Matutes Estella
Haemato-Oncology Unit, Royal Marsden Hospital and Institute of Cancer Research, 203 Fulham Road, London, SW3 6JJ, UK.
Curr Treat Options Oncol. 2007 Apr;8(2):109-16. doi: 10.1007/s11864-007-0026-0.
Splenic marginal zone lymphoma with or without villous lymphocytes (SLVL/SMZL) is a low grade B-cell lymphoma that affects patients in the sixth decade and has a median survival greater than 10 years. A substantial proportion of patients die from causes unrelated to the disease. Close to a third of the patients do not require intervention and a policy of watch and see is reasonable and recommended. There are several therapeutic options that have proved effective in these patients. Due to the natural history of the lymphoma, the main goal of all these treatments is to achieve control of the disease rather than its eradication. Retrospective designs of all documented studies, the lack of uniform response criteria and the heterogeneity in the patient's features makes interpretation of the data difficult. Splenectomy remains one of the first line options in patients fit for surgery. Amongst chemotherapy, purine analogues, in particular fludarabine in combination or not with Rituximab and Rituximab alone have a greater efficacy than alkylating agents in terms of achieving better quality of response and longer progression free survival; therefore these agents are recommended particularly in patients who are not candidates for surgery or relapse after splenectomy. In the small proportion of patients with concomitant hepatitis C virus (HCV) infection, Interferon-alpha, ribavirin or a combination of both has demonstrated a significant activity with responses correlating with clearance of HCV RNA in the blood; therefore, these agents should be considered in the therapeutic scenario as a first line in these small cohort of patients. Patients that transform to high-grade lymphoma and the minority that have TP53 abnormalities should be treated with other schedules. Prospective randomized trials would be desirable to ascertain the independent prognostic factors and the biological features that predict disease progression and drug resistance to device the optimal management and treatment for SLVL/SMZL.
伴有或不伴有绒毛淋巴细胞的脾边缘区淋巴瘤(SLVL/SMZL)是一种低度B细胞淋巴瘤,好发于60岁左右的患者,中位生存期超过10年。相当一部分患者死于与该疾病无关的原因。近三分之一的患者无需干预,“观察等待”策略是合理且推荐的。有几种治疗方案已被证明对这些患者有效。由于淋巴瘤的自然病程,所有这些治疗的主要目标是实现疾病控制而非根除。所有已记录研究的回顾性设计、缺乏统一的反应标准以及患者特征的异质性使得数据解读困难。脾切除术仍是适合手术患者的一线选择之一。在化疗药物中,嘌呤类似物,特别是氟达拉滨联合或不联合利妥昔单抗以及单独使用利妥昔单抗,在获得更好的反应质量和更长的无进展生存期方面比烷化剂更有效;因此,这些药物尤其推荐用于不适合手术或脾切除术后复发的患者。在一小部分合并丙型肝炎病毒(HCV)感染的患者中,干扰素-α、利巴韦林或两者联合已显示出显著活性,反应与血液中HCV RNA的清除相关;因此,在治疗方案中应将这些药物作为这一小部分患者的一线治疗药物考虑。转化为高级别淋巴瘤的患者以及少数有TP53异常的患者应采用其他治疗方案。需要进行前瞻性随机试验以确定独立的预后因素以及预测疾病进展和耐药性的生物学特征,从而制定SLVL/SMZL的最佳管理和治疗方案。