CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Antibacterial prophylaxis and antimicrobial stewardship in the era of innovative therapies for haematological malignancies: transplantation, cellular therapies and new drugs.
Antibacterial prophylaxis and antimicrobial stewardship in the era of innovative therapies for haematological malignancies: transplantation, cellular therapies and new drugs.
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抗菌药物预防性使用长期以来一直是接受强化化疗和造血干细胞移植(HSCT)的血液系统恶性肿瘤患者支持治疗的核心措施,尤其是在长时间且深度中性粒细胞减少的情况下。
然而,氟喹诺酮类(FQ)预防性用药的广泛使用日益引发对抗菌药物耐药性、微生物组破坏、药物相关毒性以及艰难梭菌感染的担忧,对其普遍应用提出了挑战。与此同时,血液学治疗格局正迅速演变,新型药物和细胞疗法如嵌合抗原受体(CAR)T细胞、双特异性抗体(BsAbs)、抗体-药物偶联物及免疫治疗相继引入,每种疗法均伴随独特的免疫抑制模式和感染风险。在本叙述性综述中,我们从抗菌药物管理的角度批判性地审视抗菌药物预防性用药的作用,将传统化疗和移植的证据与创新疗法的新兴数据相结合。
我们总结了当前指南建议、真实世界证据以及近期质疑常规FQ预防性用药净获益的研究,特别是在耐药率较高的环境中。还讨论了替代策略,包括非FQ药物和选择性省略预防性用药。
总体而言,现有证据支持从普遍预防性用药转向基于风险调整的个体化方法,该方法需考虑治疗方式、预期中性粒细胞减少的持续时间和深度、患者特定因素以及当地流行病学情况。在现代血液学实践中,将抗菌预防决策嵌入结构化抗菌药物管理计划中,对于平衡感染预防与长期患者安全及耐药性控制至关重要。
Antibacterial prophylaxis has long been a cornerstone of supportive care in patients with haematological malignancies undergoing intensive chemotherapy and haematopoietic stem cell transplantation (HSCT), particularly in the setting of prolonged and profound neutropenia.
However, the widespread use of fluoroquinolone (FQ) prophylaxis has increasingly raised concerns related to antimicrobial resistance, microbiota disruption, drug-related toxicity, and Clostridioides difficile infection, challenging its universal application.
At the same time, the therapeutic landscape of haematology is rapidly evolving, with the introduction of novel agents and cellular therapies such as chimeric antigen receptor (CAR) T cells, bispecific antibodies (BsAbs), antibody-drug conjugates, and immune-based treatments, each associated with distinct patterns of immunosuppression and infectious risk.
In this narrative review, we critically examine the role of antibacterial prophylaxis through the lens of antimicrobial stewardship, integrating evidence from traditional chemotherapy and transplantation with emerging data from innovative therapies.
We summarize current guideline recommendations, real-world evidence, and recent studies questioning the net benefit of routine FQ prophylaxis, particularly in settings with high resistance prevalence. Alternative strategies, including non-FQ agents and selective omission of prophylaxis, are also discussed.
Overall, available evidence supports a shift from universal prophylaxis toward a risk-adapted, individualized approach that accounts for treatment modality, expected duration and depth of neutropenia, patient-specific factors, and local epidemiology. Embedding antibacterial prophylaxis decisions within structured antimicrobial stewardship programs is essential to balance infection prevention with long-term patient safety and resistance containment in modern haematological practice.
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