Keywords
Lung cancer, Pesticides exposure, Herbicides, Insecticides, Fungicides
This article is included in the Oncology gateway.
Lung cancer, Pesticides exposure, Herbicides, Insecticides, Fungicides
See the authors' detailed response to the review by Neela Guha
See the authors' detailed response to the review by Ann C Olsson
See the authors' detailed response to the review by Matthew R Bonner
Lung cancer is a common and deadly type of cancer. In 2018, there were 2.1 million people around the world diagnosed with lung cancer, and 1.8 million died of the disease1. In 2018, Thailand had 170,495 incidences, and 114,199 deaths from lung cancer2. Besides genetic factors3, a major risk factor of lung cancer is cigarette smoking4,5. However, lung cancer was also related to other risk factors, including asbestos, crystalline silica, radon, polycyclic aromatic hydrocarbons, diesel engine exhaust particles, chromium, and nickel6,7. Previous studies have also linked cooking fumes to lung cancer8.
Results from recent studies suggested pesticide exposure as a potential risk factor of lung cancer9. The association between pesticides and lung cancer were presented around 50 years ago among grape farmers10. A large study in the United States found that lung cancer cases increase with the number of years working as a licensed pesticide applicator11. Another study in USA reported an increased risk of lung cancer among acetochlor herbicide users (RR = 1.74, 95% CI 1.07-2.84)12. In Pakistan, a study also found a strong association between pesticide exposure and lung cancer (OR = 5.1, 95% CI 3.1-8.3)13.
Some studies also linked individual pesticides to lung cancer. In the USA, a study evaluated 50 pesticides and found that seven—dicamba, metolaclor, pendimethalin, carbofuran, chlorpyrifos, diazinon, and dieldrin—to be positively associated with lung cancer14. Another study also showed a significantly increased risk of lung cancer among applicators who had been exposed to dieldrin15. Jones et al.16 reported an increased lung cancer incidence among male pesticide applicators with the highest exposure category of diazinon (OR = 1.6, 95% CI 1.11-2.31). Other individual pesticides that had been associated with lung cancer were chlopyrifos17, diazinon18, and pendimenthalin19.
Currently, there is limited evidence on the association between pesticide exposure and lung cancer and more studies are needed to confirm the association and identify more individual pesticides. According to our knowledge, the association between lung cancer and pesticides has never been studied before among Thai people. The objective of this study was to investigate the associations between pesticide exposure and lung cancer using a case-control design. The results can be used in the prevention of lung cancer, and to support global literature on the subject.
This study is a population-based case-control study. The cases refer to people diagnosed with primary lung cancer during the period of January 1, 2014 to March 31, 2017, and having at least ten years residence in Nakhon Sawan province, Thailand. Cases were selected from the database of the Thai Cancer Based Program (TCB) operated by Thai National Cancer Institute20. The TCB program requires every hospital to register cancer patients and to provide related information, e.g. types of cancer, diagnostic method, treatment information, etc.
From 299 living cases registered during the study period, 32 died during the year, 20 cases were in stage IV (undifferentiated) cancer, and the other 14 were not willing to participate in the study. After exclusion of those cases, 233 (participation rate = 77.9%) were contacted in person, and participated in this study. From 233 cases, 126 were confirmed by Computerized Tomography scan (CT scan)/ Magnetic Resonance Imaging (MRI)/ ultrasound of the whole abdomen/ Chest X-ray (CXR), 62 by histology of primary or metastasis, 21 by cytology of haematology, and 24 by history and physical examination.
Controls were neighbours who did not have lung or any other type of cancer, but were of the same gender, and age (±5 years) as the cases. In each case, two controls were selected by the interviewer using convenience sampling. In this study, data from 458 controls were used as a comparison group.
The minimum sample size to detect an OR of 1.616 was determined to be 215 for cases and 430 for controls using Kelsey’s formula21 (unmatched population base case-control study). The sample size was determined using online OpenEpi and the following assumptions: two-sided confidence level was 95%, power to detect the OR was 80%, proportion of cases with pesticide exposure was 0.522, proportion of control with exposure was 0.423, and the ratio of case to control was 1:224.
Data on pesticide exposure and other risk factors were collected using a questionnaire previously used in a study on pesticide exposure and diabetes25. The questionnaire has two major parts (provided as Extended data in English)26. Part 1 is about demographic data. We collected data on gender, age, marital status, education, occupation, living duration in the community, distances between home and farmland, exposure to air pollution (i.e., cooking smoke, working in a factory with air pollution; asbestos, diesel engine exhaust, silica, wood dust, painting and welding exposure). Data on smoking status, number of cigarettes smoked per day, and the total number of years smoked was also collected. Number of cumulative cigarettes smoked over a lifetime was calculated by multiplying the number of cigarettes smoked per day by the number of years. Those who smoked <109,500 cigarettes were considered a light smoker, while those who smoked ≥109,500 cigarettes were a heavy smoker27.
In Part 2, information on the historical use (mix or spray) of pesticides was collected. In this study, pesticides were categorized into five groups: insecticides (organochlorine, organophosphate, carbamate, and pyrethoid), herbicides, fungicides, rodenticides, and molluscicides. For each groups of pesticides, we collected data on the numbers of years and days using pesticides. The data of lifetime pesticide exposure days were then computed by multiplying the total years of exposure by the number of days per year. This study also collected data on the use of 35 individual pesticides commonly found in Thailand.
Pesticide exposure data were collected by the researcher and two village health volunteers working full times for the project. Both case and control were interviewed by the same interviewer. Prior to data collection, all interviewers were trained in how to interview and properly use the questionnaire.
Collected data were analysed using IBM SPSS Statistics (version 25) and OpenEpi (version 3.5.1). P values <0.05 were considered statistically significant. Demographic data was analysed using descriptive statistics. The associations were determined between lung cancer and groups of pesticides (herbicides, insecticides, fungicides, and molluscicides), between lung cancer and 17 individual compounds. Data were analysed with conditional and unconditional logistic regression, but the results were similar, and thus, only the results from the unconditional logistics regression are reported. Both crude and adjusted ORs with 95% confidence intervals (CIs) were presented. Adjusted ORs were analysed using multiple logistic regressions controlled for gender (male, female), age (≤54, 55–64, 65–74, and ≥75), cigarette smoking (never smoked, smoked < 109,500, smoked ≥ 109,500), occupation (farmer, non-farmer), cooking fumes exposure (yes, no), and exposure to air pollution i.e., working in factories with air pollution) (yes, no). In addition to the fundamental confounding factors, variables with statistically difference between cases and controls were included in a regression model.
Cumulative exposure days on groups of pesticides were categorized into either quartiles (Q1-Q4; Q1 being the lowest exposure and Q4 the highest) or tertile (T1-T3), depending on the number of subjects in each group. The lung cancer risk was then predicted, using non-exposed groups as a reference.
In this study, most of study participants were male with a mean age of around 65. Both cases and controls have similar gender, age, marital status, education, occupation, period of residence, distances, air pollution exposure, and cooking fume exposure. However, the cases had about twice the proportion of those who reported ever smoking a cigarette (23.6%) compared to the controls (13.6%). More detailed demographic data among case and control groups were in Table 1 and in Underlying data28.
Characteristic | Case | Control | P value** | ||
---|---|---|---|---|---|
n | % | n | % | ||
Total (any) (N = 680)* | 233 | 100.0 | 447 | 100.0 | |
Gender | 0.693 | ||||
Male | 135 | 57.9 | 266 | 59.5 | |
Female | 98 | 42.1 | 181 | 40.5 | |
Age (years) | 0.891 | ||||
≤54 | 34 | 14.6 | 71 | 15.9 | |
55–64 | 72 | 30.9 | 128 | 28.6 | |
65–74 | 72 | 30.9 | 146 | 32.7 | |
≥75 | 55 | 23.6 | 102 | 22.8 | |
Mean age (years) ± SD | 66.04 ± 10.63 | 65.37 ± 10.88 | |||
Median age (min–max) | 65.00 (37–98) | 66.00 (31–92) | |||
Marital status | 0.644 | ||||
Single | 17 | 7.3 | 27 | 6.0 | |
Married | 188 | 80.7 | 357 | 79.9 | |
Divorced/Separated | 28 | 12.0 | 63 | 14.1 | |
Education completed | 0.295 | ||||
Primary school (Grade 1–6) | 217 | 93.1 | 402 | 89.9 | |
Secondary school (Grade 7–12) | 13 | 5.6 | 40 | 8.9 | |
Undergraduate or higher | 3 | 1.3 | 5 | 1.2 | |
Occupation | 0.970 | ||||
Farmer | 131 | 56.3 | 252 | 56.3 | |
Non-farmer | 102 | 43.7 | 195 | 43.7 | |
Period of residence (years) | 0.913 | ||||
<21 | 25 | 10.7 | 45 | 10.1 | |
21–30 | 32 | 13.7 | 66 | 14.7 | |
>30 | 176 | 75.6 | 336 | 75.2 | |
Distances (m) | 0.814 | ||||
<500 | 102 | 43.8 | 197 | 44.1 | |
500–1,000 | 32 | 13.7 | 54 | 12.1 | |
>1,000 | 99 | 42.5 | 196 | 43.8 | |
Pollution exposure† | 0.636 | ||||
Yes | 116 | 49.8 | 214 | 47.9 | |
No | 117 | 50.2 | 233 | 52.1 | |
Cooking fumes exposure | 0.390 | ||||
Yes | 75 | 32.2 | 143 | 32.0 | |
No | 158 | 7.8 | 304 | 68.0 | |
Cigarette smoking | 0.003 | ||||
Never smoked | 144 | 61.8 | 298 | 66.7 | |
Smoked (current smoker or ex-smoker) | |||||
< 109,500 | 34 | 14.6 | 88 | 19.7 | |
≥ 109,500 | 55 | 23.6 | 61 | 13.6 | |
Mean (cigarettes) ± SD | 175,733±168,868 | 111,339±107,645 | |||
Median (min-max) | 109,500(5,475- 876,000) | 87,600(5,475- 812,500) | |||
Histology | |||||
Adenocarcinoma | 114 | 48.9 | |||
Squamous cell carcinoma | 17 | 7.3 | |||
Small cell carcinoma | 21 | 9.0 | |||
Large cell carcinoma | 9 | 3.9 | |||
Neoplasm, malignant | 68 | 29.2 | |||
Other and unspecified | 4 | 1.7 |
After adjusting for confounding factors, lung cancer was positively associated with historical exposure of study participants to herbicides, insecticides, and fungicides (Table 2). The adjusted variables included in the analysis were gender (male, female), age (≤54, 55–64, 65–74, ≥75), cigarette smoking (never smoked, smoked < 109,500, smoked ≥ 109,500), occupation (farmer, non-farmer), cooking fumes exposure (yes, no), and exposure to air pollution, i.e., working in factories with air pollution (yes, no). Compared with people in the non-exposed group, those in Q3-Q4 days of using herbicides had an elevated risk of lung cancer with odds ratio (OR) between 2.20 (95% CI 1.27-3.81) for people with Q3 exposure, and 3.99 (95% CI 1.62-7.11) for Q4 exposure (p < 0.001). A similar association was also found for days of insecticide use and lung cancer (OR = 2.20 for Q3, and OR = 2.24 for Q4, p 0.006). For individual compounds, lung cancer was statistically associated with a historical use dieldrin (OR = 2.56; 95% CI 1.36–4.81), chlorpyrifos (OR = 3.29; 95% CI 1.93–5.61), and carbofuran (OR = 2.10; 95% CI 1.28–3.42) (Table 3). People in Q3 and Q4 of glyphosate and paraquat exposure also showed an elevated risk of lung cancer (Table 3).
Pesticides use | Case | Control | OR (95% CI) | Adjusted OR (95% CI)* | ||
---|---|---|---|---|---|---|
n | % | n | % | |||
Total | 233 | 100.0 | 447 | 100.0 | ||
Pesticides (any) (N = 490) | ||||||
Herbicides (N = 347) | ||||||
Yes | 129 | 54.4 | 218 | 48.8 | 1.30 (0.94-1.79) | 1.34 (0.91–1.98) |
No | 104 | 44.6 | 229 | 51.2 | ||
Number of years using herbicides (N = 347) | ||||||
>30 | 23 | 9.9 | 51 | 11.4 | 1.69 (1.27-1.71) | 1.71 (1.33-1.53)** |
11–30 | 76 | 32.6 | 107 | 23.9 | 1.56 (1.07-2.27) | 1.66 (1.07-2.57)** |
1–10 | 30 | 12.9 | 60 | 13.5 | 1.10(0.67-1.80) | 1.17(0.69-2.00) |
Non-exposed | 104 | 44.6 | 229 | 51.2 | Reference | Reference |
P for trend*** | 0.045 | 0.047 | ||||
Number of days using herbicides (N = 347) | ||||||
Q4 (>960) | 52 | 22.3 | 30 | 6.7 | 3.59 (2.15-5.98) | 3.99 (1.62-7.11)** |
Q3 (501–960) | 45 | 18.5 | 50 | 10.8 | 1.88 (1.17-3.02) | 2.20 (1.27-3.81)** |
Q2 (160–500) | 23 | 10.7 | 50 | 11.6 | 1.03 (0.59-1.78) | 1.14 (0.62-2.11) |
Q1 (<160) | 9 | 3.9 | 88 | 19.7 | 0.35(0.19-0.64) | 0.39(0.20-0.74) |
Non-exposed | 104 | 44.6 | 229 | 51.2 | Reference | Reference |
P for trend*** | <0.001 | <0.001 | ||||
Insecticides (N = 305) | ||||||
Yes | 116 | 49.8 | 189 | 42.3 | 1.35 (0.98–1.86) | 1.40 (0.98–2.03) |
No | 117 | 50.2 | 258 | 57.7 | ||
Number of years using the insecticides (N = 305) | ||||||
>30 | 37 | 15.9 | 43 | 9.6 | 1.89 (1.16-3.09) | 1.82 (1.05-3.16)** |
11–30 | 63 | 27.0 | 96 | 21.5 | 1.44 (1.03-2.12) | 1.62 (1.05-2.49)** |
1–10 | 16 | 6.9 | 50 | 11.2 | 0.70(0.38-1.29) | 0.77(0.41-1.44) |
Non-exposed | 117 | 50.2 | 258 | 57.7 | Reference | Reference |
P for trend*** | 0.009 | 0.029 | ||||
Number of days using the insecticides (N = 305) | ||||||
Q4 (>1,200) | 37 | 15.9 | 39 | 8.7 | 2.17 (1.29-3.27) | 2.24 (1.33-3.72)** |
Q3 (481–1,200) | 33 | 14.1 | 34 | 7.6 | 2.13 (1.26-3.61) | 2.20 (1.24-3.89)** |
Q2 (200–480) | 28 | 12.0 | 53 | 11.9 | 1.16 (0.70-1.93) | 1.28 (0.74-2.19) |
Q1 (<200) | 18 | 7.8 | 63 | 14.1 | 0.67(0.37-1.18) | 0.72(0.40-1.31) |
Non-exposed | 117 | 50.2 | 258 | 57.7 | Reference | Reference |
P for trend*** | 0.001 | 0.006 | ||||
Fungicides (N = 116) | ||||||
Yes | 42 | 18.0 | 74 | 16.6 | 1.10 (0.73–1.68) | 1.05 (0.68–1.64) |
No | 191 | 82.0 | 373 | 83.4 | ||
Number of years using the fungicides (N = 116) | ||||||
>30 | 7 | 3.0 | 10 | 2.3 | 1.36 (0.51-3.64) | 1.05 (0.37-2.92) |
11–30 | 23 | 9.9 | 39 | 8.7 | 1.15 (0.66-1.98) | 1.13 (0.64-1.99) |
1–10 | 12 | 5.1 | 25 | 5.6 | 0.93(0.46-1.90) | 0.92(0.43-1.92) |
Non-exposed | 191 | 82.0 | 373 | 83.4 | Reference | Reference |
P for trend*** | 0.881 | 0.355 | ||||
Number of days using the fungicides (N = 116) | ||||||
Q4 (>500) | 16 | 6.8 | 13 | 2.9 | 2.40 (1.13-5.10) | 2.00 (0.91-4.40) |
Q3 (161–500) | 9 | 3.9 | 17 | 3.9 | 1.03 (0.45-2.36) | 1.01 (0.43-2.37) |
Q2 (96–160) | 9 | 3.9 | 22 | 4.9 | 0.79 (0.36-1.76) | 0.83 (0.36-1.90) |
Q1 (<96) | 8 | 3.4 | 22 | 4.9 | 0.71(0.31-1.62) | 0.68(0.29-1.590 |
Non-exposed | 191 | 82.0 | 373 | 83.4 | Reference | Reference |
P for trend*** | 0.163 | 0.189 |
*Logistic regression adjusted for gender, age (≤54, 55–64, 65–74, and ≥75), cigarette smoking (never smoked, smoked <109,500, smoked≥109,500), occupation (farmer and non–farmer), cooking fumes exposure (yes, no), and pollution exposure (working in factories with air pollution) (yes, no).
**Statistically significant (p <0.05).
***P-values for linear trends were derived using a continuous variable with midpoint value of each category.
Pesticide | Case | Control | OR (95% CI) | Adjusted OR (95% CI)* | ||
---|---|---|---|---|---|---|
n | % | n | % | |||
Total | 233 | 100.0 | 447 | 100.0 | ||
Herbicides | ||||||
Glyphosate (N = 281) | ||||||
Yes | 105 | 45.1 | 176 | 39.4 | 1.26 (0.91–1.74) | 1.29 (0.89–1.88) |
No | 128 | 54.9 | 271 | 60.6 | ||
Number of days using glyphosate | ||||||
Q4 (>1,008) | 44 | 18.9 | 26 | 5.8 | 3.58(2.11-6.07) | 3.65(2.05-6.50)** |
Q3 (401-828) | 36 | 15.5 | 33 | 7.4 | 2.30(1.37-3.87) | 2.52(1.43-4.43)** |
Q2 (161-480) | 18 | 7.7 | 37 | 8.3 | 1.02(0.56-1.87) | 1.10(0.58-2.09) |
Q1 (≤160) | 7 | 3.0 | 80 | 17.9 | 0.18(0.08-0.41) | 0.20(0.09-0.46) |
Non-exposed | 128 | 54.9 | 271 | 60.6 | Reference | Reference |
P for trend*** | <0.001 | <0.001 | ||||
Paraquat (N = 239) | ||||||
Yes | 89 | 38.2 | 150 | 33.6 | 1.22 (0.88–1.70) | 1.21 (0.85–1.73) |
No | 144 | 61.8 | 297 | 66.4 | ||
Number of days using paraquat | ||||||
Q4 (>828) | 30 | 12.9 | 29 | 6.5 | 2.11(1.22-3.66) | 2.04(1.14-3.67)** |
Q3 (401-828) | 29 | 12.4 | 32 | 7.2 | 1.85(1.08-3.18) | 1.80(1.02-3.20)** |
Q2 (145-400) | 21 | 9.1 | 35 | 7.8 | 1.19(0.67-2.12) | 1.26(0.69-2.28) |
Q1 (≤144) | 9 | 3.8 | 54 | 12.1 | 0.33(0.16-0.69) | 0.35(0.17-0.75) |
Non-exposed | 144 | 61.8 | 297 | 66.4 | Reference | Reference |
P for trend*** | <0.001 | <0.001 | ||||
2, 4-Dichlorophenoxy acetic acid (N = 117) | ||||||
Yes | 47 | 20.2 | 70 | 15.7 | 1.36 (0.90–2.04) | 1.42 (0.93–2.18) |
No | 186 | 79.8 | 377 | 84.3 | ||
Number of days using 2,4- Dichlorophenoxy acetic acid | ||||||
Q4 (>480) | 9 | 3.9 | 20 | 4.5 | 0.81(0.40-2.04) | 0.88(0.38-2.01) |
Q3 (161-480) | 11 | 4.7 | 12 | 2.7 | 1.55(0.82-3.82) | 1.58(0.79-3.78) |
Q2 (91-160) | 10 | 4.3 | 14 | 3.1 | 1.17(0.67-2.59) | 1.19(0.68-2.66) |
Q1 (≤90) | 17 | 7.3 | 24 | 5.4 | 0.59(0.25-1.39) | 0.65(0.27-1.57) |
Non-exposed | 186 | 79.8 | 377 | 84.3 | Reference | Reference |
P for trend*** | 0.095 | 0.098 | ||||
Butachlor (N = 38) | ||||||
Yes | 14 | 6.0 | 24 | 5.4 | 1.12 (0.57–2.22) | 0.88 (0.42–1.83) |
No | 219 | 94.0 | 423 | 94.6 | ||
Number of days using butachlor | ||||||
Q4 (>220) | 6 | 2.6 | 4 | 1.0 | 2.89(0.80-7.37) | 2.02(0.53-7.67) |
Q3 (101-220) | 3 | 1.3 | 5 | 1.1 | 1.15(0.27-4.89) | 0.95(0.21-4.28) |
Q2 (51-100) | 4 | 1.7 | 5 | 1.1 | 1.54(0.41-5.81) | 1.47(0.37-5.82) |
Q1 (≤50) | 1 | 0.4 | 10 | 2.2 | 0.19(0.02-1.51) | 0.19(0.02-1.52) |
Non-exposed | 219 | 94.0 | 423 | 94.6 | Reference | Reference |
P for trend*** | 0.134 | 0.154 | ||||
Propanil (N = 32) | ||||||
Yes | 11 | 4.7 | 21 | 4.7 | 1.00 (0.47–2.12) | 1.06 (0.47–2.41) |
No | 222 | 95.3 | 426 | 95.3 | ||
Number of days using propanil | ||||||
T3 (>320) | 6 | 2.6 | 10 | 2.2 | 1.21(0.80-6.30) | 1.32(0.61-6.82) |
T2 (91-320) | 3 | 1.3 | 5 | 1.1 | 1.15(0.27-4.86) | 1.29(0.29-5.60) |
T1 (≤90) | 2 | 0.8 | 6 | 1.4 | 0.63(0.12-3.19) | 0.68(0.13-3.48) |
Non-exposed | 222 | 95.3 | 426 | 95.3 | Reference | Reference |
P for trend*** | 0.379 | 0.266 | ||||
Alachlor (N= 42) | ||||||
Yes | 14 | 6.0 | 28 | 6.3 | 0.95 (0.49–1.85) | 0.91 (0.45–1.85) |
No | 219 | 94.0 | 419 | 93.7 | ||
Number of days using alachlor | ||||||
Q4 (>885) | 6 | 2.6 | 5 | 1.1 | 2.29(0.69-7.60) | 1.87(0.55-6.35) |
Q3 (341-885) | 5 | 2.2 | 5 | 1.1 | 1.91(0.54-6.67) | 1.85(0.51-6.67) |
Q2 (99-340) | 2 | 0.8 | 8 | 1.8 | 0.47(0.10-2.27) | 0.52(0.11-2.52) |
Q1 (≤98) | 1 | 0.4 | 10 | 2.3 | 0.19(0.02-1.50) | 0.17(0.02-1.39) |
Non-exposed | 219 | 94.0 | 419 | 93.7 | Reference | Reference |
P for trend*** | 0.101 | 0.099 | ||||
Insecticides | ||||||
Organochlorine insecticides | ||||||
Endosulfan (N = 79) | ||||||
Yes | 35 | 15.0 | 44 | 9.8 | 1.61 (1.00–2.60) | 1.60 (0.97–2.63) |
No | 198 | 85.0 | 403 | 90.2 | ||
Number of days using endosulfan | ||||||
Q4 (>850) | 10 | 4.3 | 10 | 2.2 | 2.03(0.83-4.97) | 2.01(0.79-5.08) |
Q3 (361-850) | 8 | 3.4 | 10 | 2.2 | 1.62(0.63-4.18) | 1.38(0.51-3.67) |
Q2 (130-360) | 8 | 3.4 | 13 | 2.9 | 1.25(0.51-3.07) | 1.31(0.52-3.30) |
Q1 (≤129) | 9 | 3.9 | 11 | 2.5 | 1.16(0.67-4.08) | 1.18(0.71-4.48) |
Non-exposed | 198 | 85.0 | 403 | 90.2 | Reference | Reference |
P for trend*** | 0.346 | 0.204 | ||||
Dieldrin (N = 44) | ||||||
Yes | 24 | 10.3 | 20 | 4.5 | 2.45 (1.32–4.53) | 2.56 (1.36–4.81)** |
No | 209 | 89.7 | 427 | 95.5 | ||
Number of days using dieldrin | ||||||
T3 (>720) | 9 | 3.9 | 6 | 1.3 | 3.06(1.07-8.72) | 3.15(1.08-9.18)** |
T2 (321-720) | 9 | 3.9 | 5 | 1.1 | 3.04(1.21-7.11) | 3.11(1.33-8.68)** |
T1 (≤320) | 6 | 2.5 | 9 | 2.1 | 1.36(0.47-3.87) | 1.36(0.47-3.95) |
Non-exposed | 209 | 89.7 | 427 | 95.5 | Reference | Reference |
P for trend*** | 0.017 | 0.022 | ||||
DDT (N = 50) | ||||||
Yes | 13 | 5.6 | 37 | 8.3 | 0.65 (0.34–1.25) | 0.67 (0.34–1.31) |
No | 220 | 94.4 | 410 | 91.7 | ||
Number of days using DDT | ||||||
T3 (>250) | 7 | 3.0 | 10 | 2.3 | 1.30(0.48-3.47) | 1.28(0.47-.50) |
T2 (121-250) | 3 | 1.3 | 12 | 2.7 | 0.46(0.13-1.66) | 0.45(0.12-1.66) |
T1 (≤120) | 3 | 1.3 | 15 | 3.3 | 0.37(0.10-1.30) | 0.41(0.11-1.46) |
Non-exposed | 220 | 94.4 | 410 | 91.7 | Reference | Reference |
P for trend*** | 0.191 | 0.151 | ||||
Organophosphate insecticides | ||||||
Chlorpyrifos (N = 70) | ||||||
Yes | 40 | 17.2 | 30 | 6.7 | 2.88 (1.74–4.76) | 3.29 (1.93–5.61)** |
No | 193 | 82.8 | 417 | 93.3 | ||
Number of days using chlorpyrifos | ||||||
T3(>720) | 15 | 6.4 | 10 | 2.2 | 3.42(1.31-6.93) | 3.42(1.47-7.96)** |
T2 (397-720) | 18 | 7.8 | 12 | 2.7 | 3.02(1.62-7.18) | 3.12(1.89-8.97)** |
T1 (≤396) | 7 | 3.0 | 8 | 1.8 | 1.89(0.67-5.28) | 1.89(0.63-5.61) |
Non-exposed | 193 | 82.8 | 417 | 93.3 | Reference | Reference |
P for trend*** | <0.001 | <0.001 | ||||
Folidol/parathion (N = 104) | ||||||
Yes | 40 | 17.2 | 64 | 14.3 | 1.24 (0.80–1.90) | 1.25 (0.78–1.99) |
No | 193 | 82.8 | 383 | 85.7 | ||
Number of days using folidol/parathion | ||||||
Q4 (>720) | 12 | 5.1 | 11 | 2.4 | 2.16(0.93-4.99) | 2.10(0.88-5.02) |
Q3 (401-1,080) | 9 | 3.9 | 7 | 1.6 | 2.05(0.93-4.15) | 2.04(0.88-4.71) |
Q2 (140-400) | 7 | 3.0 | 21 | 4.7 | 0.66(0.27-1.58) | 0.69(0.28-1.71) |
Q1 (≤139) | 12 | 5.2 | 25 | 5.6 | 0.95(0.46-1.93) | 0.95(0.85-2.01) |
Non-exposed | 193 | 82.8 | 383 | 85.7 | Reference | Reference |
P for trend*** | 0.105 | 0.105 | ||||
Mevinphos (N = 38) | ||||||
Yes | 16 | 6.9 | 22 | 4.9 | 1.42 (0.73–2.76) | 0.89 (0.22–3.65) |
No | 217 | 93.1 | 425 | 95.1 | ||
Number of days using mevinphos | ||||||
T3 (>840) | 9 | 3.9 | 8 | 1.8 | 2.44(0.95-6.29) | 2.05(0.77-5.44) |
T2 (253-840) | 5 | 2.1 | 2 | 0.4 | 2.89(0.91-5.44) | 2.53(0.84-5.53) |
T1 (≤252) | 2 | 0.9 | 12 | 2.7 | 0.16(0.22-1.26) | 0.16(0.22-1.29) |
Non-exposed | 217 | 93.1 | 425 | 95.1 | Reference | Reference |
P for trend*** | 0.065 | 0.063 | ||||
Carbamate insecticides | ||||||
Carbaryl/Savin (N = 48) | ||||||
Yes | 14 | 6.0 | 34 | 7.6 | 0.77 (0.40–1.47) | 0.89 (0.41–1.55) |
No | 219 | 94.0 | 413 | 92.4 | ||
Number of days using carbaryl/savin | ||||||
T3 (>1,050) | 7 | 3.0 | 8 | 2.2 | 1.65(0.59-4.61) | 1.71(0.59-4.94) |
T2 (321-1,050) | 5 | 2.1 | 11 | 2.6 | 0.85(0.29-2.49) | 0.87(0.29-2.63) |
T1 (≤320) | 2 | 0.9 | 15 | 1.8 | 0.25(0.15-1.10) | 0.25(0.59-4.94) |
Non-exposed | 219 | 94.0 | 413 | 92.4 | Reference | Reference |
P for trend*** | 0.130 | 0.107 | ||||
Carbofuran (N = 85) | ||||||
Yes | 43 | 18.5 | 42 | 9.4 | 2.18 (1.37–3.45) | 2.10 (1.28–3.42)** |
No | 190 | 81.5 | 405 | 90.6 | ||
Number of days using carbofuran | ||||||
Q4 (>1,200) | 11 | 4.7 | 6 | 1.4 | 4.68(1.60-13.68) | 4.57(1.53-13.57)** |
Q3 (401-1,200) | 18 | 7.7 | 5 | 1.1 | 4.52(1.15-13.06) | 4.36(1.99-13.53)** |
Q2 (101-400) | 8 | 3.5 | 14 | 3.1 | 1.21(0.50-2.95) | 1.11(0.44-2.82) |
Q1 (≤100) | 6 | 2.6 | 17 | 3.8 | 0.47(0.15-1.41) | 0.44(0.14-1.35) |
Non-exposed | 190 | 81.5 | 405 | 90.6 | Reference | Reference |
P for trend*** | <0.001 | <0.001 | ||||
Pyrethoid insecticides | ||||||
Abamectin (N = 134) | ||||||
Yes | 44 | 18.9 | 90 | 20.1 | 0.92 (0.61–1.37) | 0.82 (0.53–1.27) |
No | 189 | 81.1 | 357 | 79.9 | ||
Number of days using abamectin | ||||||
Q4 (>540) | 12 | 5.2 | 21 | 4.7 | 1.07(0.51-2.24) | 0.89(0.41-1.91) |
Q3 (361-540) | 8 | 3.4 | 16 | 3.6 | 0.94(0.39-2.24) | 0.83(.34-2.02) |
Q2 (124-360) | 14 | 6.0 | 29 | 6.5 | 0.91(0.47-1.76) | 0.79(0.39-1.58) |
Q1 (≤123) | 10 | 4.3 | 24 | 5.3 | 0.78(0.36-1.68) | 0.79(0.36-1.74) |
Non-exposed | 189 | 81.1 | 357 | 79.9 | Reference | Reference |
P for trend*** | 0.971 | 0.391 | ||||
Fungicides | ||||||
Armure/Propiconazole (N = 80) | ||||||
Yes | 29 | 12.4 | 51 | 11.4 | 1.10 (0.67–1.79) | 1.02 (0.61–1.72) |
No | 204 | 87.6 | 396 | 88.6 | ||
Number of days using Armure/propiconazole | ||||||
Q4 (>480) | 10 | 4.3 | 9 | 2.0 | 2.15(0.86-5.39) | 1.95(0.75-5.05) |
Q3 (145-480) | 8 | 3.4 | 12 | 2.7 | 1.29(0.52-3.12) | 1.01(0.39-2.60) |
Q2 (81-144) | 6 | 2.6 | 13 | 2.9 | 0.89(0.33-2.39) | 1.02(0.36-2.86) |
Q1 (≤80) | 5 | 2.1 | 17 | 3.8 | 0.57(0.20-1.56) | 0.53(0.18-1.50) |
Non-exposed | 204 | 87.5 | 396 | 88.6 | Reference | Reference |
P for trend*** | 0.349 | 0.218 | ||||
Methyl aldehyde (N = 43) | ||||||
Yes | 15 | 6.4 | 28 | 6.3 | 1.02 (0.53–1.96) | 1.03 (0.52–2.05) |
No | 218 | 93.6 | 419 | 93.7 | ||
Number of days using methyl aldehyde | ||||||
T3 (>528) | 4 | 1.7 | 16 | 3.6 | 0.48(0.15-1.45) | 0.49(0.16-1.53) |
T2 (351-528) | 4 | 1.7 | 4 | 0.9 | 1.92(0.47-4.75) | 1.77(0.42-4.44) |
T1 (≤350) | 7 | 3.0 | 8 | 1.8 | 1.68(0.36-4.69) | 1.72(0.59-4.98) |
Non-exposed | 218 | 93.6 | 419 | 93.7 | Reference | Reference |
P for trend*** | 0.284 | 0.176 |
*Logistic regression adjusted for gender, age (≤ 54, 55–64, 65–74, and ≥ 75), cigarette smoking (never smoked, smoked <109,500, smoked ≥ 109,500), occupation (farmer and non-farmer), cooking fumes exposure (yes, no) and exposure to air pollution (working in factories with air pollution) (yes, no).
**Statistically significant (p < 0.05).
The study results showed a positive association between lung cancer and the historical use of herbicides and insecticides (Table 3). The associations were in dose-response pattern and the risk of lung cancer increase with both number of years and day using the chemicals. The study also found three insecticides (dieldrin, chlorpyrifos, and carbofuran) and two herbicides (glyphosate, and paraquat) to be statistically associated with lung cancer. These results were consistent with literature indicating the potential carcinogenicity of pesticides29. In an experimental study, exposure to pesticides caused the production of reactive oxygen species (ROS), an oxygen-containing species containing an unpaired electron, such as superoxide, hydrogen peroxide, and hydroxyl radical, which are highly unstable and may cause DNA damage, protein damage, mutagenicity, necrosis, and apoptosis30. Pesticides may also increase the risk of cancer via other mechanisms including genotoxicity, tumour promotion, epigenetic effects, hormonal action and immunotoxicity31. In epidemiological study, evidence linked pesticide exposure to lung cancer are increasing, and the issue will be further discussed in the following section.
In this study, dieldrin was found to strongly associate with lung cancer and the association was in a dose-response relationship. The finding was consistent with literature. Dieldrin is an extremely persistent organic pollutant linked to many health problems, e.g., Parkinson's disease, breast cancer, affecting the immunity system, the reproductive, and nervous systems32. In the USA, the Agricultural Health Study (AHS) found seven pesticides including dicamba, metolaclor, pendimethalin, carbofuran, chlorpyrifos, diazinon, and dieldrin to be positively associated with lung cancer14. Further studies found dieldrin exposure to relate to the highest tertile of days use (RR = 5.30; 95% CI 1.50–18.60)15. After fifteen years of follow-up, the latest AHS by Bonner et al.33 found dieldrin to associate with lung cancer (OR=1.93; 95% CI: 0.70, 5.30). In Thailand, 688 tons of dieldrin was used in 1981–1990, before it was banned on May 16, 1990.
It was found that historical use of chlorpyrifos was dose-response association with lung cancer. Those who use the pesticide had 3.29 times (1.93-5.61) higher risk of lung cancer as compare to the control group. This finding was in agreement with previous studies. A study among pest control workers in Florida, USA found a long-term exposure to organophosphate and carbamate insecticides over ten years to increase mortality risk of lung cancer11. In the Agricultural Health Study, a dose response relationship was found between lung cancer and chlorpyrifos17 and diazinon18. In later studies of the AHS cohort identified chlorpyrifos as another potential risk factor17. However, the last updated results from the AHS did not support the association33. At this time, chlorpyrifos was still not banned by Thai government. On the other hand, chlorpyrifos was the primary insecticide imported to Thailand (1,193,302 kilograms in 2013)34.
This study also found a significant association between carbofuran and lung cancer (OR=2.10, 95% CI 1.28-3.42). Although previous studies did not find the association, there is some evidence suggested the potential effects of the chemical. Carbofuran (2,3-dihydro-2,2-dimethylbenzofuran-7-yl methylcarbamate) is one of the most toxic broad-spectrum carbamate insecticides. In laboratory studies, although evidence on carcinogenicity is inconclusive, carbofuran has been demonstrated to have mutagenic properties; and there are studies that have linked it to other types of cancer, e.g., lymphoma in mice3. Evidence from previous epidemiology studies were rather contradictory. In the Agricultural Health Study, the first report by Bonner et al. in 2005 found a rather strong association when lung cancer risk was compared to those in the lowest exposure category14,35. However, this association was reported to be absent in a later study in 2017 by the same author33. For other types of cancer, carbofuran has been identified as a potential cause of non-Hodgkin’s Lymphoma (NHL)36. A survey In Thailand (2012) found carbofuran to be the most commonly used pesticides in rice fields37.
Although, a rough estimation of the use of glyphosate and paraquat were not significantly associated with lung cancer, more detailed exposure data showed that people in the higher category of cumulative exposure day, especially those in a high quartile of exposure days had an elevated risk of lung cancer (Table 3). Paraquat (dipyridylium), also known as Gramoxone, is a non-selective herbicide commonly used worldwide33,38. Although, the mechanism of toxicity has not been clearly defined, research found that paraquat can cause damage to the lungs, kidneys, and the liver39. At the cellular level, paraquat can produce reactive oxygen species (ROS), the superoxide free radical, which can initiate or promote carcinogenesis40. In a case study, pulmonary fibrosis was found in the patient with paraquat poisoning41. In Thailand, paraquat was banned in May 2020.
Glyphosate [N-(phosphonomethyl) glycine, also known as Roundup] is another broad-spectrum herbicide that has been used widely in Thailand and other countries33,38. In the past decade, cancer potency of glyphosate received much attention and several comprehensive literature reviews are available42,43. In 2015, WHO revised carcinogenicity of glyphosate and classified it as “probable carcinogen”43. Laboratory studies found glyphosate to increase incidence of tumour, chromosomal damage, and oxidative stress43. Currently, evidence from epidemiological studies were limited. Although it was previously reported to relate to non-Hodgkin lymphoma, glyphosate did not relate to cancer at any sites in the large perspective Agricultural Health Study33,44,45.
The potential limitations of this type of study were the recall bias where cases and controls can recall past exposure differently. Cases tend to memorize exposure better, particularly when they know or are aware of what caused their illness46. However, with limited available information on the issues in Thailand, we did not expect participants to be aware of pesticides as causal factor for lung cancer. It was very likely that the study could have exposure misclassification due to the participants not being able to recall or name the pesticides they used in the past. In addition, data on pesticide exposure were obtained solely from the interview questionnaire without any exposure measurement. However, this information bias usually occurs evenly across a case and control group, and only has a negative effect on the association47. Selection bias might also occur when using non-random sampling or when the study sample did not represent the study population. However, in this study, data from all the lung cancer patients except those who were severely ill, were collected to minimize the bias.
This study found the occurrence of lung cancer to be associated with the historical use of pesticides. The results confirmed the association between dieldrin and chlorpyrifos and lung cancer and suggested the potential effects of carbofuran, glyphosate, and paraquat. More studies are still required to confirm the results and to identify more individual pesticides that could cause lung cancer, as well as other types of cancer. These issues should receive more attention since these chemicals have been used widely.
Figshare: Pesticide and lung cancer. https://doi.org/10.6084/m9.figshare.12356270.v428.
This project contains the following underlying data:
Figshare: Questionnaire-pesticide and lung cancer Thailand. https://doi.org/10.6084/m9.figshare.12356384.v226.
This project contains the following extended data:
Data are available under the terms of the Creative Commons Zero “No right reserved” data waiver (CC0 1.0 Public domain dedication).
First, our gratitude goes to the study participants, as without them, this study would not have been possible. We want to thank the village health volunteers for their help in data collection. We appreciate support by Dr. Adisorn Vatthanasak, chief of Nakhon Sawan Provincial Public Health Office. Thank you also to Mr. Kevin Mark Roebl of Naresuan University’s Writing Clinic for editing assistance.
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Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Partly
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: cancer epidemiology, occupational and environmental epidemiology, meta-analysis, bias analysis
Competing Interests: No competing interests were disclosed.
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Cancer epidemiology, pesticides, air pollution, occupational and environmental epidemiology
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Cancer epidemiology, pesticides, air pollution, occupational and environmental epidemiology
References
1. Marinaccio A, Consonni D, Mensi C, Mirabelli D, et al.: Authors' response: Mezei et al's "Comments on a recent case-control study of malignant mesothelioma of the pericardium and the tunica vaginalis testis".Scand J Work Environ Health. 2021; 47 (1): 87-89 PubMed Abstract | Publisher Full TextCompeting Interests: No competing interests were disclosed.
Reviewer Expertise: Cancer epidemiology, pesticides, air pollution, occupational and environmental epidemiology
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Partly
Are sufficient details of methods and analysis provided to allow replication by others?
No
If applicable, is the statistical analysis and its interpretation appropriate?
No
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Cancer epidemiology, pesticides, air pollution, occupational and environmental epidemiology
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Partly
Are sufficient details of methods and analysis provided to allow replication by others?
Partly
If applicable, is the statistical analysis and its interpretation appropriate?
Not applicable
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Occupational cancer epidemiology, lung cancer, case-control studies, cohort studies
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