Ehrenkranz Rebecca, Lam Clara, Petkov Valentina I, Dilts David, Cheng Steven, Solis Amy, Negoita Serban
J Registry Manag. 2018 Winter;45(4):161-166.
In 2017, the Surveillance, Epidemiology, and End Results (SEER) program piloted a reactive quality audit plan (r-QAP) to analyze Collaborative Stage (CS) tumor size in breast and pancreatic cancer. Preevaluation objectives were to establish procedures and analytic scope for SEER quality audits, cutoffs for data completeness/accuracy, and key decision checkpoints.
Tumor size data between 2004-2014 were selected from SEER registries for pancreatic and breast cancers, and initially assessed by site and registry for completeness. Further exploration was undertaken via cross tabulation in SEER with the American Joint Committee on Cancer (AJCC) 6th edition derived T data item to evaluate discrepancies between these closely related variables.
For both cancer sites, completeness improved between 2004 and 2014, with the proportion of known tumor size values increasing from 60.6% to 79.2% in pancreatic cancer and from 94.0% to 95.9% in breast cancer. Tumor size plausibility categories were established wherein any tumor over 100 mm for pancreatic cancer or over 200 mm for breast cancer were considered highly unlikely. Only 2% of pancreas tumors and 0.1% of breast tumors were implausibly large per site-specific cutoffs. Less than 2% of all tumor size values were potentially discrepant in cross-tabulation with AJCC 6th edition derived T for each site.
Most tumor size values appear to fall within acceptable ranges based on r-QAP activities, and implausibly large tumor size values are rare. Different natural histories and clinical presentation for pancreatic and breast cancer illustrate the need for site-specific cutoffs. Our results indicate that there are no major quality issues in the SEER research database for the CS tumor size data item in either pancreatic or breast cancer.
2017年,监测、流行病学与最终结果(SEER)项目试行一项反应性质量审核计划(r-QAP),以分析乳腺癌和胰腺癌的协作分期(CS)肿瘤大小。预评估目标是为SEER质量审核建立程序和分析范围、数据完整性/准确性的临界值以及关键决策检查点。
从SEER登记处选取2004 - 2014年间胰腺癌和乳腺癌的肿瘤大小数据,并首先按部位和登记处评估其完整性。通过在SEER中与美国癌症联合委员会(AJCC)第6版衍生的T数据项进行交叉列表进一步探究,以评估这些密切相关变量之间的差异。
对于这两种癌症部位,2004年至2014年间完整性有所提高,胰腺癌已知肿瘤大小值的比例从60.6%增至79.2%,乳腺癌从94.0%增至95.9%。确定了肿瘤大小合理性类别,其中胰腺癌任何超过100毫米或乳腺癌超过200毫米的肿瘤被视为极不可能。根据各部位特定临界值,每个部位只有2%的胰腺肿瘤和0.1%的乳腺肿瘤大小不合理地大。在与每个部位AJCC第6版衍生的T进行交叉列表时,所有肿瘤大小值中不到2%可能存在差异。
基于r-QAP活动,大多数肿瘤大小值似乎落在可接受范围内,且不合理的大肿瘤大小值很少见。胰腺癌和乳腺癌不同的自然病史和临床表现表明需要各部位特定的临界值。我们的结果表明,在SEER研究数据库中,胰腺癌或乳腺癌的CS肿瘤大小数据项不存在重大质量问题。