Freeman Esther, Semeere Aggrey, Wenger Megan, Bwana Mwebesa, Asirwa F Chite, Busakhala Naftali, Oga Emmanuel, Jedy-Agba Elima, Kwaghe Vivian, Iregbu Kenneth, Jaquet Antoine, Dabis Francois, Yumo Habakkuk Azinyui, Dusingize Jean Claude, Bangsberg David, Anastos Kathryn, Phiri Sam, Bohlius Julia, Egger Matthias, Yiannoutsos Constantin, Wools-Kaloustian Kara, Martin Jeffrey
Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Bartlett Hall 6R, 55 Fruit Street, Boston, MA, 02114, USA.
Infectious Diseases Institute, Makerere University, Kampala, Uganda.
BMC Cancer. 2016 Feb 6;16:65. doi: 10.1186/s12885-016-2080-0.
Survival after diagnosis is a fundamental concern in cancer epidemiology. In resource-rich settings, ambient clinical databases, municipal data and cancer registries make survival estimation in real-world populations relatively straightforward. In resource-poor settings, given the deficiencies in a variety of health-related data systems, it is less clear how well we can determine cancer survival from ambient data.
We addressed this issue in sub-Saharan Africa for Kaposi's sarcoma (KS), a cancer for which incidence has exploded with the HIV epidemic but for which survival in the region may be changing with the recent advent of antiretroviral therapy (ART). From 33 primary care HIV Clinics in Kenya, Uganda, Malawi, Nigeria and Cameroon participating in the International Epidemiologic Databases to Evaluate AIDS (IeDEA) Consortia in 2009-2012, we identified 1328 adults with newly diagnosed KS. Patients were evaluated from KS diagnosis until death, transfer to another facility or database closure.
Nominally, 22% of patients were estimated to be dead by 2 years, but this estimate was clouded by 45% cumulative lost to follow-up with unknown vital status by 2 years. After adjustment for site and CD4 count, age <30 years and male sex were independently associated with becoming lost.
In this community-based sample of patients diagnosed with KS in sub-Saharan Africa, almost half became lost to follow-up by 2 years. This precluded accurate estimation of survival. Until we either generally strengthen data systems or implement cancer-specific enhancements (e.g., tracking of the lost) in the region, insights from cancer epidemiology will be limited.
癌症诊断后的生存情况是癌症流行病学的一个基本关注点。在资源丰富的环境中,周围的临床数据库、市政数据和癌症登记处使在现实世界人群中进行生存估计相对简单。在资源匮乏的环境中,鉴于各种与健康相关的数据系统存在缺陷,我们从周围数据中确定癌症生存率的能力如何尚不清楚。
我们在撒哈拉以南非洲针对卡波西肉瘤(KS)解决了这个问题,卡波西肉瘤是一种随着艾滋病流行发病率激增的癌症,但该地区的生存率可能随着最近抗逆转录病毒疗法(ART)的出现而发生变化。2009年至2012年,从肯尼亚、乌干达、马拉维、尼日利亚和喀麦隆参与国际艾滋病流行病学数据库评估协会(IeDEA)联盟的33家初级保健艾滋病诊所中,我们确定了1328名新诊断为KS的成年人。对患者从KS诊断直至死亡、转至另一机构或数据库关闭进行评估。
名义上,估计22%的患者在2年内死亡,但这一估计因2年时45%的累积失访且生命状态未知而受到影响。在调整部位和CD4细胞计数后,年龄<30岁和男性与失访独立相关。
在撒哈拉以南非洲这个以社区为基础的KS诊断患者样本中,近一半患者在2年内失访。这妨碍了对生存率的准确估计。在我们普遍加强数据系统或在该地区实施针对癌症的改进措施(如追踪失访者)之前,癌症流行病学的见解将受到限制。