Brody School of Medicine, East Carolina University (ECU), Greenville, North Carolina, USA.
Division of Hematology/Oncology, Department of Internal Medicine, Brody School of Medicine, East Carolina University (ECU), Greenville, North Carolina, USA.
Cancer Rep (Hoboken). 2024 Sep;7(9):e2156. doi: 10.1002/cnr2.2156.
Squamous cell carcinoma of the prostate (SCCP) is a neoplasm that comprises fewer than 1% of all primary prostate cancer diagnoses. Given its rarity, there is a paucity of data regarding the treatment of this disease. The limited literature points to the potential of local therapy in conjunction with chemotherapy to improve patient mortality.
Using the National Cancer Initiative's Surveillance, Epidemiology, and End Results (SEER) database, a retrospective review of patients diagnosed with primary SCCP between 2000 and 2018 was performed. Patient demographics, tumor characteristics, and patient outcomes based on treatment modality were analyzed. Univariate and survival analyses were conducted with p < 0.05 indicating statistical significance.
A total of 66 patients were identified. Five-year overall survival (5y OS) was 24%; mean and median survival were 2.2 years (1.8, 2.7) and 1.2 years (0.3, 2.1), respectively. Patients with Grade I or Grade II disease had an increased 5y OS of 55% (27%, 83%). In comparison, 5y OS was 13% (-2%, 29%) for patients with Grade III and Grade IV disease (p = 0.017). Analysis of 5y OS based on disease histology revealed patients with papillary SCC had a 5y OS of 50% [9.2%, 91%], compared to 21% [9%, 34%] for patients with SCC, not otherwise specified and 0% for those with lymphoepithelial carcinoma (p = 0.048). Analysis of 5y OS stratified by treatment modality revealed no statistically significant change with any treatment (surgery, radiotherapy, and chemotherapy). No difference in 5y OS was seen between those treated with radical prostatectomy versus external beam radiation therapy.
The literature on SCCP remains sparse; the rarity of this disease limits analysis. While the investigation undertaken in this paper does not find any change in 5y OS regardless of treatment modality, the variation in 5y OS based on histologic classification of SCCP points to a potential route for the future treatment of this disease.
前列腺鳞状细胞癌(SCCP)是一种罕见的肿瘤,占所有原发性前列腺癌诊断的比例不足 1%。由于其罕见性,关于这种疾病的治疗方法的数据非常有限。有限的文献表明,局部治疗联合化疗有可能改善患者的死亡率。
利用国家癌症研究所的监测、流行病学和最终结果(SEER)数据库,对 2000 年至 2018 年间诊断为原发性 SCCP 的患者进行了回顾性分析。分析了患者的人口统计学特征、肿瘤特征以及基于治疗方式的患者结局。单变量和生存分析的 p 值<0.05 表示具有统计学意义。
共确定了 66 例患者。五年总生存率(5y OS)为 24%;平均和中位生存时间分别为 2.2 年(1.8,2.7)和 1.2 年(0.3,2.1)。I 级或 II 级疾病患者的 5y OS 增加了 55%(27%,83%)。相比之下,III 级和 IV 级疾病患者的 5y OS 为 13%(-2%,29%)(p=0.017)。根据疾病组织学分析 5y OS 发现,具有乳头状 SCC 的患者 5y OS 为 50%[9.2%,91%],而未特指的 SCC 患者为 21%[9%,34%],淋巴上皮癌患者为 0%(p=0.048)。按治疗方式分层分析 5y OS 发现,任何治疗(手术、放疗和化疗)均无统计学意义上的变化。根治性前列腺切除术与外照射放疗患者的 5y OS 无差异。
关于 SCCP 的文献仍然很少;这种疾病的罕见性限制了分析。虽然本文所进行的研究没有发现任何治疗方式的 5y OS 变化,但根据 SCCP 的组织学分类,5y OS 的变化表明了未来治疗这种疾病的潜在途径。