PO.PS01.11 · 人群科学

支持性治疗药物的使用与诊断时胰腺癌肿瘤位置相关

Use of supportive care medications is associated with pancreatic cancer tumor location at diagnosis

海报缩略图:支持性治疗药物的使用与诊断时胰腺癌肿瘤位置相关
编号 7566 展板 14 时间 4/22 09:00–12:00 区域 Section 34 主讲 Hussein Khalil, B Pharm;MS;PhD
分会场 Psychosocial and Behavioral Epidemiology, Health Services Research, Implementation Science, Pharmacoepidemiology, and Other Topics
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作者与单位 Authors & Affiliations

Hussein Khalil1, Kourtney A. D. Byrd1, Yi Guo2, Shuang Yang3, Xiwei Lou3, Lisa Scarton4, Sherise C. Rodgers5, Diana J. Wilke4, John M. Allen1

1Purdue University, West Lafayette, IN,2University of Florida College of Medicine, Gainesville, FL,3College of Medicine, University of Florida, Gainesville, FL,4University of Florida, Gainesville, FL,5Brown University, Providence, RI

摘要 Abstract

中文摘要
背景:胰腺癌(PC)常表现为随肿瘤位置而异的非特异性症状。位于体部和尾部的肿瘤常较晚出现症状,且更常伴有疼痛、恶心或恶病质。支持性治疗药物(SCMs),如精神类药物、镇痛药物、止吐药和食欲刺激剂,常用于管理这些症状,但关于处方模式是否因肿瘤位置而异所知甚少。我们评估了诊断时胰腺肿瘤位置是否与老年胰腺癌患者后续SCMs的使用相关。 方法:我们利用监测、流行病学与最终结果(SEER)-Medicare数据(2007-2019年)开展了一项回顾性队列研究。研究纳入年龄≥65岁、患有新发胰腺癌且在诊断前3个月连续拥有Medicare A、B、D部分保障的患者。在6个月内有其他癌症诊断或基线数据缺失的患者被排除。诊断前SCM使用情况通过Medicare Part D处方索赔确定。诊断时肿瘤位置分类为胰头(C250)、体部(C251)、尾部(C252)或其他(C253、C254、C257、C258、C679)。我们采用多变量logistic回归评估SCM使用与肿瘤位置之间的关联,并校正潜在混杂因素。 结果:与胰头肿瘤相比,体部肿瘤与接受大多数SCM类别的较高几率相关,包括精神类药物(任何精神类药物的OR:1.13;95% CI:1.08-1.19)、镇痛药物(任何镇痛药物的OR:1.25;95% CI:1.19-1.31)、止吐药(OR:1.08;95% CI:1.03-1.13)、食欲刺激剂(OR:1.16;95% CI:1.11-1.21)。尾部肿瘤与抗焦虑药(OR:1.07;95% CI:1.00-1.14)和非阿片类镇痛药(OR:1.25;95% CI:1.15-1.37)使用增加相关,但止吐药使用几率较低(OR:0.85;95% CI:0.81-0.89)。其他位置的肿瘤在几乎所有类别中的SCM使用几率普遍较低。 结论:诊断时胰腺癌肿瘤位置与支持性治疗药物使用的不同模式相关。胰腺体部肿瘤患者比胰头肿瘤患者更可能接受针对症状的治疗,而尾部或其他位置肿瘤患者的模式则更为多变。这些发现提示肿瘤位置可能影响支持性治疗需求,在制定个性化症状管理策略时应予以考虑。
查看英文原文 English abstract
Background: Pancreatic cancer (PC) often presents with non-specific symptoms that vary by tumor location. Tumors in the body and tail often present later and are more commonly associated with pain, nausea, or cachexia. Supportive care medications (SCMs) such as psychotropics, pain relief medications, antinausea agents, and appetite stimulants ae commonly used to manage these symptoms yet little is known about whether prescribing patterns differ by tumor location. We evaluated whether pancreatic tumor location at diagnosis is associated with subsequent use of SCMs among older adults with pancreatic cancer. Methods: We conducted a retrospective cohort study using Surveillance, Epidemiology, and End Results (SEER)-Medicare data (2007-2019). The study included patients aged ≥65 years old with incident pancreatic cancer and continuous Medicare parts A, B, and D coverage for 3 months before diagnosis. Patients with another cancer diagnosis within 6 months or missing baseline data were excluded. Pre-diagnosis SCM use was ascertained from Medicare Part D prescription claims. Tumor location at diagnosis were categorized as pancreatic head (C250), body (C251), tail (C252), or other (C253, C254, C257, C258, C679). We used multivariable logistic regression to evaluate the association between SCM use and tumor location adjusting potential confounders. Results: Compared to tumors in the pancreatic head, tumors in the body were associated with higher odds of receiving most SCM classes including psychotropic medications (OR for any psychotropic: 1.13; 95% CI: 1.08-1.19), pain medications (OR for any pain medication: 1.25; 95% CI: 1.19-1.31), anti-nausea agents (OR: 1.08; 95% CI: 1.03-1.13), appetite stimulants (OR: 1.16; 95% CI: 1.11-1.21). Tail tumors were associated with increased use of anxiolytics (OR: 1.07; 95% CI: 1.00 - 1.14) and non-opioid analgesics (OR: 1.25; 95% CI: 1.15-1.37), but lower odds of anti-nausea use (OR: 0.85; 95% CI: 0.81-0.89). Tumors in other locations generally had lower odds of SCM use across nearly all categories. Conclusion: Pancreatic cancer tumor location at diagnosis is associated with distinct patterns of supportive care medication use. Patients with tumors in the body of the pancreas were more likely to receive symptom-directed therapies than those with head tumors while those with tail or other locations had more variable patterns. These findings suggest that tumor location may influence supportive care needs and should be considered when tailoring symptom management strategies.
利益披露 Disclosure
H. Khalil, None.. K. A. D. Byrd, None.. S. Yang, None.. X. Lou, None.. S. C. Rodgers, None.. D. J. Wilke, None.. J. M. Allen, None.

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