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Effectiveness of a Wilms tumour treatment guideline adapted to local circumstances in sub-Saharan Africa: A report from Wilms Africa Phase II-CANCaRe Africa.
Fufa, Diriba; Mdoka, Cecilia; Ayalew, Mulugeta; Khofi, Harriet; Amankwah, Emmanuel; Chokwenda, Nester; Mezgebu, Esubalew; Mavinkurve-Groothuis, Annelies M C; Kamiza, Steve; Chikaphonya-Phiri, Beatrice; Wassie, Mulugeta; Atwiine, Barnabas; Branchard, Mushabe; Gorostegui, Maite; Parkes, Jeannette; Kudowa, Evaristar; Eklu, Bernice; Jator, Brian; Renner, Lorna Awo; Borgstein, Eric; Molyneux, Elizabeth; Kouya, Francine; Pritchard-Jones, Kathy; Paintsil, Vivian; Chitsike, Inam; Chagaluka, George; Israels, Trijn.
Affiliation
  • Fufa D; Pediatrics and Child Health, Jimma University, Jimma, Ethiopia.
  • Mdoka C; CANCaRe Africa, The Collaborative African Network for Childhood Cancer Care and Research, Blantyre, Malawi.
  • Ayalew M; Unit of Pediatric Hematology Oncology, University of Gondar Specialized Hospital, Gondar, Ethiopia.
  • Khofi H; CANCaRe Africa, The Collaborative African Network for Childhood Cancer Care and Research, Blantyre, Malawi.
  • Amankwah E; Paediatrics and Child Health, Kamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
  • Chokwenda N; Child Health, Korle-Bu teaching Hospital Accra, Accra, Ghana.
  • Mezgebu E; College of Health Sciences, Child and Adolescent Health, University of Zimbabwe, Harare, Zimbabwe.
  • Mavinkurve-Groothuis AMC; Pediatrics and Child Health, Jimma University, Jimma, Ethiopia.
  • Kamiza S; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Chikaphonya-Phiri B; Paediatrics and Child Health, Kamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
  • Wassie M; Paediatrics and Child Health, Kamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
  • Atwiine B; Unit of Pediatric Hematology Oncology, University of Gondar Specialized Hospital, Gondar, Ethiopia.
  • Branchard M; Mbarara University of Science and Technology, Mbarara, Uganda.
  • Gorostegui M; Mbarara University of Science and Technology, Mbarara, Uganda.
  • Parkes J; Pediatric Cancer Center Barcelona, Hospital Sant Joan de Déu, Barcelona, Spain.
  • Kudowa E; Radiotherapy, Red Cross-South Africa, Cape Town, South Africa.
  • Eklu B; Department of Statistics, Malawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
  • Jator B; Department of Child Health, School of Medicine and Dentistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
  • Renner LA; Paediatrics, Mbingo Baptist Hospital, Mbingo, Cameroon.
  • Borgstein E; Child Health, Korle-Bu teaching Hospital Accra, Accra, Ghana.
  • Molyneux E; Paediatrics and Child Health, Kamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
  • Kouya F; Paediatrics and Child Health, Kamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
  • Pritchard-Jones K; Paediatrics, Mbingo Baptist Hospital, Mbingo, Cameroon.
  • Paintsil V; University College London, London, UK.
  • Chitsike I; Department of Child Health, School of Medicine and Dentistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
  • Chagaluka G; College of Health Sciences, Child and Adolescent Health, University of Zimbabwe, Harare, Zimbabwe.
  • Israels T; Paediatrics and Child Health, Kamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
Pediatr Blood Cancer ; 71(11): e31300, 2024 Nov.
Article in En | MEDLINE | ID: mdl-39198982
ABSTRACT

BACKGROUND:

Wilms 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.

METHODS:

Wilms 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.

RESULTS:

We 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.

CONCLUSION:

Patients 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wilms Tumor / Kidney Neoplasms Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Pediatr Blood Cancer / Pediatr. blood cancer / Pediatric blood & cancer Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2024 Document type: Article Affiliation country: Ethiopia Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wilms Tumor / Kidney Neoplasms Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Pediatr Blood Cancer / Pediatr. blood cancer / Pediatric blood & cancer Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2024 Document type: Article Affiliation country: Ethiopia Country of publication: United States