Department of Internal Medicine, University of New Mexico, Albuquerque, NM, 87131, USA.
Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Ann Hematol. 2019 May;98(5):1169-1176. doi: 10.1007/s00277-018-3571-7. Epub 2019 Jan 8.
Stage I non-Hodgkin lymphoma (NHL) is rare; prognostic impact of different histologic subtypes and treatment modality is still unclear. We used the Surveillance, Epidemiology and End Results (SEER) database to evaluate survival outcomes among adult patients (age ≥ 18 years, N = 58,230) diagnosed with stage I NHL of various histologic subtypes between 1998 and 2014. Five-year disease-specific survival of patients with stage I diffuse large B cell lymphoma (DLBCL), follicular lymphoma (FL), marginal zone lymphoma (MZL), small lymphocytic lymphoma (SLL), Burkitt lymphoma (BL), mantle cell lymphoma (MCL), and peripheral T cell lymphoma (PTCL) was 82%, 92%, 95%, 89%, 78%, 77%, and 77%, respectively. The median disease-specific survival was not reached in all histologic subtypes analyzed; however, there does not appear to be a plateau in disease-specific survival of patients with stage I NHL irrespective of subtypes. Although lymphoma was the most common cause of death (40.7%), death from other cancer (17.4%) and cardiovascular disease (13.6%) were also frequent. Chemotherapy appeared favorably associated with OS in patients with DLBCL, BL, and MCL while patients with FL, MZL, SLL, and PTCL who require chemotherapy for initial treatment showed shorter OS. Patients with stage I NHL have favorable disease-specific survival; however, no plateau was seen regardless of histologic subtypes thus suggesting that patients may need attention and follow-up even in aggressive lymphomas after 5 years of remission.
I 期非霍奇金淋巴瘤(NHL)较为罕见;不同组织学亚型和治疗方式的预后影响仍不清楚。我们使用监测、流行病学和最终结果(SEER)数据库评估了 1998 年至 2014 年间诊断为 I 期 NHL 的不同组织学亚型的成年患者(年龄≥18 岁,N=58230)的生存结局。I 期弥漫性大 B 细胞淋巴瘤(DLBCL)、滤泡性淋巴瘤(FL)、边缘区淋巴瘤(MZL)、小淋巴细胞淋巴瘤(SLL)、伯基特淋巴瘤(BL)、套细胞淋巴瘤(MCL)和外周 T 细胞淋巴瘤(PTCL)患者的 5 年疾病特异性生存率分别为 82%、92%、95%、89%、78%、77%和 77%。所有分析的组织学亚型的中位疾病特异性生存率均未达到,但无论亚型如何,I 期 NHL 患者的疾病特异性生存率似乎没有平台期。尽管淋巴瘤是最常见的死亡原因(40.7%),但其他癌症(17.4%)和心血管疾病(13.6%)的死亡也很常见。化疗似乎与 DLBCL、BL 和 MCL 患者的 OS 有利相关,而需要化疗作为初始治疗的 FL、MZL、SLL 和 PTCL 患者的 OS 更短。I 期 NHL 患者的疾病特异性生存率较好;然而,无论组织学亚型如何,均未出现平台期,这表明即使在缓解 5 年后,患者可能仍需要关注和随访,即使是侵袭性淋巴瘤也是如此。