Cancer statistics 2024: All hands on deck

入射(几何) 人口学 癌症 医学 乳腺癌 老年学 疾病 癌症预防 肥胖 癌症发病率 内科学 光学 物理 社会学
作者
Don S. Dizon,Arif H. Kamal
出处
期刊:CA: A Cancer Journal for Clinicians [Wiley]
卷期号:74 (1): 8-9 被引量:91
标识
DOI:10.3322/caac.21824
摘要

The 2024 update to Cancer Statistics from the American Cancer Society estimates that over 2,000,000 people this year will hear the words, "you have cancer."1 This amounts to nearly 5500 people each day, or the equivalent to one person experiencing this every 15 seconds. This marks the first time incidence has eclipsed 2 million Americans, with more people being diagnosed at earlier stages of these diseases, when cure rates are the highest. Consequently, cancer mortality continues to decline, with an estimated 4.1 million lives saved since 1991, because of significant investments in research and screening by the National Institutes of Health, the Centers for Disease Control and Prevention, the American Cancer Society, and others. To us, four parts of the report particularly stand out. First, historically, cancer has been a disease that disproportionally affects men. However, this report demonstrates that, whereas the cancer incidence in men has been stable since the 2013, the incidence in women has ticked up since the late 1990s, attributed to higher rates of breast and uterine corpus cancers and melanoma. Thus cancer is becoming more gender-indiscriminate, with a male-to-female incidence ratio of 1.14 (95% CI, 1.136–1.143) in all ages. Many have hypothesized that differential lifestyle and risk-taking behaviors, alongside environmental exposures, resulted in higher cancer rates in men. However, as the incidence gap between genders closes, signs may point to risk factors (e.g., obesity, sedentary lifestyle) that are similarly affecting both groups, highlighting the need for a better understanding of this phenomenon. Second, although the overall cancer incidence is increasing, there are particular cancers and populations disproportionately affected. For example, whereas the rise in uterine corpus cancers in White women has increased by about 1% per year since the mid-2000s, the increase is in excess of 2% in Black, Hispanic, Asian American, and Pacific Islander people. Colorectal cancer (CRC) too shows a variability when age is considered; the declines noted in CRC are largely because of a lower rate in people older than 65 years; among those younger than 55 years, the rate continues to increase by 1% to 2% per year. Finally, men saw their rates stabilize for liver cancer and, potentially, for melanoma between 2015 and 2019, yet women saw their rates increase by 2% per year. Taken together, the report highlights how cancer cannot be over-simplified to one diagnosis, nor can we generalize these trends in a short bullet. Third, although the report highlights the tremendous advances in the treatment of hematologic and advanced solid tumor malignancies, the impact of disparities cannot be overstated. Compared with White women, for example, more Black women are diagnosed at a more advanced stage (44% vs. 23%) and have a poorer prognosis (5-year survival rate estimates of 63% vs. 84%, respectively). As the authors point out, systemic factors like disparities in guideline-concordant diagnostic and treatment protocols play a big role. Even more, it is likely that self-identification categories, such as Black, White, and Asian, mask the differences in risk and outcomes among groups. Asian, for example, may include descendants or immigrants from as many as 48 distinct countries. Whereas mortality from cancer has seen a 33% drop between 1999 and 2021, the picture is driven by deaths in older adults. A closer look in adults younger than 50 years shows that, although lung cancer death rates have fallen, they coincide with a higher rate of cancer death from CRC. CRC is now the leading cause of death in younger men and the second leading cause in younger women. Fourth, reports like this highlight the gaps and opportunities in existing databases and data-collection mechanisms. For example, as norms regarding complete data collection of sexual and gender minoritized populations evolve, so must national registries to fully appreciate the distinctive populations affected by cancer. Furthermore, we continue to have an incomplete picture of those living with metastatic disease distinct from populations considered survivors.2 Across the United States, tumor registry protocols dictate that stage is assigned at the time of initial diagnosis and is not updated if someone experiences a recurrence or develops metastatic disease. Clinically, it is important because the conversation about prognosis does not occur once; it is an ongoing conversation that changes as one's circumstances and diagnoses evolve. It is also a question that is not uncommonly asked: how many of me are there living with metastatic disease? Importantly, there are solutions to this, but this requires an update in documentation procedures. For example, the American Joint Commission on Cancer has a designation for recurrence or re-treatment, r, in its tumor, node, metastasis (TNM) system.3, 4 Although someone may be diagnosed with stage I disease at diagnosis (T1N0M0), at recurrence, they could be re-staged in a way to signify the evolution of metastatic disease (rT0N0M1). However, it is not used routinely or in standard fashion but presents an opportunity for us to collect data within a registry that could be subsequently analyzed. In summary, we continue to make progress in oncology overall, but certain ethnic, racial, age, and geographic populations face a disproportionate burden of cancer incidence and mortality. Like others, we find these health disparities wholly unacceptable and agree with the National Cancer Plan and Biden Moonshot Initiative that bold and new collaborations and thinking will be needed to produce different outcomes. As the report notes, every 15 seconds presents a real reminder of the urgency to end cancer as we know it for everyone. Don S. Dizon reports personal fees from AstraZeneca and Doximity; service on a Data and Safety Monitoring Board for Clovis Oncology, Inc., and GlaxoSmithKline, LLC; and owns stock options in Midi and Doximity, all outside the submitted work. Arif H. Kamal reports personal fees from Homebase Medical outside the submitted work and is the Chief Executive Officer of Prepped Health.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
ilk666完成签到,获得积分10
1秒前
李健的小迷弟应助刘浩然采纳,获得10
1秒前
yanglinhai完成签到 ,获得积分10
2秒前
免疫小白完成签到 ,获得积分10
2秒前
Joyo完成签到 ,获得积分10
3秒前
Flyzhang完成签到,获得积分10
3秒前
7秒前
001完成签到,获得积分10
7秒前
薏晓完成签到 ,获得积分10
7秒前
Lucas应助烂漫的白山采纳,获得10
8秒前
吕禹竺完成签到 ,获得积分10
8秒前
填海完成签到,获得积分10
8秒前
飞快的雅青完成签到 ,获得积分10
9秒前
DLJ完成签到,获得积分10
10秒前
12秒前
cwanglh完成签到 ,获得积分10
14秒前
倩倩完成签到 ,获得积分10
14秒前
怎么办完成签到 ,获得积分10
14秒前
丰富的小甜瓜完成签到,获得积分10
15秒前
刘浩然发布了新的文献求助10
17秒前
科研通AI2S应助无所谓采纳,获得10
20秒前
高佳慧发布了新的文献求助10
21秒前
23秒前
方法完成签到,获得积分10
24秒前
不安枕头完成签到 ,获得积分10
26秒前
27秒前
Sandy完成签到,获得积分10
27秒前
高贵宛海完成签到,获得积分10
30秒前
阿阿阿阿阿金完成签到 ,获得积分10
31秒前
小唐发布了新的文献求助10
34秒前
早日毕业脱离苦海完成签到 ,获得积分10
36秒前
Cynthia完成签到 ,获得积分10
37秒前
在水一方应助幸福的若枫采纳,获得10
38秒前
小柒柒完成签到,获得积分10
38秒前
向往完成签到 ,获得积分10
38秒前
韦远侵完成签到,获得积分10
39秒前
hohn完成签到,获得积分10
41秒前
huihui完成签到,获得积分10
41秒前
Brady6完成签到,获得积分10
44秒前
高分求助中
HIGH DYNAMIC RANGE CMOS IMAGE SENSORS FOR LOW LIGHT APPLICATIONS 1500
Constitutional and Administrative Law 1000
Questioning sequences in the classroom 700
Microbially Influenced Corrosion of Materials 500
Die Fliegen der Palaearktischen Region. Familie 64 g: Larvaevorinae (Tachininae). 1975 500
The Experimental Biology of Bryophytes 500
Rural Geographies People, Place and the Countryside 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5378663
求助须知:如何正确求助?哪些是违规求助? 4503041
关于积分的说明 14014978
捐赠科研通 4411712
什么是DOI,文献DOI怎么找? 2423469
邀请新用户注册赠送积分活动 1416373
关于科研通互助平台的介绍 1393834