Pancreatic Cancer Surveillance and Survival of High-Risk Individuals.

IF 28.4 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Jama Oncology Pub Date : 2024-08-01 DOI:10.1001/jamaoncol.2024.1930
Amanda L Blackford, Marcia Irene Canto, Mohamad Dbouk, Ralph H Hruban, Bryson W Katona, Amitabh Chak, Randall E Brand, Sapna Syngal, James Farrell, Fay Kastrinos, Elena M Stoffel, Anil Rustgi, Alison P Klein, Ihab Kamel, Elliot K Fishman, Jin He, Richard Burkhart, Eun Ji Shin, Anne Marie Lennon, Michael Goggins
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Abstract

Importance: Pancreatic ductal adenocarcinoma (PDAC) is a deadly disease with increasing incidence. The majority of PDACs are incurable at presentation, but population-based screening is not recommended. Surveillance of high-risk individuals for PDAC may lead to early detection, but the survival benefit is unproven.

Objective: To compare the survival of patients with surveillance-detected PDAC with US national data.

Design, setting, and participants: This comparative cohort study was conducted in multiple US academic medical centers participating in the Cancer of the Pancreas Screening program, which screens high-risk individuals with a familial or genetic predisposition for PDAC. The comparison cohort comprised patients with PDAC matched for age, sex, and year of diagnosis from the Surveillance, Epidemiology, and End Results (SEER) program. The Cancer of the Pancreas Screening program originated in 1998, and data collection was done through 2021. The data analysis was performed from April 29, 2022, through April 10, 2023.

Exposures: Endoscopic ultrasonography or magnetic resonance imaging performed annually and standard-of-care surgical and/or oncologic treatment.

Main outcomes and measures: Stage of PDAC at diagnosis, overall survival (OS), and PDAC mortality were compared using descriptive statistics and conditional logistic regression, Cox proportional hazards regression, and competing risk regression models. Sensitivity analyses and adjustment for lead-time bias were also conducted.

Results: A total of 26 high-risk individuals (mean [SD] age at diagnosis, 65.8 [9.5] years; 15 female [57.7%]) with PDAC were compared with 1504 SEER control patients with PDAC (mean [SD] age at diagnosis, 66.8 [7.9] years; 771 female [51.3%]). The median primary tumor diameter of the 26 high-risk individuals was smaller than in the control patients (2.5 [range, 0.6-5.0] vs 3.6 [range, 0.2-8.0] cm, respectively; P < .001). The high-risk individuals were more likely to be diagnosed with a lower stage (stage I, 10 [38.5%]; stage II, 8 [30.8%]) than matched control patients (stage I, 155 [10.3%]; stage II, 377 [25.1%]; P < .001). The PDAC mortality rate at 5 years was lower for high-risk individuals than control patients (43% vs 86%; hazard ratio, 3.58; 95% CI, 2.01-6.39; P < .001), and high-risk individuals lived longer than matched control patients (median OS, 61.7 [range, 1.9-147.3] vs 8.0 [range, 1.0-131.0] months; 5-year OS rate, 50% [95% CI, 32%-80%] vs 9% [95% CI, 7%-11%]).

Conclusions and relevance: These findings suggest that surveillance of high-risk individuals may lead to detection of smaller, lower-stage PDACs and improved survival.

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胰腺癌监测和高危人群的生存率。
重要性:胰腺导管腺癌(PDAC)是一种致命疾病,发病率不断上升。大多数 PDAC 在发病时无法治愈,但不建议进行人群筛查。对 PDAC 高危人群进行监测可能会导致早期发现,但其对生存的益处尚未得到证实:将监测发现的 PDAC 患者的生存率与美国全国数据进行比较:这项比较队列研究在参与胰腺癌筛查计划的多个美国学术医疗中心进行,该计划筛查具有 PDAC 家族或遗传倾向的高危人群。对比队列由年龄、性别和诊断年份与监测、流行病学和最终结果(SEER)计划相匹配的 PDAC 患者组成。胰腺癌筛查计划始于 1998 年,数据收集工作一直持续到 2021 年。数据分析从 2022 年 4 月 29 日开始,至 2023 年 4 月 10 日结束:每年进行一次内镜超声波检查或磁共振成像检查,以及标准护理手术和/或肿瘤治疗:采用描述性统计和条件逻辑回归、Cox 比例危险度回归和竞争风险回归模型对诊断时的 PDAC 分期、总生存期 (OS) 和 PDAC 死亡率进行比较。同时还进行了敏感性分析和前导时间偏差调整:共有 26 名高风险 PDAC 患者(诊断时平均 [SD] 年龄为 65.8 [9.5] 岁;15 名女性 [57.7%])与 1504 名 SEER 对照组 PDAC 患者(诊断时平均 [SD] 年龄为 66.8 [7.9] 岁;771 名女性 [51.3%])进行了比较。26 例高风险患者的原发肿瘤中位直径小于对照组患者(分别为 2.5 [范围,0.6-5.0] cm vs 3.6 [范围,0.2-8.0]cm;P 结论及意义:这些研究结果表明,对高危人群进行监测可能会发现较小、较低分期的 PDAC,从而提高存活率。
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来源期刊
Jama Oncology
Jama Oncology Medicine-Oncology
CiteScore
37.50
自引率
1.80%
发文量
423
期刊介绍: At JAMA Oncology, our primary goal is to contribute to the advancement of oncology research and enhance patient care. As a leading journal in the field, we strive to publish influential original research, opinions, and reviews that push the boundaries of oncology science. Our mission is to serve as the definitive resource for scientists, clinicians, and trainees in oncology globally. Through our innovative and timely scientific and educational content, we aim to provide a comprehensive understanding of cancer pathogenesis and the latest treatment advancements to our readers. We are dedicated to effectively disseminating the findings of significant clinical research, major scientific breakthroughs, actionable discoveries, and state-of-the-art treatment pathways to the oncology community. Our ultimate objective is to facilitate the translation of new knowledge into tangible clinical benefits for individuals living with and surviving cancer.
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