Lei K I, Leung W T, Johnson P J
Department of Clinical Oncology, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, NT.
Br J Cancer. 1994 Nov;70(5):1009-13. doi: 10.1038/bjc.1994.439.
Four of 12 Chinese patients receiving BACOP, in combination with recombinant human granulocyte colony-stimulating factor, for aggressive non-Hodgkin's lymphoma developed a rapidly progressive pneumonic illness characterised by diffuse pulmonary infiltrates and hypoxaemia. The condition proved fatal in three, and in none could an infective cause be identified. A retrospective analysis revealed only one episode of pneumonia in the previous 24 patients in whom the same BACOP regimen was administered without granulocyte colony-stimulating factor support. Granulocyte colony-stimulating factor, by augmenting white cell production, pulmonary sequestration and margination and production of toxic oxygen species, may exacerbate underlying subclinical bleomycin pulmonary toxicity. Caution should be exercised before using granulocyte-stimulating factors in bleomycin-containing regimens.
12例接受BACOP方案联合重组人粒细胞集落刺激因子治疗侵袭性非霍奇金淋巴瘤的中国患者中,有4例发生了快速进展的肺部疾病,其特征为弥漫性肺部浸润和低氧血症。3例患者病情 fatal,均未发现感染原因。回顾性分析显示,在之前24例接受相同BACOP方案但未使用粒细胞集落刺激因子支持的患者中,仅发生过1例肺炎。粒细胞集落刺激因子通过增加白细胞生成、肺部滞留和边缘化以及毒性氧物种的产生,可能会加重潜在的亚临床博来霉素肺毒性。在含博来霉素的方案中使用粒细胞刺激因子之前应谨慎。