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接受聚乙二醇化脂质体阿霉素和利妥昔单抗免疫化疗的非霍奇金淋巴瘤患者间质性肺炎的发病率。

Incidence of interstitial pneumonitis in non-Hodgkin's lymphoma patients receiving immunochemotherapy with pegylated liposomal doxorubicin and rituximab.

作者信息

Zhou Ting, Shen Qian, Peng Hui, Chao Tengfei, Zhang Lihong, Huang Liu, Yang Kaixiang, Thapa Sudip, Yu Shiying, Jiang Yongsheng

机构信息

Cancer Center of Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan, 430030, People's Republic of China.

Department of Orthopedic Surgery, Washington University, St Louis, MO, USA.

出版信息

Ann Hematol. 2018 Jan;97(1):141-147. doi: 10.1007/s00277-017-3160-1. Epub 2017 Oct 31.

Abstract

Pneumonitis is a rare but severe and potentially fatal adverse effect in chemotherapy of lymphoma. This study is aimed to investigate the incidence of interstitial pneumonitis in non-Hodgkin's lymphoma (NHL) patients receiving immunochemotherapy with pegylated liposomal doxorubicin and rituximab. Lymphoma patients were retrospectively reviewed, and eligible patients were included in this study. According to the chemotherapy regimens, patients were classified in four groups: combination of vincristine, cyclophosphamide, doxorubicin, and prednisone (CHOP group) with rituximab (RCHOP group) and combination of vincristine, cyclophosphamide, pegylated liposomal doxorubicin and prednisone (CDOP group) with rituximab (RCDOP group). Incidence and severity of interstitial pneumonitis were compared among the four groups. Among 757 patients reviewed, 207 patients were included in final analysis. Thirteen patients developed chemotherapy-induced interstitial pneumonitis, and the mean cycle of chemotherapy before the onset of pneumonitis was 4. Incidence rates of pneumonitis were 0, 1.8, 17.4, and 21.1% in CHOP, RCHOP, CDOP, and RCDOP groups, respectively (p < 0.001). The mean grades of pneumonitis were 0, 2, 2.5, and 3 in four groups, respectively (p < 0.001). After adjustment of confounders, chemotherapy regimens (OR 3.491, 95% CI 1.527-7.981, p = 0.003) and neutropenia in previous cycles (OR 2.186, 95% CI 1.281-3.731, p = 0.004) were independently associated with the incidence of pneumonitis. Interstitial pneumonitis should be highlighted in NHL patients who received more than 4 cycles of RCDOP chemotherapy regimen, especially in those who had grade 4 neutropenia in the previous cycles of chemotherapy.

摘要

肺炎是淋巴瘤化疗中一种罕见但严重且可能致命的不良反应。本研究旨在调查接受聚乙二醇化脂质体阿霉素和利妥昔单抗免疫化疗的非霍奇金淋巴瘤(NHL)患者间质性肺炎的发生率。对淋巴瘤患者进行回顾性分析,符合条件的患者纳入本研究。根据化疗方案,患者分为四组:长春新碱、环磷酰胺、阿霉素和泼尼松联合用药(CHOP组)加用利妥昔单抗(RCHOP组),以及长春新碱、环磷酰胺、聚乙二醇化脂质体阿霉素和泼尼松联合用药(CDOP组)加用利妥昔单抗(RCDOP组)。比较四组间质性肺炎的发生率和严重程度。在回顾的757例患者中,207例患者纳入最终分析。13例患者发生化疗诱导的间质性肺炎,肺炎发生前化疗的平均周期为4个周期。CHOP组、RCHOP组、CDOP组和RCDOP组的肺炎发生率分别为0、1.8%、17.4%和21.1%(p<0.001)。四组肺炎的平均分级分别为0、2、2.5和3级(p<0.001)。在调整混杂因素后,化疗方案(OR 3.491,95%CI 1.527 - 7.981,p = 0.003)和前周期的中性粒细胞减少(OR 2.186,95%CI 1.281 - 3.731,p = 0.004)与肺炎发生率独立相关。对于接受超过4个周期RCDOP化疗方案的NHL患者,尤其是在前周期化疗中有4级中性粒细胞减少的患者,应重视间质性肺炎。

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