This statistic shows the amount of registrations of newly diagnosed cases of lung cancer in England in 2021, by age group and gender. In this year, almost ************* cases were reported among men aged 70 to 74 years. It should be noted that the number of people in England in each age group varies and is therefore not necessarily a reflection of susceptibility to lung cancer.

In 2022, the mortality rate of lung cancer was the highest among those aged above 75 years of age in the European Union at ***** per 100,000 men and ***** per 100,000 women. The risk of developing lung cancer can increase by smoking, inhaling second hand smoke and exposure to asbestos.

Mortality from lung cancer (ICD-10 C33-C34 equivalent to ICD-9 162). To reduce deaths from lung cancer. Legacy unique identifier: P00508

For 2023, it was estimated that there would be 25 new lung cancer cases among those between aged 15 to 29 years old. Cancer is one of the leading causes of premature death in Canada. This statistic displays the estimated number of new lung cancer cases in Canada by age group in 2023.

Legacy unique identifier: P00508

Summary statistics of average lung cancer incidence rates and average daily smokers in percentage in 8 U.S. geographic regions, 1999–2012.

This dataset contains Cancer Incidence data for Lung Cancer (All Stages^) including: Age-Adjusted Rate, Confidence Interval, Average Annual Count, and Trend field information for US States for the average 5 year span from 2016 to 2020.Data are segmented by sex (Both Sexes, Male, and Female) and age (All Ages, Ages Under 50, Ages 50 & Over, Ages Under 65, and Ages 65 & Over), with field names and aliases describing the sex and age group tabulated.For more information, visit statecancerprofiles.cancer.govData NotationsState Cancer Registries may provide more current or more local data.TrendRising when 95% confidence interval of average annual percent change is above 0.Stable when 95% confidence interval of average annual percent change includes 0.Falling when 95% confidence interval of average annual percent change is below 0.† Incidence rates (cases per 100,000 population per year) are age-adjusted to the 2000 US standard population (19 age groups: <1, 1-4, 5-9, ... , 80-84, 85+). Rates are for invasive cancer only (except for bladder cancer which is invasive and in situ) or unless otherwise specified. Rates calculated using SEER*Stat. Population counts for denominators are based on Census populations as modified by NCI. The US Population Data File is used for SEER and NPCR incidence rates.‡ Incidence Trend data come from different sources. Due to different years of data availability, most of the trends are AAPCs based on APCs but some are APCs calculated in SEER*Stat. Please refer to the source for each area for additional information.Rates and trends are computed using different standards for malignancy. For more information see malignant.^ All Stages refers to any stage in the Surveillance, Epidemiology, and End Results (SEER) summary stage.Data Source Field Key(1) Source: National Program of Cancer Registries and Surveillance, Epidemiology, and End Results SEER*Stat Database - United States Department of Health and Human Services, Centers for Disease Control and Prevention and National Cancer Institute. Based on the 2022 submission.(5) Source: National Program of Cancer Registries and Surveillance, Epidemiology, and End Results SEER*Stat Database - United States Department of Health and Human Services, Centers for Disease Control and Prevention and National Cancer Institute. Based on the 2022 submission.(6) Source: National Program of Cancer Registries SEER*Stat Database - United States Department of Health and Human Services, Centers for Disease Control and Prevention (based on the 2022 submission).(7) Source: SEER November 2022 submission.(8) Source: Incidence data provided by the SEER Program. AAPCs are calculated by the Joinpoint Regression Program and are based on APCs. Data are age-adjusted to the 2000 US standard population (19 age groups: <1, 1-4, 5-9, ... , 80-84,85+). Rates are for invasive cancer only (except for bladder cancer which is invasive and in situ) or unless otherwise specified. Population counts for denominators are based on Census populations as modified by NCI. The US Population Data File is used with SEER November 2022 data.Some data are not available, see Data Not Available for combinations of geography, cancer site, age, and race/ethnicity.Data for the United States does not include data from Nevada.Data for the United States does not include Puerto Rico.

Mortality from lung cancer, directly age-standardised rate, persons, under 75 years, 2004-08 (pooled) per 100,000 European Standard population by Local Authority by local deprivation quintile. Local deprivation quintiles are calculated by ranking small areas (Lower Super Output Areas (LSOAs)) within each Local Authority based on their Index of Multiple Deprivation 2007 (IMD 2007) deprivation score, and then grouping the LSOAs in each Local Authority into five groups (quintiles) with approximately equal numbers of LSOAs in each. The upper local deprivation quintile (Quintile 1) corresponds with the 20% most deprived small areas within that Local Authority. The mortality rates have been directly age-standardised using the European Standard Population in order to make allowances for differences in the age structure of populations. There are inequalities in health. For example, people living in more deprived areas tend to have shorter life expectancy, and higher prevalence and mortality rates of most cancers. Lung cancer accounts for 7% of all deaths among men and in England every year and 4% of deaths among women every year. This amounts to 24% of all cancer deaths among men in England and 18% of all cancer deaths among women in England1. Reducing inequalities in premature mortality from all cancers is a national priority, as set out in the Department of Health’s Vital Signs Operating Framework 2008/09-2010/111. This indicator has been produced in order to quantify inequalities in lung cancer mortality by deprivation. This indicator has been discontinued and so there will be no further updates. Legacy unique identifier: P01406

Number and rate of new cancer cases diagnosed annually from 1992 to the most recent diagnosis year available. Included are all invasive cancers and in situ bladder cancer with cases defined using the Surveillance, Epidemiology and End Results (SEER) Groups for Primary Site based on the World Health Organization International Classification of Diseases for Oncology, Third Edition (ICD-O-3). Random rounding of case counts to the nearest multiple of 5 is used to prevent inappropriate disclosure of health-related information.

As of 2022, the age-standardized incidence rate of lung cancer among males in Polynesia was 54.7 per 100,000 population, the highest rate worldwide. The incidence rate of lung cancer among females was highest in Northern America. This statistic shows the age-standardized incidence rate of lung cancer worldwide as of 2022, by region and gender.

Summary statistics of lung cancer incidence rates for Whites in 8 U.S. geographic regions, 1999–2012 (cases per 100,000).

Deaths from lung cancer - Directly age-Standardised Rates (DSR) per 100,000 population Source: Office for National Statistics (ONS) Publisher: Information Centre (IC) - Clinical and Health Outcomes Knowledge Base Geographies: Local Authority District (LAD), Government Office Region (GOR), National, Primary Care Trust (PCT), Strategic Health Authority (SHA) Geographic coverage: England Time coverage: 2005-07, 2007 Type of data: Administrative data

Lung Cancer Deaths reports the number, crude rate, and age-adjusted mortality rate (AAMR) of deaths due to lung cancer.

This publication reports on newly diagnosed cancers registered in England during 2022. It includes this summary report showing key findings, spreadsheet tables with more detailed estimates, and a methodology document. Cancer registration estimates are provided for: • Incidence of cancer using groupings that incorporate both the location and type of cancer by combinations of gender, age, deprivation, and stage at diagnosis (where appropriate) for England, former Government office regions, Cancer alliances and Integrated care boards • Incidence and mortality (using ICD-10 3-digit codes) by gender and age group for England, former Government office regions, Cancer alliances and Integrated care boards This publication will report on 2022 cancer registrations only, trends will not be reported as the required re-stated populations for 2012 to 2020 are not expected to be published by the Office of National Statistics (ONS) until Winter 2024.

Lung cancer incidence rates by race, 1999–2012 (cases per 100,000).

Abstract Objective: To identify the socioepidemiologic and histopathologic patterns of lung cancer patients in the Middle Euphrates region. Patients and Methods: This study analyzed medical information from lung cancer patients at the Middle Euphrates Cancer Center in Iraq from January 2018 to December 2023. Demographic information (age, gender, residency, and education level) as well as clinical details (histopathological categorization) were obtained. The inclusion criteria included all confirmed lung cancer cases, while cases with inadequate data or non-lung cancer diagnosis were omitted. The data were analyzed using IBM SPSS Statistics (version 26). The data summarized using descriptive statistics, and chi-square tests used to identify correlations between categorical variables at a significance level of p < 0.05. Ethical approval was obtained from the relevant institutional review board. Results: A total of 1162 patients were included with mean age at diagnosis(64.47±11.45) years. Majority of patients are over 60 years (64.4%), followed by (40–60 years), 34%, and the least affected group is under 40 years (1.6%). Males account for the majority of cases (68%), while females about 32%, with male:female ratio that fluctuate around 2:1. Illiterate patients and those with low education levels represent the largest proportion accounting for about 87.9% of the study population. Squamous Cell Carcinoma (SCC) is the most frequent subtype (41.7%), followed closely by Adenocarcinoma (AC) at 37%, and Small Cell Lung Cancer (SCLC), 10.5%. Although SCC is the predominant subtype overall, AC incidence is increasing overtime (from 31.7% in 2018 to 41.4% in 2023) with predominance in females, younger and higher educated groups. While the percentage of SCLC and other less common subgroups remained relatively stable over time, there is a significant reduction in NSCLC-NOS diagnoses (from 11.1% in 2018 to 3.2% in 2023). Conclusions: In Iraq, specifically in the Middle Euphrates region, lung cancer is a major public health issue in the elder age groups. The two main subtypes, SCC and AC, are the main contributors, with obvious increment in AC cases in the recent years. The shifting trends indicate the urgent need for improved screening strategies, focused preventative initiatives, and customized treatment plans in view of changing risk profiles.

Data Showing - Age rates of lung cancer incidence - Plymouth - 2009 - 2013 Data and Resources Age rates of lung cancer incidence in Plymouth 2009-2013 .csv Age rates of lung cancer incidence in Plymouth 2009-2013

Number and rate of new cancer cases by stage at diagnosis from 2011 to the most recent diagnosis year available. Included are colorectal, lung, breast, cervical and prostate cancer with cases defined using the Surveillance, Epidemiology and End Results (SEER) Groups for Primary Site based on the World Health Organization International Classification of Diseases for Oncology, Third Edition (ICD-O-3). Random rounding of case counts to the nearest multiple of 5 is used to prevent inappropriate disclosure of health-related information.

Supporting figures and tables. Figure S1, Prevalence of smoking by age in 1950 birth cohort. Summary of shared input data (used by all 5 models) on smoking patterns for the US cohort born in 1950. Prevalence shown is estimated in the absence of lung cancer mortality. Version 1.0 of the Smoking History Generator (SHG) refers to published data through 2000 (Anderson, et al.), and version 1.5 supplies the 1950 birth cohort used for this analysis with data through 2009 and projections past 2009. Figure S2, Other-cause mortality, by smoking quintile, in 1950 birth cohort. These curves show the other-cause (non-lung cancer) mortality for never smokers and for current smokers by smoking quintile (Q, of cigarettes per day) for the male birth cohort of 1950, out to age 99. Former smokers are intermediate to current and never smokers. There is a similar plot for females. These were shared inputs used by all the models. Note that the rates of non-lung cancer mortality represent the US population, not trial (NLST or PLCO) participants. Figure S3, Prevalence of smoking by age in 1950 birth cohort. Output from one model showing smoking prevalence by age (calendar year), in a no screening scenario. Proportions of current/former/never smokers are in the presence of lung cancer mortality as well as all-cause mortality. Figure S4, Prevalence of smoking by age and pack-years in 1950 birth cohort. Output from one model showing smoking prevalence by category of pack-year and age. The proportion of the cohort by age that has accumulated the specified number of pack-years in the presence of lung cancer mortality and other-cause mortality. Figure S5, Incidence, no screening scenario, output from all models. For predictions past observed SEER data (over age 60) there are no observed data, but we used an age-period-cohort model to project past observed years (‘Projected’ red double line in plots below), which shows that the models are most divergent after age 85, when SEER data become most sparse. We cannot strictly compare incidence to that in prior birth cohorts since smoking patterns are dissimilar, and incidence varies by cohort. Figure S6, Mortality, no screening scenario, output from all models. The vertical line at age 90 indicates age at which all event counts (screens, deaths and deaths averted, and life years gained) were truncated for the analyses reported here. Although the models ranked programs similarly, there was variability in the total numbers of predicted lung cancer cases, deaths, and therefore lung cancer deaths prevented. The differences in rates in the no screening scenario in large part explains the predicted differences between models. The four models (E, F, S, and U) which use two-stage or multi-stage clonal expansion models have more similarly shaped curves than the fifth model (M), which does not use a clonal expansion component (see Table S1 in File S1). Figure S7, Results from all models analogous to Figure 1 in article. Figure S8, Results from all models analogous to Figure 2 in article. Figure S9, Secondary results with reduced operative candidacy with age. The dashed line denotes the efficiency frontier in the main analysis. Table S1, Additional Detail on Models. Table S2, Complete List of 120 Consensus Efficient Scenarios. Table S3, Comparison of Consensus Efficient Scenarios Identified Using Life-years Saved or Lung Cancer Deaths Avoided as Measure of Benefit. (DOCX)

Summary statistics for lung cancer incidence rates for Blacks and Whites in the Mid-South by gender, 1999–2012 (cases per 100,000).