Shimazu Yutaka, Notohara Kenji, Ueda Yasunori
Department of Hematology/Oncology, Kurashiki Central Hospital, Okayama, Japan.
Int J Hematol. 2009 Jun;89(5):577-83. doi: 10.1007/s12185-009-0289-2. Epub 2009 Apr 9.
The introduction of rituximab for diffuse large B-cell lymphoma (DLBCL) has improved the disease's overall prognosis. However, relapse in the central nervous system (CNS) is still an issue. We investigated the prognosis and risk factors of CNS recurrence in DLBCL. A total of 403 patients who were diagnosed with DLBCL without CNS involvement between January 1996 and April 2007 at our institution were included in the study. Subsequently, 42 experienced CNS relapse. Clinical information was gathered by chart review. The median disease-free interval to CNS relapse was 625 days. The mean survival periods after relapse in the cases with CNS and extra-CNS involvement were 513 and 1,615 days, respectively (P = 0.0004). Multivariate analysis identified age >60 years (P = 0.031), involvement in two or more extranodal sites (P = 0.040), bone marrow involvement (P = 0.036), an elevated serum lactate dehydrogenase (LDH) level (P = 0.016), and treatment without rituximab before CNS relapse (P = 0.027) as independent predictors of CNS relapse. We have shown that cases of DLBCL occurring in advanced age, involving two or more extranodal sites or the bone marrow, or showing an elevation of LDH have a higher risk of CNS relapse. Rituximab may prevent CNS relapse by reducing the recurrence of DLBCL at all sites. An effective CNS prophylaxis strategy should be determined according to the risk assessment of CNS relapse.
利妥昔单抗用于弥漫性大B细胞淋巴瘤(DLBCL)的治疗改善了该疾病的总体预后。然而,中枢神经系统(CNS)复发仍是一个问题。我们研究了DLBCL中枢神经系统复发的预后及危险因素。本研究纳入了1996年1月至2007年4月在我院诊断为无CNS受累的403例DLBCL患者。随后,42例发生了CNS复发。通过查阅病历收集临床信息。CNS复发的无病间隔中位数为625天。CNS受累和CNS外受累患者复发后的平均生存期分别为513天和1615天(P = 0.0004)。多因素分析确定年龄>60岁(P = 0.031)、累及两个或更多结外部位(P = 0.040)、骨髓受累(P = 0.036)、血清乳酸脱氢酶(LDH)水平升高(P = 0.016)以及CNS复发前未使用利妥昔单抗治疗(P = 0.027)为CNS复发的独立预测因素。我们发现,发生于老年、累及两个或更多结外部位或骨髓、或LDH升高的DLBCL病例CNS复发风险更高。利妥昔单抗可能通过降低DLBCL在所有部位的复发率来预防CNS复发。应根据CNS复发的风险评估确定有效的CNS预防策略。