Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Department of Neurology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Br J Haematol. 2021 Nov;195(4):561-570. doi: 10.1111/bjh.17747. Epub 2021 Aug 8.
Observational studies with long-term follow-up of patients with primary central nervous system lymphoma (PCNSL) are scarce. Patient data over a period of four decades were retrospectively analysed from databases at Nottingham University Hospitals Trust, UK. The cohort was delineated by two distinct therapeutic eras; the first from 01/01/1982 to 31/12/2010 (n = 147) and the second 01/01/2011 to 31/07/2020 (n = 125). The median age at diagnosis was significantly older in the second era compared to the first (69 and 65 years respectively, P = 0·003). The 3-, 6- and 12-month overall survival (OS) rates in the second era were significantly higher compared to the first, at 85%, 77%, 62% versus 56%, 49%, 38% respectively (log-rank test P < 0·0001). On multivariate analysis, high-dose methotrexate (HD-MTX)-based induction protocols employed in the second era were associated with improved OS compared to those used in the first [hazard ratio (HR) 0·40, 95% confidence interval (CI) 0·28-0·57]. Within the second era, superior OS rates were seen with the use of intensive HD-MTX protocols (including consolidation with high-dose chemotherapy and autologous stem cell transplantation) compared to non-intensive HD-MTX schedules (HR 0·47, 95% CI 0·22-0·99). Initiating chemotherapy within 14 days of biopsy and use of rituximab were independently associated with improved OS and progression-free survival during the second era. These data suggest that prompt treatment initiation and use of intensive HD-MTX- and rituximab-based protocols have resulted in improved survival outcomes for patients.
观察性研究中,原发性中枢神经系统淋巴瘤(PCNSL)患者的长期随访数据较为匮乏。本研究通过对英国诺丁汉大学医院信托基金的数据库进行回顾性分析,获得了长达四十年的患者数据。该队列由两个不同的治疗时代划定;第一个时代为 1982 年 1 月 1 日至 2010 年 12 月 31 日(n=147),第二个时代为 2011 年 1 月 1 日至 2020 年 7 月 31 日(n=125)。与第一个时代相比,第二个时代患者的中位诊断年龄显著更高(分别为 69 岁和 65 岁,P=0.003)。与第一个时代相比,第二个时代患者的 3 个月、6 个月和 12 个月总生存率(OS)更高,分别为 85%、77%和 62%,而分别为 56%、49%和 38%(对数秩检验 P<0.0001)。多变量分析显示,与第一个时代相比,第二个时代采用的大剂量甲氨蝶呤(HD-MTX)为基础的诱导方案与 OS 改善相关[风险比(HR)0.40,95%置信区间(CI)0.28-0.57]。在第二个时代中,与非强化 HD-MTX 方案相比,使用强化 HD-MTX 方案(包括大剂量化疗联合自体干细胞移植巩固治疗)可获得更高的 OS 率(HR 0.47,95%CI 0.22-0.99)。在第二个时代中,活检后 14 天内开始化疗和使用利妥昔单抗与 OS 和无进展生存率的改善独立相关。这些数据表明,及时开始治疗和使用强化 HD-MTX 和利妥昔单抗为基础的方案为患者带来了更好的生存结果。