在弥漫大 B 细胞淋巴瘤真实生活队列中,国际代谢预后指数优于其他基于代谢肿瘤体积的预后方法

Vibeke K.J. Vergote, Gregor Verhoef, Ann Janssens, F.J. Sherida H. Woei-a-jin, Wies Deckers, Annouschka Laenen, Thomas Tousseyn, Daan Dierickx, Christophe M. Deroose
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引用次数: 0

摘要

基线代谢肿瘤体积(MTV)是弥漫大B细胞淋巴瘤(DLBCL)的一个有希望的预后标志物。我们在现实生活中的DLBCL队列中评估了4种新型代谢风险评分的预后价值,并将它们与修订后的国际预后指数(IPI)进行了比较。方法我们纳入了2008年至2021年期间在我院确诊的一系列未经治疗的DLBCL(未另作说明)病例,这些病例均有可用的基线[18F]FDG PET/CT。我们回顾性地收集了临床数据,包括修订版 IPI 的各个组成部分。计算MTV和其他放射学特征,包括病灶播散和肿瘤体积表面比。使用四种新的代谢风险评分,包括国际代谢预后指数(IMPI)、MTV/世界卫生组织表现状态、MTV/标准化最大距离和临床 PET 模型,使用预定义的临界值计算进展风险。考虑的生存结果包括 3 年无进展生存期(PFS)、3 年进展时间(TTP)和 3 年总生存期(OS)。哈雷尔 C 指数用于评估风险评分的判别性能。建立了一个多变量模型。结果:我们共纳入了355例DLBCL,未另作规定,中位MTV为219 cm3(范围为0-5656 cm3)。在 4 个代谢风险评分中,IMPI 的 3 年 PFS、3 年 TTP 和 3 年 OS 的 C 指数最高(分别为 0.674、0.696 和 0.677)。在3年TTP方面,IMPI优于最强的临床风险评分IPI,尽管哈雷尔C指数的差异很小(0.696对0.693)。在 3 年生存期和 3 年手术期方面,IPI 的 C 指数在所有风险评分中最高(0.696 和 0.693)。IMPI、MTV/世界卫生组织表现状态和IPI评分可以识别出3年OS低于50%的低危人群(分别为43%、32%和39%)。在多变量分析中,IMPI 仍是一个独立的预后因素(P = 0.0089;危险比为 1.207;95% CI,1.048-1.389)。MTV和标准化最大距离作为连续变量时,具有最强的预后价值。在我们的分析中,肿瘤体积表面比没有显著的预后价值。结论与其他三种新型代谢风险评分相比,IMPI 具有最强的预后性能。然而,在我们的真实世界数据集中,IMPI 无法取代 IPI,因此需要进一步的前瞻性试验来比较它们的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
International Metabolic Prognostic Index Is Superior to Other Metabolic Tumor Volume–Based Prognostication Methods in a Real-Life Cohort of Diffuse Large B-Cell Lymphoma

Baseline metabolic tumor volume (MTV) is a promising prognostic marker in diffuse large B-cell lymphoma (DLBCL). We assessed the prognostic value of 4 novel metabolic risk scores in a real-life DLBCL cohort and compared them with the revised international prognostic index (IPI). Methods: We included a consecutive series of untreated DLBCL, not otherwise specified cases that were diagnosed in our hospital from 2008 to 2021 with available baseline [18F]FDG PET/CT. Clinical data were collected retrospectively, including the individual components of the revised IPI. MTV and other radiomic features, including lesion dissemination and tumor volume surface ratio, were calculated. Four novel metabolic risk scores including the international metabolic prognostic index (IMPI), the MTV/World Health Organization performance status, the MTV/standardized maximum distance, and clinical PET models were used to calculate the risk of progression using predefined cutoffs. Survival outcomes considered were 3-y progression free survival (PFS), 3-y time to progression (TTP), and 3-y overall survival (OS). The Harrell C-index was used to assess the discriminative performance of the risk scores. A multivariable model was built. Results: We included 355 DLBCL, not otherwise specified cases with a median MTV of 219 cm3 (range, 0–5,656 cm3). The IMPI had the highest C-index for 3-y PFS, 3-y TTP, and 3-y OS among the 4 metabolic risk scores (0.674, 0.696, and 0.677, respectively). For the 3-y TTP, the IMPI outperformed the strongest clinical risk score, the IPI, although the difference in the Harrell C-indices was small (0.696 vs. 0.693). Regarding the 3-y PFS and 3-y OS, the IPI has the highest C-index of all risk scores (0.696 and 0.693). The IMPI, the MTV/World Health Organization performance status, and the IPI score can recognize a poor risk group with a 3-y OS below 50% (43%, 32%, and 39%, respectively). In multivariable analysis, the IMPI remains an independent prognostic factor (P = 0.0089; hazard ratio, 1.207; 95% CI, 1.048–1.389). MTV and standardized maximum distance have the strongest prognostic values when used as a continuous variable. The tumor volume surface ratio has no significant prognostic value in our analysis. Conclusion: The IMPI has the strongest prognostic performance compared with the other 3 novel metabolic risk scores. However, in our real-world dataset, the IMPI could not replace the IPI, and further prospective trials are needed to compare their performance.

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