Optimizing outcomes for children with non-Hodgkin lymphoma in low- and middle-income countries by early correct diagnosis, reducing toxic death and preventing abandonment

被引:20
作者
Chantada, Guillermo [1 ]
Lam, Catherine G. [2 ]
Howard, Scott C. [3 ]
机构
[1] Hosp Univ Austral, Pilar, Argentina
[2] St Jude Childrens Res Hosp, Dept Global Pediat Med, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
关键词
non-Hodgkin lymphoma; Burkitt lymphoma; B-cell lymphoma; low-income countries; middle-income countries; abandonment; toxic death; ENDEMIC BURKITT-LYMPHOMA; B-CELL LYMPHOMA; CHILDHOOD-CANCER TREATMENT; SINGLE-CENTER; ADOLESCENTS; PROTOCOL; THERAPY; EXPERIENCE; LEUKEMIA; SURVIVAL;
D O I
10.1111/bjh.15785
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In high-income countries, more than 90% of children with mature B-cell lymphomas are cured with frontline therapy. However, cure requires prompt and correct diagnosis, careful risk stratification, very intense chemotherapy and meticulous supportive care, together with logistical support for patients who live far from the cancer centre or face financial barriers to receiving care. In low- and middle-income countries (LMIC), cure rates range from 20% to 70% because of lack of diagnosis, misdiagnosis, abandonment of treatment, toxic death and excess relapse with reduced-intensity regimens. Fortunately, a wide range of successful interventions in LMIC have reduced these causes of avoidable treatment failure. Public awareness campaigns have led to societal awareness of childhood cancer; telepathology has improved diagnosis, even in remote areas; subsidized chemotherapy, transportation, housing and food have reduced abandonment; and hand hygiene, nurse training programmes and health system improvements have reduced toxic death. These interventions can be deployed everywhere and at low cost, so are highly scalable. Children and adolescents with Burkitt lymphoma can be cured in all countries by making a timely correct diagnosis, applying protocols adapted to the local context, preventing abandonment of therapy and avoiding toxic death. Reducing these causes of treatment failure is feasible and highly cost-effective everywhere.
引用
收藏
页码:1125 / 1135
页数:11
相关论文
共 86 条
  • [81] Cyclophosphamide Monotherapy in Children With Burkitt Lymphoma: A Study From the French-African Pediatric Oncology Group (GFAOP)
    Traore, Fousseyni
    Coze, Carole
    Atteby, Jean-Jacques
    Andre, Nicolas
    Moreira, Claude
    Doumbe, Pierre
    Ravelomanana, Noeline
    Ye, Diarra
    Patte, Catherine
    Raquin, Marie-Anne
    Raphael, Martine
    Lemerle, Jean
    [J]. PEDIATRIC BLOOD & CANCER, 2011, 56 (01) : 70 - 76
  • [82] Burkitt lymphoma in Iraqi children: A distinctive form of sporadic disease with high incidence of EBV+ cases and more frequent expression of MUM1/IRF4 protein in cases with head and neck presentation
    Uccini, Stefania
    Al-Jadiry, Mazin F.
    Cippitelli, Claudia
    Talerico, Caterina
    Scarpino, Stefania
    Al-Darraji, Amir F.
    Al-Badri, Safaa A. F.
    Alsaadawi, Adel R.
    Al-Hadad, Salma A.
    Ruco, Luigi
    [J]. PEDIATRIC BLOOD & CANCER, 2018, 65 (12)
  • [83] The prioritisation of paediatrics and palliative care in cancer control plans in Africa
    Weaver, M. S.
    Yao, A. J. J.
    Renner, L. A.
    Harif, M.
    Lam, C. G.
    [J]. BRITISH JOURNAL OF CANCER, 2015, 112 (12) : 1845 - 1856
  • [84] Wiangnon S, 2011, ASIAN PAC J CANCER P, V12, P2215
  • [85] The impact of the methotrexate administration schedule and dose in the treatment of children and adolescents with B-cell neoplasms: a report of the BFM Group Study NHL-BFM95
    Woessmann, W
    Seidemann, K
    Mann, G
    Zimmermann, M
    Burkhardt, B
    Oschlies, I
    Ludwig, WD
    Klingebiel, T
    Graf, N
    Gruhn, B
    Juergens, H
    Niggli, F
    Parwaresch, R
    Gadner, H
    Riehm, H
    Schrappe, M
    Reiter, A
    [J]. BLOOD, 2005, 105 (03) : 948 - 958
  • [86] Yao JJA, 2013, SAMJ S AFR MED J, V103, P113, DOI [10.7196/SAMJ.6365, 10.7196/samj.6365]