经典霍奇金淋巴瘤患者血红蛋白、白蛋白、淋巴细胞和血小板(HALP)评分及血液学指标的预后评估

Pusem Patir, Kubra Cerci, Erdal Kurtoglu
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引用次数: 0

摘要

导言:霍奇金淋巴瘤(HL)占所有淋巴瘤诊断病例的 10%,占淋巴瘤相关死亡病例的 5%。准确预测霍奇金淋巴瘤的预后至关重要,尤其是考虑到 10%-20%的患者可能接受的治疗不足或过度。本研究调查了 HL 患者诊断时血红蛋白、白蛋白、淋巴细胞和血小板(HALP)评分对预后的影响:研究共纳入了147名确诊为cHL的患者,并对他们的数据进行了回顾性分析。评估了HALP评分和血液学指标[中性粒细胞-淋巴细胞比值(NLR)、淋巴细胞-单核细胞比值(LMR)和血小板-淋巴细胞比值(PLR)]作为总生存期(OS)和无病生存期(DFS)预测指标的意义:根据HALP评分和血液指标的中位值对患者进行分组。高 HALP 评分(p = 0.034)、低 NLR(p = 0.033)、高 LMR(p = 0.003)和低 PLR(p = 0.014)在早期有利组中具有统计学意义。HALP评分NLR、LMR和PLR组的DFS和OS无统计学意义:结论:免疫疗法已显著改善了 cHL 患者的生存预后,但对于 cHL 患者来说,仍然需要易于应用且可靠的预后指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Evaluation of Hemoglobin, Albumin, Lymphocyte, and Platelet (HALP) Score and Hematological Indices in Classic Hodgkin Lymphoma.

Introduction: Hodgkin lymphoma (HL) constitutes 10% of all lymphoma diagnoses and accounts for 5% of lymphoma-related deaths. Accurate prognostication in HL remains crucial, particularly given that 10%-20% of patients may receive either insufficient or excessive treatment. This study investigates the effect of hemoglobin, albumin, lymphocyte, and platelet (HALP) score, which is a marker of inflammation status and nutrition, at the time of diagnosis for the patients with HL on prognosis.

Materials and methods: A total of 147 patients diagnosed with cHL were included in the study, and their data were analyzed retrospectively. The significance of the HALP score and hematological indices [neutrophil-lymphocyte ratio (NLR), lymphocyte-monocyte ratio (LMR), and platelet-lymphocyte ratio (PLR)] as predictors of overall survival (OS) and disease-free survival (DFS) was evaluated.

Results: Patients were grouped according to median values for the HALP score and hematological indices. High HALP score (p = 0.034), low NLR (p = 0.033), high LMR (p = 0.003), and low PLR (p = 0.014) were statistically significant in the early-stage favorable group. DFS and OS were not statistically significant according to the HALP score NLR, LMR, and PLR groups.

Conclusion: The need for readily applicable, reliable prognostic markers in cHL, where immunotherapy treatments have led to significantly improved survival outcomes, remains persistent.

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