Department of Infectious Diseases, St. John Hospital and Medical Center, Detroit, MI, USA.
Clin Lymphoma Myeloma Leuk. 2012 Feb;12(1):66-9. doi: 10.1016/j.clml.2011.07.006. Epub 2011 Oct 14.
Guidelines for primary Pneumocystis jirovecii pneumonia (PCP) prophylaxis for patients with hematologic malignancy (HM) are still lacking. Our objective was to identify risk factors for PCP among patients with HM to help recognize patients who would benefit from primary PCP prophylaxis.
We performed a case-control study of adult patients with HM and negative for human immunodeficiency virus and with confirmed PCP by using cytology or histopathology from 2 medical centers over an 11-year period. Each case was matched with 4 patients without PCP by type of HM and year of treatment. We compared demographic, clinical, and laboratory data among cases and controls. Data were analyzed by using SPSS version 18.0.
Fourteen cases and 56 controls were included in the study period. No significant differences were seen in demographics between both groups. All identified patients had lymphoproliferative HM, the majority of patients (93%) had either non-Hodgkin lymphoma or chronic lymphocytic leukemia. Autoimmune diseases were more frequent in cases vs. controls (28.6% vs. 5.4% P = .01). The receipt and duration of chemotherapy were similar in both groups. Among chemotherapeutic agents, including steroids, only fludarabine was associated with increased risk for PCP (50% vs. 17.9%; P = .02). No difference was found in total or lymphocyte percentage in cases at the time of PCP diagnosis vs. nadir values in controls.
Patients with lymphoproliferative HM, specifically chronic lymphocytic leukemia and non-Hodgkin lymphoma, who are receiving fludarabine and with autoimmune disorders are at increased risk for PCP and should be considered for PCP primary prophylaxis.
目前仍缺乏血液恶性肿瘤(HM)患者原发性卡氏肺孢子虫肺炎(PCP)预防指南。我们的目的是确定 HM 患者发生 PCP 的危险因素,以帮助识别需要进行原发性 PCP 预防的患者。
我们对在两个医疗中心接受治疗的 11 年内,经细胞学或组织病理学证实的人免疫缺陷病毒阴性且患有 HM 的成年患者进行了一项病例对照研究。每个病例均与未发生 PCP 的 4 例 HM 类型和治疗年份相同的患者相匹配。我们比较了病例和对照组的人口统计学、临床和实验室数据。数据使用 SPSS 版本 18.0 进行分析。
研究期间纳入了 14 例病例和 56 例对照。两组间的人口统计学特征无显著差异。所有确诊患者均患有淋巴增生性 HM,大多数患者(93%)患有非霍奇金淋巴瘤或慢性淋巴细胞白血病。与对照组(28.6%比 5.4%,P =.01)相比,病例组更常患有自身免疫性疾病。两组患者接受和持续的化疗相似。在包括类固醇在内的化疗药物中,仅氟达拉滨与 PCP 风险增加相关(50%比 17.9%,P =.02)。与对照组的最低值相比,病例组在发生 PCP 时的总淋巴细胞或淋巴细胞百分比无差异。
患有淋巴增生性 HM(尤其是慢性淋巴细胞白血病和非霍奇金淋巴瘤)、正在接受氟达拉滨治疗且患有自身免疫性疾病的患者,发生 PCP 的风险增加,应考虑进行 PCP 一级预防。