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首页> 外文期刊>Health technology assessment: HTA >The clinical effectiveness and cost-effectiveness of different surveillance mammography regimens after the treatment for primary breast cancer: systematic reviews registry database analyses and economic evaluation.
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The clinical effectiveness and cost-effectiveness of different surveillance mammography regimens after the treatment for primary breast cancer: systematic reviews registry database analyses and economic evaluation.

机译:临床疗效和成本效益不同的监测乳房x光检查方案治疗后原发性乳腺癌:数据库分析和系统评价注册表经济评价。

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BACKGROUND: Following primary breast cancer treatment, the early detection of ipsilateral breast tumour recurrence (IBTR) or ipsilateral secondary cancer in the treated breast and detection of new primary cancers in the contralateral breast is beneficial for survival. Surveillance mammography is used to detect these cancers, but the optimal frequency of surveillance and the length of follow-up are unclear. OBJECTIVES: To identify feasible management strategies for surveillance and follow-up of women after treatment for primary breast cancer in a UK setting, and to determine the effectiveness and cost-effectiveness of differing regimens. METHODS: A survey of UK breast surgeons and radiologists to identify current surveillance mammography regimens and inform feasible alternatives; two discrete systematic reviews of evidence published from 1990 to mid 2009 to determine (i) the clinical effectiveness and cost-effectiveness of differing surveillance mammography regimens for patient health outcomes and (ii) the test performance of surveillance mammography in the detection of IBTR and metachronous contralateral breast cancer (MCBC); statistical analysis of individual patient data (West Midlands Cancer Intelligence Unit Breast Cancer Registry and Edinburgh data sets); and economic modelling using the systematic reviews results, existing data sets, and focused searches for specific data analysis to determine the effectiveness and cost-utility of differing surveillance regimens. RESULTS: The majority of survey respondents initiate surveillance mammography 12 months after breast-conserving surgery (BCS) (87%) or mastectomy (79%). Annual surveillance mammography was most commonly reported for women after BCS or after mastectomy (72% and 53%, respectively). Most (74%) discharge women from surveillance mammography, most frequently 10 years after surgery. The majority (82%) discharge from clinical follow-up, most frequently at 5 years. Combining initiation, frequency and duration of surveillance mammography resulted in 54 differing surveillance regimens for women after BCS and 56 for women following mastectomy. The eight studies included in the clinical effectiveness systematic review suggest surveillance mammography offers a survival benefit compared with a surveillance regimen that does not include surveillance mammography. Nine studies were included in the test performance systematic review. For routine IBTR detection, surveillance mammography sensitivity ranged from 64% to 67% and specificity ranged from 85% to 97%. For magnetic resonance imaging (MRI), sensitivity ranged from 86% to 100% and specificity was 93%. For non-routine IBTR detection, sensitivity and specificity for surveillance mammography ranged from 50% to 83% and from 57% to 75%, respectively, and for MRI from 93% to 100% and from 88% to 96%, respectively. For routine MCBC detection, one study reported sensitivity of 67% and specificity of 50% for both surveillance mammography and MRI, although this was a highly select population. Data set analysis showed that IBTR has an adverse effect on survival. Furthermore, women experiencing a second tumour measuring >20 mm in diameter were at a significantly greater risk of death than those with no recurrence or those whose tumour was <10 mm in diameter. In the base-case analysis, the strategy with the highest net benefit, and most likely to be considered cost-effective, was surveillance mammography alone, provided every 12 months at a societal willingness to pay for a quality-adjusted life-year of either pound20,000 or pound30,000. The incremental cost-effectiveness ratio for surveillance mammography alone every 12 months compared with no surveillance was pound4727.
机译:背景:原发性乳腺癌身体的同侧的治疗,早期检测乳房肿瘤复发(IBTR)或同侧在治疗乳腺癌和二次癌症新主要癌症的检测对侧乳房有利于生存。监视乳房x线照相术用于检测这些癌症,但最优频率监测和随访的长度不清楚。监视和管理策略后续治疗原发性后的女性乳腺癌在英国环境,并确定的有效性和成本效益不同的方案。乳腺外科医生和放射科医生识别乳房x光检查方案和电流监测告知可行的替代品;系统的证据发表评论1990年到2009年中期确定(i)临床不同的效率和成本效益监测病人的乳房x光检查方案健康状况和(2)的测试性能监测检测IBTR乳房x光检查以及异时侧乳腺癌(MCBC);(西米德兰兹郡癌症患者数据情报乳腺癌单位注册和爱丁堡数据集);系统评价结果,现有的数据集,和集中搜索特定的数据分析来确定有效性和成本效用不同的监测方案。大多数的受访者监视乳房x光检查后12个月手术(87%)或(BCS)乳房切除术(79%)。BCS或后是女性最常见的报道吗乳房切除术后(分别为72%和53%)。大多数(74%)放电妇女从监视乳房x光检查,最常见的10年之后手术。临床随访,经常在5年。结合开始,频率和持续时间监视乳房x光检查导致54个不同BCS后监测方案为女性,56岁乳房切除术后的女性。包括在临床系统的有效性审查监测乳房x光检查提供了建议生存与监测中获益不包括监测方案乳房x光检查。测试性能系统综述。IBTR检测、监测乳房x光检查灵敏度范围从64%到67%特异性从85%到97%不等。磁共振成像(MRI),灵敏度范围从86%至100%,特异性为93%。非常规IBTR检测灵敏度和用于监测乳房x光检查范围的特异性从50%到83%,从57%提高到75%,MRI分别从93%和100%分别从88%降至96%。一项研究报道,检测灵敏度为67%监测和特异性为50%乳房x光检查和核磁共振,尽管这是一个高度选择人口。IBTR对生存有负面影响。此外,女性经历第二个肿瘤测量> 20毫米直径都在明显更大的死亡风险比没有复发或那些肿瘤< 10毫米直径。净效益最高的策略,大多数可能被认为是具有成本效益的,监视乳房x光检查,每12提供个月社会支付意愿要么pound20,000质量调整生命年或pound30,000。成本效益率监测每12个月相比之下,独自乳房x光检查没有pound4727监测。

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