Brown Jennifer R, Friedberg Jonathan W, Feng Yang, Scofield Sarah, Phillips Kimberly, Dal Cin Paola, Joyce Robin, Takvorian Ronald W, Fisher David C, Fisher Richard I, Liesveld Jane, Marquis Diana, Neuberg Donna, Freedman Arnold S
Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Br J Haematol. 2009 Jun;145(6):741-8. doi: 10.1111/j.1365-2141.2009.07677.x. Epub 2009 Mar 30.
The marginal zone lymphomas (MZLs) are a recently defined group of related diseases that probably arise from a common cell of origin, the marginal zone B cell. Data on therapy for subtypes other than gastric mucosa-associated lymphoid tissue (MALT) lymphoma has been largely limited to retrospective case series. This prospective phase 2 study of fludarabine and rituximab for the treatment of marginal zone lymphomas enrolled 26 patients, 14 with nodal MZL, eight with MALT lymphomas and four with splenic MZL; 81% were receiving initial systemic therapy. Only 58% [95% confidence interval (CI) 37-77%] of patients completed the planned six cycles, due to significant haematological, infectious and allergic toxicity. Four late toxic deaths occurred due to infections [15% (95% CI 4.3-35%)], two related to delayed bone marrow aplasia and two related to myelodysplastic syndrome. Nonetheless, the overall response rate was 85% (95% CI 65-96%), with 54% complete responses. The progression-free survival at 3.1 years of follow-up is 79.5% (95% CI 63-96%). We conclude that, although concurrent fludarabine and rituximab given at this dose and schedule is a highly effective regimen in the treatment of MZLs, the significant haematological and infectious toxicity observed both during and after therapy is prohibitive in this patient population, emphasizing the need to study MZLs as a separate entity.
边缘区淋巴瘤(MZL)是一组最近定义的相关疾病,可能起源于共同的细胞来源——边缘区B细胞。除胃黏膜相关淋巴组织(MALT)淋巴瘤外,其他亚型的治疗数据在很大程度上仅限于回顾性病例系列。这项关于氟达拉滨和利妥昔单抗治疗边缘区淋巴瘤的前瞻性2期研究纳入了26例患者,其中14例为淋巴结边缘区淋巴瘤,8例为MALT淋巴瘤,4例为脾边缘区淋巴瘤;81%的患者接受初始全身治疗。由于严重的血液学、感染性和过敏性毒性,只有58%[95%置信区间(CI)37 - 77%]的患者完成了计划的六个周期治疗。发生了4例因感染导致的晚期毒性死亡[15%(95%CI 4.3 - 35%)],2例与延迟性骨髓再生障碍有关,2例与骨髓增生异常综合征有关。尽管如此,总体缓解率为85%(95%CI 65 - 96%),完全缓解率为54%。在3.1年的随访中,无进展生存率为79.5%(95%CI 63 - 96%)。我们得出结论,尽管按此剂量和疗程同时使用氟达拉滨和利妥昔单抗是治疗MZL的高效方案,但在治疗期间和治疗后观察到的严重血液学和感染性毒性在该患者群体中令人望而却步,这凸显了将MZL作为一个独立实体进行研究的必要性。