We thank Dr. Hwang et al. from Korea for their thoughtful comments on our recent article (1). Our group recently published a study in the Heart, Lung and Circulation, reporting that natural course of persistent subsolid nodules (SSNs) in the term of true growth, substantial growth and stage shift (2). In this retrospective single-center study, we enrolled 128 persistent SSNs [93 pure ground-glass nodules (GGNs) and 35 part-solid nodules (PSNs)] 3 cm or smaller from 128 participants, and reported their observation during long-term follow-ups (average of 3.57 years, maximum follow-up period of 12 years). In this study, pure GGNs exhibited median natural progression times of 7, 9, and 12 years for true growth, substantial growth, and stage shift, respectively. However, PSNs exhibited median natural progression times of 3, 3, and 9 years for true growth, substantial growth, and stage shift, respectively.
In recent years, increasing utilization of low-dose computed tomography (CT) tools for lung cancer screening has resulted in a significant portion of SSNs detected in the screening population, especially in an Asian population with the high prevalence of non-smoking related lung cancer (3,4). Overall, most patients (approx. 70%) with lung adenocarcinoma were non-smokers in Taiwan, and most patients with clinical symptoms are diagnosed at an advanced stage with poor survival outcome despite recent developments in the target therapy of late stage lung cancer over recent years (5). In the meantime, recent studies demonstrated that almost over 90% of screened lung cancers were stage I lung cancer (mostly adenocarcinoma spectrums) with the excellent prognosis in the Asian non-smoking related lung cancer screening programs (3,6).
The difference between non-screened and screened non-smoking related lung cancers make us notice the heterogeneity in growth pattern and risk factors of lung cancer (7).
According to recent literature reviews, there were high prevalence of non-smoking related lung cancers found in the Asian lung cancer screening program (3,4,6). Most patients with lung cancers diagnosed in the screening program were not eligible for National Lung Screening Trial (NLST) criteria (3,8). Previous studies have demonstrated that family history and female gender are two important risk factors with non-smoking related lung cancer (3,4). In addition, the average PM2.5 levels in Taiwan were much higher than the levels in European cities according to the European Study of Cohorts for Air pollution Effects (ESCAPE), especially in Kaohsiung city (9). This issue of expanding screening eligibility criteria may be relevant in Taiwan because of regional genetic and environmental differences. Should never-smokers at increased risk for lung cancer be screened? Recent microsimulation study by Kelvin demonstrated that never-smokers with high risk (RRs of 15 to 35) have similar to better trade-offs between benefits and harms compared with population eligible for NSLT criteria (10). However, lung cancer screening is not beneficial for most never-smokers at low risk. Comparison of eligible populations for low-dose CT screening by NLST criteria in the US and Taiwan are summarized in Figure 1 according to previous several studies (3,8,11,12). In the future, it is mandatory to investigate the proportion of real-world data on the rate of non-smoking related lung cancer in the United State and prognostic benefit in Asian non-smoking LDCT screening program.
There is a high prevalence of SSNs variant in size in the Asian non-smoking related population than in the US according to the previous studies. (16.2% in Taiwan versus 3.7–4.2% in the US) (3,13,14). However, this is the dilemma in clinical management. Over-management/over-treatment these small SSNs could lead to overdiagnosis (15). On the other hand, some patients are very anxious about these SSN lesions and worry that follow-up policy will lead to delays in lung cancer diagnosis and treatment. In this study, most GGNs have the more indolent behavior of growth pattern. Our study results are in line with 2017 Fleischer guideline recommendation (16). Wait and see policy with longer follow-up period >5 year is recommended for GGN management (2). For PSNs, they have the more aggressive behavior of growth pattern than GGNs. In addition, our study result showed that substantial growth is the high correlative with the degree of invasiveness, suggestive of substantial growth reflects the pathological invasive component of adenocarcinoma. Recent studies have demonstrated that older age, history of lung cancer, initial size 8 mm or larger, presence of a solid component, and air bronchogram were independent risk factors for subsequent SSN growth (2,17). For these pure GGNs, the most important thing is to predict potential rapid-growing lesions. In the future, to develop the prediction model integrated with clinical characters, texture or volumetric analysis on radiomic features and genetic information for GGN growth prediction is warranted (18,19).
Conflicts of Interest: The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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