首页> 外文期刊>Journal of Surgical Oncology >Survival after resection of cutaneous adnexal carcinomas with eccrine differentiation: Risk factors and trends in outcomes
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Survival after resection of cutaneous adnexal carcinomas with eccrine differentiation: Risk factors and trends in outcomes

机译:具有内分泌分化的皮肤附件癌切除术后的生存:危险因素和预后趋势

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Background Current staging systems do not specifically address cutaneous adnexal carcinomas with eccrine differentiation. Due to their rarity, prognosis and management strategies are not well established. A population-based study was performed to determine prognostic factors and survival. Methods Patients diagnosed with cutaneous adnexal carcinomas with eccrine differentiation were identified using the surveillance, epidemiology, and end results population-based cancer registry. Associations between risk factors, treatment modalities, and survival were calculated using logistical regression, Kaplan-Meier estimates and log-rank analysis. Results The incidence of distinct eccrine subtypes was determined within 1,045 patients with cutaneous adnexal tumors containing eccrine differentiation. All-cause 5-year survival (OS) was 82%, while age-adjusted survival was 94%. Patients with microcystic adnexal carcinoma had improved OS (90%) compared to patients with hidradenocarcinoma (74%), spiradenocarcinoma (77%), porocarcinoma (79%), and eccrine adenocarcinoma (81%). The majority of patients were treated with surgical excision and a small subset with surgery plus radiation, with similar OS. Patients with well-to-moderately differentiated tumors demonstrated improved OS compared to those with poorly differentiated/anaplastic disease. Conclusions Histological subtype and grade were associated with survival, and should be specified in biopsies and excised specimens. Surgical excision is appropriate, and the addition of adjuvant radiation may not be associated with survival. These results highlight survival data and high-risk prognostic factors that warrant prospective validation, and may augment current staging systems.
机译:背景技术当前的分期系统并未专门针对具有内分泌分化的皮肤附件癌。由于它们的稀有性,预后和管理策略还不完善。进行了一项基于人群的研究,以确定预后因素和生存率。方法使用监测,流行病学和最终结果以人群为基础的癌症登记系统,对诊断出患有皮肤附件附件癌并伴有内分泌分化的患者进行鉴定。使用逻辑回归,Kaplan-Meier估计和对数秩分析计算风险因素,治疗方式和生存率之间的关联。结果确定了1,045例患有内分泌分化的皮肤附件肿瘤患者中不同内分泌亚型的发生率。 5年全因生存率(OS)为82%,而按年龄调整的生存率则为94%。与囊状腺癌(74%),螺旋腺癌(77%),孢子癌(79%)和内分泌腺癌(81%)相比,微囊性附件癌患者的OS改善(90%)。大多数患者接受了手术切除,一小部分接受了手术加放疗,且OS相似。与低分化/间变性疾病相比,高分化到中等分化肿瘤的患者表现出更好的OS。结论组织学亚型和等级与生存有关,应在活检和切除的标本中注明。手术切除是适当的,辅助放疗可能与生存无关。这些结果突出了值得进行前瞻性验证的生存数据和高风险预后因素,并可能扩大当前的分期系统。

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