Risk factors and prognosis of early death in secondary hemophagocytic lymphohistiocytosis

被引:2
|
作者
Zhang, Qiaolei [1 ,2 ]
Zhu, Lixia [3 ]
Zhou, De [3 ]
Li, Li [3 ]
Xie, Wanzhuo [3 ]
Tan, Yamin [1 ,2 ]
Ye, Xiujin [3 ]
机构
[1] Univ Chinese Acad Sci, Zhejiang Canc Hosp, Dept Hematol, Canc Hosp, 38 Guangji Rd, Hangzhou 310003, Zhejiang, Peoples R China
[2] Chinese Acad Sci, Inst Canc & Basic Med IBMC, Hangzhou, Peoples R China
[3] Zhejiang Univ, Dept Hematol, Affiliated Hosp 1, Med Sch, 79 Qingchun Rd Hangzhou, Hangzhou 310003, Zhejiang, Peoples R China
关键词
Secondary hemophagocytic lymphohistiocytosis; Early death; Clinical characteristics; Risk factors; CELL LYMPHOMA; RETROSPECTIVE ANALYSIS; ADULTS;
D O I
10.1007/s00277-023-05153-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of our study was to summarize the clinical characteristics of early death patients with newly diagnosed secondary hemophagocytic lymphohistiocytosis (sHLH), analyze the risk factors of early death, and analyze the survival of patients. The clinical characteristics of 324 newly diagnosed sHLH patients admitted to the First Affiliated Hospital of Zhejiang University Medical College and Zhejiang Provincial Cancer Hospital from January 2014 to February 2021 were analyzed retrospectively. Analyze the independent risk factors of early death, compare the secondary diseases and treatment methods of patients with early death group and non early death group, and analyze the survival of all patients with sHLH. Among the 324 newly diagnosed patients with sHLH, 134 died early, with an early mortality rate of 41.4%. Comparing the clinical characteristics of patients with early death group and patients with non early death group, logistic regression model was used to conduct multifactor analysis. Age > 60 years, Plt <= 20.0 x 10(9)/L, APTT > 36.0 s and LDH > 1000.0 U/L were independent risk factors for early death of newly diagnosed sHLH patients (P < 0.05). Comparing the secondary diseases and treatment methods between early death group and non early death group, the proportion of sHLH patients secondary to lymphoma was higher in early death group than that in non early death group (P < 0.05). The proportion of sHLH patients secondary to connective tissue disease and infection was lower in early death group than that in non early death group (P < 0.05), and the proportion of sHLH patients used hormone combined chemotherapy was lower in early death group than that in non early death group (P < 0.05). The median follow-up time of all patients was 12.0 (1-65) months. The 5-year OS rates of patients with age > 60 years and age <= 60 years were 25.8% and 49.6% respectively (P < 0.001); The 5-year OS rates of patients with Plt > 20.0 x 10(9)/L and Plt <= 20.0 x 10(9)/L were 52.5% and 25.5% respectively (P < 0.001); The 5-year OS rates of patients with APTT > 36.0 s and APTT <= 36.0 s were 34.5% and 57.4% respectively (P < 0.001); The 5-year OS rates of patients with LDH > 1000.0 U/L and LDH <= 1000.0 U/L were 23.3% and 56.3% respectively (P < 0.001). Age > 60 years, Plt <= 20.0 x 10(9)/L, APTT > 36.0 s and LDH > 1000.0 U/L are independent risk factors for early death of sHLH patients. The early mortality of lymphoma associated HLH (LA-HLH) patients is high, and early use of hormone combined chemotherapy can reduce the early mortality.
引用
收藏
页码:2301 / 2308
页数:8
相关论文
共 50 条
  • [41] Risk factors of early death in pediatric hemophagocytic lymphohistocytosis: Retrospective cohort study
    Zhang, Lijun
    Dai, Lei
    Li, Deyuan
    FRONTIERS IN PEDIATRICS, 2022, 10
  • [42] Early diagnostic value of low percentage of glycosylated ferritin in secondary hemophagocytic lymphohistiocytosis
    Wang, Zhao
    Wang, Yini
    Wang, Jingshi
    Feng, Cuicui
    Tian, Liping
    Wu, Lin
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2009, 90 (04) : 501 - 505
  • [43] Early diagnostic value of low percentage of glycosylated ferritin in secondary hemophagocytic lymphohistiocytosis
    Zhao Wang
    Yini Wang
    Jingshi Wang
    Cuicui Feng
    Liping Tian
    Lin Wu
    International Journal of Hematology, 2009, 90 : 501 - 505
  • [44] Secondary Hemophagocytic Lymphohistiocytosis Presenting as Acalculous Cholecystitis
    Kandula, Manasa
    Eichenauer, Stosh
    Ahmed, Umair
    Fischer, Jacqueline
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2017, 112 : S690 - S690
  • [45] Secondary Hemophagocytic Lymphohistiocytosis in an Infant with Wolman Disease
    Bartakke, Sandip
    Nisal, Amit
    Bafna, Vibha
    Valecha, Aashna
    INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION, 2021, 37 (01) : 191 - 192
  • [46] Visceral leishmaniasis, hypertriglyceridemia and secondary hemophagocytic lymphohistiocytosis
    Claudia Colomba
    Paola Di Carlo
    Francesco Scarlata
    Chiara Iaria
    Giuseppina Barberi
    Fausto Famà
    Valeria Cama
    Antonio Cascio
    Infection, 2016, 44 : 391 - 392
  • [47] Enteric Fever Presenting as Secondary Hemophagocytic Lymphohistiocytosis
    Meenu Pandey
    Bhavna Dhingra
    Sunita Sharma
    Jagdish Chandra
    Harish Pemde
    Varinder Singh
    The Indian Journal of Pediatrics, 2012, 79 : 1671 - 1672
  • [48] Hemophagocytic lymphohistiocytosis secondary to Mycoplasma pneumoniae infection
    Ishida, Y
    Hiroi, K
    Tauchi, H
    Oto, Y
    Tokuda, K
    Kida, K
    PEDIATRICS INTERNATIONAL, 2004, 46 (02) : 174 - 177
  • [49] ACQUIRED HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS SECONDARY TO MULTIPLE MYELOMA
    Mallah, Haneen
    Vangipuram, Divya
    Solis, Ximena
    Motes, Arunee
    Islam, Ebtesam
    CHEST, 2020, 158 (04) : 971A - 971A
  • [50] Enteric Fever Presenting as Secondary Hemophagocytic Lymphohistiocytosis
    Pandey, Meenu
    Dhingra, Bhavna
    Sharma, Sunita
    Chandra, Jagdish
    Pemde, Harish
    Singh, Varinder
    INDIAN JOURNAL OF PEDIATRICS, 2012, 79 (12): : 1671 - 1672