Sobczuk Pawel, Filipowicz Paulina, Lamparski Lukasz, Kosela-Paterczyk Hanna, Teterycz Pawel, Kozak Katarzyna, Rogala Paweł, Świtaj Tomasz, Falkowski Sławomir, Rutkowski Piotr
Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Medical University of Warsaw, Warsaw, Poland.
Sci Rep. 2025 Feb 12;15(1):5247. doi: 10.1038/s41598-025-89977-z.
Trabectedin is a chemotherapeutic agent that has shown activity in the treatment of patients with soft tissue sarcomas after failure of anthracycline-based therapy and the best results were recorded in the treatment of L-sarcomas. There is a need for prognostic and predictive factors that will help clinicians with therapy selection. In this study we aim to analyze treatment results, prognostic and predictive factors in patients treated with trabectedin in routine clinical practice. We retrospectively analyzed the medical records of patients who started treatment with trabectedin between 04/2008 and 09/2021. Demographic and clinical data were extracted, and markers of systemic inflammation, including neutrophil-to-lymphocyte ratio (NLR) and systemic inflammation index (SII), were calculated. We identified 251 patients, including 174 with complete baseline laboratory data. Objective responses were noted in 10.8% of patients, and disease stabilization was noted in 49.0%. Median PFS and OS were 5.26 months and 17.98 months, respectively. In the overall population, liposarcoma and metastasis-free interval (MFI) > 10 months were predictive factors for PFS, while female sex and MFI > 10 prognostic factors for OS. Among patients with available laboratory data, the median NLR at baseline was 2.87, and SII was 1047.26. In multivariate analysis, SII ≤ 670 significantly correlated with longer PFS but not with OS. Long-term results of trabectedin treatment in Polish patients with L-sarcomas are comparable to the results of other real-world evidence studies. In conclusion, the systemic inflammation index correlates significantly with PFS, is a simple marker available for daily clinical practice to identify patients most likely to benefit from treatment.
曲贝替定是一种化疗药物,在蒽环类药物治疗失败后的软组织肉瘤患者治疗中显示出活性,在L型肉瘤治疗中取得了最佳效果。需要有助于临床医生选择治疗方案的预后和预测因素。在本研究中,我们旨在分析在常规临床实践中接受曲贝替定治疗的患者的治疗结果、预后和预测因素。我们回顾性分析了2008年4月至2021年9月开始接受曲贝替定治疗的患者的病历。提取了人口统计学和临床数据,并计算了全身炎症标志物,包括中性粒细胞与淋巴细胞比值(NLR)和全身炎症指数(SII)。我们确定了251例患者,其中174例有完整的基线实验室数据。10.8%的患者出现客观缓解,49.0%的患者病情稳定。中位无进展生存期(PFS)和总生存期(OS)分别为5.26个月和17.98个月。在总体人群中,脂肪肉瘤和无转移间期(MFI)>10个月是PFS的预测因素,而女性性别和MFI>10是OS的预后因素。在有可用实验室数据的患者中,基线时NLR的中位数为2.87,SII为1047.26。在多变量分析中,SII≤670与较长的PFS显著相关,但与OS无关。波兰L型肉瘤患者曲贝替定治疗的长期结果与其他真实世界证据研究的结果相当。总之,全身炎症指数与PFS显著相关,是一种可用于日常临床实践的简单标志物,以识别最可能从治疗中获益的患者。