Anna Gabrych, Malgorzata A Krawczyk, Malgorzata Styczewska, Weronika Lyzinska, Jadwiga Weclawek-Tompol, Iwona Dachowska-Kalwak, Bernarda Kazanowska, Malgorzata Sawicka-Zukowska, Maryna Krawczuk-Rybak, Monika Richert-Przygonska, Jan Styczynski, Julia Geisler-Paliwoda, Tomasz Szczepanski, Wioletta Bal, Radoslaw Chaber, Michal Kunc, Ewa Bien
{"title":"全身性炎症标志物在小儿软组织肉瘤中的预后作用:213例患者的多中心研究","authors":"Anna Gabrych, Malgorzata A Krawczyk, Malgorzata Styczewska, Weronika Lyzinska, Jadwiga Weclawek-Tompol, Iwona Dachowska-Kalwak, Bernarda Kazanowska, Malgorzata Sawicka-Zukowska, Maryna Krawczuk-Rybak, Monika Richert-Przygonska, Jan Styczynski, Julia Geisler-Paliwoda, Tomasz Szczepanski, Wioletta Bal, Radoslaw Chaber, Michal Kunc, Ewa Bien","doi":"10.1002/pbc.31701","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The prognostic role of systemic inflammation markers in pediatric soft-tissue sarcomas (STS) remains unclear.</p><p><strong>Procedure: </strong>This multicenter study investigated the prognostic significance of neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), C-reactive protein (CRP), and lactate dehydrogenase (LDH) in 213 pediatric patients diagnosed with STS in years 2002-2023. Patients were categorized into groups: rhabdomyosarcoma (RMS, n = 126), RMS-like (n = 57), and non-RMS (n = 30). Clinicopathological data, including complete blood counts (CBCs), CRP, and LDH levels, were collected and age-adjusted. Optimal cutoffs for predicting outcomes were determined, and the prognostic value of the inflammatory markers was assessed using Kaplan-Meier survival analysis, log-rank tests, and Cox regression models.</p><p><strong>Results: </strong>No significant differences in NLR, PLR, LMR, and CRP levels were observed between RMS, RMS-like, and non-RMS groups. However, LDH levels were significantly elevated in the RMS group compared with the RMS-like group. A consistent trend toward higher NLR, PLR, and CRP values was noted in patients with more advanced disease stages. Multivariate Cox regression analysis across the entire cohort identified CRP (HR 3.39, 95% CI 1.55-7.4, p = 0.002), NLR (HR 2.06, 95% CI 1.07-3.99, p = 0.03), and disease stage (HR = 0.49, 95% CI 0.26-0.95, p = 0.035) as independent prognostic factors for survival. Subgroup analyses revealed that the prognostic impact of these markers varied across histopathological subtypes, with limited utility in the RMS-like group.</p><p><strong>Conclusions: </strong>These findings highlight the prognostic value of systemic inflammatory markers in pediatric STS, emphasizing their potential to refine risk assessment and guide treatment.</p>","PeriodicalId":19822,"journal":{"name":"Pediatric Blood & Cancer","volume":" ","pages":"e31701"},"PeriodicalIF":2.4000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prognostic Role of Systemic Inflammatory Markers in Pediatric Soft-Tissue Sarcoma: A Multicenter Study of 213 Patients.\",\"authors\":\"Anna Gabrych, Malgorzata A Krawczyk, Malgorzata Styczewska, Weronika Lyzinska, Jadwiga Weclawek-Tompol, Iwona Dachowska-Kalwak, Bernarda Kazanowska, Malgorzata Sawicka-Zukowska, Maryna Krawczuk-Rybak, Monika Richert-Przygonska, Jan Styczynski, Julia Geisler-Paliwoda, Tomasz Szczepanski, Wioletta Bal, Radoslaw Chaber, Michal Kunc, Ewa Bien\",\"doi\":\"10.1002/pbc.31701\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The prognostic role of systemic inflammation markers in pediatric soft-tissue sarcomas (STS) remains unclear.</p><p><strong>Procedure: </strong>This multicenter study investigated the prognostic significance of neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), C-reactive protein (CRP), and lactate dehydrogenase (LDH) in 213 pediatric patients diagnosed with STS in years 2002-2023. Patients were categorized into groups: rhabdomyosarcoma (RMS, n = 126), RMS-like (n = 57), and non-RMS (n = 30). Clinicopathological data, including complete blood counts (CBCs), CRP, and LDH levels, were collected and age-adjusted. Optimal cutoffs for predicting outcomes were determined, and the prognostic value of the inflammatory markers was assessed using Kaplan-Meier survival analysis, log-rank tests, and Cox regression models.</p><p><strong>Results: </strong>No significant differences in NLR, PLR, LMR, and CRP levels were observed between RMS, RMS-like, and non-RMS groups. However, LDH levels were significantly elevated in the RMS group compared with the RMS-like group. A consistent trend toward higher NLR, PLR, and CRP values was noted in patients with more advanced disease stages. Multivariate Cox regression analysis across the entire cohort identified CRP (HR 3.39, 95% CI 1.55-7.4, p = 0.002), NLR (HR 2.06, 95% CI 1.07-3.99, p = 0.03), and disease stage (HR = 0.49, 95% CI 0.26-0.95, p = 0.035) as independent prognostic factors for survival. 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引用次数: 0
摘要
背景:全身性炎症标志物在小儿软组织肉瘤(STS)中的预后作用尚不清楚。方法:本多中心研究了2002-2023年间诊断为STS的213例儿童患者的中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)、淋巴细胞与单核细胞比值(LMR)、全身免疫炎症指数(SII)、全身炎症反应指数(SIRI)、c反应蛋白(CRP)和乳酸脱氢酶(LDH)的预后意义。患者分为横纹肌肉瘤(RMS, n = 126)、RMS样(n = 57)和非RMS组(n = 30)。收集临床病理数据,包括全血细胞计数(CBCs)、CRP和LDH水平,并进行年龄调整。确定预测结果的最佳截止点,并使用Kaplan-Meier生存分析、log-rank检验和Cox回归模型评估炎症标志物的预后价值。结果:在RMS组、RMS样组和非RMS组之间,NLR、PLR、LMR和CRP水平无显著差异。然而,与RMS样组相比,RMS组的LDH水平明显升高。在病程越晚期的患者中,NLR、PLR和CRP值的升高趋势一致。对整个队列进行多因素Cox回归分析,发现CRP (HR 3.39, 95% CI 1.55-7.4, p = 0.002)、NLR (HR 2.06, 95% CI 1.07-3.99, p = 0.03)和疾病分期(HR = 0.49, 95% CI 0.26-0.95, p = 0.035)是独立的预后因素。亚组分析显示,这些标志物对预后的影响因组织病理学亚型而异,在rms样组中应用有限。结论:这些发现强调了全身性炎症标志物在儿童STS中的预后价值,强调了它们在完善风险评估和指导治疗方面的潜力。
Prognostic Role of Systemic Inflammatory Markers in Pediatric Soft-Tissue Sarcoma: A Multicenter Study of 213 Patients.
Background: The prognostic role of systemic inflammation markers in pediatric soft-tissue sarcomas (STS) remains unclear.
Procedure: This multicenter study investigated the prognostic significance of neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), C-reactive protein (CRP), and lactate dehydrogenase (LDH) in 213 pediatric patients diagnosed with STS in years 2002-2023. Patients were categorized into groups: rhabdomyosarcoma (RMS, n = 126), RMS-like (n = 57), and non-RMS (n = 30). Clinicopathological data, including complete blood counts (CBCs), CRP, and LDH levels, were collected and age-adjusted. Optimal cutoffs for predicting outcomes were determined, and the prognostic value of the inflammatory markers was assessed using Kaplan-Meier survival analysis, log-rank tests, and Cox regression models.
Results: No significant differences in NLR, PLR, LMR, and CRP levels were observed between RMS, RMS-like, and non-RMS groups. However, LDH levels were significantly elevated in the RMS group compared with the RMS-like group. A consistent trend toward higher NLR, PLR, and CRP values was noted in patients with more advanced disease stages. Multivariate Cox regression analysis across the entire cohort identified CRP (HR 3.39, 95% CI 1.55-7.4, p = 0.002), NLR (HR 2.06, 95% CI 1.07-3.99, p = 0.03), and disease stage (HR = 0.49, 95% CI 0.26-0.95, p = 0.035) as independent prognostic factors for survival. Subgroup analyses revealed that the prognostic impact of these markers varied across histopathological subtypes, with limited utility in the RMS-like group.
Conclusions: These findings highlight the prognostic value of systemic inflammatory markers in pediatric STS, emphasizing their potential to refine risk assessment and guide treatment.
期刊介绍:
Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.