4.6 Review

Risk models for recurrence and survival after kidney cancer: a systematic review

期刊

BJU INTERNATIONAL
卷 130, 期 5, 页码 562-579

出版社

WILEY
DOI: 10.1111/bju.15673

关键词

recurrence; renal cell cancer; risk prediction; survival; prognosis; #kcsm; #KidneyCancer; #uroonc

资金

  1. Cancer Research UK Prevention Fellowship [C55650/A21464]
  2. Cancer Research UK Clinical PhD Fellowship
  3. Renal Cancer Research Fund
  4. Mark Foundation for Cancer Research
  5. Cancer Research UK Cambridge Centre [C9685/A25177]
  6. National Institute of Health Research (NIHR) Cambridge Biomedical Research Centre [BRC-1215-20014]
  7. NIHR Methods Fellowship [RM-SR-201709-009]
  8. NIHR Development and Skills Enhancement Award [NIHR301182]
  9. Medical Research Council [MC_UU_00006/6]
  10. National Institutes of Health Research (NIHR) [NIHR301182] Funding Source: National Institutes of Health Research (NIHR)

向作者/读者索取更多资源

This study systematically compared the performance of different prognostic models in predicting survival or recurrence in patients with localized renal cell cancer who underwent surgery. The study found that several models had good discriminative ability, and there was no single "best" model. When choosing a model, both the comparative performance and the availability of factors included in the model should be considered.
Objective To systematically identify and compare the performance of prognostic models providing estimates of survival or recurrence of localized renal cell cancer (RCC) in patients treated with surgery with curative intent. Materials and Methods We performed a systematic review (PROSPERO CRD42019162349). We searched Medline, EMBASE and the Cochrane Library from 1 January 2000 to 12 December 2019 to identify studies reporting the performance of one or more prognostic model(s) that predict recurrence-free survival (RFS), cancer-specific survival (CSS) or overall survival (OS) in patients who have undergone surgical resection for localized RCC. For each outcome we summarized the discrimination of each model using the C-statistic and performed multivariate random-effects meta-analysis of the logit transformed C-statistic to rank the models. Results Of a total of 13 549 articles, 57 included data on the performance of 22 models in external populations. C-statistics ranged from 0.59 to 0.90. Several risk models were assessed in two or more external populations and had similarly high discriminative performance. For RFS, these were the Sorbellini, Karakiewicz, Leibovich and Kattan models, with the UCLA Integrated Staging System model also having similar performance in European/US populations. All had C-statistics >= 0.75 in at least half of the validations. For CSS, they the models with the highest discriminative performance in two or more external validation studies were the Zisman, Stage, Size, Grade and Necrosis (SSIGN), Karakiewicz, Leibovich and Sorbellini models (C-statistic >= 0.80 in at least half of the validations), and for OS they were the Leibovich, Karakiewicz, Sorbellini and SSIGN models. For all outcomes, the models based on clinical features at presentation alone (Cindolo and Yaycioglu) had consistently lower discrimination. Estimates of model calibration were only infrequently included but most underestimated survival. Conclusion Several models had good discriminative ability, with there being no single 'best' model. The choice from these models for each setting should be informed by both the comparative performance and availability of factors included in the models. All would need recalibration if used to provide absolute survival estimates.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据