Oki Yasuhiro, Ewer Michael S, Lenihan Daniel J, Fisch Michael J, Hagemeister Fredrick B, Fanale Michelle, Romaguera Jorge, Pro Barbara, Fowler Nathan, Younes Anas, Astrow Alan B, Huang Xuelin, Kwak Larry W, Samaniego Felipe, McLaughlin Peter, Neelapu Sattva S, Wang Michael, Fayad Luis E, Durand Jean-Bernard, Rodriguez M Alma
Department of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Department of Cardiology, University of Texas MD Anderson Cancer Center, Houston, TX.
Clin Lymphoma Myeloma Leuk. 2015 Mar;15(3):152-8. doi: 10.1016/j.clml.2014.09.001. Epub 2014 Sep 28.
The present multicenter phase II trial evaluated the safety and efficacy of pegylated liposomal doxorubicin (PLD) instead of conventional doxorubicin in standard R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine [Oncovin], and prednisone) therapy for elderly patients with diffuse large B-cell lymphoma.
Patients aged > 60 years who had stage II to IV disease were included. Treatment consisted of rituximab 375 mg/m(2) intravenously (I.V.); cyclophosphamide 750 mg/m(2) IV; PLD 40 mg/m(2) (maximum, 90 mg) I.V. over 1 hour; and vincristine 2.0 mg I.V., all on day 1. Additionally prednisone, 40 mg/m(2), was given orally on days 1 to 1 to 5 (DRCOP [rituximab, cyclophosphamide, PLD, vincristine, and prednisone]). The cycles were repeated every 3 weeks for 6 to 8 cycles.
Eighty patients were enrolled and were evaluable for toxicity. The median age was 69 years. All except 1 had additional cardiac risk factors for anthracycline-induced cardiac toxicity beyond advanced age. From the intent-to-treat analysis of 79 eligible patients, the overall response rate was 86%, and the complete response rate was 78%. Cardiac events greater than grade 3 were identified in 3 patients (4%); grade 1 to 2 events, mostly asymptomatic declines in ejection fraction, were noted in another 16 patients. One death was attributed to cardiac failure. The estimated 5-year event-free and overall survival rate was 52% and 70%, respectively.
DRCOP represents an effective strategy for potentially mitigating cardiotoxicity in elderly patients with aggressive B-cell lymphoma. Future studies incorporating baseline cardiac risk assessments, long-term follow-up data, and biospecimen collection for correlative science should be undertaken.
本多中心II期试验评估了聚乙二醇化脂质体阿霉素(PLD)替代传统阿霉素用于老年弥漫性大B细胞淋巴瘤患者标准R-CHOP(利妥昔单抗加环磷酰胺、阿霉素、长春新碱[安可平]和泼尼松)治疗的安全性和疗效。
纳入年龄>60岁、疾病分期为II至IV期的患者。治疗方案包括静脉注射利妥昔单抗375mg/m²;静脉注射环磷酰胺750mg/m²;静脉注射PLD 40mg/m²(最大剂量90mg),持续1小时;静脉注射长春新碱2.0mg,均在第1天进行。此外,在第1至5天口服泼尼松40mg/m²(DRCOP[利妥昔单抗、环磷酰胺、PLD、长春新碱和泼尼松])。每3周重复1个周期,共进行6至8个周期。
80例患者入组并可进行毒性评估。中位年龄为69岁。除1例患者外,所有患者均有除高龄外的其他蒽环类药物诱导心脏毒性的心脏危险因素。从79例符合条件患者的意向性分析来看,总缓解率为86%,完全缓解率为78%。3例患者(4%)出现3级以上心脏事件;另有16例患者出现1至2级事件,主要是射血分数无症状下降。1例死亡归因于心力衰竭。估计5年无事件生存率和总生存率分别为52%和70%。
DRCOP是一种有效策略,可能减轻老年侵袭性B细胞淋巴瘤患者的心脏毒性。未来应开展纳入基线心脏风险评估、长期随访数据以及用于相关科学研究的生物样本采集的研究。