Skip to main content
BMC Cancer logoLink to BMC Cancer
. 2021 Jan 11;21:50. doi: 10.1186/s12885-020-07750-z

Current lung cancer screening guidelines may miss high-risk population: a real-world study

Guiyi Ji 1, Ting Bao 1, Zhenzhen Li 1, Huairong Tang 1, Dan Liu 2, Ping Yang 3,4, Weimin Li 2,5,6,7, Yan Huang 1,
PMCID: PMC7802250  PMID: 33430831

Abstract

Background

Despite much research published on lung cancer screening, China has had no large-scale study on the missed diagnosis of lung cancer in a health examination population. We therefore did a real-world study using the current lung cancer screening guidelines to a health examination population in China to determine the proportion of lung cancer cases that have been missed.

Methods

A real-world cohort study of screening, with the use of low-dose computed tomography, was conducted among people who took yearly health checkup in health management center of West China Hospital between 2006 and 2017. We respectively used current guidelines including lung cancer screening guidelines of the U.S. Preventive Services Task Force (USPSTF) and expert consensus on low dose spiral CT lung cancer screening in China.

Results

In a total of 15,996 participants with health examination who completed the baseline screening, 6779 (42.4%) subjects had at least one positive finding, and 142 (2.1%) cases of lung cancer were screened positive. The false positive rate was 97.9%. Of 142 lung cancer cases detected in our study, only 9.2% met the lung cancer screening guidelines proposed by the USPSTF, and 24.4% met that of China. The rates of missed diagnosis were as high as 90.8 and 75.6% respectively. In addition, we did an in-depth analysis by gender. We found that among male patients with lung cancer, the proportion of smokers was 75%, and the proportion of young people under 50 was 23.2%. Among female patients with lung cancer, the proportion of smokers was only 5.8%, and the proportion of young people under 50 was up to 33.3%.

Conclusions

The rate of missed diagnosis was as high as 90.8% applying the current lung cancer screening guidelines to the health examination population in China. Further study to determine screening guidelines for targeted populations, is warranted.

Keywords: Lung cancer, Screening, High-risk population, Health examination population, Real-world study, LDCT

Background

Lung cancer is the most frequent cancer and the leading cause of cancer death all over the world [1]. It is reported that the survival rate of lung cancer was negatively correlated with the clinical and pathological stages at the time of diagnosis [2]. Unfortunately, when symptoms appear, the disease is usually advanced and incurable [3]. The study showed that low-dose computed tomography (LDCT) can detect some tumors at early stages [4]. Many authoritative medical organizations have launched screening guidelines, which recommended lung cancer screening in high-risk groups with LDCT [57].

Generally, age and smoking are the main criteria to define high-risk groups in domestic and foreign guidelines. However, researches showed that except for smoking, the causes of lung cancer were also attributed to air pollution, environmental exposure, genetic factors [8, 9]. Although most lung cancers are caused by smoking, a lot of lung cancer cases worldwide have been reported in non-smokers [8]. If lung cancer in never smoker was considered as a separate category, it would be the seventh most common cause of cancer death around the world [10]. In addition, the incidence of lung cancer also shows a trend of youth in recent years [1113]. Young patients with lung cancer have gradually become a disease group that can not be ignored [1113].

For these reasons, the current lung cancer screening guidelines may miss some persons at high risk of lung-cancer especially young or non-smoking people [57, 14, 15]. However, there is still a lack of large-scale research on this in China. Therefore, in order to determine whether the current screening guidelines of lung cancer will lead to miss diagnosis of lung cancer cases in China, and to determine the fraction of lung cancer cases that would be missed, we did a real-world study which applied these screening guidelines to the health examination population in West China Hospital.

Methods

Trial oversight

We applied the current guidelines to the health examination population and compared them with the real world. This research, a study of screening with the use of LDCT, was conducted among the people taking yearly health checkup in health management center of West China Hospital.

Participants

Participants were enrolled and screened from June 30, 2006 through June 30, 2017. They were followed for events that occurred before December 31, 2017.

Eligible subjects did not have undergone chest imaging within 18 months before enrollment, and there were no new or aggravating cough, expectoration, hemoptysis, chest distress, dyspnea and other symptoms. Persons with any of the following conditions were excluded from this study: 1) previously received a diagnosis of unknown pulmonary nodules or malignant pulmonary nodules, masses, hilum enlargement, atelectasis; 2) a history of total or partial lobectomy; 3) history of lung cancer; 4) an unexplained weight loss of more than 5 kg in the past year. A total of 15,996 persons were enrolled. A written informed consent was obtained from every participant. Eligible participants completed a questionnaire that covered some topics, including demographic characteristics, smoking behavior, and medical history.

Guidelines

In this study, we respectively used two kinds of the current lung cancer screening guidelines including lung cancer screening guidelines of the U.S. Preventive Services Task Force (USPSTF) and expert consensus on low dose spiral CT lung cancer screening in China to the health examination population in China to determine the proportion of lung cancer cases that have been missed. The USPSTF recommended annual screening for lung cancer with LDCT in adults aged 55 to 80 years, who currently smoke or have quit within the past 15 years, and who have an at least 30 pack-years of cigarette smoking history [5, 6]. The consensus of Chinese experts suggest that annual LDCT lung-cancer screening for individuals aged 50–75 years, combining at least one of the following risk factors: 1) at least 20 pack-years of cigarette smoking history, including currently smoking or giving up smoking for less than 15 years; 2) passive smoking; 3) a history of occupational exposure, including asbestos, beryllium, uranium, radon, etc.; 4) a history of cancer or a family history of lung cancer; and 5) a history of chronic obstructive pulmonary disease (COPD) or diffuse pulmonary fibrosis [7].

Screening

Participants were invited to undergo a base-line screening. We conducted annual screenings from the next year. Participants with positive screening would be followed up, and those with negative screening would be screened in the next round.

All screening tests were conducted in accordance with a standard protocol developed by the medical physicists associated with the trial, which specified the acquisition variables and the acceptable characteristics of the machine [1618]. All computed tomography (CT) scans were performed on double row spiral CT (Somatom Emotion Duo, Siemens, Germany). Thin slice scanning with 1 mm was performed on the local lesions. All scans were obtained using a low-dose regimen, with the machine set at 120 kVp, 16 (20 mA/0.8 s) ~ 40 (50 mA/0.8 s) mAs, pitch ≤1 cm, and 0.8 s rotation time. Chest radiographs were obtained with the use of digital equipment. All the machines used for screening met the technical standards [4].

Radiologic technologists and radiologists were certified by appropriate agencies. Radiologic technologists completed training in image acquisition. Radiologists also completed training in standardized image interpretation. Two radiologists with at least 5 years of experience in thoracic radiology assessed all chest images independently. Images were assessed first in isolation and then in comparison with available historical and screening images. The comparative analysis was used to determine the outcome of the chest examination. When the interpretations of these two radiologists were different, they need to analyze repeatedly and negotiated the judgment. In addition, at least two qualified respiratory medicine and chest tumor experts from our hospital formed a diagnosis team. Based on the recommendation of radiologists and other results of physical examination, the diagnosis team made a further plan of intervention treatment. LDCT scans that could reveal any non-calcified nodule with at least 4 mm diameter were classified as positive, suspected lung cancer. Other abnormalities such as obstructive atelectasis, soft tissue or patchy clouding opacity could be classified as a positive result as well.

Medical-record abstraction

Data regarding diagnostic evaluation procedures and any associated complications for patients with positive screening tests and lung cancer were extracted from the medical records. At the same time, the pathology reports and records of operation and treatment of patients with lung cancer were also obtained. Metastatic lung cancer was excluded. The classification of histologic characteristics of the lung cancer were conducted according to the International Classification of Diseases for Oncology, 3rd Edition (ICD-O-3) [19], and the clinical stages were conducted according to the eighth edition of the Cancer Staging Manual of the American Joint Committee on Cancer (AJCC) [20].

Vital status

We have trained professionals to follow-up. A special follow-up team is responsible for ascertaining probable vital status and determining whether the cause of death was lung cancer. We have carefully distinguished between lung cancer-related deaths and those caused by diagnostic evaluation or treatment of lung cancer.

Statistical analysis

SPSS was adopted for statistical analysis. Comparisons between the group of patients with lung cancer and the group of patients without lung cancer were calculated by the chi-square test (categorical data) or the T-test (numerical data). P value < 0.05 was considered as statistically significant. Survival analysis was performed by Kaplan-Meier with ungrouped data.

Results

Characteristics of the participants

The 15,996 subjects completed baseline lung screening with LDCT from June 30, 2006 through June 30, 2017. The baseline demographic characteristics of the 15,996 participants are summarized in Table 1. The age of participants was distributed in all ages, but it was mainly over 40 years old. 11,247 (70.3%) individuals did not smoke.

Table 1.

Selected Baseline Characteristics of the Study Participants

Parameter Male, n (%) Female, n (%) Total, n (%)
Total 9801 (61.3) 6195 (38.7) 15,996 (100.0)
Age at inclusion (years)a 51.26 ± 14.76 48.80 ± 14.76 50.31 ± 14.81
< 30 545 (5.56) 586 (9.5) 1131 (7.0)
30~ 1361 (13.9) 872 (14.1) 2233 (14.0)
40~ 3119 (31.8) 2224 (35.9) 5343 (33.4)
50~ 2363 (24.1) 1196 (19.3) 3559 (22.2)
60~ 1033 (10.5) 605 (9.8) 1638 (10.2)
70~ 832 (8.5) 475 (7.7) 1307 (8.2)
≥80 548 (5.6) 237 (3.8) 785 (5.0)
Smoking status
 smoking 4697 (47.9) 52 (0.8) 4749 (29.7)
 non-smoking 5104 (52.1) 6143 (99.2) 11,247 (70.3)
 Smoking volume (pack year)a 19.24 ± 14.84 13.95 ± 25.04 19.20 ± 14.93
 < 10 894 (19.0) 13 (25.0) 907 (19.1)
 10~ 1080 (23.0) 8 (15.4) 1088 (23.0)
 20~ 841 (17.9) 1 (1.9) 842 (17.7)
 30~ 488 (10.4) 1 (1.9) 489 (10.3)
 40~ 225 (4.8) 0 (0) 225 (4.7)
 50~ 45 (1.0) 0 (0) 45 (0.9)
 ≥60 100 (2.1) 1 (1.9) 101 (2.1)
 Unknown 1024 (21.8) 28 (53.8) 1052 (22.2)
Family history of lung cancer
 Yes 163 (87.2) 181 (84.6) 401 (2.5)
 No 24 (12.8) 33 (15.4) 15,595 (97.5)
Chronic lung diseaseb
 Yes 5868 (59.9) 3450 (55.7) 9318 (58.3)
 No 3933 (40.1) 2745 (44.3) 6678 (41.7)

a Values are presented as mean ± SD (range). b Chronic lung diseases include the chronic obstructive pulmonary disease, diffuse pulmonary fibrosis, history of pulmonary tuberculosis and other respiratory diseases

Positive results of screening

In the lung cancer screening with LDCT, positive results are shown in Table 2. Of the 15,996 participants with physical examination who completed the baseline screening, 6779 subjects had at least one positive finding, with a positive rate of 42.4% (Table 2).

Table 2.

Results of Screening

Parameter Health Examination
Population
n(%)
Total No. Screened 15,996
Positive Result 6779 (42.4)
Lung cancer confirmed 142 (2.1)
T0a 86 (1.9)
T1 31 (1.9)
T2 20 (3.9)
T3 4 (3.5)
T4 1 (4.2)
Lung cancer not confirmed 6637 (97.9%)
T0a 4441 (98.1)
T1 1574 (98.1)
T2 490 (96.1)
T3 109 (96.5)
T4 23 (95.8)
Negative Result 9217 (57.6)

a The screenings were performed at 1-year intervals, with the first screening (T0) performed soon after the time of randomization

Incidence of lung cancers

The detection rates of lung cancer are summarized in Table 2. A total of 142 cases of lung cancer were screened out from the health examination population initially recruited in this research, the detection rate of lung cancer was 2.1%, and the false positive rate was 97.9% (Table 2).

We conducted this analysis in high-risk population of lung cancer. The analysis showed that based on the guidelines of the lung cancer screening proposed by the USPSTF [5, 6], of the 142 cases of lung cancer, 72 patients were aged 55–80, and 70 patients did not meet the age-standard (Table 3). In addition, the proportion of patients who met the smoking and quit-smoking standards were 8.5 and 2.1% respectively (Table 3). Only 13 cases of lung cancer met all criteria of screening (Table 3). The rate of missed diagnosis was as high as 90.8% according to the guideline of the lung cancer screening proposed by the USPSTF (Table 3).

Table 3.

The results of lung cancer screening according to the USPSTF screening guidelines

Parameter Number of lung cancer (n = 142)
Met the inclusion criteria, n(%) Not met the inclusion criteria, n(%)
Age at inclusion (years)
 A. 55 ~ 80 72 (50.7) 70 (49.3)
Smoking volume (pack year)
 B. ≥ 30 12 (8.5) 130 (91.5)
Quit smoking time (years)
 C. <  15 3 (2.1) 139 (97.9)
AB or AC 13 (9.2) 129 (90.8)

Moreover, we did the similar research in high-risk population of lung cancer based on the Chinese screening guidelines. According to the guidelines of the lung cancer screening in China [7], of the 142 cases of lung cancer, the proportion of patients who met the standards, including age, smoking, tumor history and chronic lung diseases, was 53.5, 12.7, 18.3 and 14.7%, respectively (Table 4). Just 25.4% people with lung cancer met all criteria of this guideline. The rate of missed diagnosis was 74.7% (Table 4).

Table 4.

The results of lung cancer screening according to the Chinese screening guidelines

Parameter Number of lung cancer (n = 142)
Met the inclusion criteria, n(%) Not met the inclusion criteria, n(%)
Age at inclusion (years)
 A. 50 ~ 75 76 (53.5) 66 (46.5)
Smoking volume (pack year)a
 B. ≥ 20 18 (12.7) 124 (87.3)
History of cancerb
 C. Yes 26 (18.3) 116 (81.7)
Chronic lung diseasec
 D. Yes 45 (14.7) 145 (85.3)
A(B or C or D) 36 (25.4) 106 (74.7)

aThis includes current smoking and quitting smoking less than 15 years. bThis includes a history of cancer or a family history of lung cancer. cThis includes the chronic obstructive pulmonary disease, diffuse pulmonary fibrosis, history of pulmonary tuberculosis and other respiratory diseases

Analysis of high-risk factors in lung cancer stratified by gender

Previous studies have shown that there were differences in the high-risk factors of lung cancer between different genders [10, 21, 22]. Therefore, we further investigated the high-risk factors of lung cancer by gender. As shown in Table 5, age and smoking status were high-risk factors of lung cancer in women, while in men, besides these factors, there were some other high-risk factors, such as COPD, diffuse pulmonary fibrosis, and previous history of malignant tumor (all P < 0.05). In addition, we found that the detection rate of lung cancer in women was 1.1%, significantly higher than that in men 0.7% (P = 0.021) (Table 5). In order to explore the correlation between different age stages and lung cancer, we further analyzed the risk factor of age (Table 5). The proportion of lung cancer in men under 50, 50–55, 55–75, 75–80 and over 80 years old were 23.2, 11, 42.5, 12.3 and 11.0% respectively, and those in women were 33.3, 14.5, 33.4, 8.7, 10.1% respectively (Table 5). At the same time, we also found that among patients with lung cancer in male, the proportion of smokers was 75%, and that in female lung cancer cases was only 5.8% (Table 5).

Table 5.

Analysis of high-risk factors in lung cancer stratified by gender

Characteristic Male Female
Patients with Patients without P value Patients with Patients without P value
lung cancer, n(%) lung cancer, n(%) lung cancer, n(%) lung cancer, n(%)
Total 73 (0.7) 9728 (99.3) 69 (1.1) 6126 (98.9) 0.021 b
Age (years) a 62.10 ± 13.51 51.18 ± 14.74 < 0.0001 59.17 ± 13.44 48.69 ± 14.73 < 0.0001
< 30 0 (0) 545 (5.6) 0 (0) 586 (9.6)
30~ 0 (0) 627 (6.4) 0 (0) 397 (6.5)
35~ 2 (2.7) 732 (7.5) 1 (1.4) 474 (7.7)
40~ 6 (8.2) 1497 (15.4) 8 (11.6) 1158 (18.9)
45~ 9 (12.3) 1607 (16.5) 14 (20.3) 1044 (17.0)
50~ 8 (11.0) 1288 (13.2) 10 (14.5) 710 (11.6)
55~ 4 (5.5) 1063 (10.9) 4 (5.8) 472 (7.7)
60~ 7 (9.6) 591 (6.1) 6 (8.7) 363 (5.9)
65~ 13 (17.8) 422 (4.3) 5 (7.2) 231 (3.7)
70~ 7 (9.6) 446 (4.6) 8 (11.6) 192 (3.1)
75~ 9 (12.3) 370 (3.8) 6 (8.7) 269 (4.4)
80~ 8 (11.0) 540 (5.6) 7 (10.1) 230 (3.8)
Smoking history 55 (75.3) 5299 (54.5) 0.000 4 (5.8) 52 (0.8) 0.003
Chronic obstructive pulmonary disease 24 (32.9) 1821 (18.7) 0.002 9 (13.0) 606 (9.9) 0.384
Diffuse pulmonary fibrosis 17 (23.3) 1440 (14.8) 0.042 6 (8.7) 732 (11.9) 0.407
Previous pulmonary tuberculosis 4 (5.5) 357 (3.7) 0.346 1 (1.4) 168 (2.7) 1.000
Previous history of malignant tumor 11 (15.1) 268 (2.8) < 0.0001 12 (17.4) 691 (11.3) 0.112
Family history of cancer 5 (6.8) 723 (7.4) 0.850 10 (14.5) 751 (12.3) 0.574
Number of first-degree relatives with cancer 5 (6.8) 653 (6.7) 0.371 10 (14.5) 655 (10.7) 0.478
Family history of lung cancer 2 (2.7) 185 (1.9) 0.651 1 (1.4) 213 (3.5) 0.733
Number of first-degree relatives with lung cancer 1 (1.4) 162 (1.7) 0.287 1 (1.4) 180 (2.9) 0.888

aValues are reported as mean ± SD (range). bThe detection rate of lung cancer in women is compared with that in men.

Mortality

Participants were followed-up from January 1, 2007 to January 31, 2020. The shortest follow-up time was 2.5 years, and the longest was 13 years. Up to the end of follow-up, 963 people lost their visit, the rate of which was 6.0%. There were 18 deaths of all the patients with lung cancer. The mortality rate was 12.7%. Lung cancer accounted for 55.5% of all the deaths in the study (Table 6). In addition, we plotted survival curves for patients with lung cancer (Fig. 1).

Table 6.

Causes of Death among Lung Cancer Patients

Cause of Death a Number/Total number (%)
Neoplasm of bronchus and lung 10/18 (55.5)
Respiratory illness 4/18 (22.2)
Multiple organ failure 3/18 (16.7)
Other 1/18 (5.6)

aCauses of death were categorized according to the codes in the International Classification of Diseases, 10th Revision (ICD-10)

Fig. 1.

Fig. 1

Survival curve of lung cancer patients

Discussion

The current lung cancer screening guidelines define high-risk groups in terms of age, smoking and so on [57, 23]. However, the high-risk factors of lung cancer are different between countries and regions [57, 23]. In order to know whether the current screening guidelines of lung cancer will cause missed diagnosis of lung cancer cases in the health examination population, we firstly conducted a real-world study using these screening guidelines in this Chinese population. Our results suggested that the current screening guidelines of lung cancer might miss some of the high-risk population in the health examination population. Several factors as following may contribute to this.

On the one hand, of 142 patients with lung cancer in our study, non-smokers accounted for 67.6%. In female patients with lung cancer, the proportion of non-smokers was even as high as 94.2%. Recently, a study in South Korea had reported that 84 (40.6%) out of 207 patients with lung cancer were never-smokers [24]. Moreover, a study in Japan also showed that 49.6% of patients with lung cancer occurring in never smokers might be missed if we only adopted the National Lung Screening Trial (NLST) criterion of smokers with ≥30 pack-years of smoking [25]. The different proportion of lung cancer in never smokers is probably due to different smoking prevalence of East Asian females with lung cancer (9.9% in South Korea, 17–25.6% in Japan, and 5.2% in China), which was significantly lower than that in Caucasian female patients (ranging from 53 to 91%) [2633]. Therefore, this may be the main reason why the missed diagnosis rate of lung cancer in this study is higher than that in previous studies abroad [10, 2634]. Although there were differences in the proportion of non-smoking patients with lung cancer in different countries, they all accounted for a high proportion. Therefore, according to the current lung cancer screening guidelines, this part of lung cancer cases will be missed diagnosis, especially female patients. Researches have shown that the incidence of lung cancer is related to many factors including genetic factors, smoking, environmental exposure, air pollution, and so on [9, 3542]. Generally, the vast majority (80%) of lung cancer cases are attributable to tobacco smoking [43, 44]. However, the global statistics estimate that 25% of all lung cancer cases worldwide are not due to smoking [10]. With the successful implementation of prevention and cessation programs of smoking, the proportion of lung cancer in non-smokers is expected to increase [8]. In addition, the epidemiological differences in lung cancer incidence and risk factors between Chinese and US populations suggest that inclusion of ambient air pollution exposure and gender into lung cancer risk prognostic models might better capture high-risk individuals, especially for non-smoking women [45]. Recently, a predicting lung cancer occurrence in never-smoking Asian females has been proposed [46].

On the other hand, of all lung cancers detected in our study, 28.1% patients were younger than 50 years, and 10.6% patients were older than 80 years. After further analysis by age and gender, we found that according to the age standard of lung cancer screening guidelines in China, the proportion of patients with lung cancer in men who met the criterion was 53.5%, and that in women was 47.9%. In other words, according to the Chinese standards, the proportion of male and female patients with lung cancer missed diagnosis were 46.5 and 52.1% respectively. In addition, according to age standard of lung cancer screening guidelines recommended by USPSTF, the proportion of lung cancer cases in male who met the criterion was 54.8%, and that in female was 42.1%. That is to say, based on the American Standards, the proportion of lung cancer cases missed diagnosis in men and women were 45.2 and 57.9% respectively. It can be seen that no matter which lung cancer screening guidelines you choose, there were many patients with lung cancer missed according to the age standard, especially female patients. Previous studies showed that the incidence of lung cancer in young adults were around 1.2 to 6.2% (less than 40 years), 5.3% (under 45 years), and 13.4% (less than 50 years) [4751]. Therefore, with an increasing incidence of lung cancer in young people, it have gradually become a disease group that can not be ignored [52, 53].

In addition, our study found that compared with patients with lung cancer in male, female patients with lung cancer have the following characteristics. Firstly, the detection rate of lung cancer in women is higher than that in men. Secondly, the prevalence of non-smoking lung cancer in women was much higher than that in men. Previous studies have also found that the proportion of women with non-smoking lung cancer is higher than that of men [10]. Global statistics estimate that 53% of lung cancers in female and 15% in male are not attributable to smoking [10]. Thirdly, the proportion of young people among female patients with lung cancer is higher than that among male patients with lung cancer. The feature in our study is consistent with earlier result reported in previous studies [21, 22].

Meanwhile, the result showed that there was a high rate of false positive in lung cancer screening with LDCT in our study. This was consistent with the results of the National Lung Screening Trial (NLST) [4]. Most of the false positive results might be due to the presence of non-calcified granulomas or benign intrapulmonary lymph nodes.

To our knowledge, this is the first real-world study to explore whether the current lung cancer screening guidelines are applicable to the health examination population in China. The missed diagnosis rate is very high whether using American or Chinese screening guidelines of lung cancer. Moreover, our study was a real-world cohort study with large sample size. The results could reflect the real clinical situation comprehensively and accurately. In this way, we could fully understand the gap between the guidelines and practice, and provide reference for the formulation and specification of the guidelines.

Our research also has some limitations. First, the study population mainly came from Chengdu and surrounding areas. Relevant research that includes other regions is needed. Second, our research population is mainly the staff of enterprises and institutions. Personnel structure is relatively single. We need to further enrich our personnel structure to reflect the situation more realistically. Finally, the follow-up time is too short to calculate the 5-year and 10-year survival rates together. Thus, we should extend the follow-up time to know the long-term survival rate of lung cancer.

At present, the wide-spread clinical implementation of LDCT is hampered by clinical and socio-economic limitations, and access and adherence to LDCT screening programmes in high-risk populations remains low [54]. New, more accessible screening methods might improve uptake and adherence. Recently, emerging data on the role of liquid biopsy in early-stage NSCLC suggested that ctDNA analyses might allow lung cancer detection and could be potentially integrated in currently screening programs [55].

Conclusions

This real-world study is the first research applied the current lung cancer screening guidelines to the health examination population in China. The results suggested that the rate of missed diagnosis was very high. In addition, our study also found that female patients with lung cancer have some characteristics when compared with patients with lung cancer in male. As shown in our data, further study to determine screening guidelines for targeted populations, is warranted.

Acknowledgments

We thank all study participants for their cooperation.

Abbreviations

USPSTF

U.S. preventive services task force

LDCT

Low-dose computed tomography

CT

Computed tomography

COPD

Chronic obstructive pulmonary disease

ICD-O-3

International classification of diseases for oncology, 3rd edition

AJCC

American joint committee on cancer

NLST

National lung screening trial

Authors’ contributions

GJ and YH are responsible for writing, collecting data, analysis, interpretation, revision and final approval of present article. TB, ZL, HT, DL, PY, WL are responsible for collecting data, analysis and revision. All authors have read and approved the final manuscript.

Funding

This manuscript was produced with the financial and other support of by the Research Fund for the National Key R&D Program of China (Grant No. 2017YFC0907501 and Grant No. 2017YFC0907504), National Natural Science Foundation of China (Nos. 81871890, 91859203 to W Li), and Sichuan International/Hong Kong, Macao and Taiwan Science and technology innovation cooperation project: molecular imaging research on targeted treatment of lung cancer (2018hh0161), Post-Doctor Research Project, West China Hospital, Sichuan University (2019HXBH085), Investigator-Initiated Clinicaltrial, West China Hospital, Sichuan University (HXCR20001). The funding agencies were not involved in the design and conduct of the study, nor in the collection, management, analysis, and interpretation of the data. It was not involved in the writing of the manuscript.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate

The Ethics Committee of the West China Hospital of Sichuan University, China, provided authorization for our study. Detailed information can be obtained from file No.195 approved in 2019. Written informed consent was obtained from each participant.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68:394–424. doi: 10.3322/caac.21492. [DOI] [PubMed] [Google Scholar]
  • 2.Woodard GA, Jones KD, Jablons DM. Lung Cancer staging and prognosis. Cancer Treat Res. 2016;170:47–75. doi: 10.1007/978-3-319-40389-2_3. [DOI] [PubMed] [Google Scholar]
  • 3.Flehinger BJ, Kimmel M, Polyak T, Melamed MR. Screening for lung cancer. The Mayo lung project revisited. Cancer. 1993;72:1573–1580. doi: 10.1002/1097-0142(19930901)72:5&#x0003c;1573. [DOI] [PubMed] [Google Scholar]
  • 4.Team NLSTR, Aberle DR, Adams AM, Berg CD, Black WC, Clapp JD, et al. Reduced lung-cancer mortality with low-dose computed tomographic screening. N Engl J Med. 2011;365:395–409. doi: 10.1056/NEJMoa1102873. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Moyer VA. U.S. preventive services task force. screening for lung cancer: U.S. preventive services task force recommendation statement. Ann Intern Med. 2014;160:330–338. doi: 10.7326/M13-2771. [DOI] [PubMed] [Google Scholar]
  • 6.U.S. Preventive Services Task Force. Lung cancer: screening. Recommendation summary. www.uspreventiveservicestaskforce.org. Published 2013 Accessed 2 May 2017.
  • 7.Cardiothoracic group, radiology branch, Chinese Medical Association. Expert consensus on low dose spiral CT lung cancer screening. Chin J Radiol. 2015:328–335.
  • 8.Sun S, Schiller JH, Gazdar AF. Lung cancer in never smokers--a different disease. Nat Rev Cancer. 2007;7:778–790. doi: 10.1038/nrc2190. [DOI] [PubMed] [Google Scholar]
  • 9.Akhtar N, Bansal JG. Risk factors of lung Cancer in nonsmoker. Curr Probl Cancer. 2017;41:328–339. doi: 10.1016/j.currproblcancer.2017.07.002. [DOI] [PubMed] [Google Scholar]
  • 10.Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics, 2002. CA Cancer J Clin. 2005;55:74–108. doi: 10.3322/canjclin.55.2.74. [DOI] [PubMed] [Google Scholar]
  • 11.Fidler MM, Gupta S, Soerjomataram I, Ferlay J, Steliarova-Foucher E, Bray F. Cancer incidence and mortality among young adults aged 20-39 years worldwide in 2012: a population-based study. Lancet Oncol. 2017;18:1579–1589. doi: 10.1016/S1470-2045(17)30677-0. [DOI] [PubMed] [Google Scholar]
  • 12.Kang HR, Cho JY, Lee SH, Lee YJ, Park JS, Cho YJ, et al. Role of low-dose computerized tomography in lung Cancer screening among never-smokers. J Thorac Oncol. 2019;14:436–444. doi: 10.1016/j.jtho.2018.11.002. [DOI] [PubMed] [Google Scholar]
  • 13.Peng YM, Cui HJ, Xu YB, Liu DW, Song YZ, Duan Y. A study on the incidence of lung cancer in the Sino-Japanese friendship hospital from 2005 to 2014. Chin Gen Pract. 2016;19:565–569. [Google Scholar]
  • 14.Yang P, Wang Y, Wampfler JA, Xie D, Stoddard SM, She J, et al. Trends in subpopulations at high risk for lung Cancer. J Thorac Oncol. 2016;11:194–202. doi: 10.1016/j.jtho.2015.10.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Wang Y, Midthun DE, Wampfler JA, Deng B, Stoddard SM, Zhang S, et al. Trends in the proportion of patients with lung cancer meeting screening criteria. JAMA. 2015;313:853–855. doi: 10.1001/jama.2015.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Team NLSTR, Aberle DR, Berg CD, Black WC, Church TR, Fagerstrom RM, et al. The National Lung Screening Trial: overview and study design. Radiology. 2011;258:243–253. doi: 10.1148/radiol.10091808. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Cagnon CH, Cody DD, McNitt-Gray MF, Seibert JA, Judy PF, Cody DD. Description and implementation of a quality control program in an imaging-based clinical trial. Acad Radiol. 2006;13:1431–1441. doi: 10.1016/j.acra.2006.08.015. [DOI] [PubMed] [Google Scholar]
  • 18.Gierada DS, Garg K, Nath H, Strollo DC, Fagerstrom RM, Ford MB. CT quality assurance in the lung screening study component of the National Lung Screening Trial: implications for multicenter imaging trials. AJR Am J Roentgenol. 2009;193:419–424. doi: 10.2214/AJR.08.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Fritz A, Percy C, Jack A, et al. Eds. International classification of diseases for oncology. 3rd. Geneva: World Health Organization; 2000. [Google Scholar]
  • 20.Amin MB, Edge SB, Greene FL, et al., editors. AJCC Cancer staging manual. 8. New York: Springer; 2017. [Google Scholar]
  • 21.Houston KA, Henley SJ, Li J, White MC, Richards TB. Patterns in lung cancer incidence rates and trends by histologic type in the United States, 2004-2009. Lung Cancer. 2014;86:22–28. doi: 10.1016/j.lungcan.2014.08.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Lewis DR, Check DP, Caporaso NE, Travis WD, Devesa SS. US lung cancer trends by histologic type. Cancer. 2014;120:2883–2892. doi: 10.1002/cncr.28749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Field JK, Smith RA, Aberle DR, Oudkerk M, Baldwin DR, Yankelevitz D, et al. International Association for the Study of Lung Cancer computed tomography screening workshop 2011 report. J Thorac Oncol. 2012;7:10–19. doi: 10.1097/JTO.0b013e31823c58ab. [DOI] [PubMed] [Google Scholar]
  • 24.Kim YW, Kang HR, Kwon BS, Lim SY, Lee YJ, Park JS, et al. Low-dose chest computed tomographic screening and invasive diagnosis of pulmonary nodules for lung cancer in never-smokers. Eur Respir J. 2020;56:2000177. doi: 10.1183/13993003.00177-2020. [DOI] [PubMed] [Google Scholar]
  • 25.Kakinuma R, Muramatsu Y, Asamura H, Watanabe S, Kusumoto M, Tsuchida T, et al. Low-dose CT lung cancer screening in never-smokers and smokers: results of an eight-year observational study. Transl Lung Cancer Res. 2020;9:10–22. doi: 10.21037/tlcr.2020.01.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Zhou F, Zhou C. Lung cancer in never smokers-the East Asian experience. Transl Lung Cancer Res. 2018;4:450–463. doi: 10.21037/tlcr.2018.05.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Cho J, Choi SM, Lee J, Lee CH, Lee SM, Kim DW, et al. Proportion and clinical features of never-smokers with non-small cell lung cancer. Chin J Cancer. 2017;36:20. doi: 10.1186/s40880-017-0187-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Yano T, Miura N, Takenaka T, et al. Never-smoking nonsmall cell lung cancer as a separate entity: clinicopathologic features and survival. Cancer. 2008;113(5):1012–1018. doi: 10.1002/cncr.23679. [DOI] [PubMed] [Google Scholar]
  • 29.Kosaka T, Yatabe Y, Endoh H, Kuwano H, Takahashi T, Mitsudomi T. Mutations of the epidermal growth factor receptor gene in lung cancer: biological and clinical implications. Cancer Res. 2004;64:8919–8923. doi: 10.1158/0008-5472.CAN-04-2818. [DOI] [PubMed] [Google Scholar]
  • 30.Tam IY, Chung LP, Suen WS, Wang E, Wong MC, Ho KK, et al. Distinct epidermal growth factor receptor and KRAS mutation patterns in non-small cell lung cancer patients with different tobacco exposure and clinicopathologic features. Clin Cancer Res. 2007;12:1647–1653. doi: 10.1158/1078-0432.CCR-05-1981. [DOI] [PubMed] [Google Scholar]
  • 31.Hsu LH, Chu NM, Liu CC, Tsai SYC, You DL, Ko JS, et al. Sex-associated differences in non-small cell lung cancer in the new era: is gender an independent prognostic factor? Lung Cancer. 2009;66:262–267. doi: 10.1016/j.lungcan.2009.01.020. [DOI] [PubMed] [Google Scholar]
  • 32.Mitsudomi T. Molecular epidemiology of lung cancer and geographic variations with special reference to EGFR mutations. Transl Lung Cancer Res. 2014;3:205–211. doi: 10.3978/j.issn.2218-6751.2014.08.04. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Kobrinsky NL, Klug MG, Hokanson PJ, Sjolander DE, Burd L. Impact of smoking on cancer stage at diagnosis. J Clin Oncol. 2003;21:907–913. doi: 10.1200/JCO.2003.05.110. [DOI] [PubMed] [Google Scholar]
  • 34.Ravipati HP, Mankikar R, Charaf C, Foreman M, Flenaugh E. Current lung Cancer screening guidelines may exclude high risk populations. Chest. 2014;146:593A. doi: 10.1378/chest.1994637. [DOI] [Google Scholar]
  • 35.Matakidou A, Eisen T, Houlston RS. Systematic review of the relationship between family history and lung cancer risk. Br J Cancer. 2005;93:825–833. doi: 10.1038/sj.bjc.6602769. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Spitz MR, Hong WK, Amos CI, Wu X, Schabath MB, Dong Q, et al. A risk model for prediction of lung cancer. J Natl Cancer Inst. 2007;99:715–726. doi: 10.1093/jnci/djk153. [DOI] [PubMed] [Google Scholar]
  • 37.Timofeeva MN, Hung RJ, Rafnar T. Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. Hum Mol Genet. 2012;21:4980–4995. doi: 10.1093/hmg/dds334. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Ahrendt SA, Chow JT, Yang SC, Wu L, Zhang MJ, Jen J, et al. Alcohol consumption and cigarette smoking increase the frequency of p53 mutations in non-small cell lung cancer. Cancer Res. 2000;60:3155–3159. [PubMed] [Google Scholar]
  • 39.Ragin C, Obikoya-Malomo M, Kim S, Chen Z, Flores-Obando R, Gibbs D, et al. HPV-associated lung cancers: an international pooled analysis. Carcinogenesis. 2014;35:1267–1275. doi: 10.1093/carcin/bgu038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Castro CY, Ostrowski ML, Barrios R, Green LK, Popper HH, Powell S, et al. Relationship between Epstein-Barr virus and lymphoepithelioma-like carcinoma of the lung: a clinicopathologic study of 6 cases and review of the literature. Hum Pathol. 2001;32:863–872. doi: 10.1053/hupa.2001.26457. [DOI] [PubMed] [Google Scholar]
  • 41.Shebl FM, Engels EA, Goedert JJ, Chaturvedi AK. Pulmonary infections and risk of lung cancer among persons with AIDS. J Acquir Immune Defic Syndr. 2010;55:375–379. doi: 10.1097/QAI.0b013e3181eef4f7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Kerr A, Eliason JF, Wittliff JL. Steroid receptor and growth factor receptor expression in human nonsmall cell lung cancers using cells procured by laser-capture microdissection. Adv Exp Med Biol. 2008;617:377–384. doi: 10.1007/978-0-387-69080-3_36. [DOI] [PubMed] [Google Scholar]
  • 43.Doll R, Hill AB. Smoking and carcinoma of the lung. Preliminary report. 1950. Bull World Health Organ. 1999;77:84–93. [PMC free article] [PubMed] [Google Scholar]
  • 44.Gandini S, Botteri E, Iodice S, Boniol M, Lowenfels AB, Maisonneuve P, et al. Tobacco smoking and cancer: a meta-analysis. Int J Cancer. 2008;122:155–164. doi: 10.1002/ijc.23033. [DOI] [PubMed] [Google Scholar]
  • 45.Yang D, Liu Y, Bai CX, Wang XD, Powell CA. Epidemiology of lung cancer and lung cancer screening programs in China T and the United States. Cancer Lett. 2020;468:82–87. doi: 10.1016/j.canlet.2019.10.009. [DOI] [PubMed] [Google Scholar]
  • 46.Chien LH, Chen CH, Chen TY, Chang GC, Tsai YH, Hsiao CF, et al. Predicting lung Cancer occurrence in never-smoking females in Asia: TNSF-SQ, a prediction model. Cancer Epidemiol Biomark Prev. 2020;29:452–459. doi: 10.1158/1055-9965.EPI-19-1221. [DOI] [PubMed] [Google Scholar]
  • 47.Zhang J, Chen SF, Zhen Y, Xiang J, Wu C, Bao P, et al. Multicenter analysis of lung cancer patients younger than 45 years in Shanghai. Cancer. 2010;116:3656–3662. doi: 10.1002/cncr.25100. [DOI] [PubMed] [Google Scholar]
  • 48.Subramanian J, Morgensztern D, Goodgame B, Baggstrom MQ, Gao F, Piccirillo J, et al. Distinctive characteristics of non-small cell lung cancer (NSCLC) in the young: a surveillance, epidemiology, and end results (SEER) analysis. J Thorac Oncol. 2010;5:23–28. doi: 10.1097/JTO.0b013e3181c41e8d. [DOI] [PubMed] [Google Scholar]
  • 49.Kuo CW, Chen YM, Chao JY, Tsai CM, Perng RP. Non-small cell lung cancer in very young and very old patients. Chest. 2000;117:354–357. doi: 10.1378/chest.117.2.354. [DOI] [PubMed] [Google Scholar]
  • 50.Liam CK, Lim KH, Wong CM. Lung cancer in patients younger than 40 years in a multiracial Asian country. Respirology. 2000:355–61. [PubMed]
  • 51.Ak G, Metintas M, Metintas S, Yildirim H, Erginel S, Alatas F. Lung cancer in individuals less than 50 years of age. Lung. 2007;185:279–286. doi: 10.1007/s00408-007-9021-2. [DOI] [PubMed] [Google Scholar]
  • 52.Strand TE, Malayeri C, Eskonsipo PKJ, Grimsrud TK, Norstein J, Grotmol T. Adolescent smoking and trends in lung cancer incidence among young adults in Norway 1954–1998. Cancer Causes Control. 2004;15:27–33. doi: 10.1023/B:CACO.0000016575.31651.b0. [DOI] [PubMed] [Google Scholar]
  • 53.Marugame T, Yoshimi I, Kamo K, Imamura Y, Kaneko S, Mizuno S, et al. Trends in lung cancer mortality among young adults in Japan. Jpn J Clin Oncol. 2005;35:177–180. doi: 10.1093/jjco/hyi054. [DOI] [PubMed] [Google Scholar]
  • 54.Okereke IC, Nishi S, Zhou J, Goodwin JS. Trends in lung cancer screening in the United States, 2016–2017. J Thorac Dis. 2019;11:873–881. doi: 10.21037/jtd.2019.01.105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Rolfo C, Russo A. Liquid biopsy for early stage lung cancer moves ever closer. Nat Rev Clin Oncol. 2020;17:523–524. doi: 10.1038/s41571-020-0393-z. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.


Articles from BMC Cancer are provided here courtesy of BMC

RESOURCES