Adde Magdalena, Enblad Gunilla, Hagberg Hans, Sundström Christer, Laurell Anna
Department of Oncology, Uppsala University Hospital, 751 85 Uppsala Sweden.
Med Oncol. 2006;23(2):283-93. doi: 10.1385/MO:23:2:283.
To study the effectiveness and tolerability of a dose-intensified treatment including rituximab for patients, not older than 65 yr, with high-risk aggressive B-cell lymphoma.
Thirty-eight patients with high-risk aggressive B-cell lymphoma, the majority classified as grade 2 or 3 using age-adjusted International Prognostic Index, were treated with six courses of CHOEP + rituximab on a 2-wk schedule with G-CSF d 4-11. CNS prophylaxis was administered using intravenous Ara-C as a single dose at the end of treatment.
All patients were considered responders after three courses. Thirty-one patients (82%) achieved a complete remission or a complete remission unverified. With a median follow up of 27 mo, overall and event-free survival are 79% and 60%, respectively. Treatment was given on an outpatient basis. There were no treatment- related unexpected toxic events or mortalities. Large-cell lymphoma involvement of the bone marrow was a poor prognostic sign even with this intensified treatment and 4/6 patients relapsed. CNS relapse occurred in three patients, two of whom had large cell bone marrow involvement.
Although only a short follow up, the R-CHOEP-14 regimen is promising and could be an improvement compared to conventional treatment, with acceptable toxicity. The value of intravenous Ara-C at the end of treatment can be questioned, as it did not prevent CNS relapse or affect treatment outcome.
研究包括利妥昔单抗在内的剂量强化治疗方案对65岁及以下高危侵袭性B细胞淋巴瘤患者的有效性和耐受性。
38例高危侵袭性B细胞淋巴瘤患者,多数根据年龄校正的国际预后指数被归类为2级或3级,接受了六个疗程的CHOEP +利妥昔单抗治疗,治疗方案为每2周一次,并在第4至11天给予粒细胞集落刺激因子(G-CSF)。在治疗结束时,采用静脉注射阿糖胞苷单剂量进行中枢神经系统预防。
所有患者在三个疗程后均被视为有反应者。31例患者(82%)实现了完全缓解或未经验证的完全缓解。中位随访27个月,总生存率和无事件生存率分别为79%和60%。治疗在门诊进行。没有与治疗相关的意外毒性事件或死亡。即使采用这种强化治疗,骨髓大细胞淋巴瘤受累仍是一个不良预后指标,6例患者中有4例复发。3例患者发生中枢神经系统复发,其中2例有大细胞骨髓受累。
尽管随访时间较短,但R-CHOEP-14方案很有前景,与传统治疗相比可能有所改善,且毒性可接受。治疗结束时静脉注射阿糖胞苷的价值值得怀疑,因为它未能预防中枢神经系统复发或影响治疗结果。