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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.
Atwiine, Barnabas; Mdoka, Cecilia; Branchard, Mushabe; Chagaluka, George; Fufa, Diriba; Ayalew, Mulugeta; Khofi, Harriet; Amankwah, Emmanuel; Chokwenda, Nester; Birhane, Feven; Mezgebu, Esubalew; Eklu, Bernice; Jator, Brian; Kudowa, Evaristar; Mbah, Glenn; Wassie, Mulugeta; Dondo, Vongai; Paintsil, Vivian; Pritchard-Jones, Kathy; Renner, Lorna Awo; Sung, Lillian; Kouya, Francine; Molyneux, Elizabeth; Chitsike, Inam; Israels, Trijn.
Afiliación
  • Atwiine B; Mbarara University of Science and Technology, Mbarara, Uganda.
  • Mdoka C; The Collaborative African Network for Childhood Cancer Care and Research, CANCaRe Africa, Blantyre, Malawi.
  • Branchard M; Mbarara University of Science and Technology, Mbarara, Uganda.
  • Chagaluka G; Paediatrics and Child Health, Kamuzu University of Health sciences (KUHES), Blantyre, Malawi.
  • Fufa D; Pediatrics and Child Health, Jimma University, Jimma, Ethiopia.
  • Ayalew M; Unit of Pediatric Hematology Oncology, University of Gondar Specialized Hospital, Gondar, Ethiopia.
  • Khofi H; The Collaborative African Network for Childhood Cancer Care and Research, CANCaRe Africa, 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.
  • Birhane F; Pediatrics, College of Health Sciences, Harare, Zimbabwe.
  • Mezgebu E; Unit of Pediatric Hematology Oncology, University of Gondar Specialized Hospital, Gondar, Ethiopia.
  • Eklu B; Pediatrics and Child Health, Jimma University, Jimma, Ethiopia.
  • Jator B; Paediatric Oncology, Komfo Anokye Teaching Hospital, Kumasi, Ghana.
  • Kudowa E; Paediatrics, Mbingo Baptist Hospital, Mbingo, Cameroon.
  • Mbah G; Department of Statistics, Malawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
  • Wassie M; Paediatrics, Mbingo Baptist Hospital, Mbingo, Cameroon.
  • Dondo V; Unit of Pediatric Hematology Oncology, University of Gondar Specialized Hospital, Gondar, Ethiopia.
  • Paintsil V; Pediatrics, College of Health Sciences, Harare, Zimbabwe.
  • Pritchard-Jones K; Paediatric Oncology, Komfo Anokye Teaching Hospital, Kumasi, Ghana.
  • Renner LA; Global Health, University College London, London, UK.
  • Sung L; Child Health, Korle-Bu Teaching Hospital Accra, Accra, Ghana.
  • Kouya F; Sick Children's Hospital, Toronto, Ontario, Canada.
  • Molyneux E; Paediatrics, Mbingo Baptist Hospital, Mbingo, Cameroon.
  • Chitsike I; Paediatrics and Child Health, Kamuzu University of Health sciences (KUHES), Blantyre, Malawi.
  • Israels T; Pediatrics, College of Health Sciences, Harare, Zimbabwe.
Pediatr Blood Cancer ; 71(8): e31069, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38773703
ABSTRACT

BACKGROUND:

The 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.

METHODS:

Wilms 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.

RESULTS:

We 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.

CONCLUSION:

Provision 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tumor de Wilms / Neoplasias Renales Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Africa Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Uganda

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tumor de Wilms / Neoplasias Renales Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Africa Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Uganda