CALLY指数在转移性黑色素瘤中的预后效用:建立抗pd -1治疗患者的nomogram

IF 2.8 3区 医学 Q2 ONCOLOGY
Caner Acar, Haydar Çağatay Yüksel, Gökhan Şahin, Fatma Pinar Açar, Damla Gunenc, Burçak Karaca
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引用次数: 0

摘要

背景:尽管免疫检查点抑制剂(ICIs)在转移性黑色素瘤中取得了成功,但许多患者未能获得有意义的益处,这强调了对可获得的预后生物标志物的迫切需要。c反应蛋白(CRP)-白蛋白淋巴细胞(CALLY)指数是一种免疫营养指数,在多种癌症中显示出预后价值。先前的研究表明,全身炎症和营养状况会影响ICI的疗效,这表明CALLY指数与转移性黑色素瘤的潜在相关性。本研究评估了CALLY指数在接受抗pd -1治疗的转移性黑色素瘤患者中的作用。方法:这项回顾性研究分析了2015年至2023年在埃格大学医学院接受抗pd -1单药治疗的92例转移性黑色素瘤患者。CALLY指数采用治疗前CRP、白蛋白和淋巴细胞水平计算。Kaplan-Meier分析用于估计生存结果,单因素和多因素Cox回归模型用于确定独立预后因素。然后开发了包含CALLY指数和其他重要变量的预测nomogram。结果:确定最佳CALLY指标临界值为2。低CALLY指数(≤2)患者的中位总生存期(OS)和无进展生存期(PFS)比高CALLY指数(bbb2.0)患者更差(中位OS: 9.6 vs 31.3个月,p)结论:CALLY指数是一种具有成本效益的独立预后生物标志物,可以帮助风险分层并指导接受抗pd -1治疗的转移性黑色素瘤患者的治疗决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic utility of the CALLY index in metastatic melanoma: building a nomogram for Patients on Anti-PD-1 therapy.

Background: Despite the success of immune checkpoint inhibitors (ICIs) in metastatic melanoma, many patients fail to derive meaningful benefit, underscoring the urgent need for accessible prognostic biomarkers. The C-reactive protein (CRP)-albumin-lymphocyte (CALLY) index, an immunonutritional index, has shown prognostic value in various cancers. Previous studies indicate that systemic inflammation and nutritional status influence ICI efficacy, suggesting the potential relevance of the CALLY index in metastatic melanoma. This study evaluates the CALLY index's role in metastatic melanoma patients treated with anti-PD-1 therapy.

Methods: This retrospective study analysed 92 patients with metastatic melanoma who were treated with anti-PD-1 monotherapy at Ege University's Faculty of Medicine between 2015 and 2023. The CALLY index was calculated using the pre-treatment CRP, albumin and lymphocyte levels. Kaplan-Meier analysis was used to estimate survival outcomes, and univariate and multivariate Cox regression models were employed to identify independent prognostic factors. A predictive nomogram incorporating the CALLY index and other significant variables was then developed.

Results: The optimal CALLY index cutoff was determined to be 2. Patients with a low CALLY index (≤ 2) had worse median overall survival (OS) and progression-free survival (PFS) when compared with those who had a high CALLY index (> 2) (median OS: 9.6 vs 31.3 months, p < 0.001; median PFS: 3.8 vs 10.6 months, p = 0.001). Multivariate analysis identified the CALLY index, lactate dehydrogenase above the upper limit of normal, Eastern Cooperative Oncology Group score ≥ 2, M1c/M1d staging and acral/mucosal melanoma subtypes to be independent predictors of OS. A nomogram was then constructed based on these factors, yielding a concordance index of 0.705 (95% confidence interval: 0.634-0.776). This model stratified patients into low-, intermediate- and high-risk groups, with the high-risk group showing significantly worse OS than the intermediate- and the low-risk groups (p < 0.001).

Conclusion: The CALLY index is a cost-effective and independent prognostic biomarker that can aid in risk stratification and guide treatment decisions in patients with metastatic melanoma receiving anti-PD-1 therapy.

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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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