Carcinoid Syndrome and Costs of Care During the First Year After Diagnosis of Neuroendocrine Tumors Among Elderly Patients

Oncologist. 2017 Dec;22(12):1451-1462. doi: 10.1634/theoncologist.2017-0149. Epub 2017 Jun 22.

Abstract

Background: Neuroendocrine tumors (NETs) can secrete hormonal peptides that lead to additional symptom burdens. However, it is largely unknown whether and to what extent the additional symptom burdens translate into higher costs of care. This study aimed to examine the cost pattern of elderly NET patients during the first year of diagnosis, taking into account of the carcinoid syndrome status.

Methods: We used Surveillance, Epidemiology, and End Results Medicare data to identify elderly NET patients diagnosed between January 2003 and December 2011. Patients who had at least two claims indicative of carcinoid syndrome during the 3 months before and after the NET diagnosis were considered to have carcinoid syndrome. We adopted a payer's perspective and quantified economic outcomes using the following three measures: (a) total Medicare reimbursement amount, (b) inpatient amount, and (c) outpatient amount. We used a generalized linear model (GLM) to examine the association between syndrome and costs.

Results: Our study cohort included 6,749 elderly NET well-differentiated and moderately differentiated patients. Of these patients, 5,633 (83%) were alive 1 year after diagnosis with continuous enrollment, and 1,116 (17%) died within 1 year. The multivariable GLM showed significant association between the syndrome and higher total, inpatient, and outpatient costs among the group who survived the whole year; the association was insignificant among the group who died within the first year of diagnosis.

Conclusion: This population-based study showed that NET patients with carcinoid syndrome incurred higher costs of care especially among those who survived the first year of diagnosis.

Implications for practice: This is the first population-based study that examines the health care costs associated with carcinoid syndrome among neuroendocrine tumor patients. Among patients alive throughout the first year, the unadjusted analyses showed that total median monthly costs were above $1,000 higher ($3,801 vs. $2,481) for patients with carcinoid syndrome compared with patients without. A significant association was found between carcinoid syndrome and higher total inpatient and outpatient costs among the group that survived the whole year even after controlling for clinical factors, treatment received, and demographics and neighborhood socioeconomic status; the association was insignificant among the group that died within the first year of diagnosis.

摘要

背景.神经内分泌肿瘤(NET)可分泌引发额外症状负荷的激素肽。然而, 尚不清楚额外的症状负荷是否会导致更高的医疗费用以及程度如何。本研究旨在检查NET老年患者在诊断后一年内的费用模式(将类癌综合征状态考虑在内)。

方法.研究使用了监测、流行病学和最终结果医疗保险数据来识别2003年1月至2011年12月期间被诊断患有NET的老年患者。在NET诊断前后3个月内有至少两次提示类癌综合征的索赔的患者被视为罹患类癌综合征。我们采纳了一名支付人的观点并使用以下三个指标对经济结果进行了量化:(a)医疗保险总报销金额, (b)住院费用以及(c)门诊费用。研究使用广义线性模型(GLM)检查了综合征与费用之间的相关性。

结果.研究队列包括6 749名NET高分化型和中度分化型老年患者。其中, 5 633名(83%)在诊断后一年存活内并持续入组, 1 116名(17%)在诊断后一年内死亡。多变量GLM显示在诊断后一年内存活的患者组中, 综合征与总费用、住院费用以及门诊费用较高显著相关;诊断后一年内死亡的患者组中此相关性不显著。

结论.本项基于人群的研究显示, 罹患类癌综合征的NET患者的医疗费用较高, 尤其是诊断后一年内存活的患者。

对临床实践的提示:这是首项基于人群的检查神经内分泌肿瘤患者中与类癌综合征相关的医疗费用的研究。未经校正的分析显示, 在诊断后一年内存活的患者中, 罹患类癌综合征患者的总中位月费用比无类癌综合征的患者高1 000美元(3 801美元 vs. 2 481美元)。研究发现, 即使对临床因素、接受的治疗、人口统计学以及邻近的社会经济状态进行了控制, 诊断后一年内存活的患者组中类癌综合征与总住院费用和门诊费用较高仍显著相关;但诊断后一年内死亡的患者组中相关性不明显。

Keywords: Costs; Earcinoid; Gastrointestinal; Medicare; Neuroendocrine; Surveillance, Epidemiology, and End Results.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cost-Benefit Analysis*
  • Female
  • Humans
  • Insurance Claim Review
  • Male
  • Malignant Carcinoid Syndrome / drug therapy*
  • Malignant Carcinoid Syndrome / economics
  • Malignant Carcinoid Syndrome / epidemiology
  • Medicare
  • Neuroendocrine Tumors / drug therapy*
  • Neuroendocrine Tumors / economics
  • Neuroendocrine Tumors / epidemiology
  • United States