美国癌症护理医师对真实世界证据的接受和利用:一项全国性调查。

IF 4.5 Q2 PHARMACOLOGY & PHARMACY
Thomas M Porter, Kathleen M Andersen, Wencesley Paez, Patrick Corr, Sabrina Figueiredo
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引用次数: 0

摘要

背景和目的:监管机构和政策制定者越来越多地认识到真实世界证据(RWE)是肿瘤学随机对照试验(rct)的有价值补充,但关于美国医生如何治疗癌症使用和理解RWE的数据仍然有限。该研究旨在评估美国治疗癌症的医生对RWE的态度,包括他们对解释RWE的信心和对临床决策环境的依赖。方法:2024年11月,对从美国临床肿瘤学会(ASCO)成员目录中招募的美国有执照的癌症治疗医生进行了一项横断面全国调查,采用按州人口分层的随机样本。纳入标准为积极的美国医疗执照和目前参与肿瘤患者护理。调查工具包括关于人口统计和实践特点的部分;RWE熟悉度和使用频率;RWE与RCT在治疗选择、给药和结局预测方面的比较依赖(量表范围从0到10:0 =完全依赖RCT数据,10 =完全依赖RWE);感知到的采用障碍(4分制);潜在的促进者(4分制)。分类数据汇总为计数和百分比,连续变量汇总为均值和标准差(SD)。使用卡方检验比较各组间的分类变量,使用配对t检验评估平均信赖评分的差异,使用Spearman's rho评估相关性。p < 0.05为差异有统计学意义。结果:共收到调查问卷128份。总体而言,94%的受访者(n = 120)至少“有点熟悉”RWE, 14% (n = 18)“经常”使用RWE, 3% (n = 4)报告每天使用RWE。49% (n = 63)的医生对RWE研究的解释有信心,职业生涯晚期(20年以上经验)的医生比职业生涯早期和中期的同行更缺乏信心。治疗选择(平均3.0,SD 1.7)对RWE的依赖低于给药(平均3.7,SD 2.0)或结果预测(平均3.8,SD 2.0) (p < 0.001)。最大的障碍包括调和冲突的RWE和RCT数据、数据完整性和偏倚。主要的促进因素包括改进的分析标准、指南整合和额外的培训。结论:虽然治疗癌症的美国医生对RWE的认识很高,但他们根据临床情况选择性地应用RWE,对治疗选择的依赖程度明显较低。解决对方法严谨性、数据质量和解释技能的关注可能会加强RWE与肿瘤治疗的整合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acceptance and Utilization of Real-World Evidence among Cancer Care Physicians in the USA: A National Survey.

Background and objective: Regulatory agencies and policy makers increasingly recognize real-world evidence (RWE) as a valuable complement to randomized controlled trials (RCTs) in oncology, yet data on how US physicians who treat cancer use and perceive RWE remain limited. The study aimed to assess attitudes toward RWE among US physicians who treat cancer, including their confidence in interpreting it and reliance across clinical decision contexts.

Methods: A cross-sectional national survey was administered in November 2024 to licensed US physicians who treat cancer, recruited from the American Society of Clinical Oncology (ASCO) member directory, using a random sample stratified by state population. Inclusion criteria were active US medical licensure and current involvement in oncology patient care. The survey instrument included sections on demographics and practice characteristics; RWE familiarity and usage frequency; comparative reliance on RWE versus RCTs in treatment selection, dosing, and outcome prediction (scales ranging from 0 to 10: 0 = complete reliance on RCT data, 10 = complete reliance on RWE); perceived barriers to adoption (4-point scale); and potential facilitators (4-point scale). Categorical data were summarized as counts and percentages, and continuous variables were summarized as means and standard deviations (SD). Chi-squared tests were used to compare categorical variables across groups, paired t tests were used to assess differences in mean reliance scores, and Spearman's rho was used to evaluate correlations. Statistical significance was set at p < 0.05.

Results: In total, 128 completed surveys were received. Overall, 94% of respondents (n = 120) were at least "somewhat familiar" with RWE, 14% (n = 18) used it "often," and 3% (n = 4) reported daily use. 49% (n = 63) felt confident interpreting RWE studies, with late-career physicians (> 20 years of experience) less confident than their early and mid-career peers. Reliance on RWE was lower for treatment selection (mean 3.0, SD 1.7) than for dosing (mean 3.7, SD 2.0) or outcome prediction (mean 3.8, SD 2.0) (p < 0.001). Top barriers included reconciling conflicting RWE versus RCT data, data completeness, and bias. Key facilitators included improved analytical standards, guideline integration, and additional training.

Conclusions: While awareness of RWE is high among US physicians who treat cancer, they apply it selectively on the basis of clinical context, showing notably lower reliance for treatment selection. Addressing concerns about methodological rigor, data quality, and interpretive skills may strengthen RWE's integration into oncology care.

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来源期刊
Pharmaceutical Medicine
Pharmaceutical Medicine PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.00%
发文量
36
期刊介绍: Pharmaceutical Medicine is a specialist discipline concerned with medical aspects of the discovery, development, evaluation, registration, regulation, monitoring, marketing, distribution and pricing of medicines, drug-device and drug-diagnostic combinations. The Journal disseminates information to support the community of professionals working in these highly inter-related functions. Key areas include translational medicine, clinical trial design, pharmacovigilance, clinical toxicology, drug regulation, clinical pharmacology, biostatistics and pharmacoeconomics. The Journal includes:Overviews of contentious or emerging issues.Comprehensive narrative reviews that provide an authoritative source of information on topical issues.Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by PRISMA statement.Original research articles reporting the results of well-designed studies with a strong link to wider areas of clinical research.Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Pharmaceutical Medicine may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.All manuscripts are subject to peer review by international experts. Letters to the Editor are welcomed and will be considered for publication.
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