Hannawa Idan S, Bestul Daniel J
Department of Pharmaceutical Services, Beaumont Hospital, Royal Oak, MI 48073, USA.
J Oncol Pharm Pract. 2011 Dec;17(4):381-6. doi: 10.1177/1078155210386989. Epub 2010 Nov 25.
To determine the tolerability of rituximab, specifically cytokine release syndrome/acute infusion reactions (CRS), when it is administered before or after cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy in patients with non-Hodgkin's lymphoma (NHL).
This study is a retrospective analysis of patients identified through pharmacy chemotherapy records. Inclusion criteria were diagnosis of NHL, first cycle of rituximab with CHOP or modified CHOP (mCHOP), treated between 1/1/04 and 6/30/09, age 18 years and greater, and inpatient status. Patients were excluded if their records/information were unavailable. Patients were divided into two groups based on practices observed at our institution: rituximab followed by CHOP (R-CHOP) or CHOP followed by rituximab (CHOP-R). Patient records were reviewed to determine demographic data, CRS, vital signs, evidence of chills/rigors, use of rescue medications, and rituximab infusion rates.
One-hundred thirteen patients meeting the inclusion criteria were divided into two groups: R-CHOP (n=29) and CHOP-R (n=84). R-CHOP patients experienced numerically more CRS (65.5% vs. 42.9%, p=0.0517) and significantly more chills/rigors (p=0.0376). Maximum and minimum oxygen (O(2)) saturations were significantly lower in the R-CHOP group (p=0.0444 and 0.0165, respectively). Maximum temperature was significantly higher in the R-CHOP group (p=0.0047). There was no difference between groups in use of rescue medications (p=1). R-CHOP patients required significantly more rate reductions (p=0.0431) than CHOP-R patients, although there was no difference in final tolerated rate between groups.
Patients with NHL who receive rituximab after CHOP experience significantly fewer chills/rigors, higher oxygen saturations, lower maximum temperatures, and fewer rate reductions than patients who receive rituximab before CHOP.
确定在非霍奇金淋巴瘤(NHL)患者中,利妥昔单抗在环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗之前或之后给药时的耐受性,尤其是细胞因子释放综合征/急性输液反应(CRS)。
本研究是一项通过药房化疗记录识别患者的回顾性分析。纳入标准为NHL诊断、利妥昔单抗与CHOP或改良CHOP(mCHOP)的首个疗程、2004年1月1日至2009年6月30日期间接受治疗、年龄18岁及以上且为住院状态。如果患者的记录/信息不可用则将其排除。根据在我们机构观察到的做法,将患者分为两组:利妥昔单抗后接CHOP(R-CHOP)或CHOP后接利妥昔单抗(CHOP-R)。审查患者记录以确定人口统计学数据、CRS、生命体征、寒战/发抖的证据、救援药物的使用以及利妥昔单抗输注速率。
113名符合纳入标准的患者分为两组:R-CHOP组(n = 29)和CHOP-R组(n = 84)。R-CHOP组患者在数量上经历更多的CRS(65.5%对42.9%,p = 0.0517)和明显更多的寒战/发抖(p = 0.0376)。R-CHOP组的最高和最低氧(O₂)饱和度显著更低(分别为p = 0.0444和0.0165)。R-CHOP组的最高体温显著更高(p = 0.0047)。两组在救援药物的使用上无差异(p = 1)。R-CHOP组患者比CHOP-R组患者需要显著更多的速率降低(p = 0.0431),尽管两组之间的最终耐受速率无差异。
与在CHOP之前接受利妥昔单抗的患者相比,在CHOP之后接受利妥昔单抗的NHL患者经历的寒战/发抖明显更少、氧饱和度更高、最高体温更低且速率降低更少。