Watts Caroline G, McLoughlin Kirstie G, Wade Stephen, Smit Amelia K, Soyer H Peter, Fernandez-Peñas Pablo, Whiteman David C, Guitera Pascale, Reyes-Marcelino Gillian, Canfell Karen, Cust Anne E, Caruana Michael
The Daffodil Centre, The University of Sydney, a joint venture with Cancer Council NSW, 1 King St, Newtown, Sydney, NSW, 2042, Australia.
Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.
BMC Med Inform Decis Mak. 2025 Jul 1;25(1):222. doi: 10.1186/s12911-025-03074-9.
Simulation modelling can assist with health care decision making. To inform the development and improvement of skin cancer focussed microsimulation models, we conducted a systematic review and narrative synthesis of published skin cancer models to assess the structure, parameterisation, and assumptions.
The electronic databases OVIDMedline including Embase and the Cost-Effectiveness Analysis (CEA) Registry were searched up to 7 May 2025. Studies that included microsimulation of individuals who developed or had skin cancer were eligible for inclusion. No restrictions on publication date or language were applied. The outcomes of interest were the purpose of the models, characteristics of the models and applicability for modelling skin cancer screening.
Twenty-two models were identified from the systematic review. Nineteen papers modelled melanoma, and two papers modelled keratinocyte or non-melanoma skin cancer, and one paper modelled both melanoma and keratinocyte cancer. The models were developed to assess treatment strategies (n = 10), skin cancer screening programs (n = 7), diagnostic techniques (n = 3), post-diagnosis surveillance (n = 3), preventative interventions (n = 1) and time to treatment (n = 1), with three models reporting dual aims. There was substantial variation in the simulation of the natural history of melanoma between models, with more recent models having separate natural history and clinical modules. The quality was assessed using the Quality Assessment Reporting for Microsimulation Models (QARMM) checklist and the majority of models were assessed to be of moderate quality. Limitations from these models included assuming an average tumour behaviour and constant melanoma development and progression over time. Data availability was also noted as a limitation for some models.
Most microsimulation models related to skin cancer have focused on late-stage treatment strategies. Tumour characteristics, apart from stage at diagnosis, were not accounted for in most models.
CRD42024504250.
模拟建模有助于医疗保健决策。为了为专注于皮肤癌的微观模拟模型的开发和改进提供信息,我们对已发表的皮肤癌模型进行了系统综述和叙述性综合分析,以评估其结构、参数设置和假设。
截至2025年5月7日,检索了包括Embase的电子数据库OVIDMedline和成本效益分析(CEA)注册库。纳入了对患有或发生皮肤癌的个体进行微观模拟的研究。对发表日期或语言没有限制。感兴趣的结果是模型的目的、模型的特征以及对皮肤癌筛查建模的适用性。
通过系统综述确定了22个模型。19篇论文对黑色素瘤进行了建模,2篇论文对角质形成细胞或非黑色素瘤皮肤癌进行了建模,1篇论文对黑色素瘤和角质形成细胞癌都进行了建模。这些模型的开发目的是评估治疗策略(n = 10)、皮肤癌筛查项目(n = 7)、诊断技术(n = 3)、诊断后监测(n = 3)、预防干预措施(n = 1)和治疗时间(n = 1),有3个模型报告了双重目的。不同模型对黑色素瘤自然史的模拟存在很大差异,较新的模型具有独立的自然史和临床模块。使用微观模拟模型质量评估报告(QARMM)清单对质量进行了评估,大多数模型被评估为中等质量。这些模型的局限性包括假设肿瘤行为平均化以及黑色素瘤随时间持续发展和进展。数据可用性也被指出是一些模型的局限性。
大多数与皮肤癌相关的微观模拟模型都集中在晚期治疗策略上。大多数模型没有考虑除诊断阶段外的肿瘤特征。
PROSPERO注册号:CRD42024504250。