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Repeat lung cancer screenings reveal less CXR abnormalities with different variations than first-time screening

Tatsuo Kimura

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

Shinya Fukumoto

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Akemi Nakano

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Hideki Fujii

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Yuji Nadatani

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Yukie Tauchi

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Shingo Takashima

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Yuko Nishii

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Koji, Otani

Department of Gastroenterology, Graduate School of Medicine, Osaka City University, Osaka, Japan

Naomi Ageshio

Department of Diagnostic and Interventional Radiology, Graduate School of Medicine, Osaka City University, Osaka, Japan

Tomohiro Suzumura

Department of Clinical Oncology, Graduate School of Medicine, Osaka City University, Osaka, Japan

Norifumi Kawada

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, Osaka, Japan

Department of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan

DOI: 10.15761/HPC.1000210

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Abstract

Objectives: Chest radiography (CXR) is the most common screening procedure for the detection of lung cancer. A comparative CXR review can help to detect new shadows. Participants (pts) who undergo repeated screening at the same facility as the health check-up can receive a comparative review of the CXR. It has been hypothesized that the diagnosis of CXR abnormalities in screening would be different when compared to previous CXR and when not.

Methods: We retrospectively analyzed one-year cohort derived from the ongoing MedCity21 health check-up registry. The pts with abnormalities requiring medication in CXR were invited to our clinic for chest computed tomography (CT). We compared the varieties of abnormalities on CXR between repeated and first-visit pts using chi-square tests.

Results: A total of 13,690 repeated / first visits of 7872 / 5818 (57.5 / 42.5%) pts were enrolled. The CXR abnormalities included 324 of 143 / 191 pts and 234 of 108 / 126 pts who underwent chest CT, respectively. Repeated pts had a significantly lower proportion of abnormalities in CXR that required medication than the first-visit pts (p < 0.01). CT confirmation revealed that CXR abnormalities in repeated pts were diagnosed with different variations compared to those of first-time pts. Repeated pts had a significantly lower proportion of old inflammatory changes (p=0.02) and a higher proportion of acute inflammatory shadow (p=0.02) than first-visit pts.

Conclusions: Immediate confirmation by CT revealed that CXR abnormalities in repeated pts were diagnosed with different variations compared to those of first-visit pts. A comparative review of previous CXR may be highly effective in ruling out lung cancer.

Key words

health check-up, lung cancer screening, CXR abnormalities, repeater

Abbreviations

CXR: Chest X ray; pts: participants, CT: computed tomography; LDCT: low dose CT, GGO: Ground glass opacity; MLP: Mayo Lung Project

Introduction

Lung cancer is the third most common form of cancer and the leading cause of cancer-related deaths in both men and women in Japan. Smoking, exposure to secondhand smoke, a family history of lung cancer, procedures leading to exposure to radiation such as imaging tests, environmental exposure to air pollution, and workplace exposure to asbestos and arsenic can all increase the risk of lung cancer [1]. Although avoiding risk factors may lower patient risk, it does not mean that all lung cancers can be prevented. As people age, they spend more time exposed to environmental factors, and their chances of developing cancer increase accordingly. Therefore, routine health check-ups are important. Early diagnosis improves cancer outcomes by providing care at the earliest possible stage.

The American Cancer Society recommends yearly lung cancer screening with an low-dose CT (LDCT) for certain people at higher risk of lung cancer who meet the following conditions: aged 55 to 74 years and in good health, currently smoking or having quit smoking in the past 15 years and have at least a 30 pack-year smoking history [2]. However, people who are not at higher risk of lung cancer, lung cancer must be screened using chest X ray (CXR) in residential or workplace health examinations. When previous CXR had old inflammatory shadows such as tuberculosis, calcification, and fibrotic change, it would become increasingly difficult to detect newly occurring lung cancer.

A comparative review of the CXR with the previous one helps in the detection of a new shadow. Pts who undergo repeat health check-ups at the same facility can receive a comparative review of the CXR. It has been hypothesized that the diagnosis of CXR abnormalities in screening would be different when compared to previous CXR and when not. To clarify this, we conducted a retrospective cohort study in a large Japanese population to clarify the merits of comparative review in CXR, as well as a variety of chest abnormalities in CXR screening.

Participants and methods

Study population

We analyzed one-year cohort derived from the ongoing MedCity21 health examination registry from January 1 to December 31, 2019. Participants aged 20 years or older who were receiving a course including CXR were enrolled. Our clinic, “MedCity21,” is a university outpatient clinic which performs complete health check-up. Pts with abnormalities that require medical care detected on CXR were immediately announced by call for recommendation for further examination and encouraged to visit our facility to undergo further examination by chest CT scan. The pts who previously visited MedCity21 to undergo a health check-up with CXR were called “repeated pts,” and pts who visited MedCity21 for the first time were called “first-visit pts.” This study was conducted in accordance with the tenets of the Declaration of Helsinki. The registry protocol of the MedCity21 health examination and this retrospective observational study protocol was approved by the Ethics Committee of Osaka City University Graduate School of Medicine (approval No. 2927 and No. 2020-087, respectively). We performed an opt-out option, as explained in the instructions posted on the website of our facility.

Clinical assessment

CXR was performed using a direct radiography system (Radnext 50; Hitachi Healthcare Systems Inc., Tokyo, Japan) in the posterior-anterior (120 kV, 200 mA) and lateral positions (120 kV, 320 mA). Two doctors, board-certified in internal medicine specialty, respiratory medicine, and oncology, reviewed the CXR results using 3M monochrome monitor (RadiForce GX340, EIZO Corporation, Ishikawa, Japan). For baseline screening, the results of the initial CXR were categorized into five categories according to the criteria of the Japan Society of Ningen Dock [3]: A: Normal. B: Slightly abnormal. Nothing to worry about at present, or merely a deviation from normal that is not detrimental to your health. C: Require follow-up. There is a slight problem, but it is not serious now, and if you make the necessary changes, it is easily treated. D: Medical care needed. and E: On treatment. The abnormal shadows of category D in lung fields were classified into eight items, and those outside the lung field were classified into two categories. The items included nodular shadow 5 mm in diameter, ground glass opacity (GGO), granular shadow, reticular or interstitial shadow, cystic shadow, linear shadow including atelectasis, infiltration shadow, and pleural sign (pleural thickening, effusion, and pneumothorax), mediastinum abnormality, and cardiovascular system.

CT images were reviewed by two doctors certified as radiologists or oncologists. A CT device (Supria, Hitachi Healthcare Systems Inc., Tokyo, Japan) was used at 120 kV, 30-250 mA of normal dose, scan time 0.75 S/rot, 1.25 times 16 collimation, table pitch of 1.3125, slice/interval 5 / 5 mm, and the same monitor as described above. The abnormalities in CXR were diagnosed by CT and classified into 10 items and others: old inflammatory change, nodules including GGO, granular shadow, acute inflammatory change, interstitial lung disease, pleural disease, nipples, bone shadow including bone island in the rib and spine of vertebrae, cardiovascular system, and soft tissue (fat, muscle, etc.). If an abnormality was noted on CXR but not on CT, it was classified as “no abnormality”.

Patients with small nodules should undergo tailored follow-up according to guidelines [4]. Briefly, in the CT scans, if all solid or partly solid noncalcified pulmonary nodules or GGOs were less than 10.0 mm in diameter, a follow-up CT examination was performed 3 months later. On CT, none of the nodules grew over 10.0 mm in diameter, and CT was repeated 6 months later. In principle, a patient with a nodule 10 mm in diameter or larger, or a pleural sign, was referred to a specialized outpatient at Osaka City University Hospital or another equivalent hospital for further examinations. In the case of other diseases, we referred pts to the appropriate hospitals. In each case, doctors conferred with patients to decide on a course of action. Follow-up data were retrieved from the MedCity21 health examination registry and referral letters from other hospitals at approximately 1 year of complete follow-up.

Statistical analysis

The baseline characteristics of the repeated and first-visit patients were compared using a chi-squared test. We also compared the varieties of shadows on CT scans between repeat and first-visit pts using chi-square tests. Statistical significance was set at p <0.05. Statistical analyses were conducted using GraphPad PRISM for Windows version 5.0.1 software (GraphPad Software, San Diego, CA, USA).

Results

Participant characteristics

A total of 13,690 pts was enrolled, including 6,622 men (48.4%) and 7,068 women (51.6%) (Table 1). Pts ages ranged from 20 to 90 years, with a median age of 51 years, and the 25-75 percentile was 43-60 years.   Four lung cancer cases were found. One was male and three were female. One of them was a smoker. The detection rate was 29.2 / 100,000. All cases were resected and revealed stage I adenocarcinoma. There were 7816 (57.1%) non-smokers, 3821 (27.9%) ex-smokers, 1821 (13.3%) smoked pts less than 20 cigarettes per day, and 232 (1.7%) smoked pts more than 21 cigarettes per day (15.0%). Smoking was significantly less common among women than among men (p<0.01).

Table 1. Participant’s characteristics

 

All

Male

Female

p

N

13690

6622

7068

 

Age

median (range)

51 (20-90)

52

50

N.S.

25-75 percentile

43-60

     

<65

(lung cancer)

11918

5621(1)

6297

 

>65

(lung cancer)

1772

1001

771(3)

 

Tabacco use

         

Never smoked

(lung cancer)

7816

2341(1)

5475(2)

<0.01*

Past smoker

 

3821

2728

1093

 

Current smoker 1-20/day

(lung cancer)

1821

1337

484(1)

 

Current smoker 21</day

 

232

216

16

 

*Smoking was significantly less common among women than among men (p<0.01)

The numbers of repeated and first-visit pts were 7,872 (57.5%) and 5,818 (42.5%), respectively (Figure 1). Category D in CXR included a total of 334 (2.4%) of 143 repeated pts and 191 first-visit pts. Repeated pts had a low proportion of abnormalities requiring further examination (p<0.01). After the announcement by call for recommendation for further examination, a total of 234 pts (70.1%) of 108 / 126 patients received chest CT scans in our facility.

Figure 1. The number of repeated and first-visit participants with chest X ray abnormalities requiring further examination

A: Normal. B: Slightly abnormal. C: Require follow-up. D: Medical care needed; E: On treatment

*Repeated pts had a low proportion of abnormalities requiring further examination (p<0.01).

Abnormalities detected by chest X ray

Figure 2a shows the classification of CXR abnormalities by repeated and first-visit pts. A total of 234 of 108 repeated and 126 first-visit pts who underwent chest CT scans in our clinic were analyzed for abnormalities. Nodular shadows were the most frequently noted shadows on CXR in both repeated (70.4%) pts and first-visit (71.4%) pts. The second most frequently noted shadow was a GGO in both repeated (12.0%) and first-visit (8.7%) pts. The following were granular 2.8 / 6.3%, reticular 0.0 / 4.0%, cystic 0.0 / 2.4%, linear 1.9 / 0.8%, infiltration 11.1 / 0.8%, pleural 0.9 / 2.4%, mediastinum 0.9 / 1.6%, and cardiovascular 0.0 / 1.6%, respectively. There was no significant difference in the distributions between the repeated and first-visit pts.

Figure 2. Classification of CXR abnormalities that required further examination and diagnoses by chest CT

The black and gray bars represent repeated and first-visit participants (pts), respectively. The abnormalities detected by CXR were classified into ten items (a) The most frequently noted shadows were nodular shadows in repeated (70.4%) and first-visit (71.4%) pts (*p<0.01). CT scan revealed that the CXR abnormalities could be classified into 12 items. (b) Repeated pts had a significantly lower rate of old inflammatory change of 11.1 / 22.2% (p=0.02) and a higher rate of acute inflammatory shadow of 14.8 / 4.8% (p=0.02) than first-visit pts.

Diagnoses by chest CT

CT revealed CXR abnormalities (Figure 2b). CT scan revealed that the most frequently noted shadow was a bone shadow in both sets of pts. The second most frequently noted shadow was a granular shadow in repeated pts and old inflammatory changes in first-visit pts. The third most frequently noted shadow was acute inflammatory change in repeated pts and nodules, including GGO in first-visit pts. Repeated pts had a significantly lower proportion of old inflammatory changes (p=0.02), and a higher proportion of acute inflammatory shadow than first-visit pts (p=0.02). The percentages of diagnosis of repeated/first-visit pts on chest CT were as follows: old inflammatory 11.2 / 22.2%, nodules including GGO 8.3 / 11.1%, granular 15.7 / 7.9%, acute inflammatory 14.8 / 4.8%, interstitial lung disease 0.0 / 3.2%, pleural 8.3 / 7.9%, nipple 6.5 / 1.6%, bone 19.4 / 23.0%, cardiovascular 2.8 / 7.9%, soft tissue 4.6 / 1.6%, others 2.8 / 4.0%, and no abnormality 3.7 / 6.3%, respectively.

Discussion

Repeated pts had a significantly lower proportion of abnormalities requiring further examination in CXR than the first-visit pts. Immediate confirmation by CT revealed that CXR abnormalities in repeated pts were diagnosed with different variations compared to those of first-visit pts. On CXR as category D, the repeated pts had a significantly lower proportion of old inflammatory changes and a higher proportion of acute inflammatory shadows than first-visit pts. This means that the repeated pts may benefit from a decrease in false-positives and an increase in true-positives.

For a comparative review of the previous CXR, annual visits to health check-ups are recommended. A visit interval may be estimated by the speed of tumor growth based on tumor doubling time. In a review of the natural history of lung cancer over time, the mean tumor volume doubling time is approximately 135 days for patients diagnosed during routine medical care, 150 days in screening studies involving CXR, and 480 days in screening studies involving CT [5]. Most reports show doubling times in the range of 100 to 300 days for lung cancer [6,7]. In fact, in our study, all lung cancer cases were resected and revealed stage I adenocarcinoma. Subsolid pulmonary nodules, comprising pure GGO and part-solid nodules, have a high risk of indolent malignancy [8]. Indeed, in the extended follow-up of the Mayo Lung Project (MLP), the median survival for patients with resected early-stage disease was 16.0 years in the intervention arm, versus 5.0 years in the usual-care arm, with better survival for individuals in the intervention arm [9].

In our study, CT revealed that the most frequent abnormality was bone shadow. The second most frequent abnormality was granular shadows in repeated pts and old inflammatory changes in first-visit pts. Bone shadows may or may not be visible, depending on the slight difference in body position for CXR. A granular shadow due to old tuberculosis may not change over many years. Indeed, the prostate, lung, colorectal, and ovarian cancer screening trial revealed the most common non-cancer abnormalities in CXR were granuloma (10.7%), scarring/pulmonary fibrosis (8.2%), and bone/soft tissue lesions (5.5%) [10]. 

In our study, the lung cancer detection rate was 29.2 / 100,000 and this was small compared to the incidence rate of 99.1 / 100,000 in 2017 [11]. There may be several reasons for this. First, after the announcement by call for recommendation for further examination, about 70% of the patients with CXR abnormalities in both groups visited our facility for CT scan. The remaining 30% ignored the announcement or were observed by another clinic; therefore, we could not determine a diagnosis. Second, the repeated pts exceeded the majority and had a significantly lower rate of CXR abnormalities than the first-visit patients. The lung cancer incidence among repeated pts may be lower than the statistical data. Third, since the incidence of lung cancer is extremely low, the number of lung cancer cases is small and within the margin of error.

Several limitations must be considered when interpreting our study results. This was a one-year, single-center study. However, in our facility, the 2018 cohort had no significant differences compared to the 2019 cohort in terms of participants characteristics and the distribution of shadows in CXR and diagnoses by CT, which were reported previously [12]. Second, a referral bias was considered. The repeated pts included those who had been seen three or more times. Third, CT was not included in the primary screening content in this study. Public lung cancer screening has aimed at reducing mortality in the population, but a self-paying optional complete health check-up aims for longevity in the individual. In future, in Japan, since health insurance provides additional support, most CT scans will be added. Fourth, screening tests can yield false-negative results. If we miss it once, subsequent misidentification is more likely.

In conclusion, immediate confirmation by CT revealed a difference in the proportion of CXR abnormalities between repeated and first-visit patients. We believe that regular physical examinations performed at the same facility are highly effective in ruling out lung cancer. A comparative review of previous CXR may be highly effective in avoiding unnecessary further examination. This will help improve lung cancer screening.

Author Contributions

Conceptualization: Tatsuo Kimura,

Data curation: Tatsuo Kimura, Shinya Fukumoto, Akemi Nakano, Hideki Fujii, Yuji Nadatani, Yukie Tauchi, Shingo Takashima, Yuko Nishii, Koji Otani, Naomi Ageshio

Supervision: Shinya Fukumoto, Yuji Nadatani, Norifumi Kawada,

Formal analysis: Naomi Ageshio, Tomohiro Suzumura,

Methodology: Tatsuo Kimura

Writing original draft: Tatsuo Kimura

Writing-review and editing: Tatsuo Kimura, Shinya Fukumoto, Akemi Nakano, Hideki Fujii, Yuji Nadatani, Yukie Tauchi, Shingo Takashima, Yuko Nishii, Koji Otani, Tomohiro Suzumura

Project administration: Tatsuo Kimura

Acknowledgements

The authors thank Mrs. Utsunomiya, Mr. Kusumi, and Mr. Miyao for help in data collection and Mrs. Sakama for secretary work.

Financial support statement

This work was supported by a Grant-in-Aid for Scientific Research (C) from JSPS KAKENHI 19K10579.

Conflict of interest statement

The authors declare that they have no financial conflicts of interest.

References

  1. https://www.cancer.gov/types/lung/patient/lung-prevention-pdq
  2. Wender R, Fontham ET, Barrera E, Colditz GA, Church TR, et al. (2013) American Cancer Society lung cancer screening guidelines. CA Cancer J Clin 63: 107-117. [Crossref]
  3. https://www.ningen-dock.jp/en/other/inspection
  4. Wood DE, Kazerooni EA, Baum SL, Eapen GA, Ettinger DS, et al. (2018) Lung Cancer Screening, Version 3.2018, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw 16: 412-441. [Crossref]
  5. Detterbeck FC, Gibson CJ (2008) Turning gray: the natural history of lung cancer over time. J Thorac Oncol 3: 781-792. [Crossref]
  6. Usuda K, Saito Y, Sagawa M, Sato M, Kanma K, et al. (1994) Tumor doubling time and prognostic assessment of patients with primary lung cancer. Cancer 74: 2239-2244. [Crossref]
  7. Yankelevitz DF, Kostis WJ, Henschke CI, Heelan RT, Libby DM, et al. (2003) Overdiagnosis in chest radiographic screening for lung carcinoma: frequency. Cancer 97: 1271-1275. [Crossref]
  8. Hammer MM, Palazzo LL, Kong CY, Hunsaker AR (2019) Cancer Risk in Subsolid Nodules in the National Lung Screening Trial. Radiology 293: 441-448. [Crossref]
  9. Marcus PM, Bergstralh EJ, Fagerstrom RM, Williams DE, Fontana R, et al. (2000) Lung cancer mortality in the Mayo Lung Project: Impact of extended follow-up. J Natl Cancer I 92: 1308-1316. [Crossref]
  10. Pinsky PF, Freedman M, Kvale P, Oken M, Caporaso N, et al. (2006) Abnormalities on chest radiograph reported in subjects in a cancer screening trial. Chest 130: 688-693. [Crossref]
  11. https://ganjoho.jp/reg_stat/statistics/dl/index.html#mortality
  12. Kimura T, Fukumoto S, Nakano A, Fujii H, Nadatani Y, et al. (2020) Repeat lung cancer screenings by chest X ray have a profit for the avoidance of further examinations (abstract number: OOP-5-1). In: The 27th International Health Evaluation and Promotion Association and The 4th World Congress on Ningen Dock, Yokohama, Japan.

Editorial Information

Editor-in-Chief

Kohei Akazawa
Niigata University Medical and Dental Hospital, Japan

Article Type

Research Article

Publication history

Received date: April 17, 2021
Accepted date: April 26, 2021
Published date: April 29, 2021

Copyright

©2021 Kimura T. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Kimura T, Fukumoto S, Nakano A, Fujii H, Nadatani Y, et al. (2021) Repeat lung cancer screenings reveal less CXR abnormalities with different variations than first-time screening. Health Prim Car 5: doi: 10.15761/HPC.1000210

Corresponding author

Tatsuo Kimura, M.D. Ph.D.

Department of Premier Preventive Medicine, Graduate School of Medicine, Osaka City University, 1-1-43 AbenoHARUKAS 21F, Abenosuji, Abeno-ku Osaka 545-6090, Japan.

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

Figure 1. The number of repeated and first-visit participants with chest X ray abnormalities requiring further examination

A: Normal. B: Slightly abnormal. C: Require follow-up. D: Medical care needed; E: On treatment

*Repeated pts had a low proportion of abnormalities requiring further examination (p<0.01).

Figure 2. Classification of CXR abnormalities that required further examination and diagnoses by chest CT

The black and gray bars represent repeated and first-visit participants (pts), respectively. The abnormalities detected by CXR were classified into ten items (a) The most frequently noted shadows were nodular shadows in repeated (70.4%) and first-visit (71.4%) pts (*p<0.01). CT scan revealed that the CXR abnormalities could be classified into 12 items. (b) Repeated pts had a significantly lower rate of old inflammatory change of 11.1 / 22.2% (p=0.02) and a higher rate of acute inflammatory shadow of 14.8 / 4.8% (p=0.02) than first-visit pts.

Table 1. Participant’s characteristics

 

All

Male

Female

p

N

13690

6622

7068

 

Age

median (range)

51 (20-90)

52

50

N.S.

25-75 percentile

43-60

     

<65

(lung cancer)

11918

5621(1)

6297

 

>65

(lung cancer)

1772

1001

771(3)

 

Tabacco use

         

Never smoked

(lung cancer)

7816

2341(1)

5475(2)

<0.01*

Past smoker

 

3821

2728

1093

 

Current smoker 1-20/day

(lung cancer)

1821

1337

484(1)

 

Current smoker 21</day

 

232

216

16

 

*Smoking was significantly less common among women than among men (p<0.01)