Systemic Inflammatory Indices in Second-Line Soft Tissue Sarcoma Patients: Focus on Lymphocyte/Monocyte Ratio and Trabectedin

医学 软组织肉瘤 内科学 脂肪肉瘤 小梁 肿瘤科 淋巴细胞 肉瘤 无进展生存期 胃肠病学 蒽环类 回顾性队列研究 软组织 化疗 癌症 病理 乳腺癌
作者
Valentina Fausti,Alessandro De Vita,Silvia Vanni,Virginia Ghini,Lorena Gurrieri,Nada Riva,Roberto Casadei,Marco Maraldi,Giorgio Ercolani,Davide Cavaliere,Carlo Alberto Pacilio,Federica Pieri,Flavia Foca,Alberto Bongiovanni,Nicoletta Ranallo,Sebastiano Calpona,Giovanni Luca Frassineti,Toni Ibrahim,Laura Mercatali
出处
期刊:Cancers [MDPI AG]
卷期号:15 (4): 1080-1080 被引量:22
标识
DOI:10.3390/cancers15041080
摘要

A second-line standard of treatment has not yet been identified in patients with soft tissue sarcomas (STS), so identifying predictive markers could be a valuable tool. Recent studies have shown that the intratumoral and inflammatory systems significantly influence tumor aggressiveness. We aimed to investigate prognostic values of pre-therapy neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), systemic inflammatory index (SII), progression-free survival (PFS), and overall survival (OS) of STS patients receiving second-line treatment. In this single-center retrospective analysis, ninety-nine patients with STS were enrolled. All patients received second-line treatment after progressing to anthracycline. PFS and OS curves were calculated using the Kaplan–Meier method of RNA sequencing, and CIBERSORT analysis was performed on six surgical specimens of liposarcoma patients. A high NLR, PLR, and SII were significantly associated with worse PFS (p = 0.019; p = 0.004; p = 0.006). Low LMR was significantly associated with worse OS (p = 0.006). Patients treated with Trabectedin showed a better PFS when the LMR was low, while patients treated with other regimens showed a worse PFS when the LMR was low (p = 0.0154). The intratumoral immune infiltrates analysis seems to show a correlation between intratumoral macrophages and LMR. PS ECOG. The metastatic onset and tumor burden showed prognostic significance for PFS (p = 0.004; p = 0.041; p = 0.0086). According to the histologies, PFS was: 5.7 mo in liposarcoma patients vs. 3.8 mo in leiomyosarcoma patients vs. 3.1 months in patients with other histologies (p = 0.053). Our results confirm the prognostic role of systemic inflammatory markers in patients with STS. Moreover, we demonstrated that LMR is a specific predictor of Trabectedin efficacy and could be useful in daily clinical practice. We also highlighted a possible correlation between LMR levels and the percentage of intratumoral macrophages.

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