保险状况与原发性骨和四肢软组织肉瘤的生存和治疗有关联吗?SEER数据库研究。

Anne A. Smartt, Eugene S. Jang, W. Tyler
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However, this discrepancy has not been studied in patients with primary bone and extremity soft-tissue sarcomas, a unique oncological population that typically presents late in the disease course and often requires referral and complex treatment at tertiary care centers-issues that health insurance coverage disparities could aggravate.\n\n\nQUESTIONS/PURPOSES\n(1) What is the relationship between insurance status and cause-specific mortality? (2) What is the relationship between insurance status and the prevalence of distant metastases? (3) What is the relationship between insurance status and the proportion of limb salvage surgery versus amputation?\n\n\nMETHODS\nThe Surveillance, Epidemiology, and End Results database (SEER) was used to identify a total of 12,008 patients: 4257 patients with primary bone sarcomas and 7751 patients with extremity soft-tissue sarcomas, who were diagnosed and treated between 2007 and 2014. 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Patients with primary bone and extremity soft-tissue sarcomas who were uninsured were not more likely to have distant metastases at the time of diagnosis and did not have a higher proportion of amputation surgery as compared with patients with non-Medicaid insurance. However, uninsured patients with extremity soft-tissue sarcomas still displayed reduction in disease-specific survival (HR 1.6 [95% CI 1.2 to 2.1]; p = 0.001).\n\n\nCONCLUSIONS\nDisparities manifested by differences in insurance status were correlated with an increased risk of metastasis at the time of diagnosis, reduced likelihood of treatment with limb salvage procedures, and reduced disease-specific survival in patients with primary bone or extremity soft-tissue sarcomas. Although several potentially confounding variables were controlled for, unmeasured confounding played a role in these results. 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引用次数: 25

摘要

背景:最近发表的几项基于人群的研究强调了保险状况与乳腺癌、头颈癌、睾丸癌和淋巴瘤等各种癌症患者生存率之间的关系[22,24,38,41]。一般来说,这些研究表明,没有医疗保险的患者或那些有医疗补助保险的患者比那些没有医疗补助保险的患者生存率要低。然而,这种差异尚未在原发性骨和四肢软组织肉瘤患者中进行研究,这是一种独特的肿瘤人群,通常在病程晚期出现,通常需要转诊和在三级保健中心进行复杂的治疗-健康保险覆盖范围的差异可能会加剧问题。(2)保险状况与远处转移的发生率有何关系?(3)保肢手术与截肢比例与保险状况有何关系?方法采用监测、流行病学和最终结果数据库(SEER),对2007年至2014年诊断和治疗的12,008例患者进行分析,其中4257例原发性骨肉瘤患者和7751例肢体软组织肉瘤患者。患者被分为三个保险组:非医疗补助保险、医疗补助保险和未保险。没有保险信息的患者被排除在外(原发性骨肉瘤2.7%[113例],四肢软组织肉瘤3.1%[243例])。使用Cox比例风险回归分析对患者年龄、性别、种族、民族、疾病程度(淋巴结和转移性累及)、肿瘤分级、肿瘤大小、组织学和原发肿瘤部位进行校正,评估保险状况与生存率之间的关系。结果有医疗补助保险的原发性骨肉瘤患者的疾病特异性生存率比没有医疗补助保险的患者低(风险比为1.3[95%可信区间为1.1 ~ 1.6];P = 0.003)。与没有医疗补助保险的患者相比,有医疗补助保险的肢体软组织肉瘤患者的疾病特异性生存率也降低(HR 1.2 [95% CI 1.0 ~ 1.5];P = 0.019)。原发性骨肉瘤患者(相对危险度1.8 [95% CI 1.3 ~ 2.4];p < 0.001)和四肢软组织肉瘤(RR 2.4 [95% CI 1.9 ~ 3.1];p < 0.001),在诊断时,有医疗补助保险的患者比没有医疗补助保险的患者更有可能发生远处转移。原发性骨肉瘤患者(RR 1.8 [95% CI 1.4 ~ 2.1];p < 0.001)和四肢软组织肉瘤(RR 2.4 [95% CI 1.9 ~ 3.0];p < 0.001),有医疗补助保险的患者比没有医疗补助保险的患者更容易截肢。没有医疗保险的原发性骨和四肢软组织肉瘤患者在诊断时不太可能发生远处转移,与没有医疗保险的患者相比,截肢手术的比例也不高。然而,未投保的四肢软组织肉瘤患者仍表现出疾病特异性生存率降低(HR 1.6 [95% CI 1.2 - 2.1];P = 0.001)。结论:在原发性骨或四肢软组织肉瘤患者中,保险状况差异所表现出的差异与诊断时转移风险增加、肢体保留手术治疗可能性降低以及疾病特异性生存率降低相关。虽然控制了几个潜在的混杂变量,但未测量的混杂因素在这些结果中发挥了作用。未来的研究应该寻求确定是什么因素导致了不合格的保险状况与癌症诊断后较差的生存相关的发现。候选变量可能包括医疗合并症、治疗延误、首次就诊和诊断的时间、接受治疗的类型、前往治疗的距离和交通障碍、自付负担以及教育和识字状况。这些变量几乎肯定与弱势患者群体的社会经济剥夺有关,一旦确定,就可以有针对性地进行治疗,以解决这些系统性不平等问题。证据等级:III级,治疗性研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is There an Association Between Insurance Status and Survival and Treatment of Primary Bone and Extremity Soft-Tissue Sarcomas? A SEER Database Study.
BACKGROUND Several recently published population-based studies have highlighted the association between insurance status and survival in patients with various cancers such as breast, head and neck, testicular, and lymphoma [22, 24, 38, 41]. Generally, these studies demonstrate that uninsured patients or those with Medicaid insurance had poorer survival than did those who had non-Medicaid insurance. However, this discrepancy has not been studied in patients with primary bone and extremity soft-tissue sarcomas, a unique oncological population that typically presents late in the disease course and often requires referral and complex treatment at tertiary care centers-issues that health insurance coverage disparities could aggravate. QUESTIONS/PURPOSES (1) What is the relationship between insurance status and cause-specific mortality? (2) What is the relationship between insurance status and the prevalence of distant metastases? (3) What is the relationship between insurance status and the proportion of limb salvage surgery versus amputation? METHODS The Surveillance, Epidemiology, and End Results database (SEER) was used to identify a total of 12,008 patients: 4257 patients with primary bone sarcomas and 7751 patients with extremity soft-tissue sarcomas, who were diagnosed and treated between 2007 and 2014. Patients were categorized into one of three insurance groups: insured with non-Medicaid insurance, insured with Medicaid, and uninsured. Patients without information available regarding insurance status were excluded (2.7% [113 patients] with primary bone sarcomas and 3.1% [243 patients] with extremity soft-tissue sarcomas.) The association between insurance status and survival was assessed using a Cox proportional hazards regression analysis adjusted for patient age, sex, race, ethnicity, extent of disease (lymph node and metastatic involvement), tumor grade, tumor size, histology, and primary tumor site. RESULTS Patients with primary bone sarcomas with Medicaid insurance had reduced disease-specific survival than did patients with non-Medicaid insurance (hazard ratio 1.3 [95% confidence interval 1.1 to 1.6]; p = 0.003). Patients with extremity soft-tissue sarcomas with Medicaid insurance also had reduced disease-specific survival compared with those with non-Medicaid insurance (HR 1.2 [95% CI 1.0 to 1.5]; p = 0.019). Patients with primary bone sarcomas (relative risk 1.8 [95% CI 1.3 to 2.4]; p < 0.001) and extremity soft-tissue sarcomas (RR 2.4 [95% CI 1.9 to 3.1]; p < 0.001) who had Medicaid insurance were more likely to have distant metastases at the time of diagnosis than those with non-Medicaid insurance. Patients with primary bone sarcomas (RR 1.8 [95% CI 1.4 to 2.1]; p < 0.001), and extremity soft-tissue sarcomas (RR 2.4 [95% CI 1.9 to 3.0]; p < 0.001) that had Medicaid insurance were more likely to undergo amputation than patients with non-Medicaid insurance. Patients with primary bone and extremity soft-tissue sarcomas who were uninsured were not more likely to have distant metastases at the time of diagnosis and did not have a higher proportion of amputation surgery as compared with patients with non-Medicaid insurance. However, uninsured patients with extremity soft-tissue sarcomas still displayed reduction in disease-specific survival (HR 1.6 [95% CI 1.2 to 2.1]; p = 0.001). CONCLUSIONS Disparities manifested by differences in insurance status were correlated with an increased risk of metastasis at the time of diagnosis, reduced likelihood of treatment with limb salvage procedures, and reduced disease-specific survival in patients with primary bone or extremity soft-tissue sarcomas. Although several potentially confounding variables were controlled for, unmeasured confounding played a role in these results. Future studies should seek to identify what factors drive the finding that substandard insurance status is associated with poorer survival after a cancer diagnosis. Candidate variables might include medical comorbidities, treatment delays, time to first presentation to medical care and time to diagnosis, type of treatment received, distance travelled to treatments and transportation barriers, out-of-pocket payment burden, as well as educational and literacy status. These variables are almost certainly associated with socioeconomic deprivation in a vulnerable patient population, and once identified, treatment can become targeted to address these systemic inequities. LEVEL OF EVIDENCE Level III, therapeutic study.
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