Improved outcome at end of treatment in the collaborative Wilms tumour Africa project

被引:35
作者
Israels, Trijn [1 ,2 ,3 ]
Paintsil, Vivian [4 ]
Nyirenda, Dalida [5 ]
Kouya, Francine [6 ]
Afungchwi, Glenn Mbah [7 ]
Hesseling, Peter [8 ]
Tump, Clara [9 ]
Kaspers, Gertjan [1 ,2 ,10 ]
Burns, Liz [11 ]
Arora, Ramandeep Singh [12 ]
Chagaluka, George [5 ]
Nana, Philippa [6 ]
Renner, Lorna [13 ]
Molyneux, Elizabeth [5 ]
机构
[1] Princess Maxima Ctr Paediat Oncol, Acad Outreach, Utrecht, Netherlands
[2] Princess Maxima Ctr Paediat Oncol, Dept Solid Tumours, Utrecht, Netherlands
[3] Amphia Hosp, Dept Paediat, Breda, Netherlands
[4] Komfo Anokye Teaching Hosp, Dept Child Hlth, Kumasi, Ghana
[5] Coll Med, Dept Paediat, Blantyre, Malawi
[6] Mbingo Baptist Hosp, Dept Paediat Oncol, Mbingo, Cameroon
[7] Banso Baptist Hosp, Dept Paediat, Banso, Cameroon
[8] Stellenbosch Univ, Dept Paediat & Child Hlth, Cape Town, South Africa
[9] Univ Amsterdam, Dept Artificial Intelligence, Amsterdam, Netherlands
[10] Vrije Univ Amsterdam Med Ctr, Dept Paediat Oncol, Amsterdam, Netherlands
[11] World Child Canc, Operat, London, England
[12] Max Super Specialty Hosp, Dept Pediat Oncol, New Delhi, India
[13] Univ Ghana, Dept Child Hlth, Sch Med & Dent, Accra, Ghana
关键词
adapted treatment guideline; Africa; low-income countries; regional network; survival; Wilms tumour; SUB-SAHARAN AFRICA; ONCOLOGY-GROUP GFAOP; PEDIATRIC-ONCOLOGY; CHILDREN; CANCER; ABANDONMENT; MANAGEMENT; MALAWI; CARE; CURE;
D O I
10.1002/pbc.26945
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe Collaborative Wilms Tumour (WT) Africa Project has implemented an adapted WT treatment guideline in sub-Saharan Africa as a multi-centre prospective clinical trial. A retrospective, baseline evaluation of end-of-treatment outcome was performed for a 2-year period prior to the introduction of this guideline. The collaborative project aims to reduce both treatment abandonment and death during treatment to less than 10% for improving survival. ProcedureAll participating centres obtained local Institutional Research Board (IRB) approval and implemented the adapted WT treatment guideline. End-of-treatment outcome was documented for 2 years. It was divided into alive without evidence of disease, treatment abandonment, death during treatment and persistent disease. The outcome of children enroled in the first 2 years of the prospective clinical trial has been compared to the outcome before the start of the project. ResultsOne hundred twenty-two patients were included in the baseline evaluation (2011-2012) and 133 in the first 2 years of the collaborative clinical trial (2014-2015). The percentage of patients alive without evidence of disease at the end of treatment increased from 52% (63/122) to 68% (90/133; P=0.01). Treatment abandonment decreased from 23% (28/122) to 13% (17/133; P=0.03). Death during treatment decreased from 21% (26/122) to 13% (17/133; P=0.07). ConclusionThis collaboration, using relatively simple and low-cost interventions, led to a significant decrease in treatment abandonment and increase in survival without evidence of disease at the end of treatment.
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