REVIEW ARTICLE
Carolyn C. Chang1*, Cyra-Yoonsun Kang2*, Evans M. Whitaker3, Henry Guo4, Natalie S. Lui1
1Department of Cardiothoracic Surgery, Stanford University Medical Center, Palo Alto, CA, USA; 2Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University Medical Center, Palo Alto, CA, USA; 3Lane Medical Library, Stanford School of Medicine, Palo Alto, CA, USA; 4Department of Radiology, Stanford University Medical Center, Palo Alto, CA, USA
Introduction: A growing trend of lung cancer diagnoses is occurring among Asians and Asian Americans who have never smoked, driving increased interest in implementing lung cancer screening (LCS) in this population. Current data, however, remain insufficient to support such efforts. This scoping review summarizes studies evaluating LCS using low dose computed tomography (LDCT) among Asians and Asian American nonsmokers, reporting lung cancer detection rates and highlighting the heterogeneity across studies that limits the generalizability of results.
Method: A scoping review was conducted of studies from East Asia and the United States that utilized LDCT to screen for lung cancer among Asians and Asian Americans or a subset of these populations. Data on study design, screening eligibility criteria, screening protocols, and primary outcomes, including lung cancer detection rates and stages, were extracted and summarized descriptively.
Results: A total of 1,334 studies published during 2003–2025 were identified. Of these, 28 met inclusion criteria and originated from Taiwan, Korea, Japan, China, and the United States. Among eight studies that included only Asian and Asian American individuals, four were prospective and four were retrospective. Twenty studies which included both smokers and Asian and Asian American participants were comprised of one randomized control trial, nine prospective, and ten retrospective studies. Substantial variation was observed in definitions of smoking status, screening eligibility criteria (including age thresholds), LDCT protocols, and nodule reporting and follow-up practices. Among the 28 studies, 24 reported lung cancer detection rates in the range of 0.05–4.1% among Asians and Asian Americans who had never smoked.
Conclusions: Although several studies have evaluated LCS using LDCT in Asians and Asian Americans who have never smoked, marked heterogeneity across study designs and protocols limits the ability to synthesize findings or draw meaningful conclusions. This review underscores these gaps and may inform the design and focus of future studies to guide evidence-based LCS recommendations for this population.
Key Words: lung cancer ◾ small cell lung carcinoma ◾ non-small cell lung carcinoma ◾ diagnosis ◾ screening ◾ low dose computed tomography ◾ Asian ◾ Asian American ◾ literature review
Citation: Journal of Asian Health. 2026;19(SUPPL):e123.
Copyright: © 2026 Journal of Asian Health, Inc. is published for open access under the license Creative Commons CC BY-NC 4.0 License. Authors have full copyright.
Received: June 30, 2025; Revised: October 17, 2025; Accepted: October 17, 2025; Published: January 23, 2026.
Competing interests and funding: Authors have no conflicts to declare and received no funding.
Correspondence to: Natalie S. Lui, Falk Cardiovascular Research Institute, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA. Email: natalielui@stanford.edu
While cigarette smoking remains the leading risk factor for lung cancer, approximately 20% of lung cancer deaths in the United States occur in individuals who have never smoked.1 This proportion is even higher in Asia, especially among women.2 Lung cancer is increasingly recognized to disproportionately impact Asian and Asian American women who have never smoked.3 One study suggests that Asians who have never smoked may face a risk of developing lung cancer comparable to that of high-risk smokers.4 However, these findings are difficult to interpret as the true incidence of lung cancer in individuals who have never smoked remains unclear due to the lack of smoking status data in most cancer registries.
Moreover, no established guidelines exist in Asia or the U.S. for lung cancer screening (LCS) using low dose computed tomography (LDCT) for Asians and Asian Americans who have never smoked. This gap largely stems from the fact that although LDCT screening has demonstrated survival benefits among populations with a significant smoking history,5 similar benefits have yet to be shown in Asians and Asian Americans who have never smoked. In addition, although race and sex are associated with lung cancer risk in Asians and Asian Americans who have never smoked, other contributing risk factors remain poorly understood.3 As a result, identifying the best candidates for screening continues to be a major challenge.
This challenge is evident in the differing approaches to screening taken by several Asian countries and in the U.S. In Asia, LDCT is both affordable and commonly used for routine health screening, allowing for opportunistic screening. However, broad inclusion is known to lead to over screening and overdiagnosis.6 In contrast, current U.S. guidelines from the United States Preventive Services Task Force (USPSTF) are more conservative. Studies indicate that over 75% of lung cancers in Asian populations in the U.S. are missed.7,8 Given that Asians and Asian Americans are among the largest and most diverse racial populations both in the U.S. and globally, there is a need for LCS guidelines tailored to Asians and Asian Americans who have never smoked.9,10
The first step in achieving this goal is to understand the patterns and gaps in the existing literature. In this scoping review, studies on LCS using LDCT in Asians and Asian Americans who have never smoked were assessed to detect trends in lung cancer detection rates, report study findings as related to the study populations, and to offer recommendations for future research.
Comprehensive searches of PubMed, Embase, Web of Science, and Scopus databases were iteratively developed using defined search terms and tested prior to conducting final searches (Supplemental Table 1). Inclusion and exclusion criteria were developed and tested prior to final article selection. Title and abstract screening followed by full text screening were performed by two independent reviewers. Included studies were those with primary data in either abstract form or full-text manuscripts that reported lung cancer detection rates in Asian and Asian American populations receiving LDCT (Table 1). Selected literature was limited to studies conducted in the U.S. and East Asia as several East Asian countries have implemented opportunistic screening programs and provide available data on never smoking populations.4 When overlapping study populations were identified, only the larger or more comprehensive study was included.
Once a data extraction form was developed and tested, two independent reviewers extracted data. Dispute resolution during screening and data extraction was achieved by discussion between reviewers prior to final data extraction. Literature was collected with Zotero (version 7.0, open source) reference management software and imported into Covidence systematic review software for article selection and data extraction. During data extraction, the following information was recorded: (1) details of publication (first author, year, region, study period, and study design); (2) screening eligibility and interval; (3) details of smoking (smoking status included and percentage of never or non-smokers; (4) demographics (mean age and gender); (5) family history of lung cancer; and (6) outcomes (positive screen, total lung cancer, or invasive cancer and stage 0–4).
Based on the search criteria, a total of 1,334 studies published during 2003–2025 were identified of which 71 articles were reviewed in detail and 28 studies selected for the final analysis in accordance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines11 (Figure 1). Of the final included studies, most were conducted in East Asia, including the countries of Taiwan, Korea, Japan, and China, with only one originating from the U.S. Notably, the U.S. study enrolled participants of Asian descent without specifying their regional origins.12 Among the eight studies that focused exclusively on individuals who have never smoked,12–19 four were prospective and four were retrospective (Table 2). Of the 20 studies that included both smokers and Asian and Asian American non-smokers in their screening populations,20–39 one was a randomized controlled trial, nine were prospective studies, and 10 were retrospective studies (Table 3).
| Inclusion criteria and protocol | Demographics | Results | |||||||||||||
| Author | Region | Study period | Age, yrs | LDCT interval | N | Age, mean | Male/Female (%) | FHx LC (%) | Positive screen (%) | Total lung cancer (%) | Invasive cancer (%) | Stage 0–1 (%) | Stage 2 (%) | Stage 3 (%) | Stage 4 (%) |
| Study design: Prospective | |||||||||||||||
| Li13 2025 |
Hong Kong | 2024 | 50–75 | Once | 273 | 62 | 181/ 273 (66.3) |
273 (100) | NA | NA | 3/273 (1.1) |
NA | NA | NA | NA |
| Liu14 2024 |
Taiwan | 2023 | 40–74 | Once every 3 years | 13,446 | NA | NA | NA | 949/ 13,446 (7.1) |
74/ 13,446 (0.6) |
NA | NA | NA | NA | NA |
| Shum12 2023 |
USA | 2021–2023 | 40–74 | Annual | 201 | 56.8 | 201/ 201 (100) |
83/ 201 (41.3) |
13/201 (6.5) |
NA | 3/201 (1.5) | 0/3 (0) |
2/3 (66) | 1/3 (33) | 0/3 (0) |
| Yang15 2018 |
Taiwan | 2014–2018 | 55–75 | Annual | 10,397 | 61.2 | 7,703/ 10,397 (74.1) |
4,449/ 10,397 (42.8) |
NA | 243/ 10,397 (2.3) |
198/ 10,397 (1.9) |
231/ 243 (stage I only) (95.1) |
4/243 (1.6) |
3/243 (1.2) | 5/243 (2.1) |
| Study design: Retrospective | |||||||||||||||
| Kim16 2018 |
Korea | 2002–2007 | 40–79 | Initial only | 4,365 | 51.1 | 4,365/ 4,365 (100) |
NA | NA | 22/ 4,365 (0.5) |
NA | 18/22 (81.8) |
0/22 (0) |
0/22 (0) |
2/22 (9.0) |
| Kim18 2025 |
Korea | 2009–2021 | 50–80 | Once | 21,062 | 59.8 | 16,133/ 21,062 (76.6) |
2,423/ 21,062 (11.5) |
1,291/ 21,062 (6.1) |
176,21,062(0.8) | NA | 164/ 176 (93.2) |
4/176 (2.3) | 5/176 (2.8) |
3/176 (1.7) |
| Lee19 2024 |
Korea | 2002–2022 | NA | At least once | 216,618 | NA | NA | NA | 203/ 216,618 (0.09) |
With FH 31/ 14,156 (0.2) |
NA | NA | NA | NA | NA |
| No FH 172/ 202,462 (0.08) |
|||||||||||||||
| Kim17 2023 |
Korea | 2009–2021 | 50–80 | Opportunistic | 13,084 | NA | 9,849/ 13,084 (75.3) |
NA | 2,513/ 13,084 (19.2) |
128/ 13,084 (1.0) |
NA | 111/ 128 (86.7) |
NA | NA | NA |
| Abbreviations: FHx LC = family history of lung cancer; FH = family history; MIA = minimally invasive adenocarcinoma; NS = never smokers; py = pack years; LDCT = low dose computed tomography. | |||||||||||||||
| Inclusion criteria and protocol | Demographics | Results | ||||||||||||||
| Author | Region | Study Period | Age, yrs | LDCT interval | N, total | Age, yrs | Female (%) | Never smoker (%) | FHxLC (%) | Positive screen (%) | Total lung cancer (%) | Invasive cancer (%) | Stage 0–1 (%) | Stage 2 (%) | Stage 3 (%) | Stage 4 (%) |
| Study design: Randomized control trial | ||||||||||||||||
| Rong39 2022 |
China | 2019 | 50–74 | 3 total LDCT at varying time intervals | 600 | 59.1 | 189/ 600 (31.5) |
185/ 600 (30.8) |
11/ 600 (1.8) |
131/ 600 (21.8) |
11/600 (1.8) |
MIA 2/600 (0.3) |
10/11 (90.9) |
0/11 (0) |
1/11 (9.1) |
0/11 (0) |
| Invasive adenocarcinoma 4/600 (0.7) |
||||||||||||||||
| Female NS 7/170 (4.1) |
NS- MIA 1/600 (0.2) |
NS 7/11 (63.6) |
||||||||||||||
| Subsolid 46/600 (7.7) |
Smokers 4/415 (1.0) |
Invasive adenocarcinoma 2/600 (0.3) |
||||||||||||||
| Study design: Prospective | ||||||||||||||||
| Chang20 2024 |
Taiwan | 2015–2019 | 55–75 | Annual for 2 years, biannual for 6 years | 12,011 | 61.2 | 8,868/ 12,011 (73.8) |
11,201/ 12,011 (93.3) |
6,009/ 12,011 (50.0) |
2,094/ 12,011 (17.4) |
318/ 12,011 (2.6) |
257/ 12,011 (2.1) |
307/ 318 (96.5) |
3/318 (0.9) |
3/318 (0.9) |
5/318 (1.6) |
| MIA 79/12,011 (0.7) |
||||||||||||||||
| Invasive adenocarcinoma 177/12,011 (1.5) |
||||||||||||||||
| Adenosquamous 1/12,011 (0.008) |
||||||||||||||||
| Li23 2022 |
China | 2013–2018 | High risk score 40–74 |
Once | 79,581 | 56.1 | 40,295/ 79,581 (50.6) |
31,991/ 79,581 (40.2) |
43,659/ 77,111 (56.6) |
NA | 531/ 79,581 (0.7) |
NA | 244/ 389 (62.7) |
27/ 389 (6.9) |
59/ 389 (15.2) |
59/ 389 (15.2) |
| NS 161/ 31,991 (0.5) |
||||||||||||||||
| Shao26 2022 |
China | 2021 | NA | Once | 12,360 | 58.1 | 8,169/ 12,360 (66.1) |
9,784/ 12,360 (79.2) |
329/ 12,360 (2.7) |
9,511/ 12,360 (77.0) |
86/ 12,360 (0.7) |
NA | 73/86 (84.9) | 6/86 (7.0) | 5/86 (5.8) | 2/86 (2.3) |
| NS 68/9,784 (0.7) |
||||||||||||||||
| Kakinuma22 2020 |
Japan | 2004–2012 | ≥40 | Annual | 12,114 | NS 57.9 |
4,820/ 12,114 (39.8) |
6,021/ 12,114 (49.7) |
NA | 5,155/ 12,114 (42.6) |
133/ 12,114 (1.1) |
45/ 12,114 (0.4) |
NA | NA | NA | NA |
| Smoking 58.2 | NS 66/ 6,021 (1.1) |
NS-MIA 22/6,021 (0.4) |
||||||||||||||
| Invasive adenocarcinoma 23/6,021 (0.4) |
||||||||||||||||
| Smokers- MIA 19/6,090 (0.3) |
||||||||||||||||
| Invasive adenocarcinoma 25/6,090 (0.4) | ||||||||||||||||
| Shan25 2020 |
China | 2014–2017 | ≥40 | Once | 9,084 | 55 | 3,885/ 9,084 (42.8) |
4,102/ 9,084 (45.2) |
157/ 9,084 (1.7) |
NA | 54/ 9,084 (0.6) |
NA | 53/54 (stage I–II) (98.1) |
1/54 (1.9) | 0/54 (0) | 0/54 (0) |
| NS 1,912/ 4,102 (46.6) |
NS 97/ 4,102 (2.4) |
NS 20/ 4,102 (0.5) |
||||||||||||||
| Zhang29 2020 |
China | 2012–2018 | All ages | Once | 8,392 | NA | 5,908/ 8,392 (70.4) |
7,509/ 8,392 (89.5) |
NA | NA | 179/ 8,392 (2.1) |
131/ 8,392 (1.6) |
174/ 179 (97.2) |
2/179 (1.1) | 2/179 (1.1) | 1/179 (0.6) |
| NS 167/ 7,509 (2.2) |
MIA 67/8,392 (0.8) |
|||||||||||||||
| Wu28 2016 |
Taiwan | 2013–2014 | >40 | Once | 1,763 | Male 55.5 | 734/ 1,763 (41.6) |
1,074/ 1,763 (60.9) |
297/ 1,763 (16.8) |
64/ 1,763 (3.6) |
25/ 1,763 (1.4) |
NA | 22/25 (88.0) |
2/25 (8.0) | 0/25 (0) | 1/25 (4.0) |
| Female: 57 |
NS 23/ 1,515 (1.5) |
|||||||||||||||
| Nojo24 2009 |
Japan | 2000–2007 | 40–59 | Annual | 28,687 | NA | NA | 9,405/ 28,687 (32.8) |
NA | NA | 13/28,687 (0.05) | NA | 11/13 (84.6) | 0/13 (0) | 1/13 (7.7) | 0/13 (0) |
| NS 5/9,405 (0.05) |
||||||||||||||||
| Chong21 2005 |
Korea | 1999–2003 | ≥45 | At least once | 6,406 | 55 | 876/ 6,406 (13.7) |
1,472/ 6,406 (23.0) |
NA | 2,255/ 6,406 (35.2) |
23/ 6,406 (0.4) |
NA | 13/23 (56.5) | 1/23 (4.3) |
5/23 (21.7) | 2/23 (8.7) |
| Py <20 |
||||||||||||||||
| NS 8/1472 (0.5) |
||||||||||||||||
| Study design: Retrospective | ||||||||||||||||
| Tang37 2024 |
China | 2006–2022 | ≥ 18 | Opportunistic | 30,468 | 48.9 | 13,864/30,468 (45.5) | 21,426/ 30,468 (70.3) |
4,936/3 0,468 (16.2) |
11,749/ 30,468 (38.6) |
289/ 30,468 (0.9) |
NA | Ever 73.8% |
NA | Ever 8.8% (Stage III or IV) |
|
| NS 8,321/ 21,426 (38.8) |
NS 218/ 21,426 (1.0) |
NS 78.8% |
NS 4.2% (Stage III or IV) |
|||||||||||||
| Wang38 2024 |
China | 2017–2020 | 20–80 | Once | 42,028 | NA | 17,437/42,018 (41.5) | 32,595/ 42,018 (77.6) |
NA | 1,119/ 42,018 (2.7) |
258/ 42,018 (0.6) |
NA | 225/ 258 (87.2) |
9/258 (3.5) | 9/258 (3.5) |
11/ 258 (4.3) |
| NS 880/ 32,595 (2.7) |
NS 212/ 32,595 (0.7) |
NS 190/ 258 (73.6) |
||||||||||||||
| Im32 2023 |
Korea | 2008–2018 | NA | NA | 59,094 | NA | NA | 23,089/ 59,094 (39.1) |
NA | NA | 763/ 59,094 (1.3) |
NA | NA | NA | NA | NA |
| NS 269/ 23,089 (1.2) |
||||||||||||||||
| Wang27 2023 |
China | 2013–2019 | High risk- score40–74 | Once | 11,521 | NA | 3,997/ 11,521 (34.7) |
3,636/ 11,521 (31.6) |
4,560/1 1,521 (39.6) |
NA | 197/ 11,521 (1.7) |
NA | 114/ 197 (57.9) |
NA | NA | NA |
| NS 3,636/ 3,636 (100) |
NS 2,305/ 3,636 (63.4) |
NS 54/ 3,636 (1.5) |
NS 42/54 (77.8) |
|||||||||||||
| Hamaguchi30 2021 |
Japan | 2009–2019 | ≥40 | At least once | 25,189 | NA | 10,503/ 25,189 (41.7) |
NA | NA | NA | 82/ 25,189 (0.3) |
NA | 60/82 (73.2) |
Ever 8/82 (9.8) |
Ever 3/82 (3.7) |
Ever 6/82 (7.3) |
| NS 41/NA |
NS 37/41 (90.2) |
NS 1/41 (2.4) |
NS 0/41 (0) |
NS 0/41 (0) |
||||||||||||
| Kim35 2020 |
Korea | 2009–2018 | ≥18 | Opportunistic | 37,436 | 49.5 | 13,609/37,436 (36.4) | 17,968/ 37,436 (48.0) |
NA | 6,066/ 37,436 (16.2) |
207/ 37,436 (0.6) |
NA | 159/ 207 (76.8) |
Ever 8/123 (6.5) |
Ever 11/123 (8.9) |
Ever 16/123 (13.0) |
| NS 2,908/ 17,968 (16.2) |
NS 84/ 17,968 (0.5) |
NS 75/84 (89.3) |
NS 3/84 (3.6) |
NS 3/84 (3.6) |
NS 3/84 (3.6) |
|||||||||||
| Hsu31 2018 |
Taiwan | 2013–2014 | 40–80 | Once | 1,978 | 56.6 | 894/ 1,978 (45.2) |
1,440/ 1,978 (72.8) |
404/ 1,978 (20.4) |
74/ 1,978 (3.7) |
32/ 1,978 (1.6) |
26/1,97 8 (1.3) |
29/32 (90.6) |
2/32 (6.3) |
0/32 (0%) |
1/32 (3.1) |
| MIA 6/1,978 (0.3) |
||||||||||||||||
| NS 30/ 1,440 (2.1) |
Invasive adenocarcinoma 20/1,97 8 (1.0) |
|||||||||||||||
| Kang34 2018 |
Korea | 2003–2016 | NA | Once | 28,807 | 52.1 | 29.5 | 12,176 (42.2) | NA | NA | 198/ 28,807 (0.7) |
135/ 28,807 (0.5) |
142/ 198 (71.7) |
Ever 12/ 143 (8.4) |
Ever 15/ 143 (10.5) |
Ever 25/ 143 (17.5) |
| NS 48/ 12,176 (0.4) |
||||||||||||||||
| MIA 7/12,176 (0.06) |
||||||||||||||||
| NS 55/ 12,176 (0.5) |
Invasive adenocarcinoma 11/ 12,176 (0.09) |
NS 51/55 (92.7) |
NS 2/55 (3.6) |
NS 0/55 (0) |
NS 2/55 (3.6) |
|||||||||||
| Ju33 2013 |
Korea | 2006–2011 | >55 | Once | 1,587 | 62.7 | 495/ 1,587 (31.2) |
1,092/ 1,587 (68.8) |
NA | 336/ 1,587 (21.1) |
8/336 (2.3) | NA | 5/8 (62.5) |
0/8 (0) |
1/8 (12.5) |
1/8 (12.5) |
| NS 218/ 1,092 (20.0) |
NS 4/218 (1.8) |
NS 3/4 (75.0) |
||||||||||||||
| Li36 2003 |
Japan | 1996–1999 | NA | At least once LDCT in 3 years (some had annual scans) | 7,847 | NS 64.2 |
3,559/ 7,847 (45.4) |
4,251/ 7,847 (54.2) |
NA | NA | 84/ 7,847 (1.1) |
NA | NA | NA | NA | NA |
| Smoking 68 |
NS 3,310/ 4,251 (77.9) |
NS 45/4,251 (1.1) |
||||||||||||||
| Abbreviations: FHx LC = family history of lung cancer; FH = family history; F/U = Follow up; MIA = minimally invasive adenocarcinoma; NS = never smokers; py = pack-years; LDCT = low dose computed tomography. | ||||||||||||||||
Figure 1. Literature Selection Flow Diagram.
In most of the studies, never-smoking status was not clearly defined,14–17,20,21,23–33,36,38,39 although some studies defined never-smokers as having never smoked or having smoked fewer than 100 cigarettes in a lifetime.12,13,18,19,22,34,35,37
The age range for screening eligibility varied across studies; most included individuals aged 40–74 years, though some did not specify age criteria.19,26,32,34,36 Notably, one study offered screening to participants of all ages,29 and three studies included individuals aged 18 years.35,37,38
Risk factors used to determine screening eligibility also differed across studies. Two studies recruited only women of Asian descent.12,16 A family history of any cancer or specifically lung cancer13–15,20,23,25,26,28,37,39 as well as a personal history of breast cancer,14 were considered in some studies. A history of chronic lung diseases, particularly pulmonary tuberculosis or chronic obstructive pulmonary disease was used as a qualifying factor in several studies.15,20,23,26,28,37
Information on occupational exposures, including asbestos, rubber, dust, pesticides, radiation, beryllium, uranium, and radon, were also collected to estimate their impact on lung cancer risk.23,37,39 Long-term exposure to workplace pollution14,37 and self-reported exposure to particulate matter23 were also included in some risk profiles. Several studies assessed cooking index or considered cooking without ventilation.14,15,20,39 One study used a specific risk score developed for participant Asians and Asian Americans who have never smoked to determine eligibility. The risk score uniquely considered not only environmental exposures but also lifestyle choices as well as family history.23 Three studies incorporated serum biomarkers alongside screening.12,15,22
Screening interval varied across studies and was largely dependent on the duration of the study period. Most studies implemented a one-time LDCT or conducted screening at least once during the study period13,14,16,18–21,23,25–31,33,34,36,38,39 while others performed annual screening throughout the study12,15,22,24 or offered opportunistic screening.17,35,37 One study implemented annual screening for 2 years, followed by biannual screening for 6 years.20 Variability in screening interval led to inconsistent follow-up definitions across the studies, which prevented determining time from screening to diagnosis.12,21 While some studies reported a mean or median follow-up duration, the corresponding endpoints were unclear16–18,23,24,27,28,31–33,37 and others did not specify any followup.13,14,15,22,29,30,34–36,38,39 Importantly, imaging protocols varied widely; some studies reported both collimation and slice thickness parameters,21,30,33 whereas several did not specify any imaging parameters.20,34
Positive screening results were often defined as the presence of a non-calcified nodule measuring equal to or greater than 4 mm in diameter, consistent with criteria from the U.S. based multi-center National Lung Cancer Screening Trial (NLST), funded by the National Cancer Institute/National Institutes of Health2,12,14,18,28,31,35,38,39 However, definitions of positive scans varied across studies including varying nodule size thresholds;1,15,22,25,33,34,37 some studies did not specify or report rates of positive scans.13,16,19,23,24,29,30,32,36
Pulmonary nodules detected through screening were generally classified and managed according to the Lung Imaging Reporting and Data System (Lung-RADS), a standardized classification system recognized internationally, using the most current version at the time of publication in each study;16–18,20,31,33–35 other studies did not specify classification methods 12,14,15,19,21–26,28,29,32,36–39 one study applied the guidelines from the Japanese Society of computed tomography (CT) Screening,30 and two studies used artificial intelligence–based software for nodule evaluation.13,26
Among the 28 studies, 24 reported lung cancer detection rates among Asians and Asian Americans who have never smoked, which ranged from 0.05 to 4.1%.24,39 Twelve of these studies15,20,22,25,27,29,31–33,36,39 reported rates comparable to or higher than those observed in the NLST trial.5 Most detected cases were Stage 0–1 lung cancers, with only a few diagnosed at stage 3 or 4 (Tables 2 and 3). Studies included varying subtypes of invasive adenocarcinomas across studies, with only some studies considering minimally invasive adenocarcinoma as its own classification,15,18,20,22,29,31,34,39 whereas others did not specify invasive cancer rates.14,23–28,37,38 None of the included studies reported mortality rates.
This scoping review included 28 studies of LCS with low-dose computed tomography (LDCT) in Asians and Asian Americans who have never smoked. The existing literature is marked by substantial heterogeneity, including variations in screening inclusion criteria, use and reporting of terminology (e.g. a consistent definition of never-smoker), utilization of varying screening LDCT protocols and screening intervals, follow-up reporting, and histologic stratification and staging, all of which limit meaningful comparisons and data pooling. Despite these limitations, this review of the literature highlights the comparable lung cancer detection rates among Asians and Asian Americans who have never smoked as compared with smokers,5 reinforcing the clinical relevance.
The Taiwan Lung Cancer Screening in Never-Smoker Trial (TALENT) was the largest to demonstrate high lung cancer detection rates among Asians who have never smoked.20 The results of 1-year follow up after the LDCT screening revealed a lung cancer detection rate of 2.6% in Asians who have never smoked, which is notably higher than the 1.1% observed in the U.S.-based NLST in high-risk individuals who smoked.5,20 A 2024 meta-analysis further contextualized and expanded upon the TALENT findings by comparing lung cancer risk between Asians and Asian American who have never smoked and those with a history of smoking. The analysis revealed that female individuals who have never smoked had comparable pooled-lung cancer incidence compared with individuals with a history of smoking.4
Despite elevated lung cancer detection rates, the mortality benefits (i.e. reduction in death rates through detection and intervention) of LCS among Asians and Asian Americans who have never smoked remain unclear. Current decision-making relies largely on population-based observational studies that are not sufficiently designed or powered to demonstrate mortality benefit. However, of the 28 studies, we identified one randomized controlled trial,39 which evaluated LCS in Asians and Asian Americans who have never smoked. Participants aged 50–75 years with at least one risk factor, including ≥30 pack-years of smoking with <15 years since quitting, ≥20 years of passive smoking exposure, or a family history of lung cancer in never-smokers, were randomized into three groups: no intervention; LDCT at baseline, 1 year, and 2 years; and LDCT at baseline, 1 year, and 3 years. The study reported a lung cancer detection rate of 4.1% among never-smoking females with passive smoke exposure compared with 1.0% in current smokers.39 While notable as the only apparent published RCT to date focused on Asians and Asian Americans who have never smoked, its small sample size and lack of defined follow-up limit the ability to assess mortality benefit. In the absence of demonstrated mortality benefit, advocating for screening in a historically low-risk population continues to be a major challenge. However, recent evidence has shown that an absolute reduction in late-stage cancers correlates with reduced lung cancer mortality, suggesting that stage distribution may serve as a surrogate endpoint for future studies.40
Additional concerns regarding LCS in Asians and Asian Americans who have never smoked are overdiagnosis and lead time bias (i.e. the perception that screening may have prolonged survival). A study using data from the Taiwan Cancer Registry found that after the implementation of screening in never-smoking Asian women, the incidence of early-stage lung cancer increased more than sixfold, while the rate of advanced-stage cancers remained unchanged.6 This pattern is consistent with this review’s findings that most screen-detected cancers were diagnosed at early stages (Tables 2 and 3), which suggests that LCS in this population may not have a mortality benefit. However, the prevalence of minimally invasive and invasive adenocarcinomas remains a concern and will require longer follow-up to better understand the natural history. The indolent nature of early-stage adenocarcinoma has raised the possibility of lead-time bias. Yet, emerging evidence suggests that adenocarcinoma may not always follow a predictable, stepwise progression; some lesions may behave more aggressively and unpredictably.41 In addition, the wide variability in invasive cancer detection rates across studies highlights the potential value of refining risk stratification among individuals who have never smoked. For example, one study enrolled Asians and Asian Americans who have never smoked with at least one of the following risk factors: family history of lung cancer, passive smoke exposure, history of tuberculosis or chronic obstructive pulmonary disease, a cooking index ≥110 (i.e. prolonged exposure to cooking fumes), or cooking without ventilation. This group demonstrated an invasive lung cancer detection rate of 1.9%.15
Studies underway are beginning to investigate the unique biology, genetics, and clinical behavior of lung cancer in the never smoking population.4 In parallel, several prediction models tailored for screening individuals who have never smoked are being developed and validated.42–47 These ongoing efforts can strengthen the rationale for screening the never smoking population. In the U.S., the Female Asian Never Smokers (FANS) Study seeks to identify risk factors for lung cancer among Asian American women who have never smoked.48 Complementing this effort, the Female Asian Never Smokers Screening Study (FANSS) is assessing lung cancer detection rates in Asian and Asian American women who have never smoked and has reported a 1.5% invasive cancer detection rate in preliminary findings.12 These initiatives may help refine screening strategies and inform future guidelines for this understudied population.
To enhance the generalizability of future studies, consensus is needed on the definitions of never-smokers, screening eligibility criteria, and LDCT protocols and frequency. Incorporating smoking status into large cancer registries will also be essential for accurately estimating lung cancer incidence among never-smokers and for providing more robust evidence to support current findings. Finally, large randomized controlled trials remain the gold standard for assessing mortality benefit, although their implementation is challenging due to substantial cost and time requirements.
With growing evidence of lung cancer among Asians and Asian Americans who have never smoked, concerns have emerged regarding the adequacy of current LCS paradigms, which primarily target individuals with a history of smoking. This scoping review of the current literature on screening in Asians and Asian Americans who have never smoked highlights the considerable heterogeneity across these studies, which hinders our ability to accurately assess specific screening needs of these populations. Ongoing efforts to standardize terminology, LDCT protocols, and screening frequency are critical and represent an essential first step toward generating robust evidence to support screening in these populations.
This study was exempt from institutional review board approval.