CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:EARLY DISCONTINUATION OF ANTIBIOTICS IN PEDIATRIC PATIENTS WITH LOW- AND HIGH-RISK FEBRILE NEUTROPENIA: A SINGLE-CENTRE EXPERIENCE.
EARLY DISCONTINUATION OF ANTIBIOTICS IN PEDIATRIC PATIENTS WITH LOW- AND HIGH-RISK FEBRILE NEUTROPENIA: A SINGLE-CENTRE EXPERIENCE.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
在特定 FN 儿童患者中,包括高危患者,ANC 恢复前早期停用 EAT 可能减少住院和抗生素暴露。
传统上,对于出现发热性中性粒细胞减少症(FN)的儿童癌症患者和造血干细胞移植(HSCT)受者,标准做法是维持广谱抗生素治疗,直至发热消退且中性粒细胞绝对计数(ANC)恢复。近期在成人中的研究支持在 ANC 恢复前停用经验性抗生素治疗(EAT)的安全性。然而,儿童中的数据仍然有限。
回顾性研究,纳入2022年6月至2023年8月期间因FN入院、年龄<18岁且患有癌症和/或接受HSCT的患者,这些患者在ANC 500/mm3之前停用EAT。已因有明确或疑似细菌感染来源、脓毒症而接受抗生素治疗,或已入住PICU的患者被排除。我们报告停用EAT后7天内的特征和临床结局(再入院、新发发热和新发感染),以及30天PICU入住率、感染相关死亡率和全因死亡率。
我们纳入了97例次(65例患者)FN,47例次(48.4%)发生在患有血液系统疾病(恶性或非恶性)的儿童中,包括接受过HSCT(n=8)和/或CAR-T(n=6)的患者。75.3%的例次发热持续时间少于24小时。中位EAT持续时间为3天(IQR:3-5)。ANC恢复发生在EAT停用后中位4天(IQR 2-12)。在EAT停用后7天内,11例次(11.3%)发热复发。在3/11例次中确定了感染性病因(轻度细菌性毛囊炎、可能原发性巨细胞病毒感染和侵袭性真菌感染,各n=1)。未观察到PICU入住或30天感染相关死亡率。两名患者因非感染性原因死亡。
Maintaining broad-spectrum antibiotics until resolution of fever and recovery of absolute neutrophil count (ANC) has traditionally been the standard approach for pediatric patients with cancer and for hematopoietic stem-cell transplantation (HSCT) recipients who present with febrile neutropenia (FN). Recent studies in adults support the safety of discontinuing empiric antibiotic treatment (EAT) prior to ANC recovery. However, data in children remain limited.
Retrospective study that included patients under 18 years of age with cancer and/or undergoing HSCT admitted with FN between June 2022 and August 2023, in whom EAT was discontinued prior to ANC 500/mm3. Patients already receiving antibiotics for a documented or suspected source of bacterial infection, sepsis, or admitted to PICU were excluded. We report the characteristics and clinical outcomes (readmission, new fever onset, and new infection) within 7 days of the discontinuation of EAT, as well as the 30-day PICU admission, infection-related mortality and all-cause mortality rates.
We included 97 episodes (65 patients) of FN, 47 (48.4%) occurred in children with hematologic disease (malignant or non-malignant), including patients who had received an HSCT (n=8) and/or a CAR-T (n=6). Fever lasted less than 24 hours in 75.3% of episodes. Median EAT duration was 3 days (IQR: 3-5). ANC recovery occurred at a median of 4 days (IQR 2-12) after EAT discontinuation. Fever recurred in 11 episodes (11.3%) within 7 days from EAT discontinuation. An infectious cause was identified in 3/11 episodes (mild bacterial folliculitis, probable primary Cytomegalovirus infection, and invasive fungal infection, n=1 each). No admissions to PICU or 30-day infection-related mortality were observed. Two patients died because of non-infectious causes.
Early EAT discontinuation before ANC recovery in selected pediatric patients with FN, including high-risk patients, may reduce hospitalization and antibiotic exposure.
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