Lenz Georg, Dreyling Martin, Hoster Eva, Wörmann Bernhard, Dührsen Ulrich, Metzner Bernd, Eimermacher Hartmut, Neubauer Andreas, Wandt Hannes, Steinhauer Hjalmar, Martin Sonja, Heidemann Else, Aldaoud Ali, Parwaresch Reza, Hasford Joerg, Unterhalt Michael, Hiddemann Wolfgang
Department of Internal Medicine III of the Ludwig-Maximilians University, Marchioninistrasse 15, 81377 Munich, Germany.
J Clin Oncol. 2005 Mar 20;23(9):1984-92. doi: 10.1200/JCO.2005.08.133. Epub 2005 Jan 24.
Mantle cell lymphoma (MCL) is characterized by a poor prognosis with a low to moderate sensitivity to chemotherapy and a median survival of only 3 to 4 years. In an attempt to improve outcome, the German Low Grade Lymphoma Study Group (GLSG) initiated a randomized trial comparing the combination of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) and rituximab (R-CHOP) with CHOP alone as first-line therapy for advanced-stage MCL.
One hundred twenty-two previously untreated patients with advanced-stage MCL were randomly assigned to six cycles of CHOP (n = 60) or R-CHOP (n = 62). Patients up to 65 years of age achieving a partial or complete remission underwent a second randomization to either myeloablative radiochemotherapy followed by autologous stem-cell transplantation or interferon alfa maintenance (IFNalpha). All patients older than 65 years received IFNalpha maintenance.
R-CHOP was significantly superior to CHOP in terms of overall response rate (94% v 75%; P = .0054), complete remission rate (34% v 7%; P = .00024), and time to treatment failure (TTF; median, 21 v 14 months; P = .0131). No differences were observed for progression-free survival. Toxicity was acceptable, with no major differences between the two therapeutic groups.
The combined immunochemotherapy with R-CHOP resulted in a significantly higher response rate and a prolongation of the TTF as compared with chemotherapy alone. Hence, R-CHOP may serve as a new baseline regimen for advanced stage MCL, but needs to be further improved by novel strategies in remission.
套细胞淋巴瘤(MCL)预后较差,对化疗的敏感性低至中等,中位生存期仅为3至4年。为了改善治疗效果,德国低度淋巴瘤研究组(GLSG)开展了一项随机试验,比较环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)联合利妥昔单抗(R-CHOP)与单纯CHOP作为晚期MCL一线治疗方案的疗效。
122例既往未接受治疗的晚期MCL患者被随机分配接受6个周期的CHOP方案(n = 60)或R-CHOP方案(n = 62)。年龄在65岁及以下且达到部分或完全缓解的患者再次随机分组,接受清髓性放化疗后自体干细胞移植或干扰素α维持治疗(IFNα)。所有年龄大于65岁的患者接受IFNα维持治疗。
在总缓解率(94%对75%;P = .0054)、完全缓解率(34%对7%;P = .00024)和治疗失败时间(TTF;中位时间,21个月对14个月;P = .0131)方面,R-CHOP显著优于CHOP。无进展生存期未观察到差异。毒性反应可接受,两个治疗组之间无显著差异。
与单纯化疗相比,R-CHOP联合免疫化疗导致显著更高的缓解率和TTF延长。因此,R-CHOP可作为晚期MCL的新的基础治疗方案,但需要通过缓解期的新策略进一步改进。