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A population-based study of incidence and patient survival of small cell carcinoma in the United States, 1992–2010

机译:1992-2010年美国小细胞癌发病率和患者生存率的人群研究

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Background In contrast to the well-described epidemiology and behavior of small cell lung carcinoma (SCLC), little is known about extrapulmonary small cell carcinoma (EPSCC). Methods Using data from the Surveillance, Epidemiology and End Results (SEER) Program (1992–2010), we calculated age-adjusted incidence rates (IRs), IR ratios (IRRs), annual percent change (APC), relative survival (RS), RS ratios (RSRs), and the respective 95% confidence intervals (95% CI) of SCLC and EPSCC according to primary site. We used the SEER historic stage variable that includes localized (confined to the organ of origin), regional (direct extension to adjacent organ/tissue or regional lymph nodes), and distant (discontinuous metastases) stages and combined localized and regional stages into “limited” stage. Results The incidence of SCLC (IR?=?76.3/million person-years; n?=?51,959) was 22-times that of EPSCC (IR?=?3.5; n?=?2,438). Of the EPSCC sites, urinary bladder, prostate, and uterine cervix had the highest incidence (IRs?=?0.7-0.8); urinary bladder (IRR?=?4.91) and stomach (IRR?=?3.46) had the greatest male/female disparities. Distant-to-limited stage site-specific IRRs of EPSCC were significantly elevated for pancreas (IRR?=?6.87; P?Conclusion EPSCC comprises a heterogeneous group of diseases that appears, at least in part, etiologically distinct from SCLC and is associated with more favorable stage-specific patient survival.
机译:背景技术与众所周知的小细胞肺癌(SCLC)的流行病学和行为相反,关于肺外小细胞癌(EPSCC)知之甚少。方法使用来自监测,流行病学和最终结果(SEER)计划(1992-2010年)的数据,我们计算了年龄调整后的发病率(IR),IR比率(IRR),年变化率(APC),相对生存率(RS) ,RS比率(RSR)和SCLC和EPSCC的95%置信区间(95%CI)(根据主要地点)。我们使用了SEER历史阶段变量,包括局部(仅限于起源器官),区域(直接延伸至相邻器官/组织或区域淋巴结)和远距离(间断转移)阶段,并将局部和区域阶段合并为“有限的”阶段。结果SCLC的发生率(IR = 76.3 /百万人年; n = 51959)是EPSCC的22倍(IR = 3.5; n = 2438)。在EPSCC部位中,膀胱,前列腺和子宫颈的发生率最高(IRs == 0.7-0.8)。男女性别差异最大的是膀胱(IRR≥4.91)和胃(IRR≥3.46)。胰腺EPSCC的从远至极限阶段的特定位点IRRs显着升高(IRR?=?6.87; P?结论)EPSCC包括一组异质性疾病,至少在病因学上不同于SCLC,并且与特定阶段的患者生存率更高。

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