Suppr超能文献

丹麦卫生局癌症患者治疗审查专家咨询小组的21年报告,涉及10000名癌症患者的治疗情况。

Twenty-one-year report from the Danish Health Authority Expert Advisory Panel for review of treatment of 10 000 cancer patients.

作者信息

Ladekarl Morten, Mørk Mette Louise, Albertsen Emma Skotte, Nielsen Dorte, Lassen Ulrik, Mau-Sørensen Morten, Nielsen Claus Malta, Jakobsen Anders, von der Maase Hans

机构信息

Department of Oncology and Clinical Cancer Research Center, Aalborg University Hospital, 9000 Aalborg, Denmark.

Department of Clinical Medicine, Aalborg University, 9220 Aalborg, Denmark.

出版信息

Oncologist. 2025 May 8;30(5). doi: 10.1093/oncolo/oyaf059.

Abstract

BACKGROUND

Patients with hard-to-treat or rare cancers and those not responding to standard-of-care (SoC) treatment have unmet needs. Limited access to novel drugs is an increasing additional challenge. In 2003, the Danish government adopted a Health Act to ensure that treatment of patients with life-threatening disease could be reevaluated by independent experts. The Danish Health Authority (DHA) set up an Expert Advisory Panel to provide advice on possibilities for further treatment of patients, including treatment not approved nationally. A few years later, clinical units were established that could offer unestablished treatment to patients by referral from the Panel. The treatment was first reimbursed by the Government and later by regional authorities.

MATERIALS AND METHODS

We present the structure, workflow, and impact of the Health Act for 21 years for patients with cancer. Annual reports from the DHA were the primary data source.

RESULTS

11 034 cases from 9603 cancer patients were evaluated by the Panel from 2003 to 2023, representing a median of 372 unique cases yearly. In 53%, the Panel advised on further treatment in Denmark, and of these, 56% were recommended nationally nonapproved treatment, 21% SoC treatment or workup, and 19% clinical trial participation. In 4.5% of cases, advice was given on treatment abroad. A significant decline in admissions to the Panel from a peak of 1167 patients in 2008 to 3-400 yearly from 2012 to 2017 followed the conversion of nonapproved treatments to SoC practice. A shift in drug reimbursement, independent of Panel advise, reduced the clinical impact and explained the further decline observed in admissions lately to only 51 patients in 2023.

CONCLUSIONS

This unique national scheme provided early access to treatment for patients with no further SoC options and facilitated the introduction of new cancer treatments, initiation of clinical trials, and establishment of trial units in the country. The scheme may be adapted to other countries with a public healthcare system. Results of the current report indicate that impact is dependent on delivering clinical units and reimbursement associated with the recommended treatment.

摘要

背景

患有难治性或罕见癌症的患者以及对标准治疗(SoC)无反应的患者存在未满足的需求。获得新型药物的机会有限是一个日益增加的额外挑战。2003年,丹麦政府通过了一项《健康法案》,以确保对患有危及生命疾病的患者的治疗可由独立专家重新评估。丹麦卫生当局(DHA)设立了一个专家咨询小组,就患者进一步治疗的可能性提供建议,包括未在国内获批的治疗。几年后,设立了临床单位,可根据小组的转诊为患者提供未经验证的治疗。该治疗最初由政府报销,后来由地区当局报销。

材料与方法

我们介绍了《健康法案》21年来对癌症患者的结构、工作流程和影响。DHA的年度报告是主要数据源。

结果

2003年至2023年,专家咨询小组对9603名癌症患者的11034例病例进行了评估,每年中位数为372例独特病例。在53%的病例中,小组就丹麦的进一步治疗提供了建议,其中56%被推荐接受国内未获批的治疗,21%接受标准治疗或检查,19%参与临床试验。在4.5%的病例中,就国外治疗提供了建议。随着未获批治疗转变为标准治疗实践,专家咨询小组的接诊人数从2008年的1167名患者的峰值显著下降至2012年至2017年每年的300 - 400名。与专家咨询小组的建议无关的药物报销变化降低了临床影响,并解释了最近接诊人数进一步下降至2023年仅51名患者的原因。

结论

这一独特的国家计划为没有其他标准治疗选择的患者提供了早期治疗机会,并促进了新癌症治疗方法的引入、临床试验的启动以及该国试验单位的建立。该计划可适用于其他具有公共医疗系统的国家。本报告结果表明,影响取决于提供临床单位以及与推荐治疗相关的报销。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验