Analysis of the Breast Cancer Journey in Namibia

Author:

Boucheron Pauline1,Zietsman Annelle2,Pontac Johanna2,Hansen Rolf3,Anderson Benjamin O.45,Togawa Kayo16,Macharia Peter M.789,Foerster Milena1,Schüz Joachim1,dos-Santos-Silva Isabel10,McCormack Valerie1

Affiliation:

1. International Agency for Research on Cancer, Environment and Lifestyle Epidemiology Branch, Lyon, France

2. AB May Cancer Centre, Windhoek Central Hospital, Windhoek, Namibia

3. Cancer Association of Namibia, Windhoek, Namibia

4. University of Washington, Seattle

5. World Health Organization, Geneva, Switzerland

6. National Cancer Centre Institute for Cancer Control, Division of Population Data Science, Tokyo, Japan

7. Population Health Unit, Kenya Medical Research Institute–Wellcome Trust Research Programme, Nairobi, Kenya

8. Centre for Health Informatics, Computing, and Statistics, Lancaster Medical School, Lancaster University, Lancaster, United Kingdom

9. Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium

10. Department of Non-Communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom

Abstract

ImportanceBreast cancer (BC) is the leading cancer among women in Namibia. Examining the BC journey in this multiracial country where inequalities remain large is needed to inform effective interventions to reduce BC mortality.ObjectiveTo describe the entire BC journey of Namibian women by race, utilizing the World Health Organization Global Breast Cancer Initiative (GBCI) framework.Design, Setting, and ParticipantsThis cohort study used the Namibian subset of the African Breast Cancer–Disparities in Outcomes prospective cohort. Participants were all Namibian residents with confirmed incident BC who presented at the main national public oncology center of the Windhoek Central Hospital (WCH). Follow-up started from recruitment (September 8, 2014, to October 5, 2016) and ended up to 3 years after diagnosis (December 13, 2014, to September 27, 2019). Data analysis was conducted from June 2022 to August 2023.ExposuresParticipants’ self-reported ethnicities were aggregated into 3 population groups: Black, mixed ancestry, and White.Main Outcomes and MeasuresThree-year overall survival (OS) was examined using Cox models, and summary statistics were used to describe women’s BC journey, including GBCI pillar key performance indicators: (1) early stage (TNM I or II) diagnosis (population benchmark ≥60%), (2) prompt diagnosis, ie, 60 days or less to first health care practitioner visit (population benchmark 100%), and (3) completion of recommended multimodal treatment (MT, ie, surgery plus chemotherapy) (population benchmark ≥80%).ResultsOf 405 women, there were 300 (74%) Black (mean [SD] age, 53 [15] years), 49 (12%) mixed ancestry (mean [SD] age, 53 [7] years), and 56 (14%) White (mean [SD] age, 59 [12] years) patients. Three-year OS was lowest in Black women (60% [95% CI, 54%-66%]; mixed ancestry: 80% [95% CI, 65%-89%]; White: 89% [95% CI, 77%-95%]), who had lower prevalence of early stage diagnosis (Black: 37% [95% CI, 31%-42%]; mixed ancestry and White: 75% [95% CI, 66%-83%]) and timely diagnosis (Black: 60% [95% CI, 54%-66%]; mixed ancestry and White: 77% [95% CI, 69%-85%]), while MT completion (Black: 53% [95% CI, 46%-59%]; mixed ancestry and White: 63% [95% CI, 50%-73%]) was low in all women.Conclusions and RelevanceIn this cohort study of 405 Namibian residents with BC, marked racial disparities in survival were paralleled by inequities all along the BC journey. To improve BC survival, interventions are needed to promote earlier diagnosis in Black Namibian women and to increase MT initiation and completion in all women.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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