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Who Needs Axillary Dissection After Neoadjuvant Therapy? 新辅助治疗后哪些人需要腋窝清扫?
IF 20.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-08-28 DOI: 10.1001/jamaoncol.2025.2712
Abram Recht
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引用次数: 0
Tumor-Infiltrating Lymphocytes-An Area of Standardization. 肿瘤浸润性淋巴细胞-一个标准化的领域。
IF 20.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-08-01 DOI: 10.1001/jamaoncol.2025.1849
Elif Sertesen Camoz, Ilknur Deliktas Onur, Fatih Yildiz
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引用次数: 0
Long-Term Effectiveness Associated With Fecal Immunochemical Testing for Early-Age Screening. 粪便免疫化学检测在早期筛查中的长期有效性。
IF 20.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-08-01 DOI: 10.1001/jamaoncol.2025.1433
Han-Mo Chiu, Sam Li-Sheng Chen, Chiu-Wen Su, Amy Ming-Fang Yen, Wen-Feng Hsu, Chen-Yang Hsu, Ting-Yu Lin, Yi-Chia Lee, Ming-Shiang Wu, Tony Hsiu-Hsi Chen

Importance: The rising incidence of young-onset colorectal cancer (CRC) has prompted health policymakers to consider lowering the recommended starting age for screening. However, population-based evidence supporting the long-term effectiveness of early-age screening remains limited.

Objective: To evaluate whether initiating fecal immunochemical test (FIT) screening at ages 40 to 49 years, rather than at the currently recommended age of 50 years, reduces CRC incidence and mortality.

Design, setting, and participants: This study analyzed a community-based screening cohort of Taiwanese residents aged 40 to 49 years, categorized into 4 subcohorts based on participation in early screening (age 40 to 49 years) and continuation of nationwide regular screening (50 years and older). The cohort was followed up until 2019 to compare CRC incidence and mortality across subcohorts. To mitigate self-selection bias, a delayed screening design and efficient propensity score matching was used, restricting analyses to participants attending regular screening. To validate the findings, an extended nonadherence adjustment was applied to all 4 subcohorts. Data were collected from January 2001 to December 2019, and data were analyzed from January 2021 to December 2024.

Exposures: Biennial FIT screening was initiated for the early screening group at ages 40 to 49 years and for the regular screening group at age 50 years, with follow-up continuing under Taiwan's national screening program.

Main outcomes and measures: Primary outcomes were CRC incidence and mortality rates, reported as cases per 100 000 person-years, with adjusted relative risks (aRRs) comparing early vs regular screening groups.

Results: Of 263 125 included participants, 146 796 (55.8%) were female. A total of 39 315 participated in early and regular screening, and 223 810 participated in regular screening only. The early screening group exhibited lower CRC incidence (26.1 [95% CI, 22.3-29.9] vs 42.6 [95% CI, 40.5-44.7] per 100 000 person-years) and mortality (3.2 [95% CI, 1.9-4.6] vs 7.4 [95% CI, 6.5-8.2] per 100 000 person-years). In propensity score-matched analyses, early screening significantly reduced CRC incidence (aRR, 0.79; 95% CI, 0.67-0.94) and mortality (aRR, 0.61; 95% CI, 0.38-0.98). Findings were consistent in the extended nonadherence adjustment model, showing a 25% reduction in incidence (aRR, 0.75; 95% CI, 0.72-0.77) and a 34% reduction in mortality (aRR, 0.66; 95% CI, 0.62-0.71).

Conclusions and relevance: This study found that initiating FIT screening at age 40 to 49 years was associated with further reduction in CRC mortality and incidence compared with starting screening at age 50 years. These results provide strong empirical support for lowering the CRC screening age, with substantial public health implications.

重要性:年轻发病的结直肠癌(CRC)发病率的上升促使卫生政策制定者考虑降低推荐的筛查起始年龄。然而,支持早期筛查长期有效性的基于人群的证据仍然有限。目的:评价在40 - 49岁开始粪便免疫化学试验(FIT)筛查,而不是目前推荐的50岁,是否能降低结直肠癌的发病率和死亡率。设计、环境和参与者:本研究分析了40至49岁台湾居民的社区筛查队列,根据参与早期筛查(40至49岁)和继续进行全国定期筛查(50岁及以上)分为4个亚队列。该队列随访至2019年,以比较各亚队列的CRC发病率和死亡率。为了减轻自我选择偏差,采用延迟筛选设计和有效倾向评分匹配,将分析限制在定期参加筛选的参与者。为了验证研究结果,对所有4个亚队列应用了延长的不依从调整。数据收集时间为2001年1月至2019年12月,分析时间为2021年1月至2024年12月。​主要结局和措施:主要结局是CRC发病率和死亡率,报告为每10万 000人年的病例数,并比较早期和常规筛查组的调整相对风险(arr)。结果:263名 125名纳入受试者,146名 796名(55.8%)为女性。39名 315人参加了早期和定期筛查,223名 810人只参加了定期筛查。早期筛查组CRC发病率(26.1 [95% CI, 22.3-29.9] vs 42.6 [95% CI, 40.5-44.7] / 100 000人年)和死亡率(3.2 [95% CI, 1.9-4.6] vs 7.4 [95% CI, 6.5-8.2] / 100 000人年)较低。在倾向评分匹配分析中,早期筛查显著降低了CRC发病率(aRR, 0.79;95% CI, 0.67-0.94)和死亡率(aRR, 0.61;95% ci, 0.38-0.98)。结果与扩展不依从调整模型一致,显示发生率降低25% (aRR, 0.75;95% CI, 0.72-0.77),死亡率降低34% (aRR, 0.66;95% ci, 0.62-0.71)。结论和相关性:本研究发现,与50岁开始筛查相比,在40至49岁开始筛查与CRC死亡率和发病率的进一步降低相关。这些结果为降低结直肠癌筛查年龄提供了强有力的实证支持,具有重大的公共卫生意义。
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引用次数: 0
Caring for Fasting Patients With Cancer During Ramadan. 在斋月期间照顾斋戒的癌症患者。
IF 20.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-08-01 DOI: 10.1001/jamaoncol.2025.1585
Javier Mora, Mina Bakhtiar, Nadia A Saeed, Tracy A Balboni
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引用次数: 0
Cancer Incidence and Trends in US Adults With HIV. 美国成年艾滋病毒感染者的癌症发病率和趋势
IF 20.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-08-01 DOI: 10.1001/jamaoncol.2025.1589
Cameron B Haas, Jennifer K McGee-Avila, Qianlai Luo, Ruth M Pfeiffer, Susan Gershman, Sai Cherala, Colby Cohen, Analise Monterosso, Natalie Archer, Tabassum Z Insaf, Eric A Engels, Meredith S Shiels

Importance: People with HIV are living longer due to improvements in antiretroviral therapy over the last 2 decades. Current age-specific estimates of cancer risk among people with HIV may inform cancer prevention and clinical guidelines for this population.

Objective: To estimate cancer incidence rates (IRs) using a population-based linkage of HIV and cancer registries.

Design, setting, and participants: This population-based cohort study used data from 12 US states, Washington, DC, and Puerto Rico from 2001 to 2019. People with HIV and the general population in the HIV/AIDS Cancer Match Study were included in the analysis, which occurred between October 2023 and December 2024.

Main outcomes and measures: Age-standardized IRs (per 100 000 person-years) were calculated across calendar periods (2001 to 2004, 2005 to 2009, 2010 to 2014, and 2015 to 2019) and incidence rate ratios (IRRs) across calendar periods using adjusted Poisson regression. Standardized incidence ratios (SIRs) were estimated for 2010 to 2014 and 2015 to 2019, and age group-specific cancer incidence and SIRs were estimated for 2010 to 2019.

Results: The analysis included 7.2 million person-years among 847 107 people with HIV (5.3 million person-years among males [73%]). Comparing years 2015 to 2019 to years 2010 to 2014, incidence of diffuse large B-cell lymphoma (DLBCL) decreased 23% (IRR, 0.77; 95% CI, 0.70-0.84), Kaposi sarcoma (KS) decreased 24% (IRR, 0.76; 95% CI, 0.69-0.84), Hodgkin lymphoma decreased 25% (IRR, 0.75; 95% CI, 0.65-0.86), and cancers of the lung decreased 17% (IRR, 0.83; 95% CI, 0.77-0.90) and liver decreased 25% (IRR, 0.75; 95% CI, 0.67-0.84). Among people with HIV aged 70 to 84 years, IRs were highest for cancers of the prostate (448.01; 95% CI, 404.26-495.20), lung (269.79; 95% CI, 240.86-301.24), female breast (202.29; 95% CI, 155.79-258.32), liver (82.82; 95% CI, 67.16-101.03), and colon (107.57; 95% CI, 89.61-128.08), exceeding the IRs for DLBCL (41.83; 95% CI, 30.95-55.31) and KS (15.37; 95% CI, 9.11-24.29). From 2015 to 2019, risk remained significantly elevated in people with HIV for several cancer types, including KS (SIR, 213.87; 95% CI, 198.81-229.73), Hodgkin lymphoma (SIR, 6.29; 95% CI, 5.68-6.94), DLBCL (SIR, 5.25; 95% CI, 5.25-6.01), cancers of the anus (SIR, 17.07; 95% CI, 16.01-18.17), vulva (SIR, 11.40; 95% CI, 9.60-13.44), liver (SIR, 1.89; 95% CI, 1.74-2.05), and lung (SIR, 1.59; 95% CI, 1.51-1.68). For nearly all these cancers, SIRs significantly declined with increasing age.

Conclusions and relevance: In this cohort study, significant declines in the incidence and relative risk for cancers among people with HIV demonstrate continued progress in HIV treatment and cancer prevention. These estimates may provide insight into the priorities for prevention and early detection of cancer as the population of pe

重要性:由于过去20年来抗逆转录病毒治疗的改进,艾滋病毒感染者的寿命延长了。目前艾滋病毒感染者中特定年龄的癌症风险估计可能为这一人群的癌症预防和临床指南提供信息。目的:利用基于人群的HIV和癌症登记联系来估计癌症发病率(IRs)。设计、环境和参与者:这项基于人群的队列研究使用了2001年至2019年美国12个州、华盛顿特区和波多黎各的数据。在2023年10月至2024年12月期间进行的艾滋病毒/艾滋病癌症匹配研究中,艾滋病毒感染者和普通人群被纳入分析。主要结局和测量方法:使用调整后的泊松回归计算历期(2001 - 2004年、2005 - 2009年、2010 - 2014年和2015 - 2019年)的年龄标准化IRs(每100,000 000人年)和历期的发病率比(IRRs)。对2010年至2014年和2015年至2019年的标准化发病率(SIRs)进行了估计,并对2010年至2019年的年龄组特定癌症发病率和SIRs进行了估计。结果:该分析包括847 107名HIV感染者中的720万人年(男性为530万人年[73%])。2015 - 2019年与2010 - 2014年相比,弥漫性大b细胞淋巴瘤(DLBCL)的发病率下降了23% (IRR, 0.77;95% CI, 0.70-0.84),卡波西肉瘤(KS)减少24% (IRR, 0.76;95% CI, 0.69-0.84),霍奇金淋巴瘤下降25% (IRR, 0.75;95% CI, 0.65-0.86),肺癌减少17% (IRR, 0.83;95% CI, 0.77-0.90),肝脏下降25% (IRR, 0.75;95% ci, 0.67-0.84)。在70至84岁的HIV感染者中,前列腺癌的IRs最高(448.01;95% CI, 404.26-495.20),肺(269.79;95% CI, 240.86-301.24),女性乳房(202.29;95% CI, 155.79-258.32),肝脏(82.82;95% CI, 67.16-101.03)和结肠(107.57;95% CI, 89.61-128.08),超过DLBCL的ir (41.83;95% CI, 30.95-55.31)和KS (15.37;95% ci, 9.11-24.29)。从2015年到2019年,艾滋病毒感染者罹患几种癌症的风险仍然显著升高,包括KS (SIR, 213.87;95% CI, 198.81-229.73),霍奇金淋巴瘤(SIR, 6.29;95% ci, 5.68-6.94), DLBCL (sir, 5.25;95% CI, 5.25-6.01),肛门癌(SIR, 17.07;95% CI, 16.01-18.17),外阴(SIR, 11.40;95% CI, 9.60-13.44),肝脏(SIR, 1.89;95% CI, 1.74-2.05)和肺(SIR, 1.59;95% ci, 1.51-1.68)。对于几乎所有这些癌症,SIRs都随着年龄的增长而显著下降。结论和相关性:在这项队列研究中,艾滋病毒感染者中癌症发病率和相对风险的显著下降表明艾滋病毒治疗和癌症预防的持续进展。随着艾滋病毒感染者进入癌症风险更高的年龄,这些估计可能有助于了解预防和早期发现癌症的优先事项。
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引用次数: 0
What Age Is the Best "FIT" for Colorectal Cancer Screening? 什么年龄最适合做大肠癌筛检?
IF 20.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-08-01 DOI: 10.1001/jamaoncol.2025.1361
Thejus Jayakrishnan, Andrew T Chan, Kimmie Ng
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引用次数: 0
Tumor-Infiltrating Lymphocytes-An Area of Standardization-Reply. 肿瘤浸润性淋巴细胞-标准化区域-回复。
IF 20.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-08-01 DOI: 10.1001/jamaoncol.2025.1852
Maria Vittoria Dieci, Valentina Guarneri
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引用次数: 0
JAMA Oncology. JAMA肿瘤学。
IF 28.4 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-07-01 DOI: 10.1001/jamaoncol.2024.4649
{"title":"JAMA Oncology.","authors":"","doi":"10.1001/jamaoncol.2024.4649","DOIUrl":"https://doi.org/10.1001/jamaoncol.2024.4649","url":null,"abstract":"","PeriodicalId":48661,"journal":{"name":"Jama Oncology","volume":"11 7","pages":"681"},"PeriodicalIF":28.4,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acupuncture for Nocturia in Survivors of Prostate Cancer: The NOCTURNAL Randomized Clinical Trial. 针刺治疗前列腺癌幸存者夜尿症:夜间随机临床试验。
IF 28.4 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-07-01 DOI: 10.1001/jamaoncol.2025.1199
Kevin T Liou, Sigrid Carlsson, Divya Ajay, Jaspreet S Sandhu, Yuelin Li, Q Susan Li, Felix Cheung, Kamy Chong, Allison Booher, Katherine Han, Kaitlin Lampson, Christian Nelson, Michael J Morris, Vincent P Laudone, Jun J Mao
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引用次数: 0
Are Early-Onset Cancers an Example of Accelerated Biological Aging? 早发性癌症是加速生物衰老的一个例子吗?
IF 28.4 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-07-01 DOI: 10.1001/jamaoncol.2025.1143
Jennifer L Guida, Lisa Gallicchio, Paige A Green
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引用次数: 0
期刊
Jama Oncology
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