Keywords
Lung cancer, Pesticides exposure, Herbicides, Insecticides, Fungicides
This article is included in the Oncology gateway.
Lung cancer, Pesticides exposure, Herbicides, Insecticides, Fungicides
Data were reanalyzed using new information on cigarette smoke. More information on lung cancer patients has been provided, including morphology of lung cancer and diagnostics tool for confirmation of the case. On study limitation, bias from exposure misclassification has been further discussed.
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 of 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.
Pesticide exposure might also cause 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 can also link 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 (odds ratio (OR) = 1.6, 95% confidence interval (CI) 1.11-2.31). Other individual pesticides that had been associated with lung cancer were chlopyrifos17, diazinon18, pendimenthalin19 and carbofuran20.
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 associations between pesticide exposure and lung cancer among people living in Nakhon Sawan province, Thailand. The results can be used for the prevention of lung cancer, and to support the global literature.
This study is a population-based case-control study. Cases referred 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 Thai Cancer Based Program (TCB) operated by Thai National Cancer Institute21. 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 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 hematology, and 24 by history and physical exam.
Controls were neighbors who did not have lung or any other 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 was determined to be 229 for cases and 458 for controls using Kelsey’s formula22 (unmatched population base case-control study). The assumptions used were as follows: proportion of case with pesticide exposure was 0.523, proportion of control with exposure was 0.424, and the ratio of case to control was 1:225.
Data on pesticide exposure and other risk factors were collected using a questionnaire previously used in a study on pesticide exposure and diabetes26. The questionnaire has two major parts (provided as Extended data in English)27. 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 life time 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 smoker28.
In Part 2, information on the historical use (mix or spray) of pesticides were 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 on 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. Both crude and adjusted ORs with 95% confidence intervals (CIs) were presented. Adjusted ORs were analyzed 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 quartiles (Q1-Q4; Q1 being the lowest exposure and Q4 the highest). The lung cancer risk was then predicted, using quartile 1 as a reference. For each specific pesticide, exposure data was categorized only to “ever used” and “never used”, but not the cumulative exposure days because number of subjects who reported using each pesticide was too small.
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, pollution exposure, and cigarette smoking. More detailed demographic data among case and control groups were in Table 1 and in Underlying data29.
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 lowest quartile (Q1) of number of days using herbicides, those in Q2-Q4 days of using herbicides had an elevated risk of lung cancer with odds ratio (OR) between 3.31 (95% CI 1.49–7.34) for people with Q2 exposure, and 12.58 (95% CI 5.70–27.75) for Q4 exposure (p < 0.001). A similar association was also found for days of insecticide use and lung cancer (OR = 3.96 for Q3, and OR = 4.13 for Q4, p 0.002). For fungicides, only the Q4 group had a significant risk (OR = 4.25; 95% CI 1.23–14.72). 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).
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 | 17.8 | 51 | 23.4 | 1.42 (0.83–2.41) | 1.36 (0.79–2.56) |
11–30 | 76 | 58.9 | 107 | 49.1 | 1.18 (0.67–2.09) | 1.34 (0.58–2.43.16) |
1–10 | 30 | 23.3 | 60 | 27.5 | Reference | Reference |
P-value*** | 0.192 | 0.169 | ||||
Number of days using herbicides (N = 347) | ||||||
Q4 (>960) | 52 | 40.3 | 30 | 13.8 | 10.26 (4.97–21.18) | 12.58 (5.70–27.75)** |
Q3 (501–960) | 45 | 34.9 | 50 | 22.9 | 5.38 (2.67–10.83) | 7.14 (3.32–15.33)** |
Q2 (160–500) | 23 | 17.8 | 50 | 22.9 | 2.95 (1.39–6.25) | 3.31 (1.49–7.34)** |
Q1 (<160) | 9 | 7.0 | 88 | 40.4 | Reference | Reference |
P-value*** | <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 | 31.9 | 43 | 22.7 | 2.68 (1.31–5.49) | 2.65 (1.23–5.72)** |
11–30 | 63 | 54.3 | 96 | 50.8 | 2.05 (1.07–3.91) | 2.23 (1.13–4.38)** |
1–10 | 16 | 13.8 | 50 | 26.5 | Reference | Reference |
P-value*** | 0.029 | 0.020 | ||||
Number of days using the insecticides (N = 305) | ||||||
Q4 (>1,200) | 37 | 31.9 | 39 | 20.6 | 3.18 (1.55–6.48) | 4.13 (1.27–15.14)** |
Q3 (481–1,200) | 33 | 28.5 | 34 | 18.0 | 2.94 (1.46–5.91) | 3.96 (1.21–12.97)** |
Q2 (200–480) | 28 | 24.1 | 53 | 28.1 | 1.73 (0.86–3.48) | 2.21 (0.69–7.09) |
Q1 (<200) | 18 | 15.5 | 63 | 33.3 | Reference | Reference |
P-value*** | 0.002 | 0.002 | ||||
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 | 16.6 | 10 | 13.5 | 1.45 (0.44–1.77) | 2.92 (0.30–6.03) |
11–30 | 23 | 54.8 | 39 | 52.7 | 1.22 (0.52–2.90) | 2.13 (0.42–2.32) |
1–10 | 12 | 28.6 | 25 | 33.8 | Reference | Reference |
P-value*** | 0.096 | 0.089 | ||||
Number of days using the fungicides (N = 116) | ||||||
Q4 (>500) | 16 | 38.1 | 13 | 17.6 | 3.39 (1.14–10.08) | 4.25 (1.23–14.72)** |
Q3 (161–500) | 9 | 21.4 | 17 | 23.0 | 1.45 (0.46–4.57) | 1.53 (0.41–4.73) |
Q2 (96–160) | 9 | 21.4 | 22 | 29.7 | 1.12 (0.37–3.45) | 1.22 (0.0.42–4.01) |
Q1 (<96) | 8 | 19.1 | 22 | 29.7 | Reference | Reference |
P-value*** | 0.029 | 0.022 |
Pesticide | Case | Control | OR (95% CI) | Adjusted OR (95% CI)* | ||
---|---|---|---|---|---|---|
n | % | n | % | |||
Total | 233 | 100.0 | 447 | 100.0 | ||
Herbicides | ||||||
Glyphosate | ||||||
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 | ||
Paraquat | ||||||
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 | ||
2, 4-Dichlorophenoxy acetic acid | ||||||
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 | ||
Butachlor | ||||||
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 | ||
Propanil | ||||||
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 | ||
Alachlor | ||||||
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 | ||
Insecticides | ||||||
Organochlorine insecticides | ||||||
Endosulfan | ||||||
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 | ||
Dieldrin | ||||||
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 | ||
DDT | ||||||
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 | ||
Organophosphate insecticides | ||||||
Chlorpyrifos | ||||||
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 | ||
Folidol | ||||||
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 | ||
Mevinphos | ||||||
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 | ||
Carbamate insecticides | ||||||
Carbaryl/Savin | ||||||
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 | ||
Carbofuran | ||||||
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 | ||
Pyrethoid insecticides | ||||||
Abamectin | ||||||
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 | ||
Fungicides | ||||||
Armure/Propiconazole | ||||||
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 | ||
Methyl aldehyde | ||||||
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 |
The study results showed a positive association between lung cancer and the historical use of herbicides, insecticides, and fungicides (Table 3). Herbicides and insecticides have a stronger association to lung cancer than fungicides. Compared to the Q1 group who used pesticides for less than 160 days, demonstrated lower risks of lung cancer than those in Q2 and Q3, who showed elevated risks, while Q4 had the highest risk. (Q4) (OR = 12.58, 95% CI 5.70–27.75). A similar pattern was also observed among the users of insecticides. The risk of lung cancer exponentially increased due to extended periods of using insecticides. (Q3-Q4) with OR between 3.96 (95% CI 1.21–12.97) and 4.13 (95% CI 1.27–15.14). The highest category of years using insecticides (Q4) also showed a positive association with lung cancer (OR = 4.13; 95% CI 1.27–15.14). For fungicides, a significant association was found only among fungicide users in Q4 (>500 days) (OR = 4.25; 95% CI 1.23–14.72).
These results were consistent with literature indicating the potential carcinogenicity of pesticides30. 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 apoptosis31. Pesticides may also increase the risk of cancer via other mechanisms including genotoxicity, tumor promotion, epigenetic effects, hormonal action and immunotoxicity32. In epidemiological study, evidence linked pesticide exposure to lung cancer are increasing, and the issue will be further discussed in the following section.
For individual pesticides, the study found lung cancer to be statistically associated with 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). 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 systems33. In the USA, the Agricultural Health Study 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)34. In Thailand, 688 tons of dieldrin was used in 1981–1990, before it was banned on May 16, 1990.
A study among pest control workers in Florida, USA found a long term exposure to organophosphate and carbamate insecticides to increase mortality risk of lung cancer (OR = 1.4; 95% CI 0.7–3.0) for subjects licensed from 10–19 year; OR = 2.1; 95% CI 0.8–5.5 for those licensed 20 year or more11. In the Agricultural Health Study, a dose response relationships was found between lung cancer and chlorpyrifos (RR = 2.18; 95% CI 1.31–3.64)17 and diazinon (RR = 3.46; 95% CI 1.57–7.65)18. Similar results were also replicated in later studies of the Agricultural Health Study cohort for chlorpyrifos (RR = 1.80; 95% CI 1.00–3.23), which are referring to applicators in the lowest category of exposure17. At this time, chlorpyrifos still not banned by Thai government. On the other hand, chlorpyrifos was the primary insecticide imported to Thailand (1,193,302 kilograms in 2013)35.
For carbofuran, it has demonstrated mutagenic properties in laboratory studies3. In the Agricultural Health Study, lung cancer risk of carbofuran for those with >109 days of lifetime exposure (RR = 3.05; 95% CI, 0.94–9.87) compared with those with < 109 lifetime exposure days20. In Thailand, a study reported 87 different commercial brands of insecticides which were used for 202 rice fields in Suphanburi Province (abamectin 40%, followed by chlorpyrifos 30%, and carbofuran 20%), 93 brands of plant hormones, and 56 brands of chemicals for the control of plant diseases36.
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 illness37. 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 association38. 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 of the lung cancer patients except those who were severely ill, were collected to minimize the bias.
This study found that the occurrence of lung cancer among people in Nakhon Sawan province, Thailand is associated with pesticide use. Out of 17 individual pesticides investigated, dieldrin, chlorpyrifos, and carbofuran showed significant associations with lung cancer incidence. These results are consistent with the literature from other parts of the world. Further studies should focus on identifying more individual pesticides that could cause lung cancer, as well as other types of cancer.
Figshare: Pesticide and lung cancer. https://doi.org/10.6084/m9.figshare.12356270.v329.
This project contains the following underlying data:
Figshare: Questionnaire-pesticide and lung cancer Thailand. https://doi.org/10.6084/m9.figshare.12356384.v127.
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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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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