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肢体软组织肉瘤潜在治愈性治疗后的随访费用。

Costs of follow-up after potentially curative treatment for extremity soft-tissue sarcoma.

作者信息

Goel Anupam, Christy Matthew E L, Virgo Katherine S, Kraybill William G, Johnson Frank E

机构信息

Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Int J Oncol. 2004 Aug;25(2):429-35.

Abstract

Soft-tissue sarcoma is an uncommon cancer with the potential for high rates of recurrence after initial therapy. Multiple surveillance strategies have been developed to follow patients after primary treatment. The purpose of this study was to quantify the costs associated with various published post-treatment surveillance strategies. A literature review covering the years 1982-2003 was performed to find all modern published surveillance methods for extremity soft-tissue sarcoma. Only articles describing an explicit 5-year follow-up strategy were included. Total costs of 5-year follow-up were calculated for each strategy using Medicare-allowed charges as a proxy. Thirty-four articles depicting 54 strategies were identified. Total Medicare-allowed charges in year 2003 dollars ranged from 485 dollars for follow-up of low-grade sarcoma to 21,235 dollars for follow-up of high-grade sarcoma, a 42.8-fold cost differential. The average charge for these 54 strategies was 6,401 dollars. Physical examination and chest x-ray were the most commonly used screening modalities. Several guidelines have been proposed for extremity soft-tissue sarcoma patient follow-up, most prominently those of the National Comprehensive Cancer Network. The literature has yet to reflect the consensus these guidelines suggest. This study shows wide disparity in the costs of 54 specific methods of following soft-tissue sarcoma patients. Clinical trials are needed to identify an optimal surveillance strategy, one balancing gains in survival, quality of life, costs, and societal willingness to expend resources. Such trials have not been conducted due to the rarity of extremity soft-tissue sarcomas and the costs associated with conducting long-term trials. Alternatively, prospective evaluation of imaging modalities used in follow-up should be assessed as part of other trials. Computer simulation analysis also holds great promise as an assessment tool for surveillance strategies because patient participation is not required.

摘要

软组织肉瘤是一种罕见的癌症,初始治疗后复发率可能很高。已经制定了多种监测策略来跟踪接受初始治疗后的患者。本研究的目的是量化与各种已发表的治疗后监测策略相关的成本。进行了一项涵盖1982年至2003年的文献综述,以查找所有已发表的肢体软组织肉瘤现代监测方法。仅纳入描述明确5年随访策略的文章。使用医疗保险允许的费用作为替代指标,计算每种策略的5年随访总成本。共识别出34篇描述54种策略的文章。以2003年美元计算,医疗保险允许的总费用范围从低度肉瘤随访的485美元到高度肉瘤随访的21,235美元,成本差异为42.8倍。这54种策略的平均费用为6,401美元。体格检查和胸部X光检查是最常用的筛查方式。已经提出了几项肢体软组织肉瘤患者随访指南,最著名的是美国国立综合癌症网络的指南。文献尚未反映这些指南所建议的共识。本研究表明,跟踪软组织肉瘤患者的54种特定方法的成本存在很大差异。需要进行临床试验以确定最佳监测策略,即在生存、生活质量、成本和社会资源支出意愿之间取得平衡的策略。由于肢体软组织肉瘤罕见以及进行长期试验的成本,此类试验尚未开展。或者,应将随访中使用的成像方式的前瞻性评估作为其他试验的一部分进行评估。计算机模拟分析作为监测策略的评估工具也具有很大潜力,因为无需患者参与。

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