Treatment results in children with myeloid leukemia of Down syndrome in Saudi Arabia: A multicenter SAPHOS leukemia group study

被引:2
作者
Jastaniah, Wasil [1 ,2 ,3 ]
Alsultan, Abdulrahman [4 ]
Al Daama, Saad [5 ]
Ballourah, Walid [6 ]
Bayoumy, Mohammad [7 ]
Al-Anzi, Faisal [8 ]
Al Shareef, Omar [9 ]
Abrar, Mohammed Burhan [2 ,3 ]
Al Sudairy, Reem [10 ]
Al Ghemlas, Ibrahim [11 ,12 ]
机构
[1] Umm AlQura Univ, Dept Pediat, Fac Med, Mecca, Saudi Arabia
[2] King Saud Bin Abdulaziz Univ, Princess Noorah Oncol Ctr, Jeddah, Saudi Arabia
[3] King Abdul Aziz Med City, Jeddah, Saudi Arabia
[4] King Saud Univ, Dept Pediat, Coll Med, Riyadh, Saudi Arabia
[5] King Fahad Specialist Hosp, Dammam, Saudi Arabia
[6] King Fahad Med City, Riyadh, Saudi Arabia
[7] King Faisal Specialist Hosp & Res Ctr, Jeddah, Saudi Arabia
[8] Prince Faisal Bin Bandar Canc Ctr, Qaseem, Saudi Arabia
[9] Prince Sultan Mil Med City, Riyadh, Saudi Arabia
[10] King Abdullah Specialized Childrens Hosp, King Abdulaziz Med City, Dept Pediat Hematol Oncol, Riyadh, Saudi Arabia
[11] Alfaisal Univ, Fac Med, Riyadh, Saudi Arabia
[12] King Faisal Specialist Hosp & Res Ctr, Riyadh, Saudi Arabia
关键词
Myeloid leukemia; Down syndrome; Child; Prognosis; Survival; POPULATION-BASED COHORT; ENDOGAMOUS POPULATION; PEDIATRIC-PATIENTS; CHILDHOOD-CANCER; DOSE CYTARABINE; POOLED-ANALYSIS; PARENTAL AGE; AML; RISK; CHEMOTHERAPY;
D O I
10.1016/j.leukres.2017.04.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the high incidence of Down syndrome (DS) in Arab countires, the incidence and outcomes of myeloid leukemia of DS (ML-DS) have not been studied. We evaluated 206 pediatric acute myeloid leukemia (AML) patients diagnosed between 2005 and 2012 and identified 31 (15%) ML-DS. The incidence of ML-DS was 48 per 100,000 compared to 0.6 per 100,000 for AML in non-DS children. Thus, patients with DS had 80-fold increased risk of ML-DS compared to AML in non-DS children. The median age at diagnosis was 1.8 years, male/ female ratio was 1.2, majority (84%) of patients had FAB-M7 subtype, and the cytogenetic abnormalities were normal karyotype (constitutional trisomy 21) in 48%, additional trisomy in 23%, and other aberrations in 29%. Complete remission, cumulative incidences of relapse (CIR), toxic-death, and 5-year event-free survival (EFS) rates were 96.8%, 19.4%, 13.1%, and 67.7 +/- 8.4%; respectively. In the present study, multivariate analysis revealed favorable outcome (5-year EFS 86.7 +/- 8.8%) for patients with normal karyotype. The incidence and clinical characteristics of ML-DS in Saudi patients were comparable to other reports. However, there is a need to optimize risk stratification and treatment intensity to reduce CIR and toxic death rates to further improve outcomes of patients with ML-DS.
引用
收藏
页码:48 / 54
页数:7
相关论文
共 40 条
[1]   Optimal treatment intensity in children with Down syndrome and myeloid leukaemia: data from 56 children treated on NOPHO-AML protocols and a review of the literature [J].
Abildgaard, Lotte ;
Ellebaek, Eva ;
Gustafsson, Gran ;
Abrahamsson, Jonas ;
Hovi, Liisa ;
Jonmundsson, Gudmundur ;
Zeller, Bernward ;
Hasle, Henrik .
ANNALS OF HEMATOLOGY, 2006, 85 (05) :275-280
[2]   Long-term results of an ultra low-dose cytarabine-based regimen for the treatment of acute megakaryoblastic leukaemia in children with Down syndrome [J].
Al-Ahmari, Ali ;
Shah, Niketa ;
Sung, Lillian ;
Zipursky, Alvin ;
Hitzler, Johann .
BRITISH JOURNAL OF HAEMATOLOGY, 2006, 133 (06) :646-648
[3]   Genetic dilsorders in the Arab world [J].
Al-Gazali, Lihadh ;
Hamamy, Hanan ;
Al-Arrayad, Shaikha .
BMJ-BRITISH MEDICAL JOURNAL, 2006, 333 (7573) :831-834B
[4]  
[Anonymous], ADM REG PROV POP EST
[5]   Consanguineous marriages and their effects on common adult diseases: Studies from an endogamous population [J].
Bener, Abdulbari ;
Hussain, Rafat ;
Teebi, Ahmad S. .
MEDICAL PRINCIPLES AND PRACTICE, 2007, 16 (04) :262-267
[6]  
Bener A, 2009, ASIAN PAC J CANCER P, V10, P35
[7]   Transient Abnormal Myelopoiesis and AML in Down Syndrome: an Update [J].
Bhatnagar, Neha ;
Nizery, Laure ;
Tunstall, Oliver ;
Vyas, Paresh ;
Roberts, Irene .
CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2016, 11 (05) :333-341
[8]   Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study [J].
Blink, Marjolein ;
Zimmermann, Martin ;
von Neuhoff, Christine ;
Reinhardt, Dirk ;
de Haas, Valerie ;
Hasle, Henrik ;
O'Brien, Maureen M. ;
Stark, Batia ;
Tandonnet, Julie ;
Pession, Andrea ;
Tousovska, Katerina ;
Cheuk, Daniel K. L. ;
Kudo, Kazuko ;
Taga, Takashi ;
Rubnitz, Jeffrey E. ;
Haltrich, Iren ;
Balwierz, Walentyna ;
Pieters, Rob ;
Forestier, Erik ;
Johansson, Bertil ;
van den Heuvel-Eibrink, Marry M. ;
Zwaan, C. Michel .
HAEMATOLOGICA, 2014, 99 (02) :299-307
[9]   AML patients with Down syndrome have a high cure rate with AML-BFM therapy with reduced dose intensity [J].
Creutzig, U ;
Reinhardt, D ;
Diekamp, S ;
Dworzak, M ;
Stary, J ;
Zimmermann, M .
LEUKEMIA, 2005, 19 (08) :1355-1360
[10]   Treatment strategies and long-term results in paediatric patients treated in four consecutive AML-BFM trials [J].
Creutzig, U ;
Zimmermann, M ;
Ritter, J ;
Reinhardt, D ;
Hermann, J ;
Henze, G ;
Jürgens, H ;
Kabisch, H ;
Reiter, A ;
Riehm, H ;
Gadner, H ;
Schellong, G .
LEUKEMIA, 2005, 19 (12) :2030-2042