High-grade cervical disease and cervical cancer in women aged 50 years and older compared with younger women: examining prevalence by HIV status in two large prospective cohorts in Botswana.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
29 Oct 2024
Historique:
medline: 31 10 2024
pubmed: 31 10 2024
entrez: 30 10 2024
Statut: epublish

Résumé

International guidelines recommend cervical screening cessation at age 50 following two consecutive negative screens. However, many women aged 50 and older in low-income and middle-income countries (LMICs) have not had prior opportunity to screen. We examine the prevalence of cervical dysplasia and cervical cancer stage in Botswana women aged 50+ compared with 30-49, stratified by HIV status. Secondary analysis of data from two prospective cohort studies. The screening cohort was recruited at health facilities in South East District. The cancer cohort was recruited from the primary public tertiary referral hospital and a private hospital in Gaborone, Botswana. The screening cohort included 2570 women aged 30 and older recruited from February 2021 to August 2022. Screening eligibility included anyone with a cervix and without a prior history of cervical cancer. The cancer cohort included 1520 patients diagnosed with cervical cancer who sought care at the facilities where recruitment took place from January 2015 to December 2022. The prevalence of cervical intraepithelial neoplasia (CIN)2+ and cancer stage at diagnosis was compared across age groups, stratified by HIV status. Prevalence ratios were calculated for the association between age and CIN2+/CIN3+via log-binomial regression. The prevalence of CIN2+ was similar between 30-49 years old and 50+, both among women with HIV (WWH, 15.9% and 19.3%, respectively) and without HIV (13.3% and 10.4%, respectively). Similar findings were found when CIN3+ was used as the outcome. There were no statistically significant differences in prevalence ratios (PRs) across age groups for CIN2+ (adjusted PR (aPR) WWH 1.1 (95% CI 0.80 to 1.6); aPR HIV- 0.78 (95% CI 0.45 to 1.4) nor CIN3+ (aPR WWH 1.1 (95% CI 0.70 to 1.6); aPR HIV- 0.81 (95% CI 0.40 to 1.7)). Nearly half of cervical cancer diagnoses were made in women 50+; three-quarters of cases in women without HIV were diagnosed at 50+ years. Our findings demonstrate the prevalence of high-grade cervical dysplasia and cervical cancer remains high beyond age 50 in both women with and without HIV in an LMIC context with high HIV prevalence. Screening women 50+ will allow treatment for cervical dysplasia and may provide early diagnosis of curable cervical cancer. These findings support the rapid introduction of high-performance cervical screening to increase access for women 50+. NCT04242823.

Identifiants

pubmed: 39477271
pii: bmjopen-2024-089375
doi: 10.1136/bmjopen-2024-089375
doi:

Banques de données

ClinicalTrials.gov
['NCT04242823']

Types de publication

Clinical Study Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e089375

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: RL reports support for present manuscript—NIH NCI 1K08CA271949-01. AM reports support for present manuscript—UM1TR004408 award through Harvard Catalyst. LB-M reports support for attending meetings and/or travel from MSD. PV reports payment or honoraria from Novartis, Roche, MSD; support for attending meetings and/or travel from MSD, Roche. SG reports grants from National Cancer Institute; grants or contracts from Varian Medical Systems; consulting fees from GenesisCare USA, payment or honoraria from Varian Medical Systems; stock or stock options in Harbinger Health. All other authors report no competing interests.

Auteurs

Rebecca Luckett (R)

Department of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Botswana Harvard Health Partnership, Gaborone, Botswana.
Department of Obstetrics and Gynaecology, University of Botswana, Gaborone, Botswana.
Harvard Medical School, Boston, Massachusetts, USA.
Department of Obstetrics and Gynaecology, Stellenbosch University, Cape Town, South Africa.

Bessie X Zhang (BX)

Harvard Medical School, Boston, Massachusetts, USA bessie_zhang@hms.harvard.edu.
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Annika Gompers (A)

Department of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

Jessica George (J)

Donald Bren School of Information and Computer Sciences, University of California, Irvine, California, USA.

Anna Modest (A)

Department of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

Lisa Bazzett-Matabele (L)

Department of Obstetrics and Gynaecology, University of Botswana, Gaborone, Botswana.

Peter Vuylsteke (P)

Department of Internal Medicine, University of Botswana, Gaborone, Botswana.

Maduke Kula (M)

Ministry of Health and Wellness of Botswana, Gaborone, Botswana.

Barati Monare (B)

Botswana UPenn Partnership, Gaborone, Botswana.

Matthys H Botha (MH)

Department of Obstetrics and Gynaecology, Stellenbosch University, Cape Town, South Africa.

Roger L Shapiro (RL)

Botswana Harvard Health Partnership, Gaborone, Botswana.
Harvard Medical School, Boston, Massachusetts, USA.
Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Department of Internal Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

Doreen Ramogola-Masire (D)

Department of Obstetrics and Gynaecology, University of Botswana, Gaborone, Botswana.

Surbhi Grover (S)

Botswana UPenn Partnership, Gaborone, Botswana.
Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

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