Fleszar-Pavlovic Sara E, Benzo Roberto M, Gong Rui, Browder Amber, Nawab Aria, Brito Arianna E, Merchant Nipun B, Penedo Frank J
Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA.
Psychooncology. 2025 Mar;34(3):e70135. doi: 10.1002/pon.70135.
Pancreatic cancer (PaCa) patients face a 5-year survival rate of just 13%. Most patients present with unresectable disease and endure aggressive treatments with significant chronic and debilitating side effects. PaCa patients also experience significant unmet supportive care needs (e.g., physical, psychological, informational/educational); however, limited qualitative studies have explored the specific needs of racially and ethnically diverse PaCa populations.
This study identified supportive care needs in a racially and ethnically diverse sample of PaCa survivors.
As part of a larger project to develop a psychosocial symptom management intervention, semi-structured qualitative interviews were conducted with PaCa survivors to explore the supportive care needs at diagnosis and after treatment. Qualitative data were analyzed using Rapid Qualitative Analysis, and personal/medical characteristics were analyzed using descriptive statistics.
PaCa survivors (n = 18; M = 64) participated, with the majority identifying as female (66.7%), White (88.9%), and Hispanic (55.6%). Over one-third completed interviews in Spanish. Four themes emerged: (1) information/health system needs, including difficulty understanding complex medical concepts, limited holistic care, post-treatment symptom management, and health behaviors; (2) psychosocial needs related to quality of life and relationships with family and healthcare providers; (3) physical and functional needs, including persistent side effects and lifestyle changes; and (4) positivity and gratitude.
We emphasize the themes of unmet supportive care needs in a racially and ethnically diverse sample of PaCa survivors. These findings underscore the importance of developing interventions to address these gaps and improve the overall quality of life for diverse PaCa patients.
胰腺癌(PaCa)患者的5年生存率仅为13%。大多数患者就诊时已处于无法切除的疾病阶段,并要接受激进的治疗,且伴有严重的慢性和使人衰弱的副作用。PaCa患者还存在大量未得到满足的支持性护理需求(如身体、心理、信息/教育方面);然而,针对不同种族和民族的PaCa人群的具体需求,进行的定性研究有限。
本研究确定了不同种族和民族的PaCa幸存者的支持性护理需求。
作为开发心理社会症状管理干预措施的一个更大项目的一部分,对PaCa幸存者进行了半结构化定性访谈,以探讨诊断时和治疗后的支持性护理需求。定性数据采用快速定性分析法进行分析,个人/医学特征采用描述性统计法进行分析。
共有18名PaCa幸存者(平均年龄64岁)参与,其中大多数为女性(66.7%)、白人(88.9%)和西班牙裔(55.6%)。超过三分之一的人用西班牙语完成了访谈。出现了四个主题:(1)信息/卫生系统需求,包括理解复杂医学概念困难、整体护理有限、治疗后症状管理和健康行为;(2)与生活质量以及与家人和医疗保健提供者关系相关的心理社会需求;(3)身体和功能需求,包括持续的副作用和生活方式改变;(4)积极态度和感恩。
我们强调了在不同种族和民族的PaCa幸存者样本中未得到满足的支持性护理需求主题。这些发现凸显了制定干预措施以填补这些差距并改善不同PaCa患者总体生活质量的重要性。