Breast cancer survival and survival gap apportionment in sub-Saharan Africa (ABC-DO): a prospective cohort study.


Journal

The Lancet. Global health
ISSN: 2214-109X
Titre abrégé: Lancet Glob Health
Pays: England
ID NLM: 101613665

Informations de publication

Date de publication:
09 2020
Historique:
received: 17 12 2019
revised: 18 05 2020
accepted: 20 05 2020
entrez: 23 8 2020
pubmed: 23 8 2020
medline: 5 9 2020
Statut: ppublish

Résumé

Breast cancer is the second leading cause of death from cancer in women in sub-Saharan Africa, yet there are few well characterised large-scale survival studies with complete follow-up data. We aimed to provide robust survival estimates in women in this setting and apportion the survival gaps. The African Breast Cancer-Disparities in Outcomes (ABC-DO) prospective cohort study was done at eight hospitals across five sub-Saharan African countries (Namibia, Nigeria, South Africa, Uganda, and Zambia). We prospectively recruited women (aged ≥18 years) who attended these hospitals with suspected breast cancer. Women were actively followed up by use of a telephone call once every 3 months, and a mobile health application was used to keep a dynamic record of follow-up calls due. We collected detailed sociodemographic, clinical, and treatment data. The primary outcome was 3-year overall survival, analysed by use of flexible proportional mortality models, and we predicted survival under scenarios of modified distributions of risk factors. Between Sept 8, 2014, and Dec 31, 2017, 2313 women were recruited from these eight hospitals, of whom 85 did not have breast cancer. Of the remaining 2228 women with breast cancer, 58 women with previous treatment or recurrence, and 14 women from small racial groups (white and Asian women in South Africa), were excluded. Of the 2156 women analysed, 1840 (85%) were histologically confirmed, 129 (6%) were cytologically confirmed, and 187 (9%) were clinically confirmed to have breast cancer. 2156 (97%) women were followed up for up to 3 years or up to Jan 1, 2019, whichever was earlier. Up to this date, 879 (41%) of these women had died, 1118 (52%) were alive, and 159 (7%) were censored early. 3-year overall survival was 50% (95% CI 48-53), but we observed variations in 3-year survival between different races in Namibia (from 90% in white women to 56% in Black women) and in South Africa (from 76% in mixed-race women to 59% in Black women), and between different countries (44-47% in Uganda and Zambia vs 36% in Nigeria). 215 (10%) of all women had died within 6 months of diagnosis, but 3-year overall survival remained low in women who survived to this timepoint (58%). Among survival determinants, improvements in early diagnosis and treatment were predicted to contribute to the largest increases in survival, with a combined absolute increase in survival of up to 22% in Nigeria, Zambia, and Uganda, when compared with the contributions of other factors (such as HIV or aggressive subtypes). Large variations in breast cancer survival in sub-Saharan African countries indicate that improvements are possible. At least a third of the projected 416 000 breast cancer deaths that will occur in this region in the next decade could be prevented through achievable downstaging and improvements in treatment. Improving survival in socially disadvantaged women warrants special attention. Susan G Komen and the International Agency for Research on Cancer.

Sections du résumé

BACKGROUND
Breast cancer is the second leading cause of death from cancer in women in sub-Saharan Africa, yet there are few well characterised large-scale survival studies with complete follow-up data. We aimed to provide robust survival estimates in women in this setting and apportion the survival gaps.
METHODS
The African Breast Cancer-Disparities in Outcomes (ABC-DO) prospective cohort study was done at eight hospitals across five sub-Saharan African countries (Namibia, Nigeria, South Africa, Uganda, and Zambia). We prospectively recruited women (aged ≥18 years) who attended these hospitals with suspected breast cancer. Women were actively followed up by use of a telephone call once every 3 months, and a mobile health application was used to keep a dynamic record of follow-up calls due. We collected detailed sociodemographic, clinical, and treatment data. The primary outcome was 3-year overall survival, analysed by use of flexible proportional mortality models, and we predicted survival under scenarios of modified distributions of risk factors.
FINDINGS
Between Sept 8, 2014, and Dec 31, 2017, 2313 women were recruited from these eight hospitals, of whom 85 did not have breast cancer. Of the remaining 2228 women with breast cancer, 58 women with previous treatment or recurrence, and 14 women from small racial groups (white and Asian women in South Africa), were excluded. Of the 2156 women analysed, 1840 (85%) were histologically confirmed, 129 (6%) were cytologically confirmed, and 187 (9%) were clinically confirmed to have breast cancer. 2156 (97%) women were followed up for up to 3 years or up to Jan 1, 2019, whichever was earlier. Up to this date, 879 (41%) of these women had died, 1118 (52%) were alive, and 159 (7%) were censored early. 3-year overall survival was 50% (95% CI 48-53), but we observed variations in 3-year survival between different races in Namibia (from 90% in white women to 56% in Black women) and in South Africa (from 76% in mixed-race women to 59% in Black women), and between different countries (44-47% in Uganda and Zambia vs 36% in Nigeria). 215 (10%) of all women had died within 6 months of diagnosis, but 3-year overall survival remained low in women who survived to this timepoint (58%). Among survival determinants, improvements in early diagnosis and treatment were predicted to contribute to the largest increases in survival, with a combined absolute increase in survival of up to 22% in Nigeria, Zambia, and Uganda, when compared with the contributions of other factors (such as HIV or aggressive subtypes).
INTERPRETATION
Large variations in breast cancer survival in sub-Saharan African countries indicate that improvements are possible. At least a third of the projected 416 000 breast cancer deaths that will occur in this region in the next decade could be prevented through achievable downstaging and improvements in treatment. Improving survival in socially disadvantaged women warrants special attention.
FUNDING
Susan G Komen and the International Agency for Research on Cancer.

Identifiants

pubmed: 32827482
pii: S2214-109X(20)30261-8
doi: 10.1016/S2214-109X(20)30261-8
pmc: PMC7450275
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1203-e1212

Subventions

Organisme : NCI NIH HHS
ID : R01 CA192627
Pays : United States

Informations de copyright

© 2020 International Agency for Research on Cancer; licensee Elsevier. This is an Open Access article published under the CC BY-NC-ND 3.0 IGO license which permits users to download and share the article for non-commercial purposes, so long as the article is reproduced in the whole without changes, and provided the original source is properly cited. This article shall not be used or reproduced in association with the promotion of commercial products, services or any entity. There should be no suggestion that IARC endorses any specific organisation, products or services. The use of the IARC logo is not permitted. This notice should be preserved along with the article's original URL.

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Auteurs

Valerie McCormack (V)

Section of Environment and Radiation, International Agency for Research on Cancer, Lyon, France. Electronic address: mccormackv@iarc.fr.

Fiona McKenzie (F)

Section of Environment and Radiation, International Agency for Research on Cancer, Lyon, France.

Milena Foerster (M)

Section of Environment and Radiation, International Agency for Research on Cancer, Lyon, France.

Annelle Zietsman (A)

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

Moses Galukande (M)

College of Health Sciences, Makerere University, Kampala, Uganda.

Charles Adisa (C)

Department of Surgery, Abia State University Teaching Hospital, Aba, Nigeria.

Angelica Anele (A)

Breast Oncology Unit, Federal Medical Centre, Owerri, Nigeria.

Groesbeck Parham (G)

Department of Obstetrics and Gynecology, School of Medicine, University of North Carolina, Chapel Hill, NC, USA.

Leeya F Pinder (LF)

Department of Obstetrics and Gynecology, Women and Newborn Hospital, Lusaka, Zambia; Department of Obstetrics and Gynecology, University of Washington, Seattle, WA, USA.

Herbert Cubasch (H)

Department of Surgery, University of the Witwatersrand, Johannesburg, South Africa; Chris Hani Baragwanath Academic Hospital, Johannesburg, South Africa; Non-Communicable Diseases Research Division, Wits Health Consortium, Johannesburg, South Africa.

Maureen Joffe (M)

Non-Communicable Diseases Research Division, University of the Witwatersrand, Johannesburg, South Africa; Noncommunicable Diseases Research Division, Wits Health Consortium, Johannesburg, South Africa; MRC Developmental Pathways to Health Research Unit, Department of Pediatrics, Faculty of Health Sciences, University of Witwatersrand, Johannesburg, South Africa.

Thomas Beaney (T)

Department of Primary Care and Public Health, Imperial College London, UK.

Manuela Quaresma (M)

Department of Non-Communicable Diseases Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

Kayo Togawa (K)

Section of Environment and Radiation, International Agency for Research on Cancer, Lyon, France.

Behnoush Abedi-Ardekani (B)

Section of Genetics, International Agency for Research on Cancer, Lyon, France.

Benjamin O Anderson (BO)

Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Global Health, University of Washington, Seattle, WA, USA.

Joachim Schüz (J)

Section of Environment and Radiation, International Agency for Research on Cancer, Lyon, France.

Isabel Dos-Santos-Silva (I)

Department of Non-Communicable Diseases Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

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