Koo Sophia, Baden Lindsey R
Division of Infectious Diseases, Brigham & Women's Hospital, Boston, MA 02115, USA.
J Natl Compr Canc Netw. 2008 Feb;6(2):202-13. doi: 10.6004/jnccn.2008.0017.
Immunomodulating monoclonal antibodies are a relatively new addition to the armamentarium of cancer therapeutics and have been shown to improve clinical outcomes in patients with various hematologic malignancies. Because of their targeted nature, these agents are often believed to be less immunosuppressive than standard cytotoxic chemotherapeutic agents. A clear causal association between an immunomodulating therapy and its infectious sequelae is often difficult to discern because of the burden of comorbid illness, intrinsic immunosuppression from the underlying malignancy, use in the salvage setting, and prior and concomitant use of immunosuppressive agents in this patient population. This article evaluates better-established and anecdotal infectious complications associated with major immunomodulating therapies used in hematologic malignancy and hematopoietic stem cell transplantation, including rituximab, alemtuzumab, gemtuzumab ozogamicin, infliximab, dacluzimab, and basiliximab.
免疫调节单克隆抗体是癌症治疗手段中相对较新的一类药物,已被证明可改善各种血液系统恶性肿瘤患者的临床结局。由于其靶向性,人们通常认为这些药物的免疫抑制作用比标准细胞毒性化疗药物小。由于合并症负担、潜在恶性肿瘤导致的内在免疫抑制、在挽救治疗中的应用以及该患者群体先前和同时使用免疫抑制剂,免疫调节治疗与其感染后遗症之间的明确因果关系往往难以辨别。本文评估了与血液系统恶性肿瘤和造血干细胞移植中使用的主要免疫调节疗法相关的已得到充分证实的和传闻的感染并发症,包括利妥昔单抗、阿仑单抗、吉妥珠单抗奥唑米星、英夫利昔单抗、达昔单抗和巴利昔单抗。