Evidence Synthesis Group, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK
NIHR Innovation Observatory, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
BMJ Open. 2023 Sep 28;13(9):e073306. doi: 10.1136/bmjopen-2023-073306.
To identify prognostic models for melanoma survival, recurrence and metastasis among American Joint Committee on Cancer stage I and II patients postsurgery; and evaluate model performance, including overall survival (OS) prediction.
Systematic review and narrative synthesis.
Searched MEDLINE, Embase, CINAHL, Cochrane Library, Science Citation Index and grey literature sources including cancer and guideline websites from 2000 to September 2021.
Included studies on risk prediction models for stage I and II melanoma in adults ≥18 years. Outcomes included OS, recurrence, metastases and model performance. No language or country of publication restrictions were applied.
Two pairs of reviewers independently screened studies, extracted data and assessed the risk of bias using the CHecklist for critical Appraisal and data extraction for systematic Reviews of prediction Modelling Studies checklist and the Prediction study Risk of Bias Assessment Tool. Heterogeneous predictors prevented statistical synthesis.
From 28 967 records, 15 studies reporting 20 models were included; 8 (stage I), 2 (stage II), 7 (stages I-II) and 7 (stages not reported), but were clearly applicable to early stages. Clinicopathological predictors per model ranged from 3-10. The most common were: ulceration, Breslow thickness/depth, sociodemographic status and site. Where reported, discriminatory values were ≥0.7. Calibration measures showed good matches between predicted and observed rates. None of the studies assessed clinical usefulness of the models. Risk of bias was high in eight models, unclear in nine and low in three. Seven models were internally and externally cross-validated, six models were externally validated and eight models were internally validated.
All models are effective in their predictive performance, however the low quality of the evidence raises concern as to whether current follow-up recommendations following surgical treatment is adequate. Future models should incorporate biomarkers for improved accuracy.
CRD42018086784.
确定美国癌症联合委员会(AJCC)分期 I 和 II 期手术后黑色素瘤患者的生存、复发和转移的预后模型,并评估模型性能,包括总体生存(OS)预测。
系统评价和叙述性综合。
从 2000 年至 2021 年 9 月,检索 MEDLINE、Embase、CINAHL、 Cochrane 图书馆、科学引文索引和灰色文献来源,包括癌症和指南网站。
纳入成人(≥18 岁)I 期和 II 期黑色素瘤风险预测模型的研究。结果包括 OS、复发、转移和模型性能。未对语言或出版国家进行限制。
两名配对的审查员独立筛选研究,使用关键评估清单和预测模型研究风险评估工具提取数据并评估偏倚风险,预测模型研究风险评估工具。异质预测因子阻止了统计综合。
从 28967 条记录中,纳入了 15 项研究报告的 20 个模型;8 个(I 期)、2 个(II 期)、7 个(I-II 期)和 7 个(未报告分期),但显然适用于早期阶段。每个模型的临床病理预测因子范围从 3-10 个。最常见的是:溃疡、Breslow 厚度/深度、社会人口统计学状况和部位。报告的区分值均≥0.7。校准测量显示预测和观察到的比率之间有良好的匹配。没有研究评估模型的临床实用性。8 个模型的偏倚风险较高,9 个模型的偏倚风险不明确,3 个模型的偏倚风险较低。7 个模型进行了内部和外部交叉验证,6 个模型进行了外部验证,8 个模型进行了内部验证。
所有模型在预测性能方面都很有效,但是证据质量低,令人怀疑目前手术后的随访建议是否足够。未来的模型应纳入生物标志物以提高准确性。
PROSPERO 注册号:CRD42018086784。