Real World Incidence and Etiology of Infectious Complications in Adults With Ph-Negative Acute Lymphoblastic Leukemia Treated With the Pediatric-Inspired GIMEMA LAL1913 Program. A Campus All Study

IF 3.9 4区 医学 Q2 HEMATOLOGY
Patrizia Zappasodi, Ludovica Calabretta, Virginia Valeria Ferretti, Davide Lazzarotto, Nicola Fracchiolla, Marco Cerrano, Cristina Papayannidis, Sabina Chiaretti, Maria Ilaria Del Principe, Valentina Mancini, Monia Lunghi, Fabio Forghieri, Sara Mastaglio, Michelina Dargenio, Crescenza Pasciolla, Carla Mazzone, Beatrice Sani, Fabio Guolo, Marzia Defina, Maria Ciccone, Elisa Roncoroni, Marianna Rossi, Claudia Patricia Tobar Cabrera, Gianluca Martini, Giacomo Riccaboni, Luca Arcaini, Robin Foà, Anna Candoni
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引用次数: 0

Abstract

Infections often complicate pediatric-inspired treatments for adult Philadelphia-negative acute lymphoblastic leukemia (Ph- ALL). Literature data on these complications are difficult to interpret due to the heterogeneity of types of infections analyzed or patients and treatment characteristics. A deeper insight on the infections occurring in the real life in uniformly treated ALL patients is lacking. This study investigated infectious complications in 240 newly diagnosed adult Ph- ALL patients treated in the real life according to the GIMEMA LAL1913 protocol by 18 Italian centers participating in the Campus ALL network. Incidence, etiology of microbiologically documented infections and invasive fungal infections (IFI) and mortality for infection were determined. Potential risk factors and the prophylactic strategies used during the first chemotherapy course (C1) were analyzed. Of 240 patients, 145 (60%) experienced at least one infectious episode, with bacterial infections being the most common (74.3%), followed by viral (13.9%), fungal (10.1%), and Pneumocystis jirovecii (1.7%) infections. The blood stream was the most involved site, pneumonia occurred in 14.6% of cases, half of which being fungal. Infections were prevalent during C1, affecting 40.5% of patients; IFI occurred in 12.5% of patients, most of them in C1. Risk factors for infections included older age (≥ 55 years and particularly > 65 years) and comorbidities only for IFI. The mortality rate for infection was 3.3%. Antibacterial, antiviral, antifungal, and anti-PJ prophylaxis were variably administered and did not associate with a significant reduced infection rate. In conclusion, the rate of infectious complications in the real life of adult Ph- ALL patients treated with a pediatric-inspired intensive regimen is high, mainly during induction and mostly bacterial, particularly in the bloodstream, with a high IFI rate. Older age, mainly over 65 years, is a risk factor for all types of infection. The antimicrobial prophylaxis was not associated to a reduced risk of infection.

用儿科启发的GIMEMA LAL1913项目治疗ph阴性急性淋巴细胞白血病成人感染并发症的真实世界发生率和病因学校园里所有的学习
感染常常使成人费城阴性急性淋巴细胞白血病(Ph- ALL)的儿科治疗复杂化。由于所分析的感染类型、患者和治疗特点的异质性,有关这些并发症的文献数据难以解释。对在现实生活中统一治疗的ALL患者中发生的感染缺乏更深入的了解。本研究调查了在现实生活中根据GIMEMA LAL1913协议接受治疗的240名新诊断的成人Ph- ALL患者的感染并发症,这些患者由18个参与校园ALL网络的意大利中心组成。确定了微生物学记录的感染和侵袭性真菌感染(IFI)的发生率、病因和感染的死亡率。分析首次化疗期间的潜在危险因素及预防策略。在240例患者中,145例(60%)至少经历过一次感染,其中细菌感染最常见(74.3%),其次是病毒(13.9%)、真菌(10.1%)和肺囊虫(1.7%)感染。血流是最主要的受累部位,14.6%的病例发生肺炎,其中一半为真菌性肺炎。C1期感染普遍存在,影响40.5%的患者;12.5%的患者发生IFI,主要发生在C1区。感染的危险因素包括年龄较大(≥55岁,特别是>;65岁),仅IFI有合并症。感染死亡率为3.3%。抗菌、抗病毒、抗真菌和抗pj预防是可变的,与显著降低感染率没有关联。总之,在现实生活中,接受儿科启发强化方案治疗的成人Ph- ALL患者感染并发症的发生率很高,主要是在诱导期间,大多数是细菌,特别是在血液中,IFI率很高。年龄较大,主要是65岁以上,是所有类型感染的危险因素。抗菌素预防与感染风险降低无关。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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