Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University, Torun, Bydgoszcz, Poland.
Pediatric Hematology Oncology, Department of Mother and Child, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Bone Marrow Transplant. 2023 Aug;58(8):881-892. doi: 10.1038/s41409-023-01998-2. Epub 2023 May 6.
We previously analyzed trends in incidence and factors associated with lethal complications in ALL/AML/CML patients (causes of deaths; COD-1 study). The objective of this study was the analysis of incidence and specific causes of death after HCT, with focus on infectious deaths in two time periods, 1980-2001 (cohort-1) and 2002-2015 (cohort-2). All patients with HCT for lymphoma, plasma cell disorders, chronic leukemia (except CML), myelodysplastic/myeloproliferative disorders, registered in the EBMT-ProMISe-database were included (n = 232,618) (COD-2 study). Results were compared to those in the ALL/AML/CML COD-1 study. Mortality from bacterial, viral, fungal, and parasitic infections decreased in very early, early and intermediate phases. In the late phase, mortality from bacterial infections increased, while mortality from fungal, viral, or unknown infectious etiology did not change. This pattern was similar for allo- and auto-HCT in COD-1 and COD-2 studies, with a distinct and constant lower incidence of all types of infections at all phases, after auto-HCT. In conclusion, infections were the main cause of death before day +100, followed by relapse. Mortality from infectious deaths significantly decreased, except late phase. Post-transplant mortality has significantly decreased in all phases, from all causes after auto-HCT; it has decreased in all phases after allo-HCT except late phase.
我们之前分析了 ALL/AML/CML 患者(死亡原因;COD-1 研究)致命并发症的发病趋势和相关因素。本研究的目的是分析 HCT 后发病率和特定死因,重点关注两个时期(1980-2001 年为 cohort-1,2002-2015 年为 cohort-2)的感染性死亡。所有在 EBMT-ProMISe 数据库中登记的接受 HCT 治疗的淋巴瘤、浆细胞疾病、慢性白血病(不包括 CML)、骨髓增生异常/骨髓增殖性疾病患者均纳入本研究(n=232618)(COD-2 研究)。结果与 ALL/AML/CML COD-1 研究进行了比较。在极早、早和中早期,细菌性、病毒性、真菌性和寄生虫感染的死亡率下降。在晚期,细菌性感染的死亡率增加,而真菌性、病毒性或原因不明的感染性疾病的死亡率没有变化。这种模式在 COD-1 和 COD-2 研究中的同种异体和自体 HCT 中相似,在所有阶段,自体 HCT 后所有类型感染的发生率都明显较低且保持不变。总之,感染是 100 天内死亡的主要原因,其次是复发。除晚期外,感染性死亡的死亡率显著下降。同种异体和自体 HCT 后所有阶段的移植后死亡率均显著下降,除晚期外,同种异体 HCT 后所有阶段的所有原因死亡率均下降。