Chemotherapy-Induced Peripheral Neuropathy in a Subpopulation of Mexican Pediatric Patients with Acute Lymphoblastic Leukemia

被引:1
作者
Jesus Vivas-Rosales, Irving [1 ]
Garcia-Saavedra, Liliana [2 ]
Alfonso Martin-Trejo, Jorge [3 ]
Manuel Mejia-Arangure, Juan [4 ]
Patricia Victorio-Garcia, Nora [5 ]
Herrera-Landero, Alejandro [6 ]
Carlos Nunz-Enriquez, Juan [7 ]
机构
[1] Mexican Inst Social Secur, Natl Med Ctr Siglo 21, Pediat Hosp, Dept Pediat, Mexico City, DF, Mexico
[2] Mexican Inst Social Secur, Natl Med Ctr Siglo 21, Pediat Hosp, Dept Phys Med & Rehabil, Mexico City, DF, Mexico
[3] Mexican Inst Social Secur, Natl Med Ctr Siglo 21, Pediat Hosp, Dept Hematol, Mexico City, DF, Mexico
[4] Mexican Inst Social Secur, Hlth Res Coordinat, Div Evaluat Res, Mexico City, DF, Mexico
[5] Autonomous Univ Tamaulipas, Fac Med Tampico Dr Alberto Romo Caballero, Ciudad Victoria, Mexico
[6] Mexican Inst Social Secur, Traumatol & Orthoped Hosp Lomas Verdes, Mexico City, DF, Mexico
[7] Mexican Inst Social Secur, Natl Med Ctr Siglo 21, Clin Epidemiol Res Dept, Pediat Hosp, Mexico City, DF, Mexico
关键词
Antineoplastic Agents; Children; Leukemia; Peripheral Nervous System Diseases; NEUROTOXICITY; CHILDREN; POLYNEUROPATHY; COMPLICATIONS; PATTERNS;
D O I
10.5812/ijp.11844
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Chemotherapy-induced peripheral neuropathy (CIPN) is frequent in children with acute lymphoblastic leukemia (ALL). Neurological manifestations can be grouped into one of the three functional divisions of the peripheral nervous system (PNS): sensory, motor and autonomic. One of the chemotherapeutic agents used in ALL is vincristine which has been associated with neuropathy in these children. This type of neuropathy can be transient but also leave permanent sequels that decrease patient's quality of life. Objectives: To know the frequency and type of neuropathy induced by chemotherapy in a subpopulation of Mexican pediatric patients with acute lymphoblastic leukemia. Methods: A cross-sectional study was conducted. There were included all pediatric patients with ALL diagnosed de novo from 2010 to December 31, 2013 who met the selection criteria. Descriptive statistics were used to determine the frequency and type of CIPN and information was described according to different clinical variables, type of treatment, risk classification, and ALL subtype according to the immunophenotype. Results: A total of 32 patients with acute lymphoblastic leukemia were included, mainly of early pre-B immunophenotype (93.8%), being 59.4% classified as high risk patients at the time of diagnosis. CIPN of sensory type was 78.1%, motor 34.3% and autonomic 40.6%. A significant proportion of patients (46.9%) were examined during maintenance phase. Conclusions: To our knowledge, this is the first study to report the frequency and type of CIPN in a subpopulation of Mexican children with acute lymphoblastic leukemia. Frequency of CIPN was higher than that reported in other populations. By considering that prognosis of a patient presenting CIPN could be considered as favorable after treatment suspension (in most cases), it is not always reversible and affects patient's quality of life. Therefore, it is necessary for all patients with ALL to be periodically monitored during treatment through neurological examination for detecting and immediately initiating their rehabilitation treatment.
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页数:9
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共 30 条
  • [1] Interventions for preventing neuropathy caused by cisplatin and related compounds
    Albers, J.
    Chaudhry, V
    Cavaletti, G.
    Donehower, R.
    [J]. COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2007, (01):
  • [2] Chemotherapy-induced peripheral neurotoxicity (CIPN): An update
    Argyriou, Andreas A.
    Bruna, Jordi
    Marmiroli, Paola
    Cavaletti, Guido
    [J]. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2012, 82 (01) : 51 - 77
  • [3] Chemotherapy-induced peripheral neuropathy
    Armstrong, T
    Almadrones, L
    Gilbert, MR
    [J]. ONCOLOGY NURSING FORUM, 2005, 32 (02) : 305 - 311
  • [4] Cardona AF, 2010, MED UIS, V23, P103
  • [5] CAVALETTI G, 1994, ANTICANCER RES, V14, P1287
  • [6] Neurotoxicity of chemotherapeutic and biologic agents in children with cancer
    De Braganca, Kevin C.
    Packer, Roger J.
    [J]. CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2008, 8 (02) : 114 - 122
  • [7] Díaz-Jaimes E, 2009, B MED HOSP INFANT M, V66, P529
  • [8] Distal symmetric polyneuropathy: A definition for clinical research - Report of the American Academy of Neurology, the American Association of Electrodiagnostic Medicine, and the American Academy of Physical Medicine and Rehabilitation
    England, JD
    Gronseth, GS
    Franklin, G
    Miller, RG
    Asbury, AK
    Carter, GT
    Cohen, JA
    Fisher, MA
    Howard, JF
    Kinsella, LJ
    Latov, N
    Lewis, RA
    Low, PA
    Sumner, AJ
    [J]. NEUROLOGY, 2005, 64 (02) : 199 - 207
  • [9] Fajardo-Gutierrez A, 1999, Rev Panam Salud Publica, V6, P75, DOI 10.1590/S1020-49891999000700001
  • [10] FAJARDOGUTIERRE.A, 1995, B MED HOSP INFANT M, V52, P507