Maschmeyer Georg, Bullinger Lars, Garcia-Vidal Carolina, Herbrecht Raoul, Maertens Johan, Menna Pierantonio, Pagano Livio, Thiebaut-Bertrand Anne, Calandra Thierry
Certified Cancer Center, Klinikum Ernst von Bergmann, Charlottenstrasse 72, D-14467, Potsdam, Germany.
Department of Hematology, Oncology and Tumor Immunology, Campus Virchow, Charité - Universitätsmedizin Berlin, German Cancer Consortium (DKTK), Partner Site Berlin, Berlin, Germany.
Leukemia. 2022 May;36(5):1215-1226. doi: 10.1038/s41375-022-01556-7. Epub 2022 Apr 2.
The 9th web-based European Conference on Infections in Leukemia (ECIL-9), held September 16-17, 2021, reviewed the risk of infections and febrile neutropenia associated with more recently approved immunotherapeutic agents and molecular targeted drugs for the treatment of acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). Novel antibody based treatment approaches (inotuzumab ozogamicin, gemtuzumab ozogamicin, flotetuzumab), isocitrate dehydrogenases inhibitors (ivosidenib, enasidenib, olutasidenib), FLT3 kinase inhibitors (gilteritinib, midostaurin, quizartinib), a hedgehog inhibitor (glasdegib) as well as a BCL2 inhibitor (venetoclax) were reviewed with respect to their mode of action, their immunosuppressive potential, their current approval and the infectious complications and febrile neutropenia reported from clinical studies. Evidence-based recommendations for prevention and management of infectious complications and specific alerts regarding the potential for drug-drug interactions were developed and discussed in a plenary session with the panel of experts until consensus was reached. The set of recommendations was posted on the ECIL website for a month for comments from members of EBMT, EORTC, ICHS and ELN before final approval by the panelists. While a majority of these agents are not associated with a significantly increased risk when used as monotherapy, caution is required with combination therapy such as venetoclax plus hypomethylating agents, gemtuzumab ozogamicin plus cytotoxic drugs or midostaurin added to conventional AML chemotherapy.
2021年9月16日至17日举行的第九届欧洲白血病感染网络会议(ECIL-9),回顾了与最近批准的用于治疗急性髓系白血病(AML)和急性淋巴细胞白血病(ALL)的免疫治疗药物和分子靶向药物相关的感染风险和发热性中性粒细胞减少症。基于新型抗体的治疗方法(因诺妥珠单抗、吉妥珠单抗、氟妥珠单抗)、异柠檬酸脱氢酶抑制剂(艾伏尼布、恩扎卢胺、奥图西尼布)、FLT3激酶抑制剂(吉瑞替尼、米哚妥林、奎扎替尼)、一种刺猬抑制剂(格拉斯吉布)以及一种BCL2抑制剂(维奈克拉),就其作用方式、免疫抑制潜力、当前批准情况以及临床研究报告的感染并发症和发热性中性粒细胞减少症进行了综述。在全体会议上与专家小组共同制定并讨论了关于感染并发症预防和管理的循证建议以及关于药物相互作用可能性的特定警示,直至达成共识。该套建议在ECIL网站上发布一个月,以供EBMT、EORTC、ICHS和ELN成员发表意见,然后由专家小组成员最终批准。虽然这些药物大多数作为单一疗法使用时不会显著增加风险,但在联合治疗时需要谨慎,如维奈克拉加去甲基化药物、吉妥珠单抗加细胞毒性药物或米哚妥林加入传统AML化疗。