Prevention of treatment abandonment remains an important challenge to increase survival of Wilms tumor in sub‐Saharan Africa: A report from Wilms Africa—CANCaRe Africa

Author:

Atwiine Barnabas1ORCID,Mdoka Cecilia2,Branchard Mushabe1,Chagaluka George3,Fufa Diriba4ORCID,Ayalew Mulugeta5,Khofi Harriet23,Amankwah Emmanuel6,Chokwenda Nester7,Birhane Feven5,Mezgebu Esubalew4,Eklu Bernice8,Jator Brian9,Kudowa Evaristar10,Mbah Glenn9ORCID,Wassie Mulugeta5,Dondo Vongai7,Paintsil Vivian8,Pritchard‐Jones Kathy11ORCID,Renner Lorna Awo6,Sung Lillian12,Kouya Francine9,Molyneux Elizabeth3,Chitsike Inam7,Israels Trijn23

Affiliation:

1. Mbarara University of Science and Technology Mbarara Uganda

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

3. Paediatrics and Child Health Kamuzu University of Health sciences (KUHES) Blantyre Malawi

4. Pediatrics and Child Health Jimma University Jimma Ethiopia

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

6. Child Health Korle‐Bu Teaching Hospital Accra Accra Ghana

7. Pediatrics College of Health Sciences Harare Zimbabwe

8. Paediatric Oncology Komfo Anokye Teaching Hospital Kumasi Ghana

9. Paediatrics Mbingo Baptist Hospital Mbingo Cameroon

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

11. Global Health University College London London UK

12. Sick Children's Hospital Toronto Ontario Canada

Abstract

AbstractBackgroundThe Wilms Africa studies implemented an adapted Wilm's tumor (WT) treatment protocol in sub‐Saharan Africa in two phases. Phase I began with four sites and provided out‐of‐pocket costs. Phase II expanded the number of sites, but lost funding provision. Objective is to describe the outcomes of Phase II and compare with Phase I.MethodsWilms Africa Phase I (n = 4 sites; 2014–2018) and Phase II (n = 8 sites; 2021–2022) used adapted treatment protocols. Funding for families’ out‐of‐pocket costs was provided during Phase I but not Phase II. Eligibility criteria were age less than 16 years and newly diagnosed unilateral WT. We documented patients’ outcome at the end of planned first‐line treatment categorized as treatment abandonment, death during treatment, and disease‐related events (death before treatment, persistent disease, relapse, or progressive disease). Sensitivity analysis compared outcomes in the same four sites.ResultsWe included 431 patients in Phase I (n = 201) and Phase II (n = 230). The proportion alive without evidence of disease decreased from 69% in Phase I to 54% in Phase II at all sites (p = .002) and 58% at the original four sites (p = .04). Treatment abandonment increased overall from 12% to 26% (p < .001), and was 20% (p = .04) at the original four sites. Disease‐related events (5% vs. 6% vs. 6%) and deaths during treatment (14% vs. 14% vs. 17%) were similar.ConclusionProvision of out‐of‐pocket costs was important to improve patient outcomes at the end of planned first‐line treatment in WT. Prevention of treatment abandonment remains an important challenge.

Publisher

Wiley

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