sinonasal cancer

鼻窦癌
  • 文章类型: Journal Article
    背景:晚期颅底恶性肿瘤是头颈部恶性肿瘤的异质性子集,管理往往是复杂的。最近,手术技术的范式转变和新的系统选择的出现。我们的目标是分析单个四元头颈部和颅底服务的长期结果。
    方法:对1999年至2015年间在我们机构接受治疗的127例晚期前颅底恶性肿瘤患者进行回顾性分析。研究了多个变量,以评估其对5年和10年结局的意义。
    结果:平均年龄为60.9(±12.6SD)。男性占64%,女性占36%。90%的患者患有T4疾病。中位生存时间为133个月。5年总生存率(OS)为66.2%,疾病特异性生存率(DSS)为74.7%,无复发生存率(RFS)为65.0%。十年OS为55.1%,DSS为72.1%,RFS为53.4%。组织学类型和边缘状态显著影响OS和DSS。
    结论:在过去的几十年中,晚期颅底肿瘤的外科治疗在我们的机构中取得了进展,具有可接受的生存结果和并发症发生率。组织学诊断和切缘状态是生存的主要预测因素。在目前的试验中添加新辅助系统药物可能会改善结果。
    BACKGROUND: Advanced skull base malignancies are a heterogenous subset of head and neck cancers, and management is often complex. In recent times, there has been a paradigm shift in surgical technique and the advent of novel systemic options. Our goal was to analyse the long-term outcomes of a single quaternary head and neck and skull base service.
    METHODS: A retrospective review of 127 patients with advanced anterior skull base malignancies that were treated at our institution between 1999 and 2015 was performed. Multiple variables were investigated to assess their significance on 5 and 10-year outcomes.
    RESULTS: The mean age was 60.9 (± 12.6 SD). Sixty-four percent were males and 36% were females. Ninety percent of patients had T4 disease. Median survival time was 133 months. The 5-year overall survival (OS) was 66.2%, disease-specific survival (DSS) was 74.7%, and recurrence-free survival (RFS) was 65.0%. The 10-year OS was 55.1%, DSS was 72.1%, and RFS was 53.4%. Histological type and margin status significantly affected OS & DSS.
    CONCLUSIONS: Surgical management of advanced skull base tumours has evolved over the last few decades at our institution with acceptable survival outcomes and complication rates. Histological diagnosis and margin status are the main predictors of survival. The addition of neoadjuvant systemic agents in current trials may improve outcomes.
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  • 文章类型: Journal Article
    背景:虽然罕见,鼻窦肿瘤(SNCs)具有较高的职业归因分数。
    方法:我们将基于性别的方法应用于描述性分析,发病率,和使用意大利国家鼻窦癌症登记处(ReNaTuNS:RegistroNazionaleTumoriNaso-Sinusali)的暴露模式。
    结果:该研究包括2851名SNC患者。男性(73%)比女性(27%)更容易被诊断出SNC。男性最常见的形态学是肠型腺癌(33%),而在女性中,它是鳞状细胞癌(49%)。两种性别都以鼻腔为主(50%),男性的筛窦(24%),和上颌女性(24%)。男性发病率为0.76(每100,000人年),女性为0.24,按年龄增长,更明显的是在男人身上,两者都达到了75年的顶峰。职业接触木材和皮革灰尘的频率最高(男性为41%,33%为女性)。很少有暴露是职业外或家庭的。不太可能的暴露与女性有关(57%)。
    结论:在意大利,通过允许识别和赔偿这种职业病的登记处对SNC病例进行监测很重要,许多工人接触SNC的致癌物,甚至没有意识到。考虑到这种疾病的稀有性,尤其是在女性中,ReNaTuNS可以提供一种分析性别差异的方法。
    BACKGROUND: Although rare, sinonasal cancers (SNCs) have a high occupational attributable fraction.
    METHODS: We applied gender-based approaches to descriptive analyses, incidence, and patterns of exposures using the Italian National Sinonasal Cancer Registry (ReNaTuNS: Registro Nazionale Tumori Naso-Sinusali).
    RESULTS: The study included 2851 SNC patients. SNC was diagnosed more often in men (73%) than in women (27%). The most frequent morphology in men was intestinal-type adenocarcinoma (33%), whereas in women, it was squamous cell carcinoma (49%). Nasal cavities were predominant in both genders (50%), ethmoidal sinus in men (24%), and maxillary in women (24%). Incidence rates were 0.76 (per 100,000 person-years) in men and 0.24 in women and increased by age, more evidently in men, peaking over 75 years in both. Occupational exposures to wood and leather dusts were the most frequent (41% for men, 33% for women). Few exposures were extra-occupational or domestic. Unlikely exposure was relevant in women (57%).
    CONCLUSIONS: The surveillance of SNC cases through a registry that allows for the identification of and compensation for this occupational disease is important in Italy, where numerous workers are exposed to carcinogens for SNC, without even being aware. Considering the rarity of the disease, particularly among women, the ReNaTuNS can provide a method to analyze gender differences.
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  • 文章类型: Journal Article
    该病例报告介绍了一名64岁的男性,诊断为鼻窦原发性鳞状细胞癌(SNSCC),一种罕见的侵袭性上消化道恶性肿瘤。最初,他表现为单侧复发性鼻出血。影像学和组织病理学证实了诊断。患者不遵守诊所预约导致显著的疾病进展,最终导致他不幸的死亡。该病例强调了在SNSCC中早期发现和持续监测的重要性,鉴于其非特异性早期症状和不良预后。它强调了对复发性或未解决的鼻窦主诉患者的高度怀疑的必要性,因为及时干预对于取得更好的结果至关重要。
    This case report presents a 64-year-old male diagnosed with sinonasal primary squamous cell carcinoma (SNSCC), a rare and aggressive upper aerodigestive tract malignancy. Initially, he presented with unilateral recurrent epistaxis. Imaging and histopathology confirmed the diagnosis. The patient\'s non-compliance with clinic appointments led to significant disease progression, culminating in his unfortunate demise. This case underscores the importance of early detection and continuous monitoring in SNSCC, given its nonspecific early symptoms and poor prognosis. It emphasizes the necessity for heightened suspicion in patients with recurrent or unresolved sinonasal complaints, as timely intervention is crucial for better outcomes.
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  • 文章类型: Journal Article
    背景:由于其诊断困难和组织学不同,鼻窦癌代表了一种具有挑战性的疾病。尽管进行了多学科评估和治疗,预后不良仍然存在.我们回顾性分析了在我们机构治疗的鼻窦肿瘤患者,注意组织学和现实生活中的预后。
    方法:共纳入51例连续患者。描述了临床特征。总的来说,无病,和疾病特异性生存率(OS,DFS,DSS)根据组织学进行计算。报告了Kaplan-Meyer估计曲线。
    结果:最常见的原发肿瘤是鳞状细胞癌,其次是腺癌。全球2年和5年操作系统分别为68.80%和54.58%,分别。全球2年和5年DFS分别为48.53%和29.56%,而全球2年期和5年期DSS分别为82.86%和74.57%,分别。早期和晚期癌症的中位OS分别为74个月和43个月,分别。Cox多元回归分析未显示年龄的任何统计学显着影响,舞台,或组织学对生存结果的影响。
    结论:诊断通常较晚,预后较差。适当的治疗,这总是非常多模态的,使我们能够实现略高于50%的全球5年操作系统。为了改善预后,必须进行适当的诊断以增加早期肿瘤的百分比。
    BACKGROUND: Sinonasal cancer represents a challenging disease because of its difficult diagnosis and different histology. Despite a multidisciplinary evaluation and treatments, a poor prognosis is still present. We retrospectively analyzed patients with sinonasal cancer treated in our institution, paying attention to histology and real-life prognosis.
    METHODS: A total of 51 consecutive patients were included in the study. Clinical features were described. Overall, disease-free, and disease-specific survival (OS, DFS, DSS) according to histology were calculated. Kaplan-Meyer estimator curves were reported.
    RESULTS: The most prevalent primary tumor was squamous cell carcinoma, followed by adenocarcinoma. Global 2- and 5-year OS was 68.80% and 54.58%, respectively. Global 2- and 5-year DFS was 48.53% and 29.56%, while global 2- and 5-year DSS was 82.86% and 74.57%, respectively. The median OS was 74 and 43 months for early- and late-stage cancer, respectively. The Cox multivariate regression analysis did not reveal any statistically significant effects of age, stage, or histology on survival outcomes.
    CONCLUSIONS: The diagnosis is often late and the prognosis poor. An appropriate treatment, which is always quite multimodal, allows us to achieve a global 5-year OS slightly higher than 50%. An adequate diagnosis to increase the percentage of early-stage tumors is mandatory to improve prognosis.
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  • 文章类型: Journal Article
    目的:鼻窦粘膜黑色素瘤(SNMM)是一种罕见的恶性肿瘤,以高(局部)复发率和低生存率为特征。目前缺乏对肿瘤病因的全面了解,这使得适当的肿瘤治疗复杂化。除了检查发病率的趋势,这项研究旨在评估临床特征之间的关联,治疗实践和患者结果,目的是建立可以增强SNMM管理的基线。
    方法:使用荷兰癌症登记处(NCR)的数据纳入了2001年至2021年荷兰所有新诊断的SNMM病例。
    结果:共纳入320例患者。在纳入期内,总体人群的年发病率是稳定的,年百分比变化(APC)仅为0.01%。5年总生存率(OS)和相对生存率(RS)分别为24.5%和32.4%,分别。相对存活率没有随时间增加。与单独手术相比,在手术中增加辅助放疗与较高的OS和RS无关。
    结论:鼻窦粘膜黑色素瘤是一种罕见的疾病,在2001年至2021年期间在荷兰发病率稳定。在纳入期内,生存率没有改善。该研究重申,辅助放疗似乎并不能改善患者的预后。鉴于SNMM患者的预后普遍较差,为了改善护理,应该考虑新的治疗方案。
    OBJECTIVE: Sinonasal mucosal melanoma (SNMM) is a rare malignancy, characterised by high (local) recurrence rates and poor survival. Comprehensive understanding of tumour etiology is currently lacking, which complicates adequate tumour treatment. Besides examining trends in incidence, this study aims to assess the association between clinical characteristics, treatment practices and patient outcomes, with the objective of establishing a baseline from which SNMM management can be enhanced.
    METHODS: All newly diagnosed SNMM cases in The Netherlands between 2001 and 2021 were included using data from The Netherlands Cancer Registry (NCR).
    RESULTS: A total of 320 patients were included. The annual incidence rate for the overall population was stable over the inclusion period with an annual percentage change (APC) of only - 0.01%. The 5-year overall survival (OS) and relative survival (RS) were 24.5 and 32.4%, respectively. Relative survival did not increase over time. The addition of adjuvant radiotherapy to surgery was not associated with a higher OS and RS compared to surgery alone.
    CONCLUSIONS: Sinonasal mucosal melanoma is a rare disease with stable incidence rates in the Netherlands between 2001 and 2021. There has been no improvement in survival over the course of the inclusion period. The study reaffirms that adjuvant radiotherapy does not seem to improve patient outcomes. Given the generally poor outcomes for SNMM patients, novel therapeutic options ought to be considered in order to improve care.
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  • 文章类型: Journal Article
    源自鼻腔区域上皮的恶性肿瘤称为鼻窦癌。一组高度异质性的罕见肿瘤,占所有头颈部癌症的3-5%。下一代分子谱分析的进展提高了我们对鼻窦癌复杂性的理解,并导致越来越多的不同肿瘤实体的识别。尽管取得了这些重大的进展,自1980年代以来,鼻窦癌症的治疗几乎没有发展,晚期鼻窦癌预后较差,因为通常没有靶向治疗.为了深入了解潜在的靶向治疗机会,我们对患者来源的功能性肿瘤模型进行了多组学分析,以确定与不同亚型鼻窦癌的药理学应答相关的分子特征.
    方法:患者来源的离体肿瘤模型代表四种不同的鼻窦肿瘤亚型:鼻窦肠型腺癌,鼻窦神经内分泌癌,分析包括鼻窦未分化癌和SMARCB1缺陷型鼻窦癌。将160种抗癌疗法的功能性药物筛选结果与基因组测序和肿瘤组织和离体细胞培养物的组织学分析相结合,以建立药物敏感性和包括驱动突变在内的分子特征之间的关联。
    结果:不同的鼻腔鼻窦癌亚型显示出相当不同的药物敏感性。在药物敏感性特征的基础上,每个亚型都与独特的分子特征相关.与特定基因组背景相关的治疗脆弱性得到了扩展,并通过代表不同人类癌症的癌细胞系的计算机模拟分析以及用靶向疗法治疗的鼻腔鼻窦癌症的报道案例研究进行了验证。
    结论:结果证明了了解与鼻窦肿瘤不同亚型相关的差异生物学和分子特征的重要性。患者来源的离体肿瘤模型可以成为研究这些罕见癌症并优先考虑未来临床开发和个性化医疗的靶向治疗策略的强大工具。
    Malignant tumors derived from the epithelium lining the nasal cavity region are termed sinonasal cancers, a highly heterogeneous group of rare tumors accounting for 3 - 5 % of all head and neck cancers. Progress with next-generation molecular profiling has improved our understanding of the complexity of sinonasal cancers and resulted in the identification of an increasing number of distinct tumor entities. Despite these significant developments, the treatment of sinonasal cancers has hardly evolved since the 1980s, and an advanced sinonasal cancer presents a poor prognosis as targeted therapies are usually not available. To gain insights into potential targeted therapeutic opportunities, we performed a multiomics profiling of patient-derived functional tumor models to identify molecular characteristics associated with pharmacological responses in the different subtypes of sinonasal cancer.
    METHODS: Patient-derived ex vivo tumor models representing four distinct sinonasal cancer subtypes: sinonasal intestinal-type adenocarcinoma, sinonasal neuroendocrine carcinoma, sinonasal undifferentiated carcinoma and SMARCB1 deficient sinonasal carcinoma were included in the analyses. Results of functional drug screens of 160 anti-cancer therapies were integrated with gene panel sequencing and histological analyses of the tumor tissues and the ex vivo cell cultures to establish associations between drug sensitivity and molecular characteristics including driver mutations.
    RESULTS: The different sinonasal cancer subtypes display considerable differential drug sensitivity. Underlying the drug sensitivity profiles, each subtype was associated with unique molecular features. The therapeutic vulnerabilities correlating with specific genomic background were extended and validated with in silico analyses of cancer cell lines representing different human cancers and with reported case studies of sinonasal cancers treated with targeted therapies.
    CONCLUSIONS: The results demonstrate the importance of understanding the differential biology and the molecular features associated with the different subtypes of sinonasal cancers. Patient-derived ex vivo tumor models can be a powerful tool for investigating these rare cancers and prioritizing targeted therapeutic strategies for future clinical development and personalized medicine.
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  • 文章类型: Journal Article
    背景:罕见癌症占头颈部癌症的比例不到10%,并且缺乏足够的标准化护理证据。法国罕见头颈部癌症专家网络(REFCOR)建立了一个国家数据库来收集这些罕见癌症的数据。本研究旨在描述该数据库中的患者和肿瘤特征。
    方法:在多个中心进行前瞻性数据收集。使用KaplanMeier方法和LogRank检验进行生存分析。赔率用于比较比例。
    结果:在10年的时间里,共纳入7208例患者。最常见的组织学是:非其他特定(NOS)腺癌13%,腺样囊性癌12%,罕见部位的鳞状细胞癌10%,粘液表皮样癌9%,肠型腺癌(8%)。肿瘤位于鼻窦区域(38%);唾液腺(32%);口腔/口咽/鼻咽(16%);喉/下咽(3%);耳朵(1%);其他(3%)。肿瘤主要分类为T4(23%),N0(54%),和M0(62%)。主要治疗方法包括肿瘤切除(78%)和/或放疗(63%)。唾液腺癌患者表现出更好的5年总生存率(OS)(p<0.05),与鼻窦患者相比,复发率较低,喉/下咽癌。在其他比较中没有观察到显著差异。腺泡细胞癌表现出最好的OS,而粘液黑色素瘤预后最差。
    结论:黑色素瘤,癌NOS,鼻窦无分化癌的预后仍然很差。正在努力,包括培训和指导方针,扩大网络覆盖(REFCOR,EURACAN),改善数据收集并促进个性化治疗。
    BACKGROUND: Rare cancers constitute less than 10% of head and neck cancers and lack sufficient evidence for standardized care. The French Rare Head and Neck Cancer Expert Network (REFCOR) as established a national database to collect data on these rare cancers. This study aims to describe patient and tumour characteristics in this database.
    METHODS: Prospective data collection was conducted across multiple centers. Survival analyses were performed using Kaplan Meier method and Log Rank test. Odds ratios were used for comparing proportions.
    RESULTS: A total of 7208 patients were included over a period of 10 years. The most frequent histologies were: Not Otherwise Specified (NOS) adenocarcinoma 13 %, adenoid cystic carcinoma 12 %, squamous cell carcinoma of rare locations 10 %, mucoepidermoid carcinoma 9 %, intestinal-type adenocarcinoma (8 %). Tumours were located in sinonasal area (38 %); salivary glands (32 %); oral cavity / oropharynx / nasopharynx (16 %); larynx / hypopharynx (3 %); ears (1 %); others (3 %). Tumours were predominantly classified as T4 (23 %), N0 (54 %), and M0 (62 %). Primary treatment approach involved tumour resection (78 %) and / or radiotherapy (63 %). Patients with salivary gland cancers exhibited better 5-year overall survival (OS) rates (p < 0.05), and lower recurrence rates compared to patients with sinonasal, laryngeal/ hypopharyngeal cancers. No significant differences were observed in the other comparisons. Acinar cell carcinoma demonstrated the best OS while mucous melanoma had the poorest prognosis.
    CONCLUSIONS: Melanoma, carcinoma NOS, and sinonasal undifferenciated carcinoma still have poor prognoses. Efforts are being made, including training and guidelines, to expand network coverage (REFCOR, EURACAN), improve data collection and contribute to personalized therapies.
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  • 文章类型: Journal Article
    背景:鼻前庭鳞状细胞癌(SCCNV)是一种罕见的疾病,在表述上明显不同,治疗,以及鼻腔和鼻旁窦鳞状细胞癌(SCC)的结果。然而,这些通常不单独分析。
    方法:使用荷兰癌症登记处(NCR)和荷兰全国病理学数据库(PALGA)的病理报告来鉴定2008年至2021年间荷兰所有新诊断的SCCNV病例。
    结果:共纳入763例患者。年发病率显示出显着下降趋势,年变化百分比(APC)为-3.9%。5年总生存率(OS)和无病生存率分别为69.0%和77.2%,分别。5年相对生存率为77.9%,在纳入期内略有改善。cT3分期的患者的OS似乎比cT4a分期的患者差,对TNM分类的适用性提出质疑。
    结论:鼻前庭的SCC很少见,发病率下降。建议为SCCNV引入特定的拓扑代码以提高配准精度。TNM分类似乎不适用于SCCNV,这表明需要探索其他分期方法。
    BACKGROUND: Squamous cell carcinoma of the nasal vestibule (SCCNV) is a rare disease, distinctly different in presentation, treatment, and outcome from squamous cell carcinoma (SCC) of the nasal cavity and paranasal sinuses. However, these are often not analyzed separately.
    METHODS: The Netherlands Cancer Registry (NCR) and pathology reports from the Dutch Nationwide Pathology Databank (PALGA) were used to identify all newly diagnosed SCCNV cases in the Netherlands between 2008 and 2021.
    RESULTS: A total of 763 patients were included. The yearly incidence rate displayed a significant downward trend with an annual percentage change (APC) of -3.9%. The 5-year overall survival (OS) and disease-free survival were 69.0% and 77.2%, respectively. The 5-year relative survival was 77.9% and improved slightly over the inclusion period. OS for patients who were staged cT3 appeared to be worse than those staged cT4a, calling the applicability of the TNM-classification into question.
    CONCLUSIONS: SCC of the nasal vestibule is rare, with declining incidence rates. Introducing a specific topography code for SCCNV is recommended to enhance registration accuracy. The TNM classification seems poorly applicable to SCCNV, suggesting the need to explore alternative staging methods.
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  • 文章类型: Journal Article
    背景:本研究旨在检查根治性质子束治疗(PBT)后与挽救性颅底手术相关的治疗结果和术后并发症。
    方法:回顾性分析了2002年9月至2023年5月在我们机构接受根治性PBT作为初始治疗后接受了挽救性颅底手术的9例患者。
    结果:该队列包括4名男性和5名女性,平均年龄为48.1岁。在初始治疗期间施用的平均质子剂量为68.5Gy(相对生物学有效性)。在抢救手术中,八个是前颅底手术,一个是前中颅底手术。没有观察到局部复发或围手术期死亡。术后并发症3例(33.3%),都经历过手术部位感染,其中一人也有脑脊液漏。
    结论:该研究表明,在复发性鼻窦恶性肿瘤患者中,PBT后的颅底修复手术有效地实现了局部控制和安全性。
    BACKGROUND: This study aimed to examine treatment outcomes and postoperative complications associated with salvage skull base surgery following radical proton beam therapy (PBT).
    METHODS: Nine patients who underwent salvage skull base surgery following curative PBT as the initial treatment at our institution between September 2002 and May 2023 were retrospectively reviewed.
    RESULTS: The cohort comprised four males and five females with a mean age of 48.1 years. The average proton dose administered during initial therapy was 68.5 Gy (relative biological effectiveness). Among the salvage surgeries, eight were anterior skull base surgeries, and one was an anterior middle skull base surgery. No local recurrences or perioperative deaths were observed. Postoperative complications occurred in three patients (33.3%), all experiencing surgical site infections, with one also having cerebrospinal fluid leakage.
    CONCLUSIONS: The study demonstrates that salvage skull base surgery after PBT effectively achieves local control and safety in patients with recurrent sinonasal malignancies.
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  • 文章类型: Journal Article
    BACKGROUND: Recurrent intestinal-type sinonasal adenocarcinoma (ITAC) can occur several years after primary treatment and with different histology. We aimed to clarify if such recurrences could be second primary tumors and to identify actionable mutations as targets for personalized treatment of recurrent ITAC.
    METHODS: Twelve pairs of primary and recurrent ITAC were histologically examined and analyzed by next-generation sequencing.
    RESULTS: Histological differences between primary and recurrent tumor pairs were observed in five cases. Frequent mutations included TP53, APC, TSC2, ATM, EPHA2, BRCA2, LRP1B, KRAS, and KMT2B. There was 86% concordance of somatic mutations between the tumor pairs, while four cases carried additional mutations in the recurrence.
    CONCLUSIONS: We found all cases to be clonal recurrences and not second primary tumors. Moreover, tumor pairs showed a remarkable genomic stability, suggesting that personalized treatment of a recurrence may be based on actionable molecular genetic targets observed in the primary tumor.
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