Abstract
Background
COPD is considered an independent risk factor for lung cancer. COPD and lung cancer are both very heterogeneous diseases, and the study herein investigates the link between COPD phenotypes and specific histological subtypes of lung cancer.
Methods
This case–control study comprised 2,283 patients with newly diagnosed pathological lung cancer and 2,323 non-lung cancer controls. All participants underwent pulmonary function tests. The diagnosis of COPD was based on Global Initiative for Chronic Obstructive Lung Disease criteria. Subtypes of the two diseases were categorized according to 2015 World Health Organization classification of lung cancer and computer quantification of airway collapse on maximum expiratory flow volume. ORs were estimated using logistic regression analysis.
Results
The prevalence of COPD was higher (32.8%) in lung cancer patients compared to controls (16.0%). After adjustment for age, sex, body-mass index, and smoking status, the presence of COPD significantly increased the risk of lung cancer (OR 2.88, 95% CI 2.48–3.34) and all common histological subtypes (ORs 2.04–5.26). Both emphysema-predominant and non-emphysema-predominant phenotypes of COPD significantly increased the risk of lung cancer (OR 4.43, 95% CI 2.85–6.88; OR 2.82, 95% CI 2.40–3.31). Higher risk of squamous-cell carcinoma and small-cell lung cancer was observed in patients with the emphysema-predominant than the non-emphysema-predominant phenotype (OR 1.73, 95% CI 1.03–2.89; OR 3.74, 95% CI 1.64–8.53).
Conclusion
COPD was an independent risk factor for lung cancer and all common histological subtypes. Both emphysema-predominant and non-emphysema-predominant phenotypes of COPD significantly increased the risk of lung cancer. Relative to non-emphysema-predominant phenotype of COPD, emphysema-predominant phenotype had a higher risk of squamous-cell carcinoma and small-cell lung cancer.
Keywords: lung cancer, COPD, risk, phenotype, histology
Introduction
Lung cancer and COPD are common pulmonary diseases. Lung cancer is the most common cancer and the leading cause of cancer death worldwide. In 2012, an estimated 1.8 million new cases and 1.5 million lung cancer deaths occurred globally,1,2 among which a third occurred in China.3,4 COPD is another devastating disease that causes progressive and ultimately fatal deterioration of lung function over time. In 2010, the number of COPD cases increased to 384 million worldwide.5 In China, it became a topic of increasing concern.6 COPD and lung cancer have become the third- and fifth-most common cause of deaths globally, respectively.7 The economic and social burdens associated with these diseases have indicated dramatic increases.8,9
Lung cancer and COPD are interrelated pulmonary diseases.10 They share many common risk factors, such as cigarette smoking and other inhalation hazards from occupational, domestic, or outdoor air pollution.11–15 The association between COPD and lung cancer risks has been studied extensively over the last 30 years. It has been demonstrated that reduction in forced expiratory volume in 1 second (FEV1) is associated with an increase in the risk of lung cancer.16,17 Lung cancer incidence among COPD patients with smoking history also appears very high (16.7 per 1,000 person-years).18 Moreover, epidemiological studies have found that COPD could increase the risk of lung cancer by two- to sixfold, regardless of smoking habits.19–21 Several studies have attempted to summarize possible mechanistic links between COPD and lung cancer. There are numerous arguments supporting a common physiopathology between the two diseases, such as inflammation, extracellular matrix proteolysis, oxidative stress, telomere shortening, and genetic predisposition.22–27 However, the exact mechanism connecting the two pathologies remains unclear and needs to be investigated further.
Lung cancer and COPD are heterogeneous diseases with different pathological changes. Lung cancer is characterized by abnormal cell behavior, such as increased proliferation, invasion, and angiogenesis. The World Health Organization (WHO) has classified lung cancer into several subtypes.28 On the other hand, COPD is characterized by persistent respiratory symptoms and airflow limitation. The major pathological changes in COPD include emphysema and airway remodeling.29,30 Researchers have pointed out that the heterogeneous nature of the two diseases has largely hampered progress toward uncovering this mechanistic link.24,31 There is an urgent requirement to clarify the link between COPD phenotypes and histological subtypes of lung cancer.
Generally, subtypes of lung cancer are categorized merely according to histopathology, while phenotypes of COPD can be classified in many ways, such as clinical, pathophysiologic, and radiographic methods.32,33 Traditionally, according to dominant pathological changes, patients with COPD can be divided into two most common phenotypes: emphysema-predominant and airway-predominant.34 Quantitative computed tomography (QCT) is a common diagnostic method used to derive COPD pathological phenotypes.30 However, QCT is not routinely available for patients with chronic airway disease. Furthermore, the high cost and complicated nature of the procedure limits its usage in retrospective clinical studies. Computer quantification of airway collapse (AC) on maximum expiratory flow volume (MEFV) curve is an alternative and reproducible method to predict the presence of emphysema that facilitates the identification of the emphysema-predominant phenotype of COPD.35–37
We attempted to gain insight into more specific links between lung cancer and COPD to gain an understanding of the mechanistic link between the two diseases. In this study, we validated the relationship between COPD and lung cancer risk in larger samples, and further explored the link between COPD phenotypes and the risk of specific histological subtypes of lung cancer.
Methods
Subjects
A case–control study was performed using the clinical database of Qilu Hospital, Shandong University, Jinan from 2004 to 2015. Patients with newly pathology-diagnosed lung cancer were enrolled. Non-lung cancer controls were collected from patients undergoing lung-function screening in the corresponding period. All participants underwent pulmonary function tests (PFTs) and chest CT scans. Patients were excluded if they had a history of asthma, bronchiectasis, tuberculosis, pulmonary fibrosis, or other confounding diseases. Data on age, sex, body-mass index (BMI), smoking history, lung cancer histology, chest CT, and other medical information were carefully collected for all subjects in the study. Pulmonary function-test data were exported from the MasterLab system (Jaeger, Höchberg, Germany). As a retrospective study, all data were anonymous. We declare that patients’ data were confidential and did not compromise patient interests. After the approval of the ethics committee of Qilu Hospital of Shandong University (2015091), informed consent from participants was not required.
Lung cancer diagnosis and histological classification
Lung cancer was diagnosed based on preoperative and/or postoperative histopathology reports, and was categorized as adenocarcinoma, squamous-cell carcinoma (SCC), small-cell lung cancer (SCLC), large-cell carcinoma, large-cell neuroendocrine carcinoma (LCNC), adenosquamous carcinoma, carcinoid tumors, and other histological types. SCLC, LCNC, and carcinoid tumors were grouped together into neuroendocrine tumor types according to the WHO classification of lung cancer.28 The exclusion of lung cancer in the control group was done by an experienced radiologist and pulmonologist based on chest CT scan and clinical information.
Assessment of COPD and COPD severity
All participants (lung cancer and controls) underwent PFTs performed by respiratory physicians. The Global Initiative for Chronic Obstructive Lung Disease (GOLD; 2005–2015) criteria were used to diagnose COPD and assign grades of severity: patients with postbronchodilator values of FEV1/forced vital capacity (FVC) <0.7 were classified as COPD, FEV1 ≥0.8 as mild, 0.5≤ FEV1 <0.8 moderate, 0.3≤ FEV1 <0.5 severe, and FEV1 ≤0.3 extremely severe.29
Identification of COPD phenotypes
AC on MEFV curve of diagnosed COPD patients was evaluated based on Topalovic’s method of computer quantitative measurement.36 Raw PFT data points (sampling every 40 mL volume) of MEFV curves were exported from the MasterLab system and analyzed by the computer model. AC measurements were conducted under standard procedures using a computer model based on MatLab 8.5 (MathWorks, Natick, MA, USA). The procedure was performed according to previous work.37 A few COPD patients whose raw PFT data were not available were excluded from further analysis. Studies have demonstrated that sharp AC in the MEFV curve is an indicator of emphysema.35,36 According to our previous study, AC 137° was chosen as an optimal cutoff point for categorizing COPD phenotypes: emphysema-predominant (AC ≤137°) and non-emphysema-predominant (AC >137°).
Statistical analysis
Quantitative data are expressed as means ± SD. Qualitative data are described using relative frequencies. Statistical differences between cases and controls and between-group differences were evaluated by χ2 tests or Student’s t-test. Multivariable logistic regression was used to estimate ORs and 95% CIs for lung cancer and for each histological subtype associated with COPD or COPD phenotypes. Univariate analysis was performed on age, sex, BMI, smoking status, presence of COPD, grade of COPD clinical severity, and COPD phenotype as independent variables. These variables were subsequently introduced into a multivariate model to eliminate the possibility of mutual confounding. P=0.05 was considered statistically significant. All statistical analyses were performed using SPSS version 19.0.
Results
Participant characteristics
A total of 4,606 participants were collected from March 2004 to December 2015: 2,283 lung cancer cases and 2,323 non-lung cancer controls. The characteristics of participants are shown in Table 1. There was no significant difference in age, sex, or smoking status between lung cancer patients and controls (P=0.110, 0.061, and 0.745, respectively). Significantly higher prevalence of COPD was observed in lung cancer patients (32.8% [748]) compared to controls (16% [371], P<0.001). Furthermore, similar differences between lung cancer patients and controls were revealed in each grade of COPD. Histological subtypes found were adenocarcinoma (1,120 [49.1%]), SCC (792 [34.7%]), neuroendocrine carcinoma (192 [8.4%], SCLC 152 [9.6%], LCNC 20 [0.9%], and carcinoid tumors 20 [0.9%]), large-cell carcinoma (58 [2.5%]), adenosquamous carcinoma (46 [2.0%]), and other histological types (14 [0.6%]). More than 90% of lung cancers were at an early stage (stage IA–IIB).
Table 1.
Characteristics of cases and controls
| Lung cancer cases (n=2,283) |
Non-lung cancer controls (n=2,323) |
P-value | |
|---|---|---|---|
| Age, years (mean ± SD) | 60.3±9.5 | 59.8±9.7 | 0.110 |
| Sex, n (%) | 0.061 | ||
| Male | 1,719 (75.3) | 1,804 (77.7) | |
| Female | 564 (24.7) | 519 (22.3) | |
| BMI, kg/m2 (mean ± SD) | 24.2±3.5 | 23.4±3.4 | <0.001 |
| Smoking status, n (%) | 0.745 | ||
| Current and ex-smokers | 1,225 (53.7) | 1,258 (54.2) | |
| Nonsmokers | 1,058 (46.3) | 1,065 (45.8) | |
| COPD, n (%) | |||
| No | 1,535 (67.2) | 1,952 (84.0) | <0.001 |
| Yes | 748 (32.8) | 371 (16.0) | <0.001 |
| Mild | 554 (24.3) | 305 (13.1) | <0.001 |
| Moderate | 163 (7.1) | 62 (2.7) | <0.001 |
| Severe/extremely severe | 31 (1.4) | 4 (0.2) | <0.001 |
| Histologic subtype, n (%) | |||
| Adenocarcinoma | 1,120 (49.1) | NA | |
| Squamous carcinoma | 792 (34.7) | NA | |
| Neuroendocrine carcinoma | 192 (8.4) | NA | |
| SCLC | 152 (6.6) | NA | |
| LCNC | 20 (0.9) | NA | |
| Carcinoid tumors | 20 (0.9) | NA | |
| Large-cell carcinoma | 58 (2.5) | NA | |
| Adenosquamous carcinoma | 46 (2.0) | NA | |
| Other subtypes@ | 14 (0.6) | NA | |
| Unclassified carcinoma | 61 (2.7) | NA | |
| Lung cancer stage, n (%) | |||
| I | 1,651 (72.3) | NA | |
| II | 467 (20.5) | NA | |
| III–IV | 165 (7.2) | NA |
Note:
Other subtypes include sarcomatoid carcinoma and pulmonary melanoma.
Abbreviations: BMI, body-mass index; SCLC, small-cell lung cancer; LCNC, large-cell neuroendocrine carcinoma; NA, not applicable.
Computed quantitative measurements of AC were performed on a total of 1,008 (90.1%) COPD patients (including lung cancer patients and controls). Briefly, 110 emphysema-predominant phenotypes (AC 129.2°±6.9°) and 898 non-emphysema-predominant phenotypes (AC 150.9°±7.1°) in COPD patients were identified. Patients with emphysema-predominant phenotypes had worse lung function (P<0.001), were older (P=0.024), and more of them were male (P=0.028) compared to patients with the non-emphysema-predominant phenotype. Proportions of SCC and SCLC were also significantly higher among patients with the emphysema-predominant phenotype. Other characteristics of the two phenotypes are shown in Table 2.
Table 2.
Characteristics of COPD phenotypes
| Emphysema-predominant (n=110) |
Non-emphysema-predominant (n=898) |
P-value | |
|---|---|---|---|
| Age, years (mean ± SD) | 64.6±7.8 | 62.6±8.4 | 0.024 |
| Sex, n (%) | 0.028 | ||
| Male | 104 (94.5) | 785 (87.4) | |
| Female | 6 (5.5) | 113 (12.6) | |
| BMI, kg/m2 (mean ± SD) | 23.0±3.7 | 23.3±3.4 | 0.348 |
| Smoking status, n (%) | 0.445 | ||
| Current and ex-smokers | 72 (65.5) | 622 (69.3) | |
| Nonsmokers | 38 (34.5) | 276 (30.7) | |
| AC (mean ± SD) | 129.2±6.9 | 150.9±7.1 | <0.001 |
| FEV1, L (mean ± SD) | 1.4±0.4 | 2.1±0.6 | <0.001 |
| FVC, L (mean ± SD) | 2.9±0.7 | 3.3±0.8 | <0.001 |
| FEV1/FVC, % (mean ± SD) | 50.0±9.6 | 63.2±5.5 | <0.001 |
| Lung cancer subtype, n (%) | 82 (74.5) | 596 (66.4) | |
| Adenocarcinoma | 17 (15.5) | 229 (25.5) | 0.533 |
| Squamous carcinoma | 41 (37.3) | 270 (30.1) | 0.033 |
| Neuroendocrine carcinoma | 12 (10.9) | 54 (5.9) | 0.027 |
| SCLC | 11 (10.0) | 46 (5.1) | 0.028 |
| LCNC | 1 (0.9) | 4 (0.4) | 0.366 |
| Carcinoid tumors | NA | 4 (0.4) | NA |
| Large-cell carcinoma | 3 (2.7) | 17 (1.9) | 0.404 |
| Adenosquamous carcinoma | 1 (0.9) | 7 (0.8) | 0.516 |
| Other subtypes@ | 1 (0.9) | 4 (0.4) | 0.366 |
| Unclassified carcinoma | 7 (6.4) | 15 (1.7) | 0.044 |
| Non-lung cancer, n (%) | 28 (25.5) | 302 (33.6) | 0.086 |
Note:
Other subtypes include sarcomatoid carcinoma and pulmonary melanoma.
Abbreviations: AC, airway collapse; BMI, body-mass index; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; LCNC, large-cell neuroendocrine carcinoma; SCLC, small-cell lung cancer; NA, not applicable.
Associations between COPD and lung cancer risk
Lung cancer risk factors are shown in Table 3. In univariate analysis, the presence of COPD was associated with an increased risk of lung cancer (OR 2.56, 95% CI 2.23–2.95). Multivariable logistic regression analysis revealed that after age, sex, BMI, and smoking-status adjustment, the presence of COPD was an independent risk factor for lung cancer (OR 2.88, 95% CI 2.48–3.34). After adjustment for age, sex, BMI, and smoking status, with increased COPD severity, the risk of lung cancer was significantly increased (OR 2.24, 95% CI 1.99–2.51). In the same multivariable logistic regression model, female sex was also a risk factor for lung cancer.
Table 3.
Risk factors for lung cancer
| Univariate analysis | Logistic regression@ | |||||
|---|---|---|---|---|---|---|
|
|
|
|||||
| OR | 95% CI | P-value | OR | 95% CI | P-value | |
| COPD | 2.56 | 2.23–2.95 | <0.001 | 2.88 | 2.48–3.34 | <0.001a |
| COPD grading | 2.06 | 1.84–2.29 | <0.001 | 2.24 | 1.99–2.51 | <0.001b |
| Emphysema-predominant COPD | 3.72 | 2.41–5.75 | <0.001 | 4.43 | 2.85–6.88 | <0.001c |
| Non-emphysema-predominant COPD | 2.51 | 2.15–2.93 | <0.001 | 2.82 | 2.40–3.31 | <0.001d |
| Age | 1.01 | 0.99–1.01 | 0.110 | 1.00 | 0.99–1.00 | 0.605a |
| BMI | 1.07 | 1.05–1.09 | <0.001 | 1.08 | 1.06–1.11 | <0.001a |
| Sex | 1.14 | 0.99–1.31 | 0.059 | 1.32 | 1.12–1.56 | 0.001a |
| Smoking status | 0.98 | 0.87–1.10 | 0.735 | 1.00 | 0.87–1.15 | 0.988a |
Notes:
There were four multivariable logistic regression models: COPD (dichotomous, referent non-COPD), COPD grading (continuous, increase), emphysema-predominant COPD phenotype (dichotomous, referent non-COPD), and non-emphysema-predominant COPD phenotype (dichotomous, referent non-COPD) distributed in models 1–4, respectively. Age (continuous, increase), BMI (continuous, increase), sex (dichotomous, referent male) and smoking status (dichotomous, referent nonsmoking) were common variables of models 1–4,a model 1,b model 2,c model 3,d and model 4.
Abbreviation: BMI, body-mass index.
Relationships between COPD and risk of different lung cancer subtypes
Lung cancer subtypes are presented in Table 4. After adjustment for age, sex, BMI, and smoking status, the presence of COPD indicated increased risk by two- to fivefold for each histological subtype of lung cancer compared with non-COPD. Among the most common subtypes, the odds for increased risk of SCLC were extremely high (OR 5.14, 95% CI 3.58–7.39), followed by LCNC (OR 4.35, 95% CI 1.68–11.3), SCC (OR 3.51, 95% CI 2.90–4.23), large-cell carcinoma (OR 3.41, 95% CI 1.94–5.98), and adenocarcinoma (OR 2.11, 95% CI 1.74–2.55); Additionally, the presence of COPD increased the risk of neuroendocrine lung carcinoma by 4.28-fold (OR 4.28, 95% CI 3.20–5.73). Moreover, after adjustment, with increased COPD severity, risks of the aforementioned subtypes were also significantly increased.
Table 4.
Risk factors for different histological subtypes of lung cancer@
| Squamous carcinoma& | Adenocarcinoma& | Neuroendocrine carcinoma& | SCLC& | LCNC& | |
|---|---|---|---|---|---|
| COPDa | 3.51 (2.90–4.23)# | 2.11 (1.74–2.55)# | 4.28 (3.20–5.73)# | 5.14 (3.58–7.39)# | 4.35 (1.68–11.3)# |
| COPD gradingb | 2.53 (2.20–2.29)# | 1.72 (1.49–2.00)# | 2.92 (2.41–3.61)# | 3.32 (2.61–4.22)# | 3.69 (2.04–6.68)# |
| Emphysema-predominant phenotypec | 5.96 (3.44–9.41)# | 2.01 (1.07–3.79)# | 8.73 (4.47–17.1)# | 11.9 (5.58–25.5)# | 9.80 (1.10–82.3)# |
| Non-emphysema-predominant phenotyped | 3.40 (2.78–4.17)# | 2.26 (1.85–2.77)# | 3.68 (2.76–5.08)# | 4.31 (2.89–16.8)# | 2.80 (0.85–9.18)* |
| Agea | 1.02 (1.01–1.03)# | 0.99 (0.99–1.00)* | 0.97 (0.96–0.98)# | 0.96 (0.95–0.98)# | 0.99 (0.93–1.01)* |
| BMIa | 1.08 (1.05–1.10)# | 1.09 (1.07–1.12)# | 1.07 (1.03–1.11)# | 1.07 (1.02–1.12)# | 0.99 (0.87–1.12)* |
| Sexa | 0.45 (0.33–0.61)# | 1.78 (1.48–2.16)# | 1.27 (0.87–1.87)* | 1.59 (0.99–2.55)* | 1.20 (0.36–3.98)* |
| Smoking statusa | 1.51 (1.23–1.85)# | 0.70 (0.58–0.83)# | 1.16 (0.84–1.61)* | 1.11 (0.73–1.68)* | 0.77 (0.27–2.19)* |
|
| |||||
| Carcinoid tumors& | Large-cell carcinoma& | Adenosquamous carcinoma& | Other subtypes& | Unclassified& | |
|
| |||||
| COPDa | 1.75 (0.74–6.16)* | 3.41 (1.94–5.98)# | 2.04 (1.01–4.11)# | 5.26 (1.84–18.1)# | 3.09 (1.78–5.35)# |
| COPD gradingb | 1.47 (0.63–3.45)* | 2.27 (1.53–2.71)# | 1.69 (1.03–2.79)# | 2.44 (1.17–5.09)# | 2.52 (1.78–3.59)# |
| Emphysema-predominant phenotypec | NA | 5.56 (1.55–19.9)# | 2.45 (0.27–16.8)* | 8.29 (0.88–78.5)* | 9.03 (3.16–25.8)# |
| Non-emphysema-predominant phenotyped | 2.10 (0.67–6.63)* | 3.37 (1.84–6.17)# | 1.51 (0.65–3.54)* | 3.26 (0.90–11.8)* | 2.74 (1.48–5.04)# |
| Agea | 0.98 (0.94–1.02)* | 0.99 (0.96–1.02)* | 1.01 (0.98–1.05)* | 0.99 (0.94–1.05)* | 1.02 (0.99–1.05)* |
| BMIa | 1.06 (0.94–1.19)* | 1.07 (1.00–1.16)# | 1.12 (1.03–1.21)# | 0.87 (0.74–1.03)* | 1.00 (0.93–1.08)* |
| Sexa | NA | 0.66 (0.25–1.72)* | 3.03 (1.34–6.86)# | 2.17 (0.41–11.5)* | 1.20 (0.56–2.55)* |
| Smoking statusa | 0.86 (0.31–2.45)* | 1.73 (0.89–3.35)* | 1.97 (0.90–4.33)* | 2.35 (0.52–10.6)* | 1.30 (0.70–2.43)* |
Notes:
There were four multivariable logistic regression models, and each lung cancer subtype was analyzed respectively. COPD (dichotomous, referent non-COPD), COPD grading (continuous, increase), emphysema-predominant COPD phenotype (dichotomous, referent non-COPD), and non-emphysema-predominant COPD phenotype (dichotomous, referent non-COPD) distributed in models 1–4, respectively. Age (continuous, increase), BMI (continuous, increase), sex (dichotomous, referent male) and smoking status (dichotomous, referent non-smoking) were common variables of models 1–4,a model 1,b model 2,c model 3,d and model 4.
Adjusted OR (95% CI);
P<0.05;
P>0.05.
Abbreviations: BMI, body-mass index; SCLC, small-cell lung cancer; LCNC, large-cell neuroendocrine carcinoma; NA, not applicable.
Links between COPD phenotypes and risk of specific lung cancer histological subtypes
In this study, COPD was categorized into two phenotypes: emphysema-predominant and non-emphysema-predominant. The presence of emphysema-predominant and non-emphysema-predominant COPD indicated increased risk of lung cancer by more than fourfold and twofold, respectively (OR 4.43, 95% CI 2.85–6.88; OR 2.82, 95% CI 2.40–3.31) (Table 3). Additionally, both phenotypes increased the risk of most subtypes of lung cancer, including adenocarcinoma, SCC, SCLC and large-cell carcinoma. Adjusted ORs for each subtype of lung cancer are shown in Table 4.
To clarify the difference of lung cancer risk between the two phenotypes, all non-COPD patients were removed from further analysis. Logistic regression analysis revealed that compared to patients with the non-emphysema-predominant phenotype, patients with emphysema-predominant COPD had significantly higher risk of lung cancer (adjusted OR 1.61, 95% CI 1.02–2.54), especially SCC and SCLC (adjusted OR 1.72, 95% CI 1.03–2.89; adjusted OR 3.74, 95% CI 1.64–8.53). For increased risks of other lung cancer subtypes, no significant difference was observed between the two phenotypes (Table 5).
Table 5.
Risk of specific lung cancer subtypes in the presence of emphysema-predominant phenotype of COPD relative to non-emphysema-predominant phenotype
| Emphysema-predominant phenotype of COPD@ | |||
|---|---|---|---|
|
| |||
| OR | 95% CI | P-value | |
| All subtypes | 1.61 | 1.02–2.54 | 0.043 |
| Adenocarcinoma | 0.89 | 0.46–1.71 | 0.721 |
| Squamous carcinoma | 1.73 | 1.03–2.89 | 0.038 |
| Neuroendocrine carcinoma | 3.09 | 1.50–6.35 | 0.002 |
| SCLC | 3.74 | 1.64–8.53 | 0.002 |
| LCNC | 2.94 | 0.31–28.1 | 0.349 |
| Carcinoid tumors | NA | NA | NA |
| Large-cell carcinoma | 2.24 | 0.60–8.37 | 0.230 |
| Adenosquamous carcinoma | 1.89 | 0.21–16.7 | 0.567 |
| Other subtypes | 3.28 | 0.29–37.6 | 0.340 |
| Unclassified carcinoma | 2.54 | 0.85–7.61 | 0.096 |
Notes:
Each lung cancer subtype was analyzed separately. Multivariable logistic regression model variables: emphysema-predominant phenotype of COPD (dichotomous, referent non-emphysema-predominant phenotype), age (continuous, increase), BMI (continuous, increase), sex (dichotomous, referent male), and smoking status (dichotomous, referent nonsmoking).
Abbreviations: BMI, body-mass index; SCLC, small cell-lung cancer; LCNC, large-cell neuroendocrine carcinoma; NA, not applicable.
Discussion
The present study investigated the association between COPD phenotypes and specific histological lung cancer subtypes. Compared with previous studies, this study has a number of strengths, including large sample, participants collected without specific selection, confirmed diagnosis of lung cancer and COPD, and latest methods for categorizing subtypes or phenotypes. We found that after adjustment for age, sex, BMI, and smoking status, COPD was an independent risk factor for lung cancer and all common histological subtypes. Compared to non-COPD, both emphysema-predominant and non-emphysema-predominant phenotypes of COPD significantly increased the risk of lung cancer. Moreover, we demonstrated that there were some differences among different COPD phenotypes in relation to lung cancer risk: the increased risk of SCC and SCLC was significantly higher in patients with the emphysema-predominant phenotype compared to patients with the non-emphysema-predominant phenotype.
A number of studies have reported that approximately 40%–70% of lung cancers coexist with COPD.19,38,39 In the present study, high COPD prevalence was found in 2,283 patients with lung cancer (32.8%). Even though our data appear to reveal the lowest percentages published thus far,19–21,38,39 they also appear to be very accurate. Briefly, in a previous study COPD was diagnosed using different criteria, including self-report evaluation,20 which might have led to overdiagnosis. Moreover, certain studies were performed only on smokers.19,21,40 Our lung cancer cases were not specifically selected (such as targeting population at higher risk). During subgroup analysis, we found that the prevalence of COPD in lung cancer cases was 42.4% in smokers compared to 21.8% in nonsmokers (data not shown). This was consistent with previous results. In order to avoid the potential impact of resection on lung function,41 PFTs were performed after lung cancer diagnosis but before surgery. Young et al reported that there were no significant changes in lung function before and after lung cancer diagnosis.19 As such, the results from this study should be more comparable to the prevalence of COPD in the overall lung cancer population. Besides, the prevalence of COPD in matched hospital-based controls was 16%, somewhat higher but still in line with recently published studies on COPD prevalence.6
Previous prospective studies have provided evidence for increased risk of lung cancer in the presence of COPD. Wasswa-Kintu et al demonstrated that there was an inverse relationship between lung function and lung cancer incidence in smokers.17 Furthermore, a cohort of 2,507 COPD outpatients without lung cancer was followed for a 5-year period, during which time 215 patients had developed cancer (incidence density of 16.7 per 1,000 person-years).18 Moreover, Turner et al strengthened the evidence of increased risk of COPD for lung cancer in nonsmokers.42 In the present study, we found that the presence of COPD increased the risk of lung cancer by 2.88-fold, after adjusting for age, sex, BMI, and smoking status. COPD has been reported to increase the risk of lung cancer by two to sixfold in some small case–control studies.19,38 de Torres et al observed an inverse relationship between the incidence of lung cancer and the severity of COPD.18 On the contrary, we observed that the risk of lung cancer was significantly increased following increased GOLD grade. A potential explanation is that patients with more severe COPD died at an early point during the study, revealing a decrease in the number of severe COPD patients at risk as the prospective study progressed. Nevertheless, the “survival bias” can be effectively avoided in case–control study. Besides, in this study, the same relationships were also observed in nonsmokers and female subgroups, and were consistent with the results reported by two specific population studies.40,42 The results were not in line with another study conducted in southern China in that they reported no significant relationship between previous COPD (including COPD, emphysema and chronic bronchitis) and the risk of lung cancer in nonsmokers.43 This requires a larger multicenter study to verify.
Although the aforementioned studies have confirmed that the presence of COPD increases the risk of lung cancer, they were neither designed nor powered to detect differential links between COPD and risks of histological subtypes. The most important limitation in reported studies was the small number of recorded lung cancer, insufficient to provide enough histological subtypes. A prospective study has just found SCC was the most frequent histological subtype.18 In other studies, obtaining the histological types of lung cancer was very challenging.19,42,43 Herein, lung cancer was proven by biopsy or operative histology, avoiding possible bias resulting from inaccurate diagnosis. The cases included in the study were collected over more than a decade, and they included all common lung cancer subtypes. Some subtypes are very recent, and have rarely been mentioned in similar studies, such as LCNC and neuroendocrine carcinoma, which was an important update in the latest WHO classification of lung tumors.28 Consequently, the proportion of each subtype was very close to the epidemiological distribution of lung cancer subtypes.44 We revealed that the presence of COPD indicated an increased risk of two- to five-fold for all histological subtypes, except for carcinoid tumors. The risk odds for SCLC were highest, followed by LCNC, SCC, large cell-carcinoma, and adenocarcinoma. Furthermore, the association between the risk of neuroendocrine carcinoma and COPD was studied for the first time, and the presence of COPD was found to increase the risk of neuroendocrine lung carcinoma by 4.28-fold.
Only one previous study, conducted in Taiwan, has mentioned that male and female patients with COPD had increased risks for SCC, adenocarcinoma, and SCLC. Contrary to our results, the HRs of the three subtypes were lower and very similar.45 Moreover, Papi et al reported that among smokers with NSCLC, COPD was a risk factor for SCC,21 which was also observed in our study. Besides, our results showed that female sex was also a risk factor for lung cancer. This would be mostly due to the high prevalence of adenocarcinoma in this study. Subgroup analysis showed that female sex was an independent risk factor for adenocarcinoma, not other histological subtypes. We believe ours is the first well-designed case–control study to provide ORs for risk of all histological subtypes of lung cancer according to the presence or absence of COPD.
As is well known, COPD is a very heterogeneous disease, and so the question arises: Is there any link between COPD phenotypes and the risk related to specific histological subtype of lung cancer? Previous studies have suggested that lung cancer is associated with a history of emphysema and chronic bronchitis,46–51 and emphysema and chronic bronchitis are considered traditional clinical phenotypes of COPD.32 In most studies, the diagnosis of emphysema and chronic bronchitis relied on self-report and was subject to recall bias and misclassification. In order to reduce the potential for disease misclassification, researchers have attempted to evaluate the association between computed CT evidence of emphysema and/or airflow obstruction and the risk of lung cancer. They indicated that the presence of CT evidence of emphysema could increase the risk of lung cancer by two to fourfold, but there was no or lower risk of lung cancer associated with airflow obstruction.46–49 Recently, two studies have attempted to explore the impact of COPD phenotypes categorized by QCT on lung cancer risk.51,52 Their results were inconsistent with previous studies reporting that QCT measurements of emphysema and airway dimensions were not significantly associated with lung cancer risk. This implies that methods used to determine COPD phenotypes might be very important.
In the present study, computer quantification of AC on the MEFV curve was used to categorize phenotypes: emphysema-predominant and non-emphysema-predominant.35–37 The results obtained showed that compared to non-COPD, both phenotypes independently increased the risk of overall lung cancer and most lung cancer subtypes (including adenocarcinoma, SCC, SCLC, and large-cell carcinoma). A previous cross-sectional study reported that the risk odds of SCC were significantly increased among lung cancer patients with emphysema.53 Further analysis in our study found that patients with the emphysema-predominant phenotype of COPD had higher risk of SCC and small-cell carcinoma compared with patients with the non-emphysema-predominant phenotype of COPD. Increased risk for other subtypes of lung cancer was not significantly different between the two phenotypes. To the best of our knowledge, this study is the first to successfully compare differences between the impacts of COPD phenotypes on risks related to specific histological subtypes of lung cancer.
With this study, we have presented a comprehensive evaluation of the relationship between COPD phenotypes and histological subtypes of lung cancer. Though our results would not clarify directly the specific mechanistic link between COPD and lung cancer, they can certainly provide important implications and guidance for research into the mechanism between the two diseases. On one hand, we found differences among links between COPD phenotypes and specific lung cancer histological subtypes. The strong association between SCC and emphysema-predominant phenotype of COPD can be partly explained by smoking-induced upregulated matrix metalloproteinase and excessive inflammatory and oxidative stress responses.19,21,54 SCLC is also strongly related to smoking and emphysema.13,49 As such, whether there is shared genetic susceptibility to chronic smoking-induced inflammation between SCLC and emphysema or other common mechanisms still requires more concrete research. On the other hand, COPD and its phenotypes can significantly increase the risk of almost all lung cancer subtypes. Therefore, we believe there must be some common mechanism between the pathogenesis of lung cancer and COPD that is not affected by disease heterogeneity. This hypothesis requires further studies and confirmation.
Limitations
We recognize that there were several limitations in this study. Firstly, computed quantitative measurement of AC is a reliable method to identify the emphysema-predominant phenotype of COPD, but non-emphysema-predominant phenotype may include airway-dominant and mixed phenotypes. A more precise link between the airway-dominant phenotype of COPD and lung cancer still needs further study. Secondly, PFTs of all lung cancers in this study were performed after lung cancer diagnosis. We were not able to assess the effect of lung cancer itself on lung function and the MEFV curve form, although most lung cancers in this study were at an early stage and previous research has shown no significant changes in lung function before and after lung cancer diagnosis.19 SCC and SCLC tend toward more central localization. Though Papi et al indicated that central lung cancer did not represent an increased risk of airflow limitation,21 it remains to be seen whether central lung cancer can affect the occurrence and development of emphysema. Thirdly, inhaled corticosteroids (ICSs) are commonly prescribed to COPD patients. We did not get the relevant information regarding the use of ICSs. However, several studies have demonstrated that regular ICS use in COPD patients was significantly associated with decreased lung cancer risk, especially the use of higher ICS doses (≥1,200 μg/day).55–57 Their potential role in cancer prevention should not be ignored. In addition, according to the latest classification of lung tumors, many lung SCCs of the past are now classified as adenocarcinoma.28 This study could not assess the impact of this update on the relationship between COPD and lung cancer risk. Lastly, we could not provide the lung cancer-incidence rate in the presence of COPD in this case–control study, and this remains uncertain in Chinese populations. Further well-designed prospective studies are necessary to solve these problems.
Conclusion
This study provides more evidence on the links between COPD and lung cancer. COPD is an independent risk factor for lung cancer and all common histologic subtypes. Both emphysema-predominant and non-emphysema-predominant phenotypes of COPD significantly increased the risk of lung cancer. Compared to the non-emphysema-predominant phenotype of COPD, the emphysema-predominant phenotype had a higher risk of SCC and SCLC, but not other histologic subtypes.
Acknowledgments
This work was supported by the National Natural Science Foundation of China (81370148) and the Shandong Natural Science Project (ZR2012HQ011).
Footnotes
Disclosure
The authors report no conflicts of interest in this work.
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