Cancer statistics 2024: All hands on deck

IF 503.1 1区 医学 Q1 ONCOLOGY CA: A Cancer Journal for Clinicians Pub Date : 2024-01-17 DOI:10.3322/caac.21824
Don S. Dizon MD, Arif H. Kamal MD, MBA, MHS
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To us, four parts of the report particularly stand out.</p><p>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.</p><p>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.</p><p>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.</p><p>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.<span><sup>2</sup></span> 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?</p><p>Importantly, there are solutions to this, but this requires an update in documentation procedures. 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Abstract

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.

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2024 年癌症统计数据:全员参与
据美国癌症协会(American Cancer Society)发布的《2024 年癌症统计数据》更新版估计,今年将有超过 200 万人听到 "你得了癌症 "这句话1 ,这相当于每天有近 5500 人,或相当于每 15 秒就有一个人听到这句话。这标志着美国人的癌症发病率首次突破 200 万,越来越多的人在这些疾病的早期阶段就被确诊,而此时的治愈率是最高的。因此,癌症死亡率持续下降,自 1991 年以来,由于美国国立卫生研究院、疾病控制和预防中心、美国癌症协会等机构在研究和筛查方面的大量投资,估计挽救了 410 万人的生命。首先,从历史上看,癌症一直是一种严重影响男性的疾病。然而,这份报告表明,自 2013 年以来,男性的癌症发病率一直保持稳定,而女性的发病率自 20 世纪 90 年代末以来却一直在上升,原因是乳腺癌、子宫体癌和黑色素瘤的发病率较高。因此,癌症越来越不分性别,各年龄段的男女发病率比为 1.14(95% CI,1.136-1.143)。许多人假设,不同的生活方式和冒险行为以及环境暴露导致男性患癌率较高。然而,随着两性发病率差距的缩小,一些迹象可能表明,风险因素(如肥胖、久坐不动的生活方式)同样影响着这两个群体,这就凸显了更好地理解这一现象的必要性。其次,尽管癌症的总体发病率在上升,但一些特定的癌症和人群却受到了不成比例的影响。例如,自 2000 年代中期以来,白人妇女的子宫癌发病率每年增长约 1%,而黑人、西班牙裔、亚裔美国人和太平洋岛民的增幅则超过 2%。考虑到年龄因素,结肠直肠癌(CRC)的发病率也出现了变化;CRC 发病率下降的主要原因是 65 岁以上人群的发病率较低;55 岁以下人群的发病率则继续以每年 1%-2%的速度增长。最后,2015 年至 2019 年期间,男性的肝癌发病率趋于稳定,黑色素瘤的发病率也可能趋于稳定,而女性的发病率则每年上升 2%。第三,尽管报告强调了血液学和晚期实体瘤恶性肿瘤治疗的巨大进步,但差异的影响也不容忽视。例如,与白人妇女相比,更多的黑人妇女被诊断为晚期(44% 对 23%),而且预后较差(5 年生存率估计值分别为 63% 对 84%)。正如作者所指出的那样,系统性因素,如与指南相一致的诊断和治疗方案的差异,起了很大的作用。此外,黑人、白人和亚裔等自我认同类别很可能掩盖了不同群体之间的风险和结果差异。例如,亚裔可能包括来自多达 48 个不同国家的后裔或移民。虽然癌症死亡率在 1999 年至 2021 年间下降了 33%,但这主要是由于老年人的死亡造成的。仔细观察 50 岁以下成年人的情况可以发现,虽然肺癌死亡率有所下降,但与此同时,CRC 的癌症死亡率却在上升。目前,CRC 是年轻男性的主要死因,也是年轻女性的第二大死因。第四,此类报告凸显了现有数据库和数据收集机制的不足和机遇。例如,随着有关性少数群体和性别少数群体完整数据收集规范的发展,国家登记处也必须充分了解受癌症影响的特殊群体。此外,我们对转移性疾病患者的了解仍不全面,他们有别于被认为是幸存者的人群。2 在美国,肿瘤登记协议规定,分期是在初次诊断时指定的,如果患者复发或出现转移性疾病,分期将不再更新。在临床上,这一点非常重要,因为关于预后的对话不是一次就能完成的;它是一个持续的对话,会随着个人情况和诊断的变化而变化。这也是一个经常被问到的问题:我有多少人患有转移性疾病?重要的是,有办法解决这个问题,但这需要更新记录程序。例如,美国癌症联合委员会(American Joint Commission on Cancer)在其肿瘤、结节、转移(TNM)系统中对复发或再治疗(r)进行了指定。
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
CiteScore
873.20
自引率
0.10%
发文量
51
审稿时长
1 months
期刊介绍: CA: A Cancer Journal for Clinicians" has been published by the American Cancer Society since 1950, making it one of the oldest peer-reviewed journals in oncology. It maintains the highest impact factor among all ISI-ranked journals. The journal effectively reaches a broad and diverse audience of health professionals, offering a unique platform to disseminate information on cancer prevention, early detection, various treatment modalities, palliative care, advocacy matters, quality-of-life topics, and more. As the premier journal of the American Cancer Society, it publishes mission-driven content that significantly influences patient care.
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