肝细胞癌经动脉化疗栓塞患者的再校准生存预测

Alessandro Cucchetti, Edoardo G. Giannini, Cristina Mosconi, Maria Corina Plaz Torres, Giulia Pieri, Fabio Farinati, Gian Ludovico Rapaccini, Maria Di Marco, Eugenio Caturelli, Rodolfo Sacco, Giuseppe Cabibbo, Claudia Campani, Andrea Mega, Maria Guarino, Antonio Gasbarrini, Gianluca Svegliati-Baroni, Francesco Giuseppe Foschi, Gabriele Missale, Alberto Masotto, Gerardo Nardone, Giovanni Raimondo, Gianpaolo Vidili, Maurizia Rossana Brunetto, Vito Sansone, Marco Zoli, Francesco Azzaroli, Franco Trevisani, the ITA.LI.CA Study Group
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引用次数: 3

摘要

TACE前预测模型用于评估肝细胞癌(HCC)经动脉化疗栓塞(TACE)治疗患者的预后。然而,在进入临床实践之前,模型应该证明它发挥了有用的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Recalibrating survival prediction among patients receiving trans-arterial chemoembolization for hepatocellular carcinoma

Background & Aims

The Pre-TACE-Predict model was devised to assess prognosis of patients treated with trans-arterial chemoembolization (TACE) for hepatocellular carcinoma (HCC). However, before entering clinical practice, a model should demonstrate that it performs a useful role.

Methods

We performed an independent external validation of the Pre-TACE model in a cohort that differs in setting and time period from the one that generated the original model. Data from 826 patients treated with TACE for naïve HCC (2008-2018) were used to assess calibration and discrimination of the Pre-TACE-Predict model.

Results

The four risk-categories identified by the Pre-TACE-Predict model had gradient monotonicity, with median survivals of 52.0, 36.2, 29.9, and 14.1 months respectively. However, predicted survivals systematically underestimated observed survivals (R2: 0.667). A recalibration was adopted maintaining fixed the prognostic index and modifying the baseline survival function. This resulted in an almost perfect calibration (R2: 0.995) in all the four risk categories. Cox regressions showed that aetiology and macrovascular invasion, included in the Pre-TACE-Predict model, had no prognostic impact in the present study population, and that coefficients for tumour size and multiplicity were overestimated. The c-index was similar to that of the m-HAP-III, but higher than those of HAP, m-HAP-II and the six-and-twelve models.

Conclusions

The recalibration of Pre-TACE-Predict model improved the estimation of survival probabilities of HCC patients treated with TACE. The highest discriminatory ability of the Pre-TACE-model in comparison to other available models, together with risk stratification and recalibration, makes it the best prognostic tool currently available for these patients.

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