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本文引用的文献

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Estimation of Lead Time via Low-Dose CT in the National Lung Screening Trial.在国家肺癌筛查试验中通过低剂量CT评估提前期
J Healthc Inform Res. 2018 Jun 12;2(4):353-366. doi: 10.1007/s41666-018-0027-8. eCollection 2018 Dec.
2
Population modeling of tumor growth curves and the reduced Gompertz model improve prediction of the age of experimental tumors.肿瘤生长曲线的群体建模和简化的 Gompertz 模型提高了对实验性肿瘤年龄的预测。
PLoS Comput Biol. 2020 Feb 25;16(2):e1007178. doi: 10.1371/journal.pcbi.1007178. eCollection 2020 Feb.
3
Reduced Lung-Cancer Mortality with Volume CT Screening in a Randomized Trial.随机试验中 CT 容积筛查降低肺癌死亡率
N Engl J Med. 2020 Feb 6;382(6):503-513. doi: 10.1056/NEJMoa1911793. Epub 2020 Jan 29.
4
Lung cancer mortality reduction by LDCT screening-Results from the randomized German LUSI trial.低剂量计算机断层扫描(LDCT)筛查降低肺癌死亡率-来自德国 LUSI 随机试验的结果。
Int J Cancer. 2020 Mar 15;146(6):1503-1513. doi: 10.1002/ijc.32486. Epub 2019 Jun 20.
5
Prolonged lung cancer screening reduced 10-year mortality in the MILD trial: new confirmation of lung cancer screening efficacy.MILD 试验证实:延长肺癌筛查时间可降低 10 年死亡率,再次确认肺癌筛查的有效性。
Ann Oncol. 2019 Jul 1;30(7):1162-1169. doi: 10.1093/annonc/mdz117.
6
growth of 60 non-screening detected lung cancers: a computed tomography study.60 例非筛查性检出肺癌的生长情况:一项 CT 研究。
Eur Respir J. 2018 Apr 12;51(4). doi: 10.1183/13993003.02183-2017. Print 2018 Apr.
7
Baseline and annual repeat rounds of screening: implications for optimal regimens of screening.基线和年度重复筛查轮次:对最佳筛查方案的影响。
Eur Radiol. 2018 Mar;28(3):1085-1094. doi: 10.1007/s00330-017-5029-z. Epub 2017 Oct 5.
8
Mortality, survival and incidence rates in the ITALUNG randomised lung cancer screening trial.ITALUNG 随机肺癌筛查试验中的死亡率、生存率和发病率。
Thorax. 2017 Sep;72(9):825-831. doi: 10.1136/thoraxjnl-2016-209825. Epub 2017 Apr 4.
9
Low-dose computed tomography for lung cancer screening: comparison of performance between annual and biennial screen.低剂量计算机断层扫描肺癌筛查:年度筛查与两年筛查性能比较。
Eur Radiol. 2016 Nov;26(11):3821-3829. doi: 10.1007/s00330-016-4228-3. Epub 2016 Feb 11.
10
Long-Term Follow-up Results of the DANTE Trial, a Randomized Study of Lung Cancer Screening with Spiral Computed Tomography.DANTE 试验的长期随访结果,一项使用螺旋 CT 进行肺癌筛查的随机研究。
Am J Respir Crit Care Med. 2015 May 15;191(10):1166-75. doi: 10.1164/rccm.201408-1475OC.

肺癌筛查的前置时间长度。

Duration of lead time in screening for lung cancer.

机构信息

Department of Medicine (retired), Hadassah Medical Center, PO Box 3894, 91037, Jerusalem, Israel.

出版信息

BMC Pulm Med. 2021 Jan 6;21(1):4. doi: 10.1186/s12890-020-01385-3.

DOI:10.1186/s12890-020-01385-3
PMID:33407288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7788818/
Abstract

BACKGROUND

Screening for lung cancer has used chest radiography (CR), low dose computed tomography (LDCT) and sputum cytology (SC). Estimates of the lead time (LT), i.e., the time interval from detection of lung cancer by screening to the development of symptoms, have been derived from longitudinal studies of populations at risk, tumor doubling time (DT), the ratio between its prevalence at the first round of screening and its annual incidence during follow-up, and by probability modeling derived from the results of screening trials.

OBJECTIVE

To review and update the estimates of LT of lung cancer.

METHODS

A non-systematic search of the literature for estimates of LT and screening trials. Search of the reference sections of the retrieved papers for additional relevant studies. Calculation of LTs derived from these studies.

RESULTS

LT since detection by CR was 0.8-1.1 years if derived from longitudinal studies; 0.6-2.1 years if derived from prevalence / incidence ratios; 0.2 years if derived from the average tumor DT; and 0.2-1.0 if derived from probability modeling. LT since detection by LDCT was 1.1-3.5 if derived from prevalence / incidence ratios; 3.9 if derived from DT; and 0.9 if derived from probability modeling. LT since detection of squamous cell cancer by SC in persons with normal CR was 1.3-1.5 if derived from prevalence/incidence ratios; and 2.1 years if derived from the DT of squamous cell cancer.

CONCLUSIONS

Most estimates of the LT yield values of 0.2-1.5 years for detection by CR; of 0.9-3.5 years for detection by LDCT; and about 2 years or less for detection of squamous cell cancer by SC in persons with normal CR. The heterogeneity of the screening trials and methods of derivation may account for the variability of LT estimates.

摘要

背景

肺癌筛查使用了胸部 X 光摄影(CR)、低剂量计算机断层扫描(LDCT)和痰液细胞学检查(SC)。通过对处于风险中的人群进行纵向研究、肿瘤倍增时间(DT)、首轮筛查时的患病率与随访期间年度发病率的比值,以及通过筛查试验的结果得出的概率模型,对领先时间(LT)进行了估计,即通过筛查发现肺癌到出现症状的时间间隔。

目的

回顾和更新肺癌 LT 的估计值。

方法

对 LT 和筛查试验的文献进行非系统性检索。检索检索到的论文的参考文献部分以获取其他相关研究。从这些研究中计算 LT。

结果

如果源自纵向研究,则源自 CR 检测的 LT 为 0.8-1.1 年;如果源自患病率/发病率比值,则为 0.6-2.1 年;如果源自平均肿瘤 DT,则为 0.2 年;如果源自概率模型,则为 0.2-1.0 年。如果源自患病率/发病率比值,则源自 LDCT 检测的 LT 为 1.1-3.5 年;如果源自 DT,则为 3.9 年;如果源自概率模型,则为 0.9 年。如果源自 SC 检测的 CR 正常的人鳞状细胞癌,则 LT 为 1.3-1.5 年,如果源自患病率/发病率比值,则为 2.1 年;如果源自鳞状细胞癌的 DT,则为 2.1 年。

结论

大多数 LT 估计值为 CR 检测的 0.2-1.5 年;LDCT 检测的 0.9-3.5 年;CR 正常的人通过 SC 检测的鳞状细胞癌为 2 年或更短。筛查试验和推导方法的异质性可能是 LT 估计值变化的原因。