首页> 外文期刊>Journal of Clinical Oncology >Rituximab added to first-line mitoxantrone, chlorambucil, and prednisolone chemotherapy followed by interferon maintenance prolongs survival in patients with advanced follicular lymphoma: an East German Study Group Hematology and Oncology Study.
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Rituximab added to first-line mitoxantrone, chlorambucil, and prednisolone chemotherapy followed by interferon maintenance prolongs survival in patients with advanced follicular lymphoma: an East German Study Group Hematology and Oncology Study.

机译:一线米托蒽醌,苯丁酸氮芥和泼尼松龙化学疗法加用利妥昔单抗后再进行干扰素维持治疗可延长晚期滤泡性淋巴瘤患者的生存期:东德血液学和肿瘤学研究小组。

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PURPOSE: Rituximab has been shown to be active in follicular lymphoma (FL), both as monotherapy and in combination with chemotherapy. We conducted a randomized trial comparing mitoxantrone, chlorambucil, and prednisolone (MCP) chemotherapy plus rituximab with MCP alone. PATIENTS AND METHODS: Previously untreated patients with stage III or IV CD20+ indolent or mantle cell lymphoma were randomly assigned to either eight 28-day cycles of MCP plus rituximab (R-MCP; n = 181) or eight cycles of MCP alone (n = 177). All patients who achieved a complete or partial remission were treated with interferon maintenance until relapse. Herein, we report the results from the primary analysis population of patients with FL, who constituted the majority of patients (56%) recruited to the trial (n = 201; R-MCP, n = 105; MCP, n = 96). RESULTS: Rates of overall and complete response were significantly higher in the R-MCP arm than the MCP arm (overall response, 92% v 75%, respectively; P = .0009; complete response, 50% v 25%, respectively; P = .004). With a median follow-up time of 47 months, median event-free survival (EFS) and progression-free survival (PFS) times were significantly prolonged with R-MCP compared with MCP (EFS, not reached v 26 months, respectively; P < .0001; PFS, not reached v 28.8 months, respectively; P < .0001), and overall survival (OS) was significantly improved with R-MCP compared with MCP (4-year OS rate, 87% v 74%, respectively; P = .0096). CONCLUSION: The R-MCP regimen significantly improves complete and overall response rates, EFS, PFS, and OS in patients with previously untreated advanced FL, without a clinically significant increase in toxicity.
机译:目的:利妥昔单抗已被证明在滤泡性淋巴瘤(FL)中是有效的,既可作为单一疗法,也可与化学疗法联用。我们进行了一项随机试验,比较了米托蒽醌,苯丁酸氮芥和泼尼松龙(MCP)化疗加利妥昔单抗与单独MCP的比较。患者和方法:先前未接受治疗的III期或IV期CD20 +惰性或套细胞淋巴瘤患者被随机分配至MCP加利妥昔单抗的8个28天周期(R-MCP; n = 181)或单独的MCP 8个周期(n = 177)。所有达到完全或部分缓解的患者均接受干扰素维持治疗直至复发。本文中,我们报告了FL患者的主要分析人群的结果,这些患者占该试验的大多数患者(56%)(n = 201; R-MCP,n = 105; MCP,n = 96)。结果:R-MCP组的总体和完全缓解率显着高于MCP组(总体缓解率分别为92%v 75%; P = 0.0009;完全缓解率分别为50%v 25%; P = .004)。中位随访时间为47个月,与MCP相比,R-MCP显着延长了无事件生存(EFS)和无进展生存(PFS)的中位时间(EFS,分别未达到26个月; P <.0001; PFS,未达到28.8个月; P <.0001),与MCP相比,R-MCP显着改善了总生存期(OS)(4年OS率分别为87%和74%) ; P = .0096)。结论:R-MCP方案可显着改善先前未接受治疗的晚期FL患者的完全和总体缓解率,EFS,PFS和OS,且临床上无明显的毒性增加。

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