Department of Haematology, Clinical Cancer Research Centre, Aalborg University Hospital, Aalborg, Denmark.
Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Am J Hematol. 2023 Mar;98(3):388-397. doi: 10.1002/ajh.26803. Epub 2023 Jan 1.
Peripheral T-Cell Lymphomas (PTCLs) are rare, aggressive lymphomas with poor outcomes, but limited-stage disease is infrequent and not well-described. This study reports outcomes and prognostic factors in limited-stage nodal PTCLs in a binational population-based setting. Patients were identified from the Danish and Swedish lymphoma registries. Adults diagnosed with limited-stage nodal PTCL (stage I-II) and treated with CHOP(-like) therapy ±radiotherapy between 2000 and 2014 were included. Medical records were reviewed by local investigators. A total of 239 patients with a median age of 62 years were included; 67% received 6-8 cycles of CHOP(-like) therapy and 22% received 3-4 cycles, of which 59% also received radiotherapy. Autologous stem cell transplant consolidation was administered to 16% of all patients. Median follow-up was 127 months with 5-years overall survival (OS) of 58% (95% CI: 53-65) and progression-free survival (PFS) of 53% (95% CI: 47-59). In multivariable analysis, age ≥ 60 years and B-symptoms were unfavorable and ALK+ anaplastic large cell T-Cell lymphoma was favorable for survival outcomes. There was no difference in treatment-specific outcome (3-4 cycles vs. 6-8 cycles of CHOP(-like) ± radiotherapy). Low-risk patients (age < 60 without B-symptoms) had a 5-year OS of 77% (95% CI 67-89%). In the present study of limited-stage nodal PTCL, survival after curative intent chemotherapy +/- radiotherapy was inferior to that of limited-stage diffuse large B-cell lymphoma, but a subgroup of young patients without B-symptoms had very good outcomes. Treatment outcomes after 3-4 cycles versus 6-8 cycles of CHOP(-like) therapy were comparable.
外周 T 细胞淋巴瘤(PTCLs)是一种罕见的侵袭性淋巴瘤,预后较差,但局限性疾病并不常见,也未得到充分描述。本研究报告了在一个双国家人群为基础的环境中局限性结外 PTCL 患者的结局和预后因素。从丹麦和瑞典的淋巴瘤登记处中识别出患者。本研究纳入了 2000 年至 2014 年间诊断为局限性结外 PTCL(I-II 期)且接受 CHOP(-样)治疗±放疗的成年人。由当地研究人员对病历进行了审查。共纳入了 239 例中位年龄为 62 岁的患者;67%的患者接受了 6-8 个周期的 CHOP(-样)治疗,22%的患者接受了 3-4 个周期的治疗,其中 59%的患者还接受了放疗。16%的患者接受了自体干细胞移植巩固治疗。中位随访时间为 127 个月,5 年总生存率(OS)为 58%(95%CI:53-65),无进展生存率(PFS)为 53%(95%CI:47-59)。多变量分析显示,年龄≥60 岁和 B 症状是不利的,ALK+间变性大细胞 T 细胞淋巴瘤对生存结局有利。治疗特异性结局(3-4 个周期与 6-8 个周期的 CHOP(-样)±放疗)之间没有差异。低危患者(年龄<60 岁且无 B 症状)的 5 年 OS 率为 77%(95%CI 67-89%)。在本研究中,局限性结外 PTCL 患者接受根治性化疗±放疗后的生存率低于局限性弥漫性大 B 细胞淋巴瘤,但无 B 症状的年轻患者亚组具有非常好的结局。3-4 个周期与 6-8 个周期 CHOP(-样)治疗后的治疗结局相当。