Reunamo Taina, Kalashnikov Ilja, Lahtela Kreetta, Pollari Marjukka, Viisanen Leevi, Mannisto Susanna, Jyrkkiö Sirkku, Leppä Sirpa
Department of Oncology, Turku University Hospital and University of Turku, Wellbeing Services County of Southwest Finland, Turku, Finland.
Research Programs Unit, Faculty of Medicine, University of Helsinki, P.O. Box 180, 00029, Helsinki, Finland.
Sci Rep. 2025 Jul 25;15(1):27077. doi: 10.1038/s41598-025-12596-1.
Peripheral T-cell lymphomas (PTCLs) represent a heterogeneous group of rare malignancies with poor survival; however, population-based long-term survival data remain limited. We conducted a nationwide study to estimate overall survival (OS) and relative survival (RS) among 915 patients diagnosed with PTCLs from 2002 - 2018 (57% males, median age 67 years) using the Finnish Cancer Registry. The most common subtypes included PTCL not otherwise specified (PTCL NOS; 37%), angioimmunoblastic T-cell lymphoma (AITL; 27%), and ALK-anaplastic large cell lymphoma (ALK-ALCL; 12%). Age > 60 years at diagnosis, advanced stage, and male sex were associated with poorer OS. Five-year OS and RS were better in patients with ALK + ALCL compared with PTCL NOS (5-year OS: 85% vs 30%). Patients with ALK- ALCL had a favorable 5-year OS compared to PTCL NOS (46% vs 30%), while those with enteropathy-associated T-cell lymphoma (EATL) demonstrated worse OS (15%). There was no improvement in RS from 2002 - 2012 to 2013 - 2018. OS was better in patients (excluding ALK + ALCL) receiving high-dose chemotherapy (HDCT) compared to those for whom HDCT was not planned (HR 0.61; 95% CI 0.47 - 0.80). We conclude that RS did not improve during the study period; however, consolidation with HDCT for eligible patients resulted in favorable survival.
外周T细胞淋巴瘤(PTCL)是一组异质性罕见恶性肿瘤,生存率较低;然而,基于人群的长期生存数据仍然有限。我们利用芬兰癌症登记处进行了一项全国性研究,以估计2002年至2018年期间915例诊断为PTCL的患者(57%为男性,中位年龄67岁)的总生存期(OS)和相对生存期(RS)。最常见的亚型包括未另行指定的PTCL(PTCL NOS;37%)、血管免疫母细胞性T细胞淋巴瘤(AITL;27%)和ALK-间变性大细胞淋巴瘤(ALK-ALCL;12%)。诊断时年龄>60岁、晚期和男性与较差的OS相关。与PTCL NOS相比,ALK+ALCL患者的5年OS和RS更好(5年OS:85%对30%)。与PTCL NOS相比,ALK-ALCL患者的5年OS较好(46%对30%),而肠病相关T细胞淋巴瘤(EATL)患者的OS较差(15%)。2002年至2012年至2013年至2018年期间RS没有改善。与未计划接受大剂量化疗(HDCT)的患者相比,接受HDCT的患者(不包括ALK+ALCL)的OS更好(HR 0.61;95%CI 0.47-0.80)。我们得出结论,在研究期间RS没有改善;然而,对符合条件的患者进行HDCT巩固治疗可带来良好的生存效果。