Department of Neurology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA.
Department of Neurology, Weill Cornell Medical College, New York, NY, USA.
J Neurooncol. 2019 Sep;144(3):553-562. doi: 10.1007/s11060-019-03257-1. Epub 2019 Aug 3.
The standard treatment for primary central nervous system lymphoma (PCNSL) involves induction methotrexate-based chemotherapy with or without consolidation whole brain radiotherapy (WBRT). As WBRT carries a substantial risk for cognitive impairment, alternative consolidation treatments have been used to reduce neurotoxicity, including reduced-dose WBRT (rdWBRT) or high-dose chemotherapy with autologous stem cell transplant (HDC-ASCT). In this study, we characterized cognitive functions in PCNSL patients achieving long-term remission following rdWBRT or HDC-ASCT.
PCNSL patients completed cognitive evaluations at diagnosis, post-induction chemotherapy, and yearly up to 5 years following rdWBRT or HDC-ASCT. Quality of life (QoL), white matter (WM) disease, and cortical atrophy (CA) on MRI were assessed at similar intervals.
Performance was impaired on most cognitive tests at diagnosis. Linear mixed model analyses in each group showed statistically significant improvement from baseline up to year 3 in attention/executive functions, graphomotor speed, and memory; however, there was a decline in attention/executive functions and memory after year 3 in both groups. WM abnormalities increased over time in both groups, but more patients treated with rdWBRT developed CA and WM changes. There were no significant longitudinal group differences in cognitive performance or QoL.
Results indicated improvement in cognitive function up to 3 years post-treatment, but a decline at later time points and an increase in brain structure abnormalities in both groups. The findings suggest that rdWBRT and HDC-ASCT may be associated with delayed neurotoxicity in progression-free patients and underscore the need for long-term follow-up to characterize cognitive dysfunction in PCNSL patients.
原发性中枢神经系统淋巴瘤(PCNSL)的标准治疗包括诱导甲氨蝶呤为基础的化疗联合或不联合全脑放疗(WBRT)巩固治疗。由于 WBRT 会导致认知功能障碍的风险较大,因此已经使用替代巩固治疗来降低神经毒性,包括低剂量 WBRT(rdWBRT)或大剂量化疗联合自体干细胞移植(HDC-ASCT)。在这项研究中,我们对接受 rdWBRT 或 HDC-ASCT 巩固治疗后达到长期缓解的 PCNSL 患者的认知功能进行了研究。
PCNSL 患者在诊断时、诱导化疗后以及 rdWBRT 或 HDC-ASCT 后每年进行认知评估,直至 5 年。在类似的时间间隔评估 MRI 上的生活质量(QoL)、白质(WM)疾病和皮质萎缩(CA)。
在诊断时,大多数认知测试的表现都受到了损害。每组的线性混合模型分析显示,在注意力/执行功能、手写字速度和记忆方面,从基线到第 3 年有统计学意义的改善;然而,在两组中,在第 3 年后注意力/执行功能和记忆都有所下降。两组的 WM 异常随时间推移而增加,但接受 rdWBRT 治疗的患者中有更多的患者出现了 CA 和 WM 改变。在认知表现或 QoL 方面,两组之间没有显著的纵向组间差异。
结果表明治疗后 3 年内认知功能有所改善,但在后期时间点有所下降,两组患者的脑结构异常都有所增加。这些发现表明,rdWBRT 和 HDC-ASCT 可能与无进展生存患者的迟发性神经毒性有关,并强调需要长期随访以明确 PCNSL 患者的认知功能障碍。