Effectiveness of a Wilms tumour treatment guideline adapted to local circumstances in sub‐Saharan Africa: A report from Wilms Africa Phase II—CANCaRe Africa

Author:

Fufa Diriba1ORCID,Mdoka Cecilia2,Ayalew Mulugeta3,Khofi Harriet24,Amankwah Emmanuel5,Chokwenda Nester6,Mezgebu Esubalew1,Mavinkurve‐Groothuis Annelies M. C.7ORCID,Kamiza Steve4,Chikaphonya‐Phiri Beatrice4,Wassie Mulugeta3,Atwiine Barnabas8ORCID,Branchard Mushabe8,Gorostegui Maite9,Parkes Jeannette10ORCID,Kudowa Evaristar11,Eklu Bernice12,Jator Brian13,Renner Lorna Awo5,Borgstein Eric4,Molyneux Elizabeth4,Kouya Francine13,Pritchard‐Jones Kathy14ORCID,Paintsil Vivian12,Chitsike Inam6,Chagaluka George4,Israels Trijn24ORCID

Affiliation:

1. Pediatrics and Child Health Jimma University Jimma Ethiopia

2. CANCaRe Africa The Collaborative African Network for Childhood Cancer Care and Research Blantyre Malawi

3. Unit of Pediatric Hematology Oncology University of Gondar Specialized Hospital Gondar Ethiopia

4. Paediatrics and Child Health Kamuzu University of Health Sciences (KUHeS) Blantyre Malawi

5. Child Health Korle‐Bu teaching Hospital Accra Accra Ghana

6. College of Health Sciences Child and Adolescent Health University of Zimbabwe Harare Zimbabwe

7. Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands

8. Mbarara University of Science and Technology Mbarara Uganda

9. Pediatric Cancer Center Barcelona Hospital Sant Joan de Déu Barcelona Spain

10. Radiotherapy Red Cross‐South Africa Cape Town South Africa

11. Department of Statistics Malawi Liverpool Wellcome Research Programme Blantyre Malawi

12. Department of Child Health School of Medicine and Dentistry Kwame Nkrumah University of Science and Technology Kumasi Ghana

13. Paediatrics Mbingo Baptist Hospital Mbingo Cameroon

14. University College London London UK

Abstract

AbstractBackgroundWilms tumour (WT) is one of the cancer types targeted by the Global Initiative for Childhood Cancer (GICC). The objective of this study was to describe the outcomes of Wilms Africa Phase II in sub‐Saharan Africa.MethodsWilms Africa Phase II used a comprehensive WT treatment protocol in a multi‐centre, prospective study conducted in eight hospitals in Ethiopia (2), Ghana (2), Malawi, Cameroon, Zimbabwe and Uganda. Eligibility criteria were: age younger than 16 years, unilateral WT, diagnosed between 1 January 2021 and 31 December 2022.ResultsWe included 230 WT patients, median age 3 years, 53% male. Median maximum tumour diameter at diagnosis was 13.6 cm and 33% of patients had metastatic disease. Nephrectomy was performed in 71% of patients, of whom 21% had a tumour rupture. Two‐year event‐free survival (EFS) was 41.3% ± 3.9% after a median follow‐up of 17 months (range: 1–33 months), with treatment abandonment considered an event. Treatment abandonment occurred in 26% and death during treatment in 14%. Disease relapse occurred in 10%. Two‐year EFS of the 26 patients who received radiotherapy was 64.5% ± 9.7% with no reported disease relapse.ConclusionPatients continue to present late with advanced WT in sub‐Saharan Africa, and their survival is below the 60% GICC target. Prevention of treatment abandonment and treatment‐related mortality remain important. Earlier diagnosis and access to radiotherapy are expected to decrease disease‐related mortality.

Funder

Foundation S

Publisher

Wiley

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