Introduction
As the life expectancy of our population increases, there is a greater incidence of oesophagogastric cancer, particularly in the elderly population [
1,
2]. Treatment is complex and resource intensive and usually includes adjuvant therapy combined with complex foregut resection [
3‐
5].
Foregut resection in the elderly is generally undertaken with caution due to increased frailty, greater comorbidities and impaired nutritional status. While it would be reasonable to assume that older patients undergoing oesophagogastric resection would have higher rates of perioperative complication [
6,
7], the available evidence is limited and conflicting. Some retrospective studies support the idea that elderly patients suffer more post-operative medical complications [
8], and subsequently higher rates of mortality [
9], though opposing evidence indicates comparable morbidity and mortality rates [
10,
11]. Available data are further confounded by the use of adjuvant therapies which may result in higher complication rates in the elderly and therefore are frequently omitted [
12‐
14].
The aim of this study was to ascertain whether increased age, over 75 years, has an adverse effect on post-operative, short-term, outcomes in patients undergoing oesophagogastric resection.
Materials and methods
A single unit cohort study of patients undergoing curative resection for oesophagogastric cancer between 2002 and 2020 at two co-located hospitals was undertaken (Royal North Shore and North Shore Private hospitals). Ethics approval was given by the Human Research Ethics Committee of the New South Wales Northern Sydney Local Health District, HREC reference number 2022/ETH00802. Patients with oesophagogastric cancer who underwent curative surgical resection in our unit were retrospectively identified from a prospectively collated database. Patients undergoing resection for benign disease or where concurrent laryngeal resection was performed were excluded from the study.
The database included patient characteristics (age, sex, smoking status), the American Society of Anesthesiologists (ASA) grade of the patient [
15], comorbidities, operative details, use of adjuvant therapy, type and stage of disease. Post-operative data included length of stay (LOS), unplanned return to theatre, unplanned ICU admission, unplanned reintubation, unplanned readmission to hospital, in-hospital mortality, and 30- and 90-day mortality. Specific surgical complications recorded included anastomotic leak, haemorrhage, intra-abdominal abscess, wound infection and chylothorax. Non-surgical complications included respiratory, cardiac and thrombo-embolic. Collected data were examined with a focus on age greater than 75 years, and 75 years or younger.
Treatment and perioperative data collected early in this series were based on the data set from the Association of Upper Gastrointestinal Surgeons of the United Kingdom and Ireland (AUGIS), and severity of complications was recorded using the Clavien-Dindo grading system [
16]. Later in the series, details of complications were recorded according to the International Oesophagectomy Complications Consensus Group [
17].
Pre-treatment staging comprised of CT and FDG PET scans. Staging laparoscopy was performed for those patients with gastric or junctional cancer. Patients were routinely discussed at a multidisciplinary team meeting. Patients with a gastric malignancy, or a Siewart type 3 oesophagogastric junctional cancer, underwent a total or subtotal gastrectomy. Oesophageal resection in this series was either via open Ivor Lewis resection or hybrid thoracoscopic 3 stage resection dependent on tumour location. Thoracic epidural and on table extubation were routine. Surgery was performed by the two senior authors (SL and GS) or trainees under their supervision.
Categorical variables were presented as counts and percentages and analysed using Fishers’ exact or Chi-square tests. Continuous variables were expressed as mean and standard deviation for normally distributed data and analysed using T tests. Continuous variables which were not normally distributed were expressed as median and range and analysed using Mann–Whitney U test. Association of variables with complications following oesophagectomy were assessed using logistic regression. All univariable analyses with p value < 0.2 were included in the multivariable model after testing for collinearity. Backward elimination was used as the variable selection method. The results were presented with an odds ratio (OR), 95% confidence interval (CI) and a corresponding p value.
Results
There were 466 consecutive patients included in this analysis of which 277 underwent oesophagectomy and 189 underwent gastrectomy. Of these patients, 22% were aged over 75 (
n = 104); 14% of the oesophageal cohort (
n = 39/277) and 34% of the gastric cohort (
n = 65/189). Patient characteristics are outlined in Tables
1 and
2. Patients aged over 75, in both the oesophagectomy and gastrectomy cohorts, were more likely to be ASA grade 3 or higher (
p = 0.002 and
p = 0.005, respectively) and more frequently had pre-existing cardiovascular and neurological comorbidities. Tables
3 and
4 outline the treatment received, the histopathology and staging (TNM) of both oesophagectomy and gastrectomy patients. There were 103 patients with oesophageal cancer who underwent an Ivor Lewis resection, and 174 patients had a hybrid 3-stage resection (Table
3 37% vs. 63%). Amongst those with gastric cancer, 77 patients underwent a total gastrectomy, and 112 had either a subtotal (
n = 104) or a distal gastrectomy (
n = 8) (Table
4 41% vs. 59%).
Table 1
Oesophagectomy patient characteristics by age
Median Age (Range) | 67(34–85) | | | |
Sex, n (%) | | | | 0.960 |
Male | 221(79.8) | 190(79.8) | 31(79.5) | |
Female | 56(20.2) | 48(20.2) | 8(20.5) | |
ASA Grade, n (%) | | | | 0.002 |
1 or 2 | 157(56.7) | 144(60.5) | 13(33.3) | |
3 or 4 | 120(43.3) | 94(39.5) | 26(66.7) | |
COPD, n (%) | 33(11.9) | 25(10.5) | 8(20.5) | 0.074 |
HTN, n (%) | 78(28.2) | 68(28.6) | 10(25.6) | 0.706 |
CAD, n (%) | 41(14.8) | 30(12.6) | 11(28.2) | 0.011 |
Arrhythmia, n (%) | 28(10.1) | 20(8.4) | 8(20.5) | 0.020 |
Diabetes, n (%) | 33(11.9) | 29(12.2) | 4(10.3) | 0.999 |
PE/DVT, n (%) | 12(4.3) | 10(4.2) | 2(5.1) | 0.679 |
TIA/CVA, n (%) | 10(3.6) | 5(2.1) | 5(12.8) | 0.001 |
Smoking, n (%) | 20(7.2) | 20(8.4) | 0(0.0) | 0.088 |
Renal, n (%) | 6(2.2) | 6(2.5) | 0(0.0) | 0.600 |
Table 2
Gastrectomy patient characteristics by age
Median Age (Range) | 71(30–91) | | | |
Sex, n (%) | | | | 0.088 |
Male | 112(59.3) | 68(54.8) | 44(67.7) | |
Female | 77(40.7) | 56(45.2) | 21(32.3) | |
ASA Grade, n (%) | | | | 0.005 |
1 or 2 | 108(57.1) | 80(64.5) | 28(43.1) | |
3 or 4 | 81(42.9) | 44(35.5) | 37(56.9) | |
COPD, n (%) | 4(2.19) | 2(1.6) | 2(3.1) | 0.609 |
HTN, n (%) | 59(31.2) | 31(25.0) | 28(43.1) | 0.011 |
CAD, n (%) | 22(11.6) | 10(8.1) | 12(18.5) | 0.034 |
Arrhythmia, n (%) | 15(7.9) | 6(4.8) | 9(13.9) | 0.030 |
Diabetes, n (%) | 24(12.7) | 13(10.5) | 11(16.9) | 0.207 |
PE/DVT, n (%) | 9(4.8) | 4(3.2) | 5(7.7) | 0.279 |
TIA/CVA, n (%) | 6(3.2) | 1(0.8) | 5(7.7) | 0.019 |
Smoking, n (%) | 15(7.9) | 12(9.7) | 3(4.6) | 0.269 |
Renal, n (%) | 7(3.7) | 3(2.4) | 4(6.2) | 0.235 |
Table 3
Oesophagectomy treatment and histopathological details by age
Neoadjuvant therapy, n (%) | | | | 0.753 |
Chemo-radiotherapy | 120(43.3) | 103(43.3) | 17(43.6) | |
Chemotherapy | 97(35.0) | 85(35.7) | 12(30.8) | |
None | 60(21.7) | 50(21.0) | 10(25.6) | |
Adjuvant chemotherapy, n (%) | 43(15.5) | 39(16.4) | 4(10.3) | 0.327 |
Hospital, n (%) | | | | 0.296 |
Public | 76(27.4) | 68(28.6) | 8(20.5) | |
Private | 201(72.6) | 170(71.4) | 31(79.5) | |
Procedure, n (%) | | | | 0.860 |
Ivor Lewis | 103(37.2) | 88(37.0) | 15(38.5) | |
3 Stage | 174(62.8) | 150(63.0) | 24(61.5) | |
Pathological T Stage, n (%) | | | | 0.34 |
T0 | 28(10.1) | 24(10.1) | 4(10.3) | |
T1 | 80(28.9 | 64(26.9 | 16(41.0 | |
T2 | 42(15.1) | 36(15.1) | 6(15.4) | |
T3 | 114(41.2) | 103(43.3) | 11(28.2) | |
T4 | 13(4.7) | 11(4.6) | 2(5.1) | 0 |
Pathological N Stage, n (%) | | | | 0.96 |
N0 | 157(56.7) | 134(56.3) | 23(59.0) | |
N1 | 79(28.5) | 69(29.0) | 10(25.6) | |
N2 | 25(9.0) | 21(8.8) | 4(10.3) | |
N3 | 16(5.8) | 14(5.9) | 2(5.1) | 0 |
Histopathology, n (%) | | | | 0.325 |
Adenocarcinoma | 227(82.0) | 192(80.7) | 35(89.7) | |
Squamous cell carcinoma | 43(15.5) | 40(16.8) | 3(7.7) | |
Other | 7(2.5) | 6(2.5) | 1(2.6) | |
Table 4
Gastrectomy treatment and histopathological details by age
Neoadjuvant chemotherapy, n (%) | 71(37.6) | 55(44.4) | 16(24.6) | 0.008 |
Adjuvant chemotherapy, n (%) | 62(32.8) | 55(44.4) | 7(10.8) | < 0.001 |
Hospital, n (%) | | | | 0.658 |
Public | 76(40.6) | 51(41.8) | 25(38.5) | |
Private | 111(59.4) | 71(58.2) | 40(61.5) | |
Gastrectomy, n (%) | | | | 0.163 |
Distal or Subtotal | 112(59.3) | 69(55.7) | 43(66.2) | |
Total or Extended total | 77(40.7) | 55(44.3) | 22(33.8) | |
Lymph node dissection, n (%) | | | | 0.145 |
D1 or D1 + | 139(73.5) | 87(70.2) | 52(80.0) | |
D2 | 50(26.5) | 37(29.8) | 13(20.0) | |
Pathological T Stage, n (%) | | | | 0.191 |
T0 | 9(4.8) | 7(5.6) | 2(3.1) | |
T1 | 55(29.1) | 41(33.1) | 14(21.5) | |
T2 | 32(16.9) | 16(12.9) | 16(24.6) | |
T3 | 62(32.8) | 41(33.1) | 21(32.3) | |
T4 | 31(16.4) | 19(15.3) | 12(18.5) | |
Pathological N Stage, n (%) | | | | 0.196 |
N0 | 96(50.8) | 63(50.8) | 33(50.8) | |
N1 | 37(19.6) | 22(17.8) | 15(23.1) | |
N2 | 24(12.7) | 20(16.1) | 4(6.1) | |
N | 32(16.9) | 19(15.3) | 13(20.0) | |
Histopathology, n (%) | | | | 0.301 |
Adenocarcinoma | 179(94.7) | 115(92.8) | 64(98.5) | |
Neuroendocrine | 3(1.6) | 3(2.4) | 0(0.0) | |
Other | 7(3.7) | 6(4.8) | 1(1.5) | |
Oesophagectomy cohort
Older patients undergoing oesophagectomy were as likely to receive adjuvant therapy as the younger cohort (Table
3). LOS in the older group was 17 days versus 15 days in the younger cohort although there was no statistical difference (
p = 0.301).
There was no difference in mortality rates between the two cohorts; 30- and 90-day mortality rates in the older cohort were 2.6% and 2.6% (
n = 1) and in the younger cohort 1.3% (
n = 3) and 2.5% (
n = 6), respectively (Table
5).
Table 5
Oesophagectomy outcomes by age
Overall post-op Complications, n (%) | 147 (53.1) | 120 (50.4) | 27 (69.2) | 0.029 |
Intra-op Complications, n (%) | 6 (2.2) | 5 (2.1) | 1 (2.6) | 0.999 |
Surgical Complications, n (%) | 96 (34.7) | 83 (34.9) | 13 (33.3) | 0.851 |
Non-Surgical Complications, n (%) | 97 (35.0) | 74 (31.1) | 23 (59.0) | 0.001 |
Blood Transfusion, n (%) | 47 (17.0) | 37 (15.6) | 10 (25.6) | 0.120 |
Unplanned return to OR, n (%) | 88 (31.8) | 77 (32.3) | 11 (28.2) | 0.606 |
Unplanned ICU admission, n (%) | 44 (15.9) | 35 (14.7) | 9 (23.1) | 0.185 |
Unplanned readmission, n (%) | 17 (6.1) | 16 (6.7) | 1 (2.6) | 0.482 |
Reintubation required, n (%) | 21 (7.6) | 18 (7.6) | 3 (7.7) | 0.999 |
Tracheostomy required, n (%) | 4 (1.4) | 4 (1.7) | 0 (0.0) | 0.999 |
In-hospital Mortality, n (%) | 6 (2.2) | 5 (2.1) | 1 (2.6) | 0.999 |
30-day Mortality, n (%) | 4 (1.4) | 3 (1.3) | 1 (2.6) | 0.457 |
90-day Mortality, n (%) | 7 (2.5) | 6 (2.5) | 1 (2.6) | 0.999 |
Median LOS (days) and range | 15 (5–160) | 15 (5–160) | 17 (8–67) | 0.301 |
Clavien Dindo Grade, n (%) | | | | 0.795 |
Grade 1 | 9 (6.1) | 7 (5.8) | 2 (7.4) | |
Grade 2 | 46 (31.3) | 36 (30.0) | 10 (37.0) | |
Grade 3a or 3b | 68 (46.3) | 58 (48.4) | 10 (37.0) | |
Grade 4a or 4b | 19 (12.9) | 15 (12.5) | 4 (14.8) | |
Grade 5 | 5 (3.4) | 4 (3.3) | 1 (3.7) | |
Patients over 75 were more likely to develop post-operative complications (
p = 0.029), and they were more likely to be non-surgical (
p = 0.001) (Table
5). Of those non-surgical complications cardiac (specifically cardiac arrythmias) and thrombo-embolic (DVT/PE) adverse events were comparatively more common (
p = < 0.001 and
p = 0.017 respectively) (Appendix Table
8).
There was no difference in rates of surgical complications between age groups of oesophagectomy patients (Appendix Table
9). A conduit or anastomotic leak occurred in 39/277 patients (14.1%), 8/103 (7.8%) of whom had an Ivor Lewis versus 31/174 (17.2%) who had a 3-stage oesophagectomy (
p = 0.020). Leaks in the 3-stage oesophagectomy group were predominately due to necrosis of the tip of the conduit rather than a leak from the anastomosis.
Univariable analyses are presented in Appendix Tables
10 and
11 for all complications and non-surgical complications for oesophagectomy patients. On multivariable analysis, ASA grade 3 or 4 (OR 1.85, 95% CI 1.13–3.03,
p = 0.015), an operation performed in our public hospital (OR 1.78, 95% CI 1.02–3.11,
p = 0.043) and a 3-stage oesophagectomy (OR 1.97, 95% CI 1.19–3.26, p = 0.009) were predictive for increased rates of all post-operative complications (surgical and non-surgical). Whilst age over 75 years, surgery performed in our public hospital and a 3-stage oesophagectomy, were predictive of non-surgical complications (Table
6 and Appendix Table
12).
Table 6
Oesophagectomy; multivariable analysis for all complications
ASA Grade | | | 0.015 |
1 or 2 | Reference | | |
3 or 4 | 1.85 | 1.13–3.03 | |
Hospital | | | 0.043 |
Private | Reference | | |
Public | 1.78 | 1.02–3.11 | |
Procedure | | | 0.009 |
Ivor Lewis | Reference | | |
3 Stage | 1.97 | 1.19–3.26 | |
Gastrectomy cohort
Gastrectomy patients more likely received neoadjuvant or adjuvant systemic therapy if they were 75 years or younger (
p = 0.008 and
p = < 0.001) (Table
4). Patients over 75 had a greater LOS (median 13 days vs. 12 days,
p = 0.006). There was no difference in post-operative complications between age groups (Table
7). An anastomotic leak occurred in 16/189 patients (8.5%); 10/124 (8.1%) of those patients were aged 75 years or under, and 6/65 (9.2%) were over 75 (
p = 0.784).
Table 7
Gastrectomy outcomes by age
Overall post-op Complications, n (%) | 58(30.7) | 36(29.0) | 22(33.9) | 0.495 |
Intra-op Complications, n (%) | 4(2.1) | 1(0.8) | 3(4.6) | 0.118 |
Surgical Complications, n (%) | 32(16.9) | 22(17.7) | 10(15.4) | 0.681 |
Non-Surgical Complications, n (%) | 44(23.3) | 25(20.2) | 19(29.2) | 0.161 |
Unplanned return to OR, n (%) | 15(7.9) | 9(7.3) | 6(9.2) | 0.634 |
Unplanned ICU admission, n (%) | 21(11.1) | 13(10.5) | 8(12.3) | 0.705 |
Unplanned admission, n (%) | 13(6.9) | 10(8.1) | 3(4.6) | 0.548 |
In-hospital Mortality, n (%) | 2(1.1) | 1(0.8) | 1(1.5) | 0.999 |
30-day Mortality, n (%) | 2(1.1) | 1(0.8) | 1(1.5) | 0.999 |
90-day Mortality, n (%) | 3(1.6) | 1(0.8) | 2(3.1) | 0.272 |
Median LOS (days) and range | 12(7–232) | 12(7–232) | 13(8–172) | 0.006 |
Clavien Dindo Grade, n (%) | | | | 0.650 |
Grade 1 | 8(13.8) | 6(16.7) | 2(9.1) | |
Grade 2 | 28(48.3) | 15(41.7) | 13(59.1) | |
Grade 3a or 3b | 11(19.0) | 7(19.4) | 4(18.2) | |
Grade 4a or 4b | 9(15.5) | 7(19.4) | 2(9.1) | |
Grade 5 | 2(3.4) | 1(2.8) | 1(4.5) | |
There was no difference between age groups in rates or severity of complications, and 30- and 90- day mortality. 30- and 90-day mortality rates in the older cohort were 1.5% (
n = 1) and 3.1% (
n = 2) and in the younger cohort 0.8% and 0.8% (
n = 1) respectively (Table
7).
Discussion
The risk of complications following treatment for oesophgogastric malignancy is not insignificant and overall survival rates are low [
18,
19]. The influence of the patient’s age as a predictor of complication following foregut resection would seem likely from an intuitive viewpoint. The literature regarding this however has been contradictory; some suggest advanced age is a predictor for morbidity and mortality [
9,
20] while others do not corroborate this [
10,
11,
21]. Surgeons should be pragmatic in their approach to the elderly patient when offering surgical resection, with particular consideration of patients’ functional baseline [
22] as well as their pre-existing comorbidities. Providing accurate peri-operative mortality and complication rates to patients, allowing informed decision making, is essential. The aim of our study was therefore to scrutinise short-term outcomes in elderly patients undergoing oesophagogastric resection within our institution.
In our series, elderly patients were more likely to have a higher ASA grade and more pre-treatment comorbidities. Advanced age was a predictor for non-surgical complications in those undergoing an oesophagectomy, specifically they were more likely to develop cardiac arrythmia and thromboembolic complications. Prophylactic beta blockade has been purported to prevent atrial fibrillation following oesophagectomy, however, due to conflicting evidence for and against the use of beta blockers, our institution has not adopted this for routine practice [
23‐
25]. Despite some evidence for prolonged use of post-discharge DVT prophylaxis it has not been the policy of our treating group to mandate post-discharge DVT prophylaxis in all our resected patients. It is well recognised that patients undergoing neoadjuvant chemotherapy develop deep venous thrombosis during their treatment [
26] and our results raise the question as to whether routine screening for DVT may be appropriate following neoadjuvant chemotherapy. Our data show that increased age did not confer an increased risk of complications in patients undergoing gastrectomy. At our institution, for patients undergoing oesophagogastric resection, it appears that age has not been a factor in determining post-operative mortality.
Along with higher ASA grade and type of oesophageal resection, patients undergoing oesophageal resection in our public facility had higher complication rates than patients in our private facility. Trainee surgeons performing oesophagogastric resection were supervised by the consultant surgeon authors. The surgical and anaesthetic approach and post-operative care were identical in both co-located facilities. No other factors predicting a higher risk of complication were able to be identified in this group of patients. This disparity in complication rates is the subject of ongoing evaluation in our unit.
Curative treatment of oesophagogastric malignancy is challenging for patients, carers, and health care professionals. Overall 5-year survival rates for oesophageal cancer are around 10–22% [
27], and 33% for gastric cancer [
28]. Identifying patients in whom rates of complication may be sufficiently high to not recommend curative treatment is critical.
The authors recognise limitations to this study, including the retrospective design. This was mitigated by prospective collection of data and therefore no recall bias, no exclusion of appropriate patients and a large study size. The study spanned 18 years with standardised surgical data collected by two surgeons throughout. During this timeframe however the treatment paradigm for these malignancies has evolved and we understand this may have impacted the peri-operative outcomes. The data are from a single institution, and future work could look to collaborate in a multi-centre approach. It has not been our practice to routinely assess patient frailty prior to offering treatment however, there is an increasing body of evidence that frailty may be a more accurate predictor of perioperative outcome than age [
29‐
31]. A number of clinical and radiological scoring systems have been developed with a view to risk stratification [
32‐
34], an example being the Edmonton Frail Scale which is a validated and practical screening tool for frailty [
35]. Perhaps a specific adaptation of these methods that is applicable to geriatric patients undergoing workup for curative treatment of oesophagogastric malignancy may become clinically relevant in the future. An obvious limitation of our study is that of selection bias. All patients referred to our unit for consideration of curative resection were presented at our Multidisciplinary team meeting. Not all patients with localised disease within our referral network were discussed at our meeting. Conceivably, if an elderly patient was diagnosed with oesophageal malignancy and it was felt by the diagnosing gastroenterologist or the patient’s general practitioner that the patient was unfit for surgery, they may not have been referred for discussion. Unfortunately, it is therefore impossible to calculate a denominator of patients which includes patients over 75 with potentially curable disease who were not offered resection. While this absence of a denominator detracts from the strength of our study, we believe our conclusion that resection should be offered to selected elderly patients is valid.
Conclusion
This study shows that curative surgical resection can be offered safely to elderly patients without significant adverse outcomes, or increased peri-operative morbidity, and with acceptable post-operative mortality rates. Age alone is not a reliable predictor of poor outcomes, and therefore our unit will continue to offer surgery, including the use of adjuvant therapies, to select patients over the age of 75. Improving methods for identifying patients at greater risk of complications following oesophagogastric resection should be a priority for clinicians into the future.
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