Park Silvia, Kang Cheol-In, Chung Doo Ryeon, Peck Kyong Ran, Kim Won Seog, Kim Seok Jin
Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Division of Infectious Diseases, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Cancer Res Treat. 2015 Jul;47(3):448-57. doi: 10.4143/crt.2014.034. Epub 2014 Nov 3.
Rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) is the standard chemotherapy in diffuse large B-cell lymphoma (DLBCL) patients. Although febrile neutropenia (FN) is the major toxicity of this regimen, non-neutropenic fever (NNF) becomes an emerging issue.
We analyzed clinical features and outcomes of febrile complications from 397 patients with newly diagnosed DLBCL who were registered in the prospective cohort study. They had completed R-CHOP between September 2008 and January 2013.
Thirty-nine patients (9.8%) had NNF whereas 160 patients (40.3%) had FN. Among them, 24 patients (6.0%) had both during their treatment. Compared to frequent occurrence of initial FN after the first cycle (> 50% of total events), more than 80% of NNF cases occurred after the third cycle. Interstitial pneumonitis comprised the highest proportion of NNF cases (54.8%), although the causative organism was not identified in the majority of cases. Thus, pathogen was identified in a limited number of patients (n=9), and Pneumocystis jiroveci pneumonia (PJP) was the most common. Considering that interstitial pneumonitis without documented pathogen could be clinically diagnosed with PJP, the overall rate of PJP including probable cases was 4.5% (18 cases from 397 patients). The NNF-related mortality rate was 10.3% (four deaths from 39 patients with NNF) while the FN-related mortality rate was only 1.3%.
NNF was observed with incidence of 10% during R-CHOP treatment, and showed different clinical manifestations with respect to the time of initial episode and causes.
利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)是弥漫性大B细胞淋巴瘤(DLBCL)患者的标准化疗方案。尽管发热性中性粒细胞减少症(FN)是该方案的主要毒性,但非中性粒细胞减少性发热(NNF)正成为一个新出现的问题。
我们分析了前瞻性队列研究中登记的397例新诊断DLBCL患者发热并发症的临床特征和结局。他们在2008年9月至2013年1月期间完成了R-CHOP治疗。
39例患者(9.8%)发生NNF,而160例患者(40.3%)发生FN。其中,24例患者(6.0%)在治疗期间两者均发生。与第一个周期后初始FN的频繁发生(>总事件的50%)相比,超过80%的NNF病例发生在第三个周期后。间质性肺炎在NNF病例中占比最高(54.8%),尽管大多数病例中未鉴定出致病微生物。因此,在少数患者(n=9)中鉴定出病原体,耶氏肺孢子菌肺炎(PJP)是最常见的。考虑到无病原体记录的间质性肺炎可临床诊断为PJP,包括可能病例在内的PJP总发生率为4.5%(397例患者中有18例)。NNF相关死亡率为10.3%(39例NNF患者中有4例死亡),而FN相关死亡率仅为1.3%。
在R-CHOP治疗期间观察到NNF发生率为10%,并且在初始发作时间和病因方面表现出不同的临床表现。