Halaas Jeffrey L, Moskowitz Craig H, Horwitz Steven, Portlock Carol, Noy Ariela, Straus David, O'Connor Owen A, Yahalom Joachim, Zelenetz Andrew D
Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Leuk Lymphoma. 2005 Apr;46(4):541-7. doi: 10.1080/10428190400029932.
Treatment of diffuse large B-cell lymphoma (DLBCL) with CHOP-21 (cyclophosphamide 750 mg/m2, doxorubicin 50 mg/m2, vincristine 1.4 mg/m2, prednisone 100 mg for 5 days every 21 days) results in long-term remission in approximately 45% of patients. Recent phase III trials have demonstrated improved survival by modifying CHOP either through adding rituximab or shortening the time between cycles to 14 days. These studies prompted our institution to treat newly diagnosed patients with DLBCL refusing or not eligible for protocol-based therapy with R-CHOP-14. In this single-institution retrospective analysis, we report our results with this regimen. Forty-nine patients with newly diagnosed DLBCL and ineligible or refusing protocol-based therapy were retrospectively identified. Patients were treated with 6-8 cycles of R-CHOP-14 given with filgrastim and prophylactic antibiotics. The main toxicities with R-CHOP-14 were hematological and neurological and were not unexpected. There were no treatment-related deaths. Patients received 90% of planned cytotoxic drug density. The complete remission/complete remission uncertain (CR/CRu) rate was 82.2%. At a median follow-up of 24 months, the event-free survival was 80% and overall survival 90%. These results demonstrate R-CHOP-14 can be given to patients safely and short-term results regarding survival are promising. Whether adding rituximab and increasing dose intensity improves survival over either alone will require randomized studies.
采用CHOP-21方案(环磷酰胺750 mg/m²、多柔比星50 mg/m²、长春新碱1.4 mg/m²、泼尼松100 mg,每21天服用5天)治疗弥漫性大B细胞淋巴瘤(DLBCL),约45%的患者可实现长期缓解。近期的III期试验表明,通过添加利妥昔单抗或将周期时间缩短至14天来改良CHOP方案,可提高生存率。这些研究促使我们机构采用R-CHOP-14方案治疗拒绝或不符合基于方案治疗条件的新诊断DLBCL患者。在这项单机构回顾性分析中,我们报告了该方案的治疗结果。回顾性纳入了49例新诊断的DLBCL患者,这些患者不符合或拒绝基于方案的治疗。患者接受了6 - 8个周期的R-CHOP-14治疗,并给予非格司亭和预防性抗生素。R-CHOP-14的主要毒性为血液学和神经学毒性,且在意料之中。没有与治疗相关的死亡病例。患者接受了计划细胞毒性药物剂量的90%。完全缓解/完全缓解不确定(CR/CRu)率为82.2%。中位随访24个月时,无事件生存率为80%,总生存率为90%。这些结果表明,R-CHOP-14可安全地用于患者,且生存方面的短期结果很有前景。添加利妥昔单抗和增加剂量强度是否比单独使用其中任何一种更能提高生存率,这需要进行随机研究。