非特异性 T 细胞淋巴瘤:单中心研究结果。

I Kriachok, I Tytorenko, N Shudrak, O Aleksik, Ya Stepanishyna, T Kadnikova, Ya Pastushenko, N Shokun, T Rudiyk, M Bushuieva
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引用次数: 0

摘要

背景:非特异性外周T细胞淋巴瘤(PTCL-NOS)是外周T细胞淋巴瘤(PTCL)中最常见的亚型。它约占所有 PTCL 的 25%,占所有淋巴瘤的 15%以上。文章介绍了乌克兰首次对PTCL-NOS患者进行前瞻性研究的结果。研究的目的是分析 PTCL 患者的发病率和所接受的治疗,评估总生存期和无进展生存期,并确定预测治疗反应的因素:对2018年2月至今确诊为外周PTCL-NOS的31名患者的数据进行了分析。T细胞淋巴肿瘤根据2016年WHO分类进行诊断。治疗方案与ESMO和NCCN指南一致。90%以上的患者接受了以蒽环类药物为基础的治疗方案(CHOP;CHOEP--环磷酰胺、多柔比星、依托泊苷、长春新碱、泼尼松)。38.70%的患者(12 人)采用了以 CHOP 为基础的初始治疗方案,58.06%的患者(18 人)添加了依托泊苷:根据恶性淋巴瘤反应标准(Cheson,2008年,2014年)评估反应。治疗总反应率为58.06%(n = 18),其中29.03%的患者有完全反应,29.03%的患者有部分反应。3.44%的患者病情稳定,41.37%的患者病情恶化。12个月和24个月的生存率分别为75.44%和50.81%。12个月和24个月无进展生存率分别为47.68%和33.1%。Ki-67过表达(> 65%)是一个负面预后因素:结论:乌克兰的一项人口研究得出的PTCL治疗结果与欧洲其他研究的结果相似,但所有这些研究的结果都不尽如人意。需要开展进一步研究,制定新的检查和治疗策略,以改善治疗效果。重点应放在对具有有利和不利临床因素的 PTCL 患者的一线治疗效果进行比较的务实临床试验上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NOT OTHERWISE SPECIFIED T-CELL LYMPHOMA: OUTCOMES OF A SINGLE CENTER STUDY.

Background: The peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) is the most common subtype of peripheral T-cell lymphoma (PTCL). It constitutes approximately 25% of all PTCLs and accounts for more than 15% of all lymphomas. The results of the first Ukrainian prospective study of patients with PTCL-NOS are presented in the article. The aim of the study was to analyze the morbidity of PTCL patients and the treatment performed, to evaluate overall survival and progression-free survival, and to determine the factors that predict the treatment response.

Patients and methods: An analysis was performed on the data of 31 patients diagnosed with peripheral PTCL-NOS from February 2018 to the present. T-cell lymphoid neoplasms were diagnosed according to the 2016 WHO classification. The treatment regimens were in alignment with ESMO and NCCN guidelines. More than 90% of patients were prescribed anthracycline-based regimens (CHOP; CHOEP - cyclophosphamide, doxorubicin, etoposide, vincristine, prednisone). An initial treatment was performed with CHOP-based regimens in 38.70% (n = 12) of patients, with the addition of etoposide in 58.06% of patients (n = 18).

Results: The response was assessed according to the response criteria for malignant lymphoma (Cheson, 2008, 2014). The overall response to therapy was 58.06% (n = 18), with complete responses in 29.03% of patients and partial responses in 29.03% of patients. The stabilization of the disease occurred in 3.44%, while the disease progression in 41.37% of patients. The 12-month and 24-month survival rates were 75.44% and 50.81%, respectively. The 12-month and 24-month progression-free survivals were 47.68% and 33.1%, respectively. Ki-67 overexpression (> 65%) was a negative prognostic factor.

Conclusions: The results of the treatment of PTCL obtained in a Ukrainian population study are similar to those in other European studies, all of which remain unsatisfactory. Further research is required to develop a new strategy for examination and therapy to improve treatment outcomes. The emphasis should be placed on the pragmatic clinical trials comparing the efficacy of first-line treatment in PTCL patients with both favorable and unfavorable clinical factors.

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