康替唑胺治疗血液系统恶性肿瘤患者革兰氏阳性细菌感染的有效性和安全性:一项回顾性研究。

IF 3 3区 医学 Q2 INFECTIOUS DISEASES
Ruihua Mi, Luyang Chang, Lin Chen, Lin Wang, Yixuan Ma, Jia Liu, Dongbei Li, Xudong Wei
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引用次数: 0

摘要

目的:康替唑胺是一种恶唑烷类抗生素,其抗菌活性与利奈唑胺相当,具有降低血液学毒性的明显优势。本回顾性分析旨在评估康特唑胺治疗血液病患者革兰氏阳性细菌感染(GPI)的安全性和有效性。方法:回顾性分析2022年4月至2024年6月在河南省肿瘤医院接受化疗或造血干细胞移植(HSCT)后接受康唑胺治疗至少3天的确诊或疑似GPI的成人血液病患者。综合数据收集包括人口统计变量、治疗方案、感染概况、微生物学数据和临床结果。结果:共纳入132例患者(47.5±18.0岁),男性61.4%。血液系统恶性肿瘤的治疗策略包括联合化疗加靶向治疗(41.7%)、单独化疗(37.9%)和造血干细胞移植(20.5%)。60.6%为发热性中性粒细胞减少症。一半以上的感染发生在治疗后一个月内,主要影响肺部和皮肤/软组织。2例患者在接受康替唑胺治疗前并发血流感染(BSI)。康替唑胺治疗的中位时间为12天,72.7%的患者将其作为初始治疗。使用康唑胺的理由包括复杂的皮肤和软组织感染(cSSTI)、既往治疗失败、不良反应和禁忌症。临床有效率为70.6% (95% CI: 62.7% ~ 78.5%),其中肺炎为64.4% (95% CI: 52.2% ~ 76.6%),皮肤或软组织感染为74.6% (95% CI: 63.0% ~ 86.1%),发热性中性粒细胞减少为69.3% (95% CI: 58.9% ~ 79.8%)。17例患者(12.9%)出现不良事件。12例新发/加重恶心或上腹不适,7例呕吐;这些可能与镇静剂有关。未观察到康替唑胺相关的血液学不良事件、视神经或周围神经病变。结论:康替唑胺对这些患者似乎很有希望,但需要大规模的前瞻性研究来证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of contezolid in the treatment of Gram-positive bacterial infections in patients with hematological malignancies: a retrospective study.

Purpose: Contezolid, an oxazolidinone antibiotic, is recognized for its comparable antimicrobial activity to linezolid, with a distinct advantage of reduced hematological toxicity. This retrospective analysis aims to evaluate the safety and efficacy profile of contezolid in the treatment of Gram-positive bacterial infections (GPI) in hematological patients.

Methods: A retrospective analysis was conducted on adult hematological patients with confirmed or suspected GPI who received contezolid for at least three days following chemotherapy or hematopoietic stem cell transplantation (HSCT) at Henan Cancer Hospital between April 2022 and June 2024. Comprehensive data collection included demographic variables, treatment protocols, infection profiles, microbiological data, and clinical outcomes.

Results: The study included 132 patients (47.5 ± 18.0 years), 61.4% male. Treatment strategies for hematological malignancies included combination chemotherapy with targeted therapy (41.7%), chemotherapy alone (37.9%), and HSCT (20.5%). 60.6% had febrile neutropenia. More than half of the infections occurred within one month after treatment, predominantly affecting the lungs and skin/soft tissue. Two patients had concurrent bloodstream infections (BSI) prior to receiving contezolid treatment. The median contezolid treatment was 12 days, 72.7% had it as initial treatment. The rationale for contezolid utilization includes complicated skin and soft-tissue infections (cSSTI), prior treatment failure, adverse reactions, and contraindications. Clinical effective rate was 70.6% (95% CI: 62.7% - 78.5%), with 64.4% (95% CI: 52.2% - 76.6%) in pneumonia, 74.6% (95% CI: 63.0% - 86.1%) in skin or soft tissue infections, and 69.3% (95% CI: 58.9% - 79.8%) in febrile neutropenia. Seventeen patients (12.9%) had adverse events. Twelve had new-onset/aggravated nausea or epigastric discomfort, and seven had vomiting; these may relate to contezolid. No contezolid-related hematological adverse events, optic or peripheral neuropathy were observed.

Conclusions: Contezolid seems promising for these patients, but large-scale prospective studies are needed for confirmation.

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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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