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利妥昔单抗联合化疗治疗 B 细胞淋巴瘤患者中基于 PCR 的诊断方法使肺孢子菌肺炎发生率降低。

Low incidence of pneumocystis pneumonia utilizing PCR-based diagnosis in patients with B-cell lymphoma receiving rituximab-containing combination chemotherapy.

机构信息

Department of Pharmacy Services, Mayo Clinic, Rochester, Minnesota.

Department of Pharmacy, Spectrum Health, Grand Rapids, Michigan.

出版信息

Am J Hematol. 2016 Nov;91(11):1113-1117. doi: 10.1002/ajh.24499. Epub 2016 Aug 22.

Abstract

Recent literature has demonstrated concern over the risk of Pneumocystis jirovecii pneumonia (PJP) when administering rituximab with combination chemotherapy such as in R-CHOP; however, the exact risk and potential need for prophylaxis is unknown. We sought to determine the incidence of PJP infection following R-CHOP administration in patients with B-cell lymphoma. Consecutive patients diagnosed with B-cell lymphoma receiving R-CHOP were evaluated from chemotherapy initiation until 180 days after the last administration. The primary outcome was cumulative incidence of PJP infection. Secondary endpoints included the association of rituximab, prednisone and subsequent chemotherapy with PJP infection risk. A total of 689 patients (53% male, median age 66 years) were included. Seventy-three percent of patients completed at least 6 cycles of R-CHOP treatment. Median rituximab and prednisone cumulative doses were 3950 mg and 5325 mg, respectively. Median daily prednisone dose through end of treatment was 45 mg (range 7.6 mg to 119 mg). The cumulative incidence of PJP was 1.51% (95% CI 0.57-2.43, at maximum follow-up of 330 days), below 3.5%, the conventional threshold for prophylaxis. Univariate analysis did not detect a statistically significant association between PJP and rituximab, steroids, or receipt of additional chemotherapy in this patient population. Our results demonstrate a low occurrence of Pneumocystis pneumonia during R-CHOP treatment of B-cell lymphoma and argue against universal anti-Pneumocystis prophylaxis in this setting. Further investigations should focus on targeted anti-Pneumocystis prophylaxis for patients presenting with high-risk baseline characteristics or when receiving rituximab-inclusive intensive combination chemotherapy regimens as treatment for other aggressive lymphoma subtypes. Am. J. Hematol. 91:1113-1117, 2016. © 2016 Wiley Periodicals, Inc.

摘要

最近的文献表明,在接受利妥昔单抗联合化疗(如 R-CHOP)治疗时,存在发生肺孢子菌肺炎(PJP)的风险,但确切的风险和潜在预防需求尚不清楚。我们旨在确定接受 R-CHOP 治疗的 B 细胞淋巴瘤患者发生 PJP 感染的发生率。从化疗开始到最后一次给药后 180 天,对连续诊断为 B 细胞淋巴瘤并接受 R-CHOP 治疗的患者进行评估。主要结局是 PJP 感染的累积发生率。次要终点包括利妥昔单抗、泼尼松和随后的化疗与 PJP 感染风险的关系。共纳入 689 例患者(53%为男性,中位年龄 66 岁)。73%的患者至少完成了 6 个周期的 R-CHOP 治疗。利妥昔单抗和泼尼松的累积剂量中位数分别为 3950mg 和 5325mg,中位日剂量泼尼松分别为 45mg(范围为 7.6-119mg)。在最大随访 330 天的情况下,PJP 的累积发生率为 1.51%(95%CI0.57-2.43),低于 3.5%,这是预防的常规阈值。单变量分析未发现 PJP 与利妥昔单抗、类固醇或在该患者人群中接受额外化疗之间存在统计学显著关联。我们的研究结果表明,在接受 R-CHOP 治疗 B 细胞淋巴瘤期间,发生肺孢子菌肺炎的发生率较低,因此在这种情况下不支持普遍使用预防性抗肺孢子菌治疗。进一步的研究应集中于针对具有高基线特征的患者或在接受包含利妥昔单抗的强化联合化疗方案治疗其他侵袭性淋巴瘤亚型时,进行靶向性抗肺孢子菌预防。Am.J.Hematol.91:1113-1117,2016。©2016WileyPeriodicals,Inc.

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