia, Derewicz Diana, Gheorghișan-Gălățeanu Ancuța-Augustina, Dumitru Adrian Vasile, Ciongariu Ana Maria, Costache Mariana
Department of Pathology, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.
Department of Pathology, University Emergency Hospital, 050098 Bucharest, Romania.
Biomedicines. 2023 Sep 23;11(10):2616. doi: 10.3390/biomedicines11102616.
Thick cutaneous melanomas (Breslow depth > 4 mm) are locally advanced tumors, generally associated with poor prognosis. Nevertheless, these tumors sometimes display unpredictable behavior. This study aims to analyze clinical and histopathological features that can influence the prognosis of thick melanomas. This is a retrospective study on 94 thick primary cutaneous melanomas diagnosed between 2012 and 2018 that were followed-up for at least five years to assess disease progression and survival. We evaluated the age, gender, tumor location, histological subtype, Breslow depth, Clark level, resection margins, mitotic index, the presence/absence of ulceration, necrosis, regression, microsatellites, neurotropism, lymphovascular invasion, and the pattern of tumor-infiltrating lymphocytes, and their association with disease progression and survival. By conducting univariate analysis, we found that progression-free survival (PFS) was significantly associated with female gender, the superficial spreading melanoma (SSM) subtype, mitotic index, necrosis, microsatellites, and perineural invasion. Overall survival (OS) was significantly associated with female gender, Breslow depth, SSM subtype, necrosis, microsatellites, and perineural invasion. Through multivariate Cox proportional hazards regression, we found that the only factors associated with PFS were Breslow depth, necrosis, microsatellites, and perineural invasion, while the factors associated with OS were Breslow depth, necrosis, microsatellites, and perineural invasion. Certain histopathological features such as Breslow depth, necrosis, microsatellites, and perineural invasion could explain differences in disease evolution. This is one of the first studies to demonstrate an association between necrosis and perineural invasion and outcomes in patients with thick melanomas. By identifying high-risk patients, personalized therapy can be provided for improved prognosis.
厚皮黑色素瘤( Breslow深度>4mm)是局部进展期肿瘤,通常预后较差。然而,这些肿瘤有时表现出不可预测的行为。本研究旨在分析可影响厚黑色素瘤预后的临床和组织病理学特征。这是一项对2012年至2018年间诊断的94例厚原发性皮肤黑色素瘤进行的回顾性研究,这些患者至少随访了五年以评估疾病进展和生存情况。我们评估了年龄、性别、肿瘤位置、组织学亚型、Breslow深度、Clark分级、切除切缘、有丝分裂指数、溃疡、坏死、消退、微卫星、嗜神经现象、淋巴管浸润以及肿瘤浸润淋巴细胞的模式,以及它们与疾病进展和生存的关联。通过单因素分析,我们发现无进展生存期(PFS)与女性性别、浅表扩散型黑色素瘤(SSM)亚型、有丝分裂指数、坏死、微卫星和神经周围侵犯显著相关。总生存期(OS)与女性性别、Breslow深度、SSM亚型、坏死、微卫星和神经周围侵犯显著相关。通过多变量Cox比例风险回归分析,我们发现与PFS相关的唯一因素是Breslow深度、坏死、微卫星和神经周围侵犯,而与OS相关的因素是Breslow深度、坏死、微卫星和神经周围侵犯。某些组织病理学特征,如Breslow深度、坏死、微卫星和神经周围侵犯,可以解释疾病演变的差异。这是首批证明坏死和神经周围侵犯与厚黑色素瘤患者预后之间存在关联的研究之一。通过识别高危患者,可以提供个性化治疗以改善预后。