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Original article
Association between age, deprivation and specific comorbid conditions and the receipt of major surgery in patients with non-small cell lung cancer in England: A population-based study
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  1. Aurélien Belot1,
  2. Helen Fowler1,
  3. Edmund Njeru Njagi1,
  4. Miguel-Angel Luque-Fernandez1,
  5. Camille Maringe1,
  6. Winnie Magadi1,
  7. Aimilia Exarchakou1,
  8. Manuela Quaresma1,
  9. Adrian Turculet1,
  10. Michael D Peake2,3,4,
  11. Neal Navani5,6,
  12. Bernard Rachet1
  1. 1 Cancer Survival Group, Department of Non-Communicable Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK
  2. 2 Department of Respiratory Medicine, University Hospitals of Leicester, Leicester, UK
  3. 3 National Cancer Registration and Analysis Service, Public Health England, London, UK
  4. 4 Centre for Cancer Outcomes, University College London Hospitals, London, UK
  5. 5 UCL Respiratory, University College London, London, UK
  6. 6 Department of Thoracic Medicine, University College London Hospital, London, UK
  1. Correspondence to Dr Aurélien Belot, Cancer Survival Group, Department of Non-Communicable Disease Epidemiology, London School of Hygiene & Tropical Medicine, London WC1E 7HT, UK; aurelien.belot{at}lshtm.ac.uk

Abstract

Introduction We investigated socioeconomic disparities and the role of the main prognostic factors in receiving major surgical treatment in patients with lung cancer in England.

Methods Our study comprised 31 351 patients diagnosed with non-small cell lung cancer in England in 2012. Data from the national population-based cancer registry were linked to Hospital Episode Statistics and National Lung Cancer Audit data to obtain information on stage, performance status and comorbidities, and to identify patients receiving major surgical treatment. To describe the association between prognostic factors and surgery, we performed two different analyses: one using multivariable logistic regression and one estimating cause-specific hazards for death and surgery. In both analyses, we used multiple imputation to deal with missing data.

Results We showed strong evidence that the comorbidities ‘congestive heart failure’, ‘cerebrovascular disease’ and ‘chronic obstructive pulmonary disease’ reduced the receipt of surgery in early stage patients. We also observed gender differences and substantial age differences in the receipt of surgery. Despite accounting for sex, age at diagnosis, comorbidities, stage at diagnosis, performance status and indication of having had a PET-CT scan, the socioeconomic differences persisted in both analyses: more deprived people had lower odds and lower rates of receiving surgery in early stage lung cancer.

Discussion Comorbidities play an important role in whether patients undergo surgery, but do not completely explain the socioeconomic difference observed in early stage patients. Future work investigating access to and distance from specialist hospitals, as well as patient perceptions and patient choice in receiving surgery, could help disentangle these persistent socioeconomic inequalities.

  • lung cancer
  • surgical treatment
  • population-based data
  • socioeconomic inequalities
  • comorbidities

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Key messages

What is the key question?

  • What is the association between specific comorbid conditions and the receipt of major surgical treatment in patients with non-small cell lung cancer (NSCLC), and does it explain socioeconomic inequalities in the receipt of treatment?

What is the bottom line?

  • We showed strong evidence that (i) the comorbidities ‘congestive heart failure’, ‘cerebrovascular disease’ and ‘chronic obstructive pulmonary disease’ reduced the rate of surgery in patients with early stage NSCLC, and (ii) after adjusting for covariates such as age, stage and performance status, socioeconomic inequalities in receiving surgical treatment remain.

Why read on?

  • Using population-based data, we quantified the association between specific comorbid conditions and the receipt of surgery, and showed that socioeconomic inequalities in receiving major surgical treatment persist, even after accounting for the main prognostic factors (stage, performance status, specific comorbid conditions).

Introduction

Lung cancer is the leading cause of cancer death in the UK for both men and women: in 2014, >19 000 deaths were observed in men and >16 000 in women, corresponding to age-standardised mortality rates of 89.69 and 60.52 per 100 000 person-years, respectively.1 Despite encouraging decreasing age-standardised incidence in lung cancer,1 it remains a major public health issue given its poor prognosis; for patients diagnosed in England between 2010 and 2014, the 1-year age-standardised net survival probability was estimated at 34% in men and 40% in women, those figures being 11% and 16% at 5 years.2

Different studies have reported socioeconomic inequalities, with a consistently lower survival for the more deprived patients.3–5 Disentangling the reasons behind these socioeconomic inequalities remains a topic of active research. One aspect to consider is any variation in patient characteristics between socioeconomic groups. For example, studies that have examined the prevalence of comorbidity according to socioeconomic group found that while comorbidity, or indeed multimorbidity, was most prevalent in the elderly, it was also found in younger patients of lower socioeconomic status.6 7 Moreover, some authors have suggested that variations in surgical resection rates and more generally in access to treatment could partly explain those inequalities.8–12 Understanding which factors are associated with the probability to receive major surgical treatment could help further improve the surgical resection rate, and thus lung cancer survival.8 In addition to the central role of tumour stage at diagnosis, the role of comorbidities is often studied using the summarised Charlson score.9–11 Thus, the question regarding the association between specific individual comorbid conditions and the probability to receive major surgery remains unresolved. We hypothesise that patients with comorbidities have lower probability of receiving surgery than patients without comorbidities. Conversely, we hypothesise that patients diagnosed with an early stage tumour and whose health status is good should be very likely to receive a surgical treatment with curative intent. Moreover, controlling for these specific comorbidities will allow assessment of whether the association between socioeconomic deprivation and treatment remains.

We aim here to quantify the association between patient and tumour factors and the probability to receive major surgical treatment for patients diagnosed with non-small cell lung cancer (NSCLC) in England in 2012, with a particular emphasis on the roles played by specific comorbid conditions and deprivation.

Methods

Data

Data were obtained from the National Cancer Registry at the Office for National Statistics13 for all adults (aged 15–99 years) diagnosed with a first primary malignant NSCLC (all ICD-O-3 morphology codes except those between 8041 and 8045, behaviour /3) in 2012 in England. Patients diagnosed with a lung cancer for which the morphology was malignant neoplasm not otherwise specified (NOS) or epithelial neoplasms NOS, were also included. All patients have been followed up until the 31 December 2015 by the National Health Service Central Register, to update each patient’s vital status (alive, emigrated, dead or not traced). Data were further linked to the National Lung Cancer Audit (NLCA) data,14 using successively different combinations of patient identifier variables to ensure successful matching of same patients in the two datasets.15 The NLCA data captured information on several tumour and patient-related factors, such as (i) the tumour’s T, N, M (coding the size, the node and the metastasis components of stage, respectively), (ii) the patient’s performance status (PS), (iii) whether a PET-CT scan was performed (yes/no) and (iv) the surgical procedure undertaken with the intention of curing the patient.14 PET-CT scan is recommended prior to surgery as it provides more accurate staging information, in particular detecting metastatic disease unidentified by other imaging investigations. We applied a previously developed algorithm to derive for each tumour a summarised four-category stage at diagnosis variable using information from the NLCA in the first instance, and from the national cancer registry data if no information were present in the NLCA data.16

For each patient with NSCLC, we used the inpatient, outpatient and Accident and Emergency Hospital Episode Statistics (HES) datasets to derive prevalence indicators of the 17 comorbid conditions of the Charlson Comorbidity Index, in addition to obesity.17 We focused on comorbidities that would influence fitness to undergo major surgery, namely myocardial infarction, congestive heart failure, peripheral vascular disease, cerebrovascular disease and Chronic Obstructive Pulmonary Disease (COPD).18 To retrieve information on comorbidity, we used a 6-year window up to 6 months before diagnosis, checking the diagnostic fields of the HES data to identify whether any of the aforementioned comorbidities had been recorded during this period.17

The primary source of information for the major surgical treatment was the NLCA data, supplemented with information from the HES data where the former was unavailable. In both datasets, information on surgery (with the corresponding date) was recorded using the Office of Population Censuses and Surveys Classification of Interventions and Procedures (fourth version (OPCS-4)).19 We preset a time window of 30 days before diagnosis and 180 days after diagnosis to identify the first major surgical treatment received for each patient. The categorisation of surgery as ‘major’ was made according to the OPCS-4 codes recorded for the procedure, and was based on definitions of ‘surgery with curative intent’ devised from extensive input from clinicians and oncologists and endorsed by the Site-Specific Clinical Reference Groups of the National Cancer Intelligence Network (see online supplementary appendix 1).20 Where patients had surgery before the recorded cancer diagnosis date, we recoded their time from diagnosis to surgery as 1 day for the time-to-event analysis (see ’Analysis' section).

Supplementary file 1

We measured deprivation using the Income Domain from the 2010 England Indices of Multiple Deprivation (IMD) defined at the Lower Super Output Area level (average population of 1500).21 The Income Domain score is a combination of five indicators, and it measures the proportion of the population in an area experiencing deprivation related to low income. It ranges from 0% to 77%21 (ie, the higher the more deprived, see online supplementary appendix figure S2) and is named ‘deprivation score’ hereafter. More details on the different deprivation measures and the way they are calculated could be found here (https://www.gov.uk/government/statistics/english-indices-of-deprivation-2010).

Analysis

The studied prognosis factors were sex, age at diagnosis, deprivation score, PS, stage at diagnosis, a binary variable indicating if a PET/PET-CT scan was performed and five binary variables indicating the presence of specific comorbid conditions.

We performed two types of analysis to describe the receipt of surgery while controlling for the prognostic factors. First, we used a logistic regression model with major surgery (yes/no) as the outcome (analysis 1). However, some patients may have died before having had a chance to receive surgery. Second, we modelled the two cause-specific hazards (ie, one for surgery and one for death) using the semi-parametric Cox model (analysis 2). We analysed the first event with the corresponding time-to-event, thus accounting for the competing risk of death22: patients who died without receiving surgery were censored for the surgery-specific rate. Conversely, patients who received surgery were censored at their time of surgery when estimating the death-specific rate. As the time window for the surgery went up to a maximum of 180 days, patients alive without surgery after 180 days were censored at that time.

In each analysis, the predictors were defined as follows: for the continuous variables age at diagnosis and deprivation score, we assumed non-linear associations using flexible functional forms (quadratic splines with one inflection point around the median, ie, at 70 years for the age at diagnosis, and at 0.1 for the deprivation score); from the original PS14 coded according to the WHO classification (indicating a person’s status relating to activity/disability), we recoded this variable in two groups: good (0 or 1) versus poor (2, 3 and 4); the four-category variable for stage at diagnosis was dichotomised in two groups: early stage (stage 1 and 2) versus late stage (3 and 4). It would be expected that patients with good PS and early tumour stage would be offered surgery as the first-choice treatment. Finally, we assumed an interaction between all the variables and the binary indicator defining early versus late stage.

To deal with the issue of missing data, we performed multiple imputation (MI) using the ‘Substantive-Model Compatible Fully Conditional Specification’ method,23 under the Missing At Random assumption24 (meaning that the probability of missing data in the particular covariate is dependent on the observed data, ie, the other covariates and the outcome, but not additionally on the unobserved value of the particular covariate). The variables PET-CT scan, stage and PS had missing information, up to 30% of missing values for the PET-CT scan variable. These three variables being binary, we used a logistic regression model for the imputation including as variables all the prognostic factors defining the linear predictor (see above) in addition to the outcome (ie, the binary surgery variable for analysis 1 or the time and the type of event for analysis 2). We generated 30 imputed datasets.25

To assess the strength of the association between the outcome and the deprivation score, we performed a likelihood ratio test (LRT) on each imputed dataset by comparing a model that included the deprivation score (in its non-linear form and with the interaction) with one that did not. Each of the 30 LRT statistics were compared with a Χ2 distribution with 6 df. We also used a joint Wald test from the estimated parameters obtained after MI to assess the strength of the association between the outcome (either binary or time-to-event) and the deprivation score.

We repeated the steps detailed above on the complete case data (using only the data from patients having no missing information in any of the variables), which is usually called a ‘sensitivity analysis’; it allows to assess how variables the results are to the missing data mechanism assumed, and thus how much caution may be needed in interpreting them.26

Results

Study population

The study population were 31 351 patients diagnosed with NSCLC in England in 2012 (11 030 adenocarcinomas: 35%, 3442 large cells: 11%, 7058 squamous cells: 23% and 9821 other histological subtypes: 31%). The percentage of successful linkage between the cancer registry data (the core data) and the NLCA data was 83%, and it was higher than 99% for linkage with the HES data. From these patients, 4850 received surgery (table 1). The mean age was 72.8 years overall, the group who received surgery were younger on average (68.4 compared with 73.6 years). Sixty-eight per cent of NSCLC were diagnosed with an advanced stage, 9% stage being missing. Information of PET-CT scan and PS was also missing for 30% and 24% of patients, respectively. COPD was the most prevalent comorbidity (22%) with much lower prevalence observed for all other comorbidities (between 5.2% and 6.4%).

Table 1

Characteristics of patients diagnosed with non-small cell lung cancer in England in 2012

Results from analysis 1: the multivariable logistic regression

The strongest predictor of the odds of receiving surgery was stage: the adjusted odds of receiving surgery for advanced stage patients was 0.01 times that of early stage patients (odds ratio (OR) 0.01, 95% confidence interval (CI) 0.007 to 0.014) (table 2). This was expected because surgery is rarely offered to advanced stage patients. However, it indicates evidence of the quality and the validity of the dataset. Interactions between binary stage (early/advanced) and all other factors included in the logistic model enabled the parameter estimates for early and advanced stage to be interpreted separately, and we focus on interpreting the results among early stage patients unless otherwise stated. A poor PS (2, 3 or 4) dramatically reduced the odds of receiving surgery (OR 0.15, 95% CI 0.13 to 0.17). A recorded diagnosis of congestive heart failure, cerebrovascular disease or COPD was strongly associated with reduced odds of receiving surgery (OR 0.55, 95% CI 0.40 to 0.74, OR 0.58, 95% CI 0.45 to 0.76 and OR 0.50, 95% CI 0.43 to 0.57, respectively). By contrast, having had a PET-CT scan was associated with an increased odds of receiving surgery (OR 3.65, 95% CI 3.08 to 4.33). Women had higher odds of having surgery compared with men (OR 1.22, 95% CI 1.08 to 1.38).

Table 2

Adjusted* ORs of receiving surgery with corresponding 95% CIs within each stage-specific stratum†, and estimated (i) after multiple imputation and (ii) only using complete cases

The probability to receive surgery for both early and advanced stage patients without any comorbidities, with good PS and who had a PET-CT scan performed is provided for men with low deprivation (score of 0.1) by age at diagnosis (figure 1A). We observed a clear association between a patients’ age and the probability of receiving surgery with a dramatic decrease after 75 years: the probability to receive surgery for a patient aged 50 years was 87.9% (95% CI 85.4 to 90.0) compared with 65.2% (95% CI 61.9 to 68.3) at 80 years (figure 1A).

Figure 1

Predicted probability of receiving major surgery with 95% CI for early stage (solid line) and advanced stage (dashed line) in male patients with non-small cell lung cancer without any comorbidities, with good performance status, having had a PET-CT scan: (A) according to age at diagnosis with a deprivation score of 0.1 or (B) according to deprivation score with an age at diagnosis of 70 years. Results are based on the multivariable logistic regression. The ranges of age at diagnosis and deprivation score were limited to the 2.5th and 97.5th percentile of the observed distribution.

The probability to receive surgery for both early and advanced stage patients aged 70 years at diagnosis by deprivation score is provided for men (figure 1B). The joint Wald test showed evidence of differences on the probability to receive surgery by deprivation (p<0.01 of the Χ2 test comparing models with and without deprivation score). This was also confirmed by the 30 LRT, all showing strong association between surgery and deprivation score. Overall, we observed decreasing probability of surgery from least to most deprived patients in early stage patients (figure 1B): the probability to receive surgery was 86.0% (95% CI 83.1 to 88.4) for patients living in areas with 3% of people with low income (ie, deprivation score of 0.03, less deprived) compared with 78.6% (95% CI 75.7 to 81.3) for patients living in areas with 40% of people with low income (ie, a deprivation score of 0.4, more deprived). Such difference was not observed in advanced stage patients for whom the probability to receive surgery was estimated around 16% for all deprivation scores (figure 1B).

The multivariable regression model does not include interactions between sex and age at diagnosis nor between sex and deprivation score. This leads to patterns of predicted probabilities of surgery for women similar to men, while at a different absolute level, by age and deprivation; we reported the predicted probability to receive surgery for both early and advanced stage patients without any comorbidities, with good PS and who had a PET-CT scan performed for women with a deprivation score of 0.1 according to age at diagnosis (see online supplementary appendix figure S1a), and for women aged 70 years at diagnosis according to deprivation score (see online supplementary appendix figure S1b).

Comparing the results with those obtained with the complete case analysis, we observed a similar overall pattern of results, with slight differences in some point estimates (table 2). These differences were expected as when we explored the missing data mechanism, we found that the probability of missing data for PS and for PET-CT scan was strongly associated with the outcome variable after controlling for other covariables. Such an observation of the missing data mechanism implied that the analysis based on complete cases would be expected to be biased.24

Results of analysis 2: competing risks analysis

The competing risk analysis corroborated the results obtained with the multivariable logistic regression, with a low HR of receiving surgery for all advanced stage patients and for patients with poor PS in both early and advanced stage of diagnosis (table 3). The estimated HRs associated with comorbidities also showed strong evidence of a lower rate of receiving surgery for patients with congestive heart failure, cerebrovascular disease and COPD in early stage patients. The mortality rate was clearly associated with stage: advanced stage patients had a mortality rate 3.34 (95% CI 2.60 to 4.27) times higher than patients with an early stage diagnosis. A poor PS increased the mortality rate in both early and advanced stage patients. None of the comorbid conditions showed any strong association with mortality.

Table 3

Adjusted* HRs of receiving surgery and of death with corresponding 95% CIs within each stage-specific stratum†, and estimated (i) after multiple imputation and (ii) only using complete cases

The rate of receiving surgery decreased dramatically for older patients (figure 2A): early stage patient aged 80 years at diagnosis had around half the rate of receiving surgery of early stage patients aged 70 years (HR 0.57, 95% CI 0.54 to 0.60). Furthermore, we found strong evidence of an association between the rate of receiving surgery and deprivation score from both the joint Wald test and the 30 LRTs. The rate of receiving surgery for an early stage deprived patient (deprivation score of 0.4) was 12% lower than that of a less deprived patient (deprivation score of 0.1, HR 0.88, 95% CI 0.80 to 0.97) (figure 2B). We observed a clear association with age for both stage groups (figure 3A), but no association with deprivation score (figure 3B) on the hazard of death without surgery. From the complete case analysis, we reported similar patterns with slight differences in some point estimates (table 3).

Figure 2

Adjusted HR of receiving major surgery with 95% CI for early stage (solid line) and advanced stage (dashed line) in male patients with non-small cell lung cancer without any comorbidities, with good performance status, having had a PET-CT scan: (A) according to age at diagnosis with a deprivation score of 0.1 or (B) according to deprivation score with an age at diagnosis of 70 years. Results are based on the competing risks analysis using semi-parametric Cox models. The ranges of age at diagnosis and deprivation score were limited to the 2.5th and 97.5th percentile of the observed distribution.

Figure 3

Adjusted HR of death with 95% CI for early stage (solid line) and advanced stage (dashed line) in male patients with non-small cell lung cancer without any comorbidities, with good performance status, having had a PET-CT scan: (A) according to age at diagnosis with a deprivation score of 0.1 or (B) according to deprivation score with an age at diagnosis of 70 years. Results are based on the competing risks analysis using semi-parametric Cox models. The ranges of age at diagnosis and deprivation score were limited to the 2.5th and 97.5th percentile of the observed distribution.

Discussion

This study found strong evidence of an inverse association between the receipt of surgery and the comorbidities congestive heart failure, cerebrovascular disease and COPD in patients with early stage NSCLC. We also observed an important fall in the receipt of surgery with increasing age at diagnosis. Despite adjusting for these prognostic factors, the receipt of surgery still also depended on the deprivation score: more deprived patients have a lower probability of receiving surgical treatment compared with less deprived patients. Stage at diagnosis and the patient’s PS were confirmed as the strongest predictors for receiving major surgery while there was a clear association between having had a PET-CT scan and the receipt of major surgery.

One major strength of the study is the use of population-based cancer registry data linked to NLCA data and HES data, which provided an enriched source of information describing the probability to receive surgery among patients with NSCLC diagnosed in England in 2012. We focused on patients with NSCLC as surgery is the recommended treatment in contrast to small-cell lung carcinomas, where the primary treatment is usually chemotherapy. We benefited from algorithms that made the best use of our data,16 17 and enabled information on stage at diagnosis and specific type of comorbidities to be included as predictors for the probability to receive surgery. We assumed that the measurement of detailed information on important prognostic factors such as comorbidities, stage, PET-CT scan and PS were either properly recorded (ie, no measurement error nor misclassification) or properly retrieved using the developed algorithms. We analysed an area-based measure for deprivation21; it has the advantage of encapsulating both the individual (SES) and the greater environment where the patient lives.27

The study dealt with the problem of missing data using a MI technique, which properly accounts for the presence of non-linear functional forms for the continuous variable, as well as interactions between variables.23 This is another strength of this work as we found other studies that either discarded missing data28 29 or treated them as another category,10 11 30 although neither of these approaches are recommended. As we were expecting a strong association between stage at diagnosis and the outcome, we assumed an interaction between stage and all the other prognostic factors, which was particularly insightful for interpreting results among early stage lung cancer. We analysed continuous variables (age and deprivation score) in their existing form, allowing the depiction of their continuous gradual association with the receipt of surgery through flexible functional forms (such as splines, as used here). Under the assumption of the missing at random missingness mechanism, results from the multiple imputation are unbiased.24

In the multivariable logistic regression, the outcome was receiving surgery yes/no. The group of patients who did not receive surgery within the first 6 months following diagnosis are a mixture of (i) patients who were alive and not surgically treated and (ii) patients who died during the first 6 months without receiving surgery. This last group being not ‘at risk’ of receiving surgery complicates the interpretation.31 The competing risk analysis allowed us to distinguish the two different event types (surgery or death), whichever came first.22 In both analyses, we used a model parametrisation that allows for interpretation of the parameter estimates for the early and the advanced stage groups separately, due to the interaction between early/advanced stage and all the other variables. The results from both analyses led to the same findings, which were consistent with results previously published. First, the stage at diagnosis was the strongest predictor of receiving surgery.10 The patient’s PS and the indication of a PET-CT scan performed32 were also strongly associated with surgery. The persisting differences observed between the less and more deprived patients in their receipt of major surgery was also found in some other studies,8 11 33–36 with the exception of the study by Rich et al.30 However, in this latter study, the authors dealt with the missing data problem differently from us, as they created an additional category ‘missing’, which may lead to biased estimation.37 38 We also observed an important decrease in the probability to receive surgery in older patients,39 40 even if their benefit in receiving surgical treatment was equivalent to that of their younger counterparts.41 Indeed, as stressed by Chambers et al, 41

several prospective and large population studies have shown unanimously that patients >70 years of age respond as well as younger patients in all outcome measures pertaining to morbidity, mortality and quality of life postoperatively, and should receive aggressive surgical management if considered fit for surgery, in accordance with the British Thoracic Society guidelines.

We showed strong evidence of lower odds of having major surgery in patients with congestive heart failure, cerebrovascular disease and COPD in patients with early stage NSCLC, consistently with a population-based study conducted in the USA,29 while another study conducted in the Netherlands did not find an association between comorbidity conditions and treatment received for patients with NSCLC.40 However, a limitation of the study is related to the information used for comorbidity, which is derived from the HES datasets.17 Thus, we do not know the comorbidity status for patients who never attended secondary care, and assume they do not have any comorbidities. This could also be the case in an instance where comorbid patients attend hospital, but their comorbidities are erroneously not disclosed in hospital records. So, our measure of comorbidity-specific conditions could underestimate the level of comorbidity at a population level. However, we focused on the more severe comorbidities that are likely to limit fitness for surgery and thus, we would expect the majority of patients with these more serious ‘grades’ of illnesses to have been admitted to hospital at some stage. Having had a PET-CT scan could be considered as a possible mediator (thus being on the causal pathway) between deprivation and receipt of surgery and between comorbidities and receipt of surgery. We therefore performed a supplementary sensitivity analysis (using a competing-risks method of analysis and focusing on the receipt of surgery, see ’Methods' section) without adjusting on the PET-CT scan variable to evaluate the consistency of the results. The adjusted HRs of receiving surgery were quite similar to those presented in table 3 and in figure 2, and the main conclusions remained unchanged (data not shown). Those additional results suggest that having had a PET-CT scan performed played a minor role on the socioeconomic differences to receive surgery.

It appears that further investigation is warranted to understand why the more deprived patients have a lower probability of receiving surgery compared with the less deprived patients, and also why there is an extremely large gradient in receiving surgery according to the age at diagnosis. An approach would be to describe the patient choice, as this is always a major factor in whether treatment, especially surgical treatment, is carried out. It may well be that older and more deprived patients are less likely to agree to surgical treatment. Perceptions of treatments, wishes, levels of engagement with healthcare and understanding of risks of benefits of surgery—all of which affect patient choice—may vary by socioeconomic level. Travel issues (eg, costs and time to travel) may well also come into play in these groups of patients. A study conducted in Australia showed that the longer the distance to a specialist hospital the lower the chance of receiving surgery.42 A comparable investigation would be to assess urban-rural difference in access to treatment and receipt of surgery, as reported in the USA and in Ireland,28 43 as well as whether a patient was first seen at a thoracic surgical centre.30 Crawford et al showed distance from surgical centre and socioeconomic deprivation were additive in their association with lower resection rates in a study from Yorkshire in the UK.35 Therefore, an interesting step forward would be to describe patient choice according to the main patient characteristics (including age and deprivation level). This could be informative in identifying key learning points, such as highlighting the need to focus on either improving access to tertiary services, providing clear information to help inform patient choice and evaluating financial barriers to undergoing surgery (eg, transport costs/leave from work).

Acknowledgments

The authors would like to thank three anonymous reviewers for their comments, which helped to improve the manuscript. The authors would also like to thank Francisco Javier Rubio from the Cancer Survival Group of the London School of Hygiene & Tropical Medicine for interesting discussion on the topic.

References

Footnotes

  • Contributors AB and BR developed the concept and design of the study. AB, HF, M-AL-F, CM, WM and AT were involved in the data preparation and the data linkage. AB carried out the data analysis and wrote the manuscript. All authors interpreted the data, drafted and critically revised the manuscript. All authors read and approved the final version of the manuscript.

  • Funding This research was supported by Cancer Research UK (grant number C7923/A18525).

  • Disclaimer The findings and conclusions in this report are those of the authors and do not necessarily represent the views of Cancer Research UK.

  • Competing interests None declared.

  • Ethics approval The authors have obtained the ethical and statutory approvals required for this research (PIAG 1-05(c)/2007; ECC 1-05(a)/2010); ethical approval updated 6 April 2017 (REC 13/LO/0610).

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Author note The authors attest that they have obtained appropriate permissions and paid any required fees for use of copyright protected materials.

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