Kurtin Sandra, Woodward Susan, Kolb Erin, Snyder Shonna, Hull Shawna
From University of Arizona Cancer Center, Tucson, Arizona.
Moffitt Cancer Center, Tampa, Florida.
J Adv Pract Oncol. 2025 May 4:1-11. doi: 10.6004/jadpro.2025.16.7.13.
Symptom burden is the primary driver for patients with indolent systemic mastocytosis (ISM) to seek medical care, whether or not they are diagnosed.
This descriptive study aimed to describe the advanced practitioner (AP) and ISM patient perspective relative to the symptom burden of ISM, multidisciplinary diagnosis and management of ISM, barriers to symptom management, strategies for collaborative management of ISM, and communicative health literacy in patients with ISM.
An ISM patient survey and AP survey were developed by an AP-led steering committee incorporating validated tools to measure symptom burden, symptom burden impact, barriers, and strategies for improving symptom burden. Surveys were embedded in Qualtrics and were deployed by Conexiant to a convenience sample of AP members of the Advanced Practitioner Society for Hematology/Oncology (APSHO), AP members of the American Initiative in Mast Cell Diseases, and patients affiliated with The Mast Cell Disease Society between December 22, 2024, and February 3, 2025.
50 APs and 53 ISM patients completed 100% of the questions on the corresponding surveys. The symptom burden described using the Indolent Systemic Mastocytosis Symptom Assessment Form (ISM-SAF) to identify the symptoms that are most common, most challenging, and have the greatest impact on quality of life aligns with published data for patients in this survey. Only 24% ( = 13) of ISM patients indicated their disease was well controlled, while 76% of APs indicated greater than 50% of their ISM patients had well-controlled disease ( = 38). Most APs (68%) in the survey indicated they saw one to five ISM patients per year but were comfortable with managing ISM-related symptoms (54%, = 27). Practice patterns for triage, multidisciplinary management, and shared decision-making are described.
This is the first ISM symptom burden-focused survey to provide a direct comparison of patient responses to those of APs in hematology/oncology and allergy and immunology. Indolent systemic mastocytosis symptom burden measurement and symptom burden reduction remain challenging, with several barriers and gaps identified in this study. The APSHO Toolkit for Systemic Mastocytosis, developed in parallel to this study, provides an AP-focused resource for overcoming some of the barriers and gaps identified in this study.
症状负担是惰性系统性肥大细胞增多症(ISM)患者寻求医疗护理的主要驱动因素,无论他们是否被诊断出来。
这项描述性研究旨在描述高级执业者(AP)和ISM患者对于ISM症状负担、ISM的多学科诊断与管理、症状管理障碍、ISM协作管理策略以及ISM患者的沟通健康素养的看法。
由一个由AP主导的指导委员会制定了一份ISM患者调查问卷和一份AP调查问卷,其中纳入了经过验证的工具来测量症状负担、症状负担影响、障碍以及改善症状负担的策略。调查问卷嵌入Qualtrics平台,并由Conexiant公司分发给血液学/肿瘤学高级执业者协会(APSHO)的AP成员、肥大细胞疾病美国倡议组织的AP成员以及肥大细胞疾病协会的附属患者,调查时间为2024年12月22日至2025年2月3日。
50名AP和53名ISM患者完成了相应调查问卷上的所有问题。使用惰性系统性肥大细胞增多症症状评估表(ISM-SAF)描述的症状负担,以确定最常见、最具挑战性且对生活质量影响最大的症状,与本调查中患者的已发表数据一致。只有24%(n = 13)的ISM患者表示其疾病得到良好控制,而76%的AP表示他们超过50%的ISM患者疾病得到良好控制(n = 38)。调查中的大多数AP(68%)表示他们每年诊治1至5名ISM患者,但对管理与ISM相关的症状感到得心应手(54%,n = 27)。描述了分诊、多学科管理和共同决策的实践模式。
这是第一项以ISM症状负担为重点的调查,旨在直接比较患者与血液学/肿瘤学以及过敏和免疫学领域AP的回答。惰性系统性肥大细胞增多症的症状负担测量和症状负担减轻仍然具有挑战性,本研究中发现了一些障碍和差距。与本研究同时开发的APSHO系统性肥大细胞增多症工具包,为克服本研究中发现的一些障碍和差距提供了一个以AP为重点的资源。