Identification of significant risks in pediatric acute lymphoblastic leukemia (ALL) through machine learning (ML) approach

被引:27
作者
Mahmood, Nasir [1 ,2 ]
Shahid, Saman [3 ]
Bakhshi, Taimur [3 ]
Riaz, Sehar [4 ,5 ]
Ghufran, Hafiz [4 ,5 ]
Yaqoob, Muhammad [5 ,6 ]
机构
[1] Univ Hlth Sci UHS, Dept Biochem Human Genet & Mol Biol, Lahore, Pakistan
[2] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON, Canada
[3] Natl Univ Comp & Emerging Sci NUCES, Fdn Adv Sci & Technol FAST, Dept Sci & Humanities, Lahore, Pakistan
[4] Childrens Hosp, Sch Allied Hlth Sci, Lahore, Pakistan
[5] Inst Child Hlth, Lahore, Pakistan
[6] Childrens Hosp, Dept Med Genet, Lahore, Pakistan
关键词
Pediatric ALL; Machine learning (ML); Classification and regression trees (CART); Platelets; Hemoglobin; Environmental factors; CHILDHOOD LEUKEMIA; GENETIC POLYMORPHISMS; DRINKING-WATER; CHROMOSOMAL-ABNORMALITIES; THROMBOTIC COMPLICATIONS; SOCIOECONOMIC-STATUS; CHILDREN; SUSCEPTIBILITY; POPULATION; MUTATIONS;
D O I
10.1007/s11517-020-02245-2
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Pediatric acute lymphoblastic leukemia (ALL) through machine learning (ML) technique was analyzed to determine the significance of clinical and phenotypic variables as well as environmental conditions that can identify the underlying causes of child ALL. Fifty pediatric patients (n = 50) included who were diagnosed with acute lymphoblastic leukemia (ALL) according to the inclusion and exclusion criteria. Clinical variables comprised of the blood biochemistry (CBC, LFTs, RFTs) results, and distribution of type of ALL, i.e., T ALL or B ALL. Phenotypic data included the age, sex of the child, and consanguinity, while environmental factors included the habitat, socioeconomic status, and access to filtered drinking water. Fifteen different features/attributes were collected for each case individually. To retrieve most useful discriminating attributes, four different supervised ML algorithms were used including classification and regression trees (CART), random forest (RM), gradient boosted machine (GM), and C5.0 decision tree algorithm. To determine the accuracy of the derived CART algorithm on future data, a ten-fold cross validation was performed on the present data set. The ALL was common in children of age below 5 years in male patients whole belonged to middle class family of rural areas. (B-ALL) was most frequent as compared with T-ALL. The consanguinity was present in 54% of cases. Low levels of platelets and hemoglobin and high levels of white blood cells were reported in child ALL patients. CART provided the best and complete fit for the entire data set yielding a 99.83% model fit accuracy, and a misclassification of 0.17% on the entire sample space, while C5.0 reported 98.6%, random forest 94.44%, and gradient boosted machine resulted in 95.61% fitting. The variable importance of each primary discriminating attribute is platelet 43%, hemoglobin 24%, white blood cells 4%, and sex of the child 4%. An overall accuracy of 87.4% was recorded for the classifier. Platelet count abnormality can be considered as a major factor in predicting pediatric ALL. The machine learning algorithms can be applied efficiently to provide details for the prognosis for better treatment outcome. Graphical Identification of significant risks in pediatric acute lymphoblastic leukemia (ALL) through machine learning (ML) approach.
引用
收藏
页码:2631 / 2640
页数:10
相关论文
共 64 条
  • [1] Abdeldaim AM, 2018, STUD COMPUT INTELL, V730, P131, DOI 10.1007/978-3-319-63754-9_7
  • [2] Castro-Jiménez MA, 2011, PREV CHRONIC DIS, V8
  • [3] Outcome of treatment in children with philadelphia chromosome-positive acute lymphoblastic leukemia
    Aricò, M
    Valsecchi, MG
    Camitta, B
    Schrappe, M
    Chessells, J
    Baruchel, A
    Gaynon, P
    Silverman, L
    Janka-Schaub, G
    Kamps, W
    Pui, CH
    Masera, G
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (14) : 998 - 1006
  • [4] Thrombosis in children with acute lymphoblastic leukemia - Part I. Epidemiology of thrombosis in children with acute lymphoblastic leukemia
    Athale, UH
    Chan, AKC
    [J]. THROMBOSIS RESEARCH, 2003, 111 (03) : 125 - 131
  • [5] Five Most Common Prognostically Important Fusion Oncogenes are Detected in the Majority of Pakistani Pediatric Acute Lymphoblastic Leukemia Patients and are Strongly Associated with Disease Biology and Treatment Outcome
    Awan, Tashfeen
    Iqbal, Zafar
    Aleem, Aamer
    Sabir, Noreen
    Absar, Muhammad
    Rasool, Mahmood
    Tahir, Ammara H.
    Basit, Sulman
    Khalid, Ahmad Mukhtar
    Sabar, Muhammad Farooq
    Asad, Sultan
    Ali, Agha Shabbir
    Mahmood, Amer
    Akram, Muhammad
    Saeed, Tariq
    Saleem, Arsalan
    Mohsin, Danish
    Shah, Ijaz Hussain
    Khalid, Muhammad
    Asif, Muhammad
    Haq, Riazul
    Iqbal, Mudassar
    Akhtar, Tanveer
    [J]. ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (11) : 5469 - 5475
  • [6] Risk factors for acute leukemia in children: A review
    Belson, Martin
    Kingsley, Beverely
    Holmes, Adrianne
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 2007, 115 (01) : 138 - 145
  • [7] Influence of race and socioeconomic status on outcome of children treated for childhood acute lymphoblastic leukemia
    Bhatia, S
    [J]. CURRENT OPINION IN PEDIATRICS, 2004, 16 (01) : 9 - 14
  • [8] Dexamethasone versus prednisone and daily oral versus weekly intravenous mercaptopurine for patients with standard-risk acute lymphoblastic leukemia: a report from the Children's Cancer Group
    Bostrom, BC
    Sensel, MR
    Sather, HN
    Gaynon, PS
    La, MK
    Johnston, K
    Erdmann, GR
    Gold, S
    Heerema, NA
    Hutchinson, RJ
    Provisor, AJ
    Trigg, ME
    [J]. BLOOD, 2003, 101 (10) : 3809 - 3817
  • [9] Activating NOTCH1 mutations predict favorable early treatment response and long-term outcome in childhood precursor T-cell lymphoblastic leukemia
    Breit, Stephen
    Stanulla, Martin
    Flohr, Thomas
    Schrappe, Martin
    Ludwig, Wolf-Dieter
    Tolle, Gabriele
    Happich, Margit
    Muckenthaler, Martina U.
    Kulozik, Andreas E.
    [J]. BLOOD, 2006, 108 (04) : 1151 - 1157
  • [10] Environmental and genetic risk factors for childhood leukemia: Appraising the evidence
    Buffler, PA
    Kwan, ML
    Reynolds, P
    Urayama, KY
    [J]. CANCER INVESTIGATION, 2005, 23 (01) : 60 - 75