Disparities in breast cancer survival between women with and without HIV across sub-Saharan Africa (ABC-DO): a prospective, cohort study.
Journal
The lancet. HIV
ISSN: 2352-3018
Titre abrégé: Lancet HIV
Pays: Netherlands
ID NLM: 101645355
Informations de publication
Date de publication:
03 2022
03 2022
Historique:
received:
30
06
2021
revised:
13
11
2021
accepted:
07
12
2021
pubmed:
5
3
2022
medline:
15
3
2022
entrez:
4
3
2022
Statut:
ppublish
Résumé
Studies have shown increased mortality among women living with HIV diagnosed with breast cancer compared with HIV-negative women with breast cancer. We aimed to examine how this HIV differential varies by patient or breast tumour characteristics. The African Breast Cancer-Disparities in Outcomes (ABC-DO) study is a prospective cohort of women (aged ≥18 years) with incident breast cancer recruited consecutively at diagnosis (2014-17) from hospitals in Namibia, Nigeria, South Africa, Uganda, and Zambia. Detailed clinical and epidemiological data, including self-reported or tested HIV status, were collected at baseline. Participants were actively followed up via telephone calls every 3 months. The primary outcome was all-cause mortality, assessed in all women who had at least one updated vital status after baseline interview. Using Cox regression, we examined differences in overall survival by HIV status in the cohort, and across country and patient subgroups, adjusted for age, tumour grade, and tumour stage at cancer diagnosis. Between Sept 8, 2014, and Dec 31, 2017, we recruited 2154 women with primary breast cancer, 519 of whom were excluded due to their countries having small numbers of women with HIV for comparison. Among the remaining 1635 women, 313 (19%) were living with HIV, 1184 (72%) were HIV negative, and 138 (9%) had unknown HIV status. At breast cancer diagnosis, women with HIV were younger and had lower body-mass index (BMI) than their HIV-negative counterparts, but had similar tumour stage, grade, and receptor subtypes. At the end of the follow-up (Jan 1, 2019), a higher proportion of women with HIV (137 [44%] of 313) had died than had HIV-negative women (432 [37%] of 1184). Crude 3-year survival was 9% lower for women with HIV (46% [95% CI 40-53]) than for HIV-negative women (55% [52-59]; hazard ratio (HR) 1·41 [1·15-1·74]). The HIV survival differential did not differ by age, BMI, tumour subtype, or tumour grade, but was stronger in women with non-metastatic disease (3-year survival 52% HIV-positive vs 63% HIV-negative women, adjusted HR 1·65 [1·30-2·10]), whereas women with metastatic cancer had low survival, regardless of HIV status. The larger survival deficit among women with HIV with non-metastatic breast cancer calls for a better understanding of the reasons underlying this differential (eg, biological mechanisms, health behaviours, detrimental HIV-breast cancer treatment interactions, or higher HIV background mortality) to inform strategies for reducing mortality among this patient group. Susan G Komen, International Agency for Research on Cancer, National Cancer Institute, and UK-Commonwealth Scholarships.
Sections du résumé
BACKGROUND
Studies have shown increased mortality among women living with HIV diagnosed with breast cancer compared with HIV-negative women with breast cancer. We aimed to examine how this HIV differential varies by patient or breast tumour characteristics.
METHODS
The African Breast Cancer-Disparities in Outcomes (ABC-DO) study is a prospective cohort of women (aged ≥18 years) with incident breast cancer recruited consecutively at diagnosis (2014-17) from hospitals in Namibia, Nigeria, South Africa, Uganda, and Zambia. Detailed clinical and epidemiological data, including self-reported or tested HIV status, were collected at baseline. Participants were actively followed up via telephone calls every 3 months. The primary outcome was all-cause mortality, assessed in all women who had at least one updated vital status after baseline interview. Using Cox regression, we examined differences in overall survival by HIV status in the cohort, and across country and patient subgroups, adjusted for age, tumour grade, and tumour stage at cancer diagnosis.
FINDINGS
Between Sept 8, 2014, and Dec 31, 2017, we recruited 2154 women with primary breast cancer, 519 of whom were excluded due to their countries having small numbers of women with HIV for comparison. Among the remaining 1635 women, 313 (19%) were living with HIV, 1184 (72%) were HIV negative, and 138 (9%) had unknown HIV status. At breast cancer diagnosis, women with HIV were younger and had lower body-mass index (BMI) than their HIV-negative counterparts, but had similar tumour stage, grade, and receptor subtypes. At the end of the follow-up (Jan 1, 2019), a higher proportion of women with HIV (137 [44%] of 313) had died than had HIV-negative women (432 [37%] of 1184). Crude 3-year survival was 9% lower for women with HIV (46% [95% CI 40-53]) than for HIV-negative women (55% [52-59]; hazard ratio (HR) 1·41 [1·15-1·74]). The HIV survival differential did not differ by age, BMI, tumour subtype, or tumour grade, but was stronger in women with non-metastatic disease (3-year survival 52% HIV-positive vs 63% HIV-negative women, adjusted HR 1·65 [1·30-2·10]), whereas women with metastatic cancer had low survival, regardless of HIV status.
INTERPRETATION
The larger survival deficit among women with HIV with non-metastatic breast cancer calls for a better understanding of the reasons underlying this differential (eg, biological mechanisms, health behaviours, detrimental HIV-breast cancer treatment interactions, or higher HIV background mortality) to inform strategies for reducing mortality among this patient group.
FUNDING
Susan G Komen, International Agency for Research on Cancer, National Cancer Institute, and UK-Commonwealth Scholarships.
Identifiants
pubmed: 35245508
pii: S2352-3018(21)00326-X
doi: 10.1016/S2352-3018(21)00326-X
pmc: PMC9031563
mid: NIHMS1793903
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e160-e171Subventions
Organisme : World Health Organization
ID : 001
Pays : International
Organisme : NCI NIH HHS
ID : R01 CA192627
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA250012
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
World Health Organization; 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 WHO endorses any specific organisation, products or services. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL.
Déclaration de conflit d'intérêts
Declaration of interests We declare no competing interests.
Références
Int J Cancer. 2018 Dec 1;143(11):2732-2740
pubmed: 29992553
J Natl Cancer Inst. 2011 May 4;103(9):753-62
pubmed: 21483021
Int J Cancer. 2015 Mar 1;136(5):E359-86
pubmed: 25220842
Cancer Epidemiol Biomarkers Prev. 2017 Jul;26(7):1027-1033
pubmed: 28619832
J Acquir Immune Defic Syndr. 2005 Jul 1;39(3):293-9
pubmed: 15980688
AIDS. 2021 Mar 15;35(4):605-618
pubmed: 33394680
AIDS. 2013 Nov 28;27(18):2933-42
pubmed: 23921614
BMJ Open. 2016 Aug 23;6(8):e011390
pubmed: 27554102
EClinicalMedicine. 2019 Nov 26;17:100205
pubmed: 31891138
Int J Cancer. 2018 Apr 15;142(8):1568-1579
pubmed: 29197068
Breast Cancer Res. 2019 Aug 13;21(1):93
pubmed: 31409419
J Clin Oncol. 2015 Jul 20;33(21):2376-83
pubmed: 26077242
Cancer. 2019 Aug 15;125(16):2868-2876
pubmed: 31050361
Ann Oncol. 2014 Oct;25(10):1901-1914
pubmed: 24769692
Lancet Glob Health. 2020 Sep;8(9):e1203-e1212
pubmed: 32827482
BMC Infect Dis. 2019 Aug 13;19(1):715
pubmed: 31409277
J Glob Oncol. 2017 Apr;3(2):114-124
pubmed: 28706996
Am J Epidemiol. 2020 Oct 1;189(10):1185-1196
pubmed: 32383449
Int J Cancer. 2020 Mar 1;146(5):1208-1218
pubmed: 31087650
Lancet. 2018 Mar 17;391(10125):1023-1075
pubmed: 29395269
Ann Surg Oncol. 2010 Jun;17(6):1471-4
pubmed: 20180029
J Glob Oncol. 2016 Mar 30;2(5):284-291
pubmed: 28717714
PLoS Med. 2009 Apr 28;6(4):e1000066
pubmed: 19399157
JAMA Oncol. 2019 Sep 01;5(9):e191742
pubmed: 31369037
Cancer Epidemiol. 2018 Feb;52:120-127
pubmed: 29306221
Breast Cancer Res Treat. 2013 Jul;140(1):177-86
pubmed: 23801159
Breast. 2019 Feb;43:123-129
pubmed: 30550925