Department of Pathology, School of Medicine, Kurume University, Kurume, Japan.
Department of Hematology, Shimane University Hospital, Izumo, Japan.
Cancer Med. 2024 Feb;13(3):e6793. doi: 10.1002/cam4.6793. Epub 2024 Jan 17.
Peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) is a heterogeneous disease that can be classified into the PTCL-TBX21 and PTCL-GATA3 subtypes.
In this study, we compared the clinicopathological features of PTCL-NOS in a Japanese cohort, classified using an IHC algorithm.
One hundred patients with PTCL-NOS were categorized as having PTCL-TBX21 (n = 55), PTCL-GATA3 (n = 24), or PTCL-unclassified (n = 21). When comparing PTCL-TBX21 and PTCL-GATA3, PTCL-TBX21 showed significantly lower CD4 positivity (p = 0.047), lower counts of high endothelial venules (p = 0.032), and a tendency for a better response to initial treatment (p = 0.088). Gene expression analysis using the nCounter system showed higher expression of tumor immunity-related genes, such as PD-L1, LAG3, and IDO1, in PTCL-TBX21 than in PTCL-GATA3. PTCL-GATA3 had significantly worse overall survival (OS) than those with PTCL-TBX21 (p = 0.047), although a similar tendency was observed for progression-free survival (PFS) (p = 0.064). PTCL-GATA3 was a prognostic factor for OS in univariate analysis (HR 2.02; 95% CI, 1.09-3.77; p = 0.027), although multivariate analysis did not show significance (HR 2.07; 95% CI, 0.93-4.61; p = 0.074). In the PFS analysis, PTCL-GATA3 was an independent prognostic factor by univariate analysis (HR 1.96; 95% CI, 1.08-3.56; p = 0.027) and multivariate analysis (HR 2.34; 95% CI, 1.07-5.11; p = 0.032).
The classification of PTCL-NOS into PTCL-TBX21 and PTCL-GATA3 is useful for predicting the prognosis of Japanese patients and stratifying the administration of tumor immune checkpoint inhibitors in clinical practice.
非特指外周 T 细胞淋巴瘤(PTCL-NOS)是一种异质性疾病,可分为 PTCL-TBX21 和 PTCL-GATA3 亚型。
本研究比较了采用免疫组化算法分类的日本队列中 PTCL-NOS 的临床病理特征。
100 例 PTCL-NOS 患者分为 PTCL-TBX21(n=55)、PTCL-GATA3(n=24)或 PTCL 未分类(n=21)。与 PTCL-TBX21 相比,PTCL-GATA3 患者 CD4 阳性率明显较低(p=0.047),高内皮静脉计数较低(p=0.032),初始治疗反应较好(p=0.088)。使用 nCounter 系统进行的基因表达分析显示,PTCL-TBX21 中与肿瘤免疫相关的基因,如 PD-L1、LAG3 和 IDO1 的表达较高。PTCL-GATA3 的总生存期(OS)明显低于 PTCL-TBX21(p=0.047),尽管无进展生存期(PFS)也有类似趋势(p=0.064)。PTCL-GATA3 是单因素分析中 OS 的预后因素(HR 2.02;95%CI,1.09-3.77;p=0.027),但多因素分析无统计学意义(HR 2.07;95%CI,0.93-4.61;p=0.074)。在 PFS 分析中,PTCL-GATA3 是单因素分析(HR 1.96;95%CI,1.08-3.56;p=0.027)和多因素分析(HR 2.34;95%CI,1.07-5.11;p=0.032)中的独立预后因素。
将 PTCL-NOS 分为 PTCL-TBX21 和 PTCL-GATA3 有助于预测日本患者的预后,并在临床实践中分层使用肿瘤免疫检查点抑制剂。