Is there ageism in oncology?

SMJ 2003: 48(1) 17-20

David Austin , Medical Student , University of Aberdeen

Elizabeth M Russell, Emeritus Professor of Social Medicine , University of Aberdeen

 

Address for correspondence and reprints:

Professor Elizabeth Russell

Department of Public Health , Medical School , Polwarth Building , Foresterhill , Aberdeen  AB25 2ZD

Phone and fax: 01224 861216

Email: e.m.russell@abdn.ac.uk

 

Abstract

Study Objective: To use routine data to explore age-related decision making in the hospital management of colorectal cancer.

Design: Retrospective analysis of linked Scottish cancer registry and hospital discharge data for colorectal cancer.

Setting: All Scottish general hospitals.

Participants: All patients on the Scottish colorectal cancer registry 1992-6 (n=15,299).

Main Results:  Histological verification was used to indicate the “gold standard” of investigation.  Definitive surgery and chemotherapy were used as indicators of treatment received. After adjusting for demographic factors, tumour sub-site, co-morbidity and route of first admission, increasing age was associated with markedly decreased rates of histological verification, surgery and chemotherapy. It is still not possible to be sure whether there is ageism in the management of older patients with colorectal cancer. However, the rate of histological verification fell markedly with increasing age, making it questionable whether decisions to treat were based on best clinical practice at the time. Differences observed between this study and clinical trial data may represent the margin of ageism between everyday clinical practice and controlled conditions.

Conclusions : The value of this analysis lies in the fact that the data come from routine clinical practice rather than special studies. The improved content of Scottish cancer register and the ability to link it to hospital care provides a useful baseline for monitoring adherence to clinical guidelines.

 

Keywords:   Ageism, colorectal cancer, cancer registration, data linkage, clinical guidelines.

Introduction

National statistics indicate that five-year survival from all cancers is worse in older patients even when reduced life expectancy is accounted for1.  Turner et al.2 summarised disparities between age groups in investigation, treatment and outcome in cancer.  She reviewed the evidence for and against attributing them to age-based decisions not to treat, but was unable to reach a conclusion on the underlying reasons.

 

The principles of the NHS oppose age-based rationing, and any explicit priorities have favoured older patients either directly or indirectly because they are the main sufferers of cancer and heart disease, which are two current priorities3-5.  Traditionally, doctors have been trained that clinical need is the only stated criterion on which care should be determined.  Age-based  decisions to limit treatment that are not justifiable on grounds of clinical need can therefore be regarded as ageist.  Age Concern feels that ageism exists within the NHS6, yet there is little empirical data to back-up this claim. 

 

Using routine data, this study took a different approach to Turner and aimed to determine whether age related differences in hospital management of cancer patients were clinically justifiable or not. Colorectal cancer was chosen as the tracer condition so that the justification of clinical decisions could be related to available and accepted guidance on good clinical practice7 .  A recent systematic review of surgery for colorectal cancer found that, although overall survival after colorectal cancer surgery decreased with age, there was no significant difference in cancer-related mortality with age in those who underwent curative surgery8. Neither was there a greater level of co-morbidity (as judged by the presence of conditions such as diabetes and hypertension) with increasing age in the 84% who had surgery, although probably there was more co-morbidity in the 16% who did not. However, the proportion whose tumours had been staged fell significantly with age, which suggests that in the older old patients something other than stage was used as the basis for deciding whether or not to undertake curative surgery. Current evidence is that

·          Although the systematic review showed that stage of tumour at presentation increases with age, this trend reflected only a deficit of Stage A and an excess of Stage D. Other studies have shown no difference in stage at presentation. However, the number of patients with unknown stage increases with age8-11

·        Age of patient alone is not a predictor for poor survival or complication rates after surgery11-15

·          Older patients respond as well to chemotherapy as do younger patients, although they are under represented in clinical trials and data on toxicity and quality of life is poor 16,17

 

Thus, on the basis of this evidence, there is no a priori reason for managing older patients differently solely on account of their age. The issue for best practice is the correct selection of patients according to their clinical condition rather than the simplistic approach of assuming that older patients will always fare worse and therefore may not merit aggressive management. 

 

The studies in the systematic review were, by definition, prospective audit or research, usually in relatively controlled conditions. In Scotland, because of the record linkage system for all hospital discharges that has existed for at least 20 years, there is a rare opportunity to analyse routine hospital patient care longitudinally regardless of where or by whom it was given. This study therefore examined the care of colorectal cancer patients in all Scottish hospitals to see whether any differences by age could be justified on clinical grounds. It was also recognised that the study would provide a baseline for future audit of this care in the light of the increasing use of clinical guidelines for good practice 7.

 

Methods

The data set was the Scottish cancer registration records for all patients aged over 17, diagnosed between 1st January 1992 and 31st December 1996 (n=15299).  Computerised probability linking was carried out by ISD Scotland to connect patients to their individual episodes of care collected through the Scottish Morbidity Record inpatient and day case form (SMR 01).  SMR 01 details were selected if they contained a diagnosis of colorectal cancer and were within the time frame of one year pre-registration to one-year post registration.

 

Excluded were patients with missing deprivation category (n=123), missing link numbers (n=182), anal cancers (n=235) and patients who were not admitted to hospital (including death certificate only registrations, n=1983).  The revised data set contained 12776 patients.

 

The results were adjusted for co-morbid conditions that may affect survival and therefore treatment choice. The method of adjustment was that used in the Scottish Clinical Outcome Indicators for all cancers18.  Hospital admissions with a principal diagnosis of any of seven conditions deemed to be relevant to cancer prognosis were used as the basis for this variable. The conditions were diabetes, hypertension, ischaemic heart disease, other heart disease, cerebro-vascular disease, respiratory disease and arthritis, and the period of two years before to one month after cancer registration was defined as a clinically relevant time frame.  The co-morbidity variable had three levels: "no admissions", "one admission" or "two admissions" for any of the relevant conditions.

 

Tumour sub-site was also identified as a clinically relevant factor that is known to vary with age. .  Sub-site was coded into the categories “right” (caecum to transverse colon), “left” (splenic flexure to sigmoid colon), “rectal” (rectosigmoid junction, rectal ampulla) and “unspecified”.

 

Emergency admission is known to be associated with a poorer outcome in colorectal cancer9,19,20, although the reasons are unclear. Route of first inpatient admission for colorectal cancer was therefore used as one indicator of poor prognosis. Sex and deprivation (measured by the Carstairs index of deprivation, DEPCAT21) were included to allow adjustment for socio-demographic factors that might affect the interpretation.   Attempts were also made to adjust for poor overall fitness. Patients whose registration was based only on death certification and those with no inpatient record of care were removed as being many of the "sickest" patients.

 

This study used three main indicators of clinical outcome.  Histological verification (from the cancer registration data set) to indicate extent of investigation; the "gold standard" of investigation for colorectal cancer is a pathological diagnosis.  Definitive surgery (coded for on SMR 01) to indicate potentially curative procedures; all patients with a resectable tumour should be considered for surgery7.  Chemotherapy (coded for on SMR 01 as procedure X35.2) to indicate adjuvant and palliative treatment; chemotherapy should be considered for all patients with Dukes stage C or with advanced disease 7. 

 

SPSS for Windows was used for all analyses.  Age was initially cross-tabulated against each main outcome to give an indication of the unadjusted pattern of care.  Five age-bands (17-54,55-64, 65-74, 75-84 and 85+) were used for all the analyses.  All relevant variables (age, comorbidity, sub-site, type of admission, sex and deprivation category) were then entered into a logistic regression (LR) analysis for each of the outcome variables.  Only differences significant at the 5% level are reported.

Results

The mean age of patient was 70.9 (SD ±12.11), range 17-107.  Right-sided and unspecified tumours were the more common tumours in older groups, and both co-morbidity and emergency admission increased with increasing age.  Deprivation levels were similarly distributed at each age-band and males were affected proportionately more than females at younger ages.

 

The percentage of patients whose tumours were histologically verified decreased with age (Mann-Whitney p<0.001,Table 1) The proportion of verified patients (mean 90.6%, n=11581) in the youngest group was 95.5%, compared with 88.1% in the 75-84 category and 78.1% in the 85+ category. When adjusted for all other relevant factors, increased age remained a negative predictor for histological verification: 75-84 year olds were 2.7 times less likely (LR p<0.0001) and 85+ year olds 4.8 times less likely (LR p<0.0001) to be histologically verified when compared to the youngest group (Figure 1).

 

The percentage of patients receiving definitive (ie potentially curative) surgery (mean 78.1%, n=9977) decreased with age (Mann-Whitney p<0.001, Table 1).  After adjusting for the relative influence of other relevant factors, age continued to be a statistically significant negative predictor.   Compared to the youngest age band, 75-84 year olds were 20% less likely to receive definitive surgery (LR p=0.003) and patients of 85 and over were 55% less likely to receive definitive surgery (LR p<0.0001, Figure 2).

 

Approximately one-third (32.8%) of 17-54 year olds and one-fifth (18.5%) of 55-64 year olds received chemotherapy (Table 1).  Very few patients over 75 received chemotherapy: at 75-84 - only 47 patients (1.4%) - and at 85 and over only 1 patient in Scotland (0.1%) received the treatment (Mann-Whitney p<0.001). The overall mean was 10.6% (n=1351). When adjusted for all other relevant factors, increasing age remained a statistically significant negative predictor for receiving chemotherapy (Figure 3).

 

Discussion

Our results show striking age associated differences in the investigation and treatment of colorectal cancer. Even when adjusted for clinical and demographic factors, older patients showed decreased rates of histological verification, potentially curative surgery, and chemotherapy. The rate of potentially curative surgery was similar to that found in the systematic review8. However, the percentages of cancers in the Scottish routine data that were not histologically verified were higher at all ages than the percentages of unstaged cancers in the review.

What makes this study valuable is the extent of coverage that the Scottish routine data allow and the unique insight into the pattern of care within the health service.  While criticism can be levelled at large scale retrospective studies and a cautious approach to interpretation should be maintained 22, the results from the study merit debate. The unique methods of linkage of ISD data were set up in the 1990s specifically for the purpose of mapping trends and analysing comparative information.  Scotland's cancer registration system compares favourably with those in other countries.  Case ascertainment is believed to be about 95%, data linkage is highly accurate (error rate <1%), and coding for procedure is also thought to be correct in over 96% of cases18, 23.  Future use of linked SMR 06 data in Scotland has since been further improved by the addition of variables indicating stage at presentation and grade of tumour

 

This addition permitted a post hoc analysis of cancer registration (SMR 06) data for 1997 to examine the percentage distribution of stage by age at presentation. When the patients not investigated were excluded, stage did not vary with age (Figure4).  Compared to the recent systematic review data 8, unknown stage was more likely at all ages but especially in the 75-84 age group, in whom 15.6% in Scotland in 1992-96 were not staged (Table 2) compared with only 9% in the review (covering studies from 1988-2000).

A further comparison between the 1992-96 data and the systematic review showed that, while the overall rate of potentially curative surgery was similar (78% in Scotland compared to 75% in the review), in Scotland this fell from 81% in the 65-74 age group to 61% in those aged 85 plus. In the systematic review, the comparable fall was from 75% to 67%. If these comparisons are accurate, they may reflect differences between special studies and routine practice that may be at the margin of ageism rather than of best clinical practice.

 

Attempts to correct for co-morbidity were hampered by the lack of a validated measure in colorectal cancer.  The co-morbidity indicator used is based on principal diagnosis on hospital admission for conditions other than colorectal cancer, because principal diagnosis is more likely to be accurately and completely recorded than are concomitant diagnoses at the time of the cancer admission, and because the Scottish record linkage system means that all such admissions in Scotland will be captured. ISD sample audits have found no systematic bias in completeness of such capture.  However, these admissions were recorded only over the two prior years and so missed  co-morbidity not investigated or treated in hospital during that time. Also, severity of the co-morbid events is unknown.

 

Despite these limitations, the chosen co-morbidity indicator showed variation with age, histological verification, chemotherapy and definitive surgery and therefore appeared to have some face validity and be a useful, if not fully comprehensive, indicator of co-morbidity in colorectal cancer.

Thus, linkage of cancer registration and hospital episode data provides a very much larger data set than does either alone, and covers all Scottish hospitals regardless of participation in special studies or audits. The ability to adjust the data set also considerably enhances its utility even although no one has yet devised a reliable measure of co-morbidity. This analysis confirms the existence of age-related variations in care that may be greater than those found in special studies. This analysis should act as a baseline for comparison with subsequent years, during which both more accurate staging data and a growth in explicit clinical guidelines have become available.

 

 


Acknowledgements

We are extremely grateful to the Cancer Intelligence Unit at ISD for all their help, and especially Diane Stockton, without whom the several analyses would not have been possible.  Gordon Prescott provided much needed statistical help. DA is grateful to PPP Healthcare for his student grant.


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