Reinwald Mark, Boch Tobias, Hofmann Wolf-Karsten, Buchheidt Dieter
Department of Hematology and Oncology, Mannheim University Hospital, University of Heidelberg, Mannheim, Germany.
Biomark Insights. 2016 Apr 21;10(Suppl 3):55-68. doi: 10.4137/BMI.S22430. eCollection 2015.
Infectious complications are a major cause of morbidity and mortality in patients with hemato-oncological diseases. Although disease-related immunosuppression represents one factor, aggressive treatment regimens, such as chemotherapy, stem cell transplantation, or antibody treatment, account for a large proportion of infectious side effects. With the advent of targeted therapies affecting specific kinases in malignant diseases, the outcome of patients has further improved. Nonetheless, dependent on the specific pathway targeted or off-target activity of the kinase inhibitor, therapy-associated infectious complications may occur. We review the most common and approved kinase inhibitors targeting a variety of hemato-oncological malignancies for their immunosuppressive potential and evaluate their risk of infectious side effects based on preclinical evidence and clinical data in order to raise awareness of the potential risks involved.
感染性并发症是血液肿瘤疾病患者发病和死亡的主要原因。尽管疾病相关的免疫抑制是一个因素,但积极的治疗方案,如化疗、干细胞移植或抗体治疗,是感染性副作用的主要原因。随着影响恶性疾病中特定激酶的靶向治疗的出现,患者的预后进一步改善。尽管如此,根据激酶抑制剂的特定靶向途径或脱靶活性,仍可能发生与治疗相关的感染性并发症。我们回顾了针对各种血液肿瘤恶性肿瘤的最常见且已获批的激酶抑制剂的免疫抑制潜力,并根据临床前证据和临床数据评估其感染性副作用风险,以提高对潜在风险的认识。