Trends in national and ethnic burden of ovarian cancer mortality in South Africa (1999-2018): a population based, age-period-cohort and join point regression analyses.

IF 3.4 2区 医学 Q2 ONCOLOGY BMC Cancer Pub Date : 2025-03-20 DOI:10.1186/s12885-025-13735-7
Gbenga Olorunfemi, Elena Libhaber, Oliver C Ezechi, Eustasius Musenge
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Abstract

Ovarian cancer is the most lethal and third leading cause of gynaecological cancers globally and in South Africa (SA). However, its current mortality trends have not been evaluated in most sub-Saharan African Countries including South Africa that is currently undergoing epidemiological and health transitions. We evaluate the trends in the ovarian cancer mortality rates in SA over 20 years (1999-2018).

Methods: Crude (CMR) and age standardised mortality rates (ASMR) of ovarian cancer was calculated based on national mortality data of South Africa. The overall and ethnic trends of ovarian cancer mortality among women aged 15 years and older from 1999 to 2018 was assessed using the Join point regression model, while Age-period-cohort regression analysis was conducted to evaluate the underlying impact of age, period and cohort on ovarian cancer mortality.

Results: In all, 12,721 ovarian cancer deaths were reported in South Africa from 1999 to 2018 and the mortality rates increased from 2.34 to 3.21 per 100,00 women at 1.8% per annum. In 2018, the overall mean age at ovarian cancer death in South Africa was 62.30 ± 14.96 years while the mean age at death among Black women (58.07 ± 15.56 years), was about 11 years earlier than among White women (69.48 ± 11.71 years). In 2018, the White ethnic group (4.93 deaths per 100,000 women) had about doubled the ovarian cancer ASMR for the non-Whites (Indian/Asians, 2.92/100,000 women, mixed race, 2.49/100,000 women and Black women (2.36/ 100,000 women). All the ethnic groups had increased ASMR with Black women (Average annual percent change, [AAPC]: 4.7%, P-value < 0.001) and Indian/Asian women (AAPC: 2.5%, P-value < 0.001) having the highest rise. Cohort mortality risk ratio of ovarian cancer increased with successive birth cohort from 0.35 among 1924-1928 birth cohorts to 3.04 among 1999-2003 cohort and the period mortality risk increased by about 13% and 7.5% from 1999 to 2003 to 2004-2008 (RR: 0.87, 95% CI: 0.80-0.94), and from 2004 to 2008 to 2009-2013 (RR: 1.075, 95% CI:1.004-1.152) respectively. The longitudinal age analysis revealed that ovarian cancer increased with age, but there was an exponential increase from 55 years.

Conclusions: Our study showed that there was increasing trends in ovarian cancer mortality among all the South African ethnic groups, driven partly by increasing cohort and period mortality risks. We therefore highlight the huge burden of ovarian cancer in SA and the need for targeted intervention. Public health interventions geared towards reducing ovarian cancer mortality should be instituted and ethnic disparity should be incorporated in the cancer control policy.

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南非卵巢癌死亡率的国家和种族负担趋势(1999-2018):基于人群、年龄期队列和连接点回归分析
卵巢癌是全球和南非(SA)妇科癌症的最致命和第三大原因。然而,包括南非在内的大多数撒哈拉以南非洲国家目前的死亡率趋势尚未得到评估,这些国家目前正在经历流行病学和卫生转型。我们评估了南非20年来(1999-2018年)卵巢癌死亡率的趋势。方法:根据南非国家死亡率数据,计算卵巢癌粗死亡率(CMR)和年龄标准化死亡率(ASMR)。采用连接点回归模型评估1999年至2018年15岁及以上女性卵巢癌死亡率的总体趋势和民族趋势,并进行年龄-时期-队列回归分析,评估年龄、时期和队列对卵巢癌死亡率的潜在影响。结果:从1999年到2018年,南非总共报告了12721例卵巢癌死亡,死亡率从每10万名妇女2.34例上升到3.21例,每年增长1.8%。2018年,南非卵巢癌死亡的总体平均年龄为62.30±14.96岁,而黑人女性的平均死亡年龄(58.07±15.56岁)比白人女性(69.48±11.71岁)早约11岁。2018年,白人(每10万名女性中有4.93人死亡)的卵巢癌ASMR是非白人(印度/亚洲人,2.92/10万名女性,混血儿,2.49/10万名女性和黑人女性(2.36/ 10万名女性)的两倍左右。结论:我们的研究表明,在所有南非族裔群体中,卵巢癌死亡率都有上升趋势,部分原因是队列和时期死亡风险的增加。因此,我们强调了SA中卵巢癌的巨大负担和有针对性干预的必要性。应采取旨在降低卵巢癌死亡率的公共卫生干预措施,并将种族差异纳入癌症控制政策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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