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. 2022 Nov 30;12:1032443. doi: 10.3389/fonc.2022.1032443

Gastrectomy for cancer beyond life expectancy. A comprehensive analysis of oncological gastric surgery in Germany between 2008 and 2018

Maximilian Berlet 1, Marie-Christin Weber 1, Philipp-Alexander Neumann 1, Helmut Friess 1, Daniel Reim 1,*
PMCID: PMC9747770  PMID: 36531049

Abstract

Introduction

Major gastric surgery for distal esophageal and gastric cancer has a strong impact on the quality of life, morbidity, and mortality. Especially in elderly patients reaching their life expectancy, the responsible use and extent of gastrectomy are imperative to achieve a balance between harm and benefit. In the present study, the reimbursement database (German Diagnosis Related Groups (G-DRG) database) of the Statistical Office of the Federal Republic of Germany was queried to evaluate the morbidity and mortality of patients aged above or below 75 years following gastrectomy.

Material and methods

All patients in Germany undergoing subtotal gastrectomy (ST), total gastrectomy (T), or gastrectomy combined with esophagectomy (TE) for gastric or distal esophageal cancer (International Statistical Classification of Diseases and Related Health Problems Version 10 (ICD-10) C15.2, C15.5, and C16.0–C16.9) between 2008 and 2018 were included. Intraoperative and postoperative complications as well as comorbidities, in-hospital mortality, and the extent of surgery were assessed by evaluating ICD-10 and operation and procedure key (Operationen- und Prozedurenschlüssel) codes.

Results

A total of 67,389 patients underwent oncologic gastric resection in Germany between 2008 and 2018. In total, 21,794 patients received ST, 41,825 received T, and 3,466 received TE, respectively. In 304 cases, the combinations of these, in fact, mutually exclusive procedures were encoded. The proportion of patients aged 75 years or older was 51.4% (n = 11,207) for ST, 32.6% (n = 13,617) for T, and 28.1% (n = 973) for TE. The in-hospital mortality of elderly patients was significantly increased in all three groups. (p < 0.0001) General complications such as respiratory failure (p = 0.0054), acute renal failure (p < 0.0001), acute myocardial failure (p < 0.0001), and the need for resuscitation (ST/T: p < 0.0001/TE: p = 0.0218) were significantly increased after any kind of gastrectomy. Roux-en Y was the most commonly applied reconstruction technique in both young and elderly patients. Regarding lymphadenectomy, systematic D2 dissection was performed less frequently in older patients than in the younger collective in the case of ST and T as well as D3 dissection. Peritonectomy and hyperthermic intraperitoneal chemotherapy were uncommon in elderly patients alongside ST and T compared to younger patients (p < 0.0001).

Conclusion

The clinical outcome of major oncological gastric surgery is highly dependent on a patient’s age. The elderly show a tremendously increased likelihood of in-hospital mortality and morbidity.

Keywords: elderly patients, gastrectomy, gastric cancer, esophageal cancer, clinical outcome, comorbidity, mortality

Introduction

Oncologic resection for gastric cancer by either partial or total gastrectomy is the main pillar of curative treatment aside from multimodal therapies in advanced stages, which may be a critical matter from numerous aspects. On one hand, an oncologically radical approach is important in order to achieve R0 resection (1), but, on the other hand, gastrectomy is correlated to a high mortality rate of up to 20% (2). In particular, age-related aspects regarding surgery for gastric cancer have not been adequately investigated yet. Thus, most studies only focus on surgical technique and cancer specifications and do not cover the entire collective of elderly patients requiring therapy for gastric cancer (3, 4). Articles related to elderly gastrectomy patients usually address the best surgical technique in terms of minimally invasive and robotic-assisted surgery (57). With regard to stratification by age, several aspects are of particular interest. For example, perioperative mortality and the probability of other postoperative complications must be weighed against current life expectancy without surgery (8). Recent study collectives are mostly small in number. In addition, the results being published may be biased due to the fact that these studies are mostly reporting on patient cohorts from specialized treatment centers not representing common clinical nationwide practice. Therefore, a systematic analysis of large case numbers is urgently needed to evaluate the influence of age on the surgical outcome related to major gastric surgery, especially when life expectancy is reached. The aim of the present study was to evaluate the clinical outcomes of patients aged beyond the average life expectancy undergoing surgery for gastric cancer in a population-based study using a structured query of the German Diagnosis Related Groups (G-DRG) database of the German Statistical Office (DESTATIS). The complete database is accessible only for selected researchers and contains all the diagnoses and medical procedures of inpatients treated in German hospitals, which were encoded according to the International Classification of Diseases version 10 with the German modification (ICD-10-GM) and the German operation and procedure key (‘Operationen- und Prozedurenschlüssel’, OPS) (9).

Material and methods

All patients with gastric and distal esophageal cancer (ICD C15.2, C15.5, and C16.0–C16.9) receiving major gastric surgery in terms of subtotal gastrectomy (ST, OPS 5-435, 5-436), total gastrectomy (T, OPS 5-437), and total gastrectomy with esophageal resection (TE, OPS 5-438) in Germany between 2008 and 2018 were included. The parameters queried comprised comorbidity, reconstruction technique, the extent of lymphadenectomy (LAD), adjunctive therapy and organ resection, intraoperative and postoperative adverse events, and perioperative mortality. These factors were then analyzed for age dependency by setting a cutoff at 75 years. Patients younger than this age were assigned to group L75 (‘less than 75 years’), and older patients were assigned to group G75 (‘greater or equal to 75 years’). Intraoperative and postoperative complications were defined according to the international consensus on complications after gastrectomy for cancer (10). The source code for the query of the G-DRG database was created in the SAS programming language, as required by DESTATIS (9). The same program code was executed separately for each year of interest. Diagnoses and complications were defined using the most appropriate ICD-10 and OPS codes available (see the supplement for details). Statistical analysis was then performed using R statistical software version 3.6 without additional packages (11). To calculate significance, the Wilcoxon rank sum test was used for the Charlson comorbidity scores and the chi-square test and Fisher’s exact test were applied to nominal scaled parameters. In case of multiple testing, Bonferroni correction was used to adjust p-values. The particular statistical tests applied to the data and the absolute subgroup sizes are depicted in each table and figure. Relative frequencies are given for mortality, complications, the reconstruction technique, LAD, and adjunctive therapy. The Charlson index for comorbidity is reported as the mean and standard deviation for each collective and year. The significance level was set at 5%.

Results

A total of 67,389 patients with gastric or distal esophageal cancer underwent major gastric resection in Germany during the observation period (ST: 21,794/T: 41,825/TE: 3,466/combinations of OPS codes for ST, T, or TE: 304 cases). The proportion of patients with an age of 75 years or more (G75) was 51.4% (n = 11,207) for ST, 32.6% (n = 13,617) for T, and 26.9% for TE (n = 973).

For the analysis of comorbidity, the Charlson comorbidity index in its classic version was calculated for both collectives (12). For each individual year and each type of gastric resection, there was a significantly higher score found in the elderly group ( Table 1 ).

Table 1.

Charlson comorbidity score of patients undergoing major gastric surgery in Germany between 2008 and 2018.

Group Parameter 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 p-value
<75 ST Mean 4.77 4.89 5.15 4.98 5.11 5.32 5.44 5.5 5.22 5.4 5.58 graphic file with name fonc-12-1032443-i001.jpg
sd 3.2 3.23 3.4 3.34 3.37 3.45 3.46 3.57 3.62 3.49 3.56
n 1,144 1,095 1,012 969 962 946 945 946 848 869 851
T Mean 4.77 4.9 5.17 5.13 5.2 5.46 5.49 5.64 5.56 5.79 5.64
sd 3.32 3.34 3.45 3.45 3.44 3.53 3.51 3.57 3.5 3.54 3.48
n 2,887 2,774 2,661 2,598 2,475 2,395 2,843 2,701 2,382 2,314 2,178
TE Mean 4.5 5.41 4.94 5.38 5.23 5.86 5.74 6.17 5.73 6.05 5.88
sd 3.27 3.41 3.3 3.16 3.56 3.71 3.41 3.59 3.45 3.56 3.51
n 140 179 135 148 150 152 214 194 403 406 372
≥75 ST Mean 6.76 7.16 7.49 7.21 7.46 7.54 7.71 7.96 7.9 7.87 7.96
sd 3.07 3.24 3.34 3.31 3.41 3.31 3.48 3.61 3.47 3.64 3.57
n 1,167 1,089 1,016 988 987 984 1,029 1,057 945 992 953
T Mean 6.89 6.99 7.39 7.37 7.44 7.79 7.86 7.79 8.12 7.97 8
sd 3.26 3.22 3.43 3.42 3.4 3.52 3.56 3.51 3.62 3.55 3.57
n 1,205 1,208 1,108 1,197 1,208 1,237 1,380 1,385 1,297 1,228 1,164
TE Mean 7.44 6.81 7.21 7.24 8 7.88 7.14 7.82 7.88 8.25 8.47
sd 3.21 3.38 3.11 3.37 3.6 3.48 3.1 4.1 3.61 3.53 3.67
n 57 54 56 54 48 59 71 79 164 173 158

< 75: patients, younger than 75 years, ≥ 75: patients with an age of 75 years or older, ST, subtotal gastrectomy, T, total gastrectomy, TE, combined total gastrectomy and esophageal resection, mean, mean of the Charlson comorbidity index, sd, standard deviation of the Charlson comorbidity index, n, number of patients in the particular group; the Wilcoxon rank sum test with Bonferroni adjustment was used for statistical testing with a level of significance set at 5%. The difference between L75 and G75 was significant for each single year under study.

The bold values represent the mean values.

The pattern of reconstruction techniques, in terms of the use of Billroth II (BII), analog to Billroth II (aBII), Roux en Y-like (RY), or other (O) reconstruction, was almost the same in both age groups with slight differences regarding modified techniques. Nevertheless, the number of BII reconstructions was higher in elderly patients undergoing ST (30.7 vs. 26.2%). Following all gastric resection types, RY was the most frequently used technique in both groups ( Figures 1A, B ). Regarding LAD, systematic D2 LAD was the most frequently used procedure after total gastrectomy and gastrectomy combined with esophagectomy in patients <75 years and ≥75 years. D3 dissection was performed less commonly in the G75 collective (ST: 3.2 vs. 5.7%/T: 6.8 vs. 9.2%/TE: 7.9 vs. 11.6%) After subtotal resection, LAD strategies other than straight systematic D2 or D3 LAD were used in 51.4% (L75) and 62.1% (G75) including partly D2 or D3 dissection, respectively ( Figures 1C, D ).

Figure 1.

Figure 1

ST: subtotal gastrectomy, T: total gastrectomy, TE: gastrectomy combined with esophagectomy, BII: Billroth II reconstruction, aBII reconstruction analogue to Billroth II, RY: Roux en-Y reconstruction, O: other reconstruction technique, D2 LAD: straight D2 lymphadenectomy, D3 LAD: straight D3 lymphadenectomy, Other LAD: extent of lymphadenectomy other than straight systematic D2 or D3, Chi-square test with Bonferroni adjustment was applied for statistical testing. The significance level was set at 5%.

While the type of reconstruction did not differ substantially between the two age groups, the extent of further therapy and additional organ resection appeared to be markedly divergent. Less aggressive approaches were observed for pancreatic resection after subtotal and total gastrectomy (ST: 1.3 vs. 2.3%, OR 0.58, CI95% 0.46–0.71, p < 0.0001/T: 3.6 vs. 4.5%, OR 0.80, CI95% 0.72–0.89, p = 0.0005). Partial or total adrenalectomy was less frequently performed in the G75 group alongside total gastrectomy (0.4 vs. 0.9%, OR 0.48, CI95% 0.35–0.64, p < 0.0001). In contrast, there was no significant difference between the two groups in terms of splenectomy for subtotal and total gastrectomy or combined gastrectomy and esophagectomy. Most extensive methods, such as peritonectomy and hyperthermic intraperitoneal chemotherapy (HIPEC), were used rarely in elderly patients in association with all three types of gastric surgery ( Table 2 ).

Table 2.

Adjunctive therapy and organ resection alongside oncological gastric resection in elderly patients in Germany between 2008 and 2018.

Adjunctivetherapy Subtotal gastrectomy (ST) Total gastrectomy (T) Total gastrectomy and esophageal resection (TE)
< 75 y ≥ 75 y < 75 y ≥ 75 y < 75 y ≥ 75 y
n % n % OR CI95% p-value n % n % OR CI95% p-value n % n % OR CI95% p-value
Pancreatic
resection
239
(10,587)
2.3% 147
(11,207)
1.3% 0.58 0.46–0.71 <0.0001 1,270
(28,208)
4.5% 494
(13,617)
3.6% 0.80 0.72–0.89 0.0005 147
(2,493)
5.9% 41
(863)
4.8% 0.79 0.54–1.14 1.0000
Liver
resection
609
(10,587)
5.8% 570
(11,207)
5.1% 0.88 0.78–1.00 0.6508 1,791
(28,208)
6.3% 771
(13,617)
5.7% 0.89 0.81–1.00 0.1282 179
(2,493)
8.4% 77
(919)
7.2% 1.18 0.88–1.57 1.0000
Splenectomy 206
(10,587)
1.9% 267
(11,207)
2.4% 1.23 1.00–1.49 0.6040 2,898
(28,208)
10.3% 1,412
(13,617)
10.4% 1.01 0.94–1.08 1.0000 317
(2,493)
12.7% 119
(973)
12.2% 0.96 0.76–1.20 1.0000
Peritonectomy 108
(9,443)
1.1% 23
(6,044)
0.4% 0.33 0.20–0.52 <0.0001 741
(28,208)
2.6% 118
(12,412)
0.95% 0.36 0.29–0.43 < 0.0001 75
(2,279)
3.2% 0
(161)
0.0% 0.1801
HIPEC 58
(9,443)
1.1% 0
(9,087)
0.0% <0.0001 568
(25,321)
2.2% 21
(11,204)
0.19% 0.08 0.05–0.13 < 0.0001 33
(1,316)
2.5% 0
(471)
0.0% 0.0014
Colon
resection
398
(10,587)
3.8% 434
(11,207)
3.9% 1.03 0.89–1.90 1.0000 1,224
(28,208)
4.3% 623
(13,617)
4.6% 1.06 0.95–1.67 1.0000 114
(2,493)
4.6% 36
(812)
4.4% 0.97 0.64–1.43 1.0000
Adrenalectomy 21
(5,523)
0.38% 16
(5,988)
0.27% 0.70 0.34–1.41 1.0000 252
(28,208)
0.9% 53
(12,409)
0.4% 0.48 0.35–0.64 < 0.0001 42
(2,149)
2.0% 3
(592)
0.5% 0.26 0.05–0.80 0.2136

ST, subtotal gastrectomy; T, total gastrectomy; TE, total gastrectomy in combination with esophageal resection; HIPEC, hyperthermic intraperitoneal chemotherapy; <75 y, patients younger than 75 years; ≥75 y, patients at an age of 75 years or more; n, absolute number of patients; the numbers in brackets delineate the overall collective after indexing by the Statistical Office; OR, odds ratio; CI95%, 95% confidence interval; Fisher’s exact test with the Bonferroni adjustment of p-values was used for statistical testing. The level of significance was set at 5%.

The bold values denote statistical significance at P <0.05 level.

General and surgical complications were subgrouped into intraoperative and postoperative adverse events according to the international consensus of complications after gastrectomy for cancer (10). The intraoperative course in terms of unintended injury to anatomic structures such as solid organs and blood vessels, during ST and T was slightly increased in elderly patients. (ST: 1.7 vs. 1.2%, OR 1.43, CI95% 1.14–1.81, p = 0.0173/T: 2.2 vs. 1.7%, OR 1.28, CI95% 1.10–1.48, p = 0.0109) Intraoperative bleeding and the need for interruption of surgery were not impacted by age ( Table 3A ).

Table 3.

Intraoperative and postoperative general and surgical complications in elderly patients undergoing oncological gastric resection in Germany between 2008 and 2018.

A Intraoperative Subtotal gastrectomy (ST) Total gastrectomy (T) Total gastrectomy and esophageal resection (TE)
< 75 y ≥ 75 y < 75 y ≥ 75 y < 75 y ≥ 75 y
n % n % OR CI95% p-value n % n % OR CI95% p-value n % n % OR CI95% p-value
Unintended intraoperative
damage to vessels or organs
128
(10,587)
1.2% 193
(11,207)
1.7% 1.43 1.14–1.81 0.0173 486
(28,208)
1.7% 298
(13,617)
2.2% 1.28 1.10–1.48 0.0109 50
(2,174)
2.3% 17
(467)
3.6% 1.60 0.85–2.86 0.9378
Intraoperative bleeding 474
(10,587)
4.5% 543
(11,207)
4.8% 1.09 0.96–1.24 1.0000 1,236
(28,208)
4.4% 677
(13,617)
5.0% 1.14 1.04–1.26 0.0676 139
(2,341)
5.9% 54
(812)
6.7% 1.13 0.80–1.57 1.0000
Interruption of the
planned procedure
30
(5,488)
0.5% 35
(7,193)
0.49% 0.89 0.53–1.50 1.0000 87
(28,208)
0.3% 43
(9,987)
0.4% 1.40 0.95–2.04 0.7965 0
(924)
0.0% 0
(450)
0.0%
B Postoperative
general
Subtotal gastrectomy (ST) Total gastrectomy (T) Total gastrectomy and esophageal resection (TE)
<75 y ≥75 y <75 y ≥75 y <75 y ≥75 y
n % n % OR CI95% p-value n % n % OR CI95% p-value n % n % OR CI95% p-value
Apoplexy 55
(8,656)
0.64% 122
(11,207)
1.1% 1.72 1.24–2.41 0.0275 106
(28,208)
0.38% 99
(13,617)
0.73% 1.94 1.46–2.58 0.1081 10
(1,399)
0.71% 3
(738)
0.41% 0.57 0.09–2.21 1.0000
Need for resuscitation 160
(10,587)
1.5% 293
(11,207)
2.6% 1.75 1.44–2.14 < 0.0001 479
(28,208)
1.7% 457
(13,617)
3.4% 2.01 1.76–2.29 < 0.0001 69
(2,341)
2.9% 51
(919)
5.5% 1.93 1.30–2.84 0.0218
Myocardial infarction 206
(10,587)
1.9% 356
(11,207)
3.2% 1.65 1.39–1.98 < 0.0001 629
(28,208)
2.2% 535
(13,617)
3.9% 1.79 1.59–2.02 < 0.0001 80
(2,493)
3.2% 52
(919)
5.7% 1.81 1.23–2.21 0.0642
Cardiac dysrhythmia 167
(10,587)
1.6% 435
(11,207)
3.9% 2.52 2.10–3.04 < 0.0001 571
(28,208)
2.0% 544
(13,617)
4.0% 2.01 1.78–2.27 < 0.0001 91
(2,493)
3.7% 56
(902)
6.2% 1.75 1.22–2.49 0.0762
Acute myocardial failure 219
(10,587)
2.1% 714
(11,207)
6.4% 3.22 2.76–3.77 < 0.0001 488
(28,208)
1.7% 803
(13,617)
5.9% 3.56 3.17–4.00 < 0.0001 44
(2,279)
1.9% 66
(866)
7.6% 4.19 2.79–6.34 < 0.0001
Pulmonary embolism 167
(10,587)
1.6% 195
(11,207)
1.7% 1.10 0.89–1.37 1.0000 523
(28,208)
1.9% 261
(13,617)
1.9% 1.03 0.88–1.20 1.0000 65
(2,070)
3.1% 22
(733)
3.0% 0.95 0.55–1.58 1.0000
Respiratory failure 1092
(10,587)
10.3% 1,595
(11,207)
14.2% 1.44 1.32–1.57 < 0.0001 3,407
(28,208)
12.1% 2,420
(13,617)
17.8% 1.57 1.48–1.67 < 0.0001 489
(2,493)
19.6% 249
(973)
25.6% 1.41 1.17–1.68 0.0054
Need for tracheostomy 231
(10,587)
2.2% 273
(11,207)
2.4% 1.12 0.93–1.34 1.0000 778
(28,208)
2.8% 515
(13,617)
3.8% 1.39 1.23–1.55 < 0.0001 128
(2,493)
5.1% 65
(973)
6.7% 1.32 0.95–1.81 1.0000
Need for prolonged
intubation
29
(7,848)
0.37% 27
(5,110)
0.53% 1.43 0.81–2.51 1.0000 101
(25,813)
0.39% 54
(9,915)
0.54% 1.39 0.98–1.96 1.0000 17
(1,759)
0.97% 3
(446)
0.67% 0.69 0.12–2.42 1.0000
Liver dysfunction 466
(10,587)
4.4% 548
(11,207)
4.9% 1.11 0.98–1.27 1.0000 1,428
(28,208)
5.1% 832
(13,617)
6.1% 1.22 1.11–1.33 < 0.0001 159
(2,493)
6.4% 53
(764)
6.9% 1.09 0.77–1.52 1.0000
Acute renal insufficiency 530
(10,587)
5.0% 1,077
(11,207)
9.6% 2.02 1.80–2.25 < 0.0001 1,406
(28,208)
5.0% 1,422
(13,617)
10.4% 2.22 2.06–2.40 < 0.0001 198
(2,493)
7.9% 131
(973)
13.5% 1.80 1.41–2.29 0.0001
Infection 1,152
(10,587)
10.9% 1,826
(11,207)
16.3% 1.59 1.47–1.73 < 0.0001 3124
(28,208)
11.1% 2,157
(13,617)
15.8% 1.51 1.42–1.60 < 0.0001 301
(2,493)
12.1% 166
(973)
17.1% 1.50 1.21–1.85 0.0058
C gastrectomy (ST) Total gastrectomy (T) Total gastrectomy and esophageal resection (TE)
<75 y ≥75 y <75 y ≥75 y <75 y ≥75 y
n % n % OR CI95% p-value n % n % OR CI95% p-value n % n % OR CI95% p-value
Need for
blood transfusion
2,918
(8,348)
35.0% 4,987
(8,951)
55.7% 2.34 2.20–2.49 < 0.0001 8,563
(22,547)
38.0% 6,323
(11,204)
56.4% 2.12 2.02–2.22 < 0.0001 835
(2,174)
38.4% 468
(862)
54.3 1.90 1.61–2.24 < 0.0001
Bowel obstruction 184
(10,587)
1.7% 218
(11,207)
1.9% 1.12 0.91–1.37 1.0000 354
(28,208)
1.3% 176
(13,617)
1.3% 1.03 0.85–1.24 1.0000 20
(1,565)
1.3% 10
(619)
1.6% 1.27 0.53–2.86 1.0000
Bowel perforation 47
(9,443)
0.5% 94
(11,207)
0.84% 1.69 1.17– 2.46 0.0882 194
(28,208)
0.69% 153
(13,617)
1.1% 1.64 1.32–2.04 0.0002 11
(1,357)
0.81% 0
(159)
0.0% 1.0000
Duodenal leak 23
(6,660)
0.35% 24
(6,239)
0.38% 1.11 0.60–2.07 1.0000 22
(15,675)
0.14% 25
(7,403)
0.34% 2.41 1.30–4.49 0.0826 3
(1,312)
0.23% 3
(914)
0.33% 1.44 0.19–10.7 1.0000
Anastomotic leakage1 281
(5,405)
5.2% 313
(5,960)
5.3% 1.01 0.85–1.19 1.0000 1,090
(14,813)
7.4% 756
(7,691)
9.8% 1.37 1.24–1.51 < 0.0001 182
(1,741)
10.4% 85
(704)
12.1% 1.18 0.88–1.56 1.0000
Pancreatic fistula 563
(10,587)
5.3% 559
(11,207)
5.0% 0.93 0.82–1.06 1.0000 1,796
(28,208)
6.4% 818
(13,617)
6.0% 0.94 0.86–1.02 1.0000 193
(2,493)
7.7% 64
(919)
7.0% 0.89 0.65–1.20 1.0000
Pancreatitis 45
(8,679)
0.52% 32
(8,279)
0.39% 0.74 0.45–1.20 1.0000 115
(28,208)
0.41% 66
(13,617)
0.48% 1.19 0.86–1.63 1.0000 7
(1,392)
0.5% 0
(667)
0.0% 1.0000
Need for abdominal
drainage
397
(10,587)
3.7% 433
(11,207)
3.9% 1.03 0.89–1.19 1.0000 1,144
(28,208)
4.0% 619
(13,617)
4.5% 1.12 1.01–1.25 0.6243 129
(2,493)
5.2% 49
(737)
6.6% 1.31 0.90–1.85 1.0000
Impaired gastric
emptying
3
(3,876)
0.08% 16
(6,144)
0.26% 3.37 0.96–18.07 1.0000
Other complications 1,904
(10,587)
18.0% 2183
(11,207)
19.5% 1.10 1.02–1.18 0.1473 5,461
(28,208)
19.4% 2,969
(13,617)
21.8% 1.16 1.10–1.22 < 0.0001 576
(2,493)
23.1% 233
(973)
23.9% 1.05 0.88–1.25 1.0000

ST, subtotal gastrectomy; T, total gastrectomy; TE, total gastrectomy in combination with esophageal resection; <75 y, patients younger than 75 years; ≥75 y, patients at an age of 75 years or more; n, absolute number of patients; the numbers in brackets delineate the overall collective after indexing by the Statistical Office; OR, odds ratio; CI95%, 95% confidence interval; 1The ICD-10-GM code for anastomotic leakage was just introduced in 2013; Fisher’s exact test with the Bonferroni adjustment of p-values was used for statistical testing. The level of significance was set at 5%.

The bold values denote statistical significance at P < 0.05 level.

Significant differences between the two groups, L75 and G75, were found in the postoperative course. General complications such as respiratory and acute renal failure, acute myocardial dysfunction, and the need for resuscitation were increased after subtotal and total gastrectomy in G75. In addition, elderly patients were significantly more susceptible to infections after all three types of gastric resection were studied ( Table 3B ).

Regarding specific surgical complications, the elderly had a significantly increased need for blood transfusions after each type of surgery. Furthermore, older patients showed an increased risk of bowel perforation (1.1 vs. 0.69%, OR 1.64, CI95% 1.32–2.04, p < 0.0002) and anastomotic leakage (9.8 vs. 7.4%, OR 1.37, CI95% 1.24–1.51, p < 0.0001) if they received total gastrectomy ( Table 3C ).

In-hospital mortality in elderly patients was higher after all three types of gastrectomy compared with the L75 group. (ST: 11.0 vs. 4.36%, OR 2.71, CI95% 2.42–3.03, p < 0.0001/T: 11.9 vs. 4.23%, OR 3.05, CI95% 2.82–3.30, p < 0.0001/TE: 13.9 vs. 5.86%, OR 2.59, CI95% 1.99–3.35, p < 0.0001) ( Table 4 )

Table 4.

In-hospital mortality following oncological gastric surgery in elderly patients in Germany between 2008 and 2018.

< 75 y ≥ 75 y
n In-hospital death Mortality n In-hospital death Mortality OR CI95% p-value
ST 10,587 462 4.36% 11,207 1,233 11.0% 2.71 2.42–3.03 <0.0001
T 28,208 1,193 4.23% 13,617 1,618 11.9% 3.05 2.82–3.30 <0.0001
TE 2,493 146 5.86% 916 127 13.9% 2.59 1.99–3.35 <0.0001

ST, subtotal gastrectomy; T, total gastrectomy; TE, total gastrectomy in combination with esophageal resection; <75 y, patients younger than 75 years; ≥75 y, patients at an age of 75 years or more; n, absolute number of patients; OR, odds ratio; CI95%: 95% confidence interval, Fisher’s exact test with the Bonferroni adjustment of p-values was used for statistical testing. The level of significance was set at 5%.

Discussion

The present study assessed differences in outcome after major oncologic gastric surgery among patients aged 75 years and older in Germany between 2008 and 2018 based on the G-DRG database of the German Federal Statistical Office (DESTATIS). Significant differences were found in particular with respect to postoperative morbidity and mortality.

Comorbidity was measured using the Charlson comorbidity index. The elderly collective scored significantly higher compared to younger patients stratified by each kind of gastric resection and each single year under study. Obviously, the difference is biased by the fact that the age of a particular patient is part of the calculation formula for the Charlson comorbidity index itself. An age between 80 and 89 years adds 4 points to the score, and an age of more than 90 years contributes to even 5 points, respectively. Nevertheless, the mean score suggests a 10-year mortality of 47% in the L75 group and 79% in the G75 collective solely based on comorbidity profile without considering the surgeries performed, indicating a certain vulnerability among the elderly group (12). For this reason, especially if life expectancy is reached, preoperative comorbidities and clinical circumstances must thoroughly be taken into account when planning major gastric resection for cancer in elderly patients.

The pattern of reconstruction techniques was rather similar in both groups. Merely after ST, there were more BII-like reconstructions performed in the elderly, and, after T, a slightly increased rate of reconstruction techniques ‘other than BII and RY’ was seen in this group. All in all, the age does not influence the choice of reconstruction technique fundamentally. Unfortunately, the current version of the OPS does not reflect the whole range of possible reconstruction techniques in detail. As case numbers in western Europe are not comparable to that in Asia, the implementation of new reconstruction approaches and their representation in the relevant coding systems are still hampered (13).

Regarding LAD, straight D2 and D3 LAD seems to be applied less frequently to elderly patients. Instead, other strategies like partial D2 or D3 LAD are more common in this group (see the supplement for the exact code definition used for the query). The fact that LAD is performed to an altered extent in elderly gastric cancer patients is already known and has been shown to be appropriate in Asian populations (14). The influence on the clinical outcome of adapted LAD in elderly patients in a western collective cannot fully be uncovered by the presented study. However, recent research suggests that standard D2 gastrectomy can safely be applied even to elderly patients (15, 16). Further research and clear recommendations are urgently needed on this field, as the presented data suggest, that D2 LAD seems to be applied hesitantly to patients older than 75 years, which may influence the oncologic outcome. Nonetheless, D2 dissection rates were surprisingly low although D2 LAD was adopted as a standard surgical procedure in the local guidelines. It may be speculated that D2 is either not performed according to the guideline recommendations or that the coding was not done appropriately. The influence of modified LAD on postoperative outcomes, therefore, cannot be finally evaluated in the setting of this analysis.

Another indicator of an adapted approach in elderly patients is the lower rate of additive organ resections such as pancreatic resection and peritonectomy. In addition, HIPEC is applied less frequently to the G75 collective. A less aggressive approach in gastric surgery for the elderly has been observed previously, as a reduction in the dimension of treatment may significantly improve the complication profile and should be considered in these patients (17). The data indicate an already-present clear consideration about the kind and extent of adjunctive surgery in daily clinical practice. Thus, pancreatic resection in the case of ST and T and adrenalectomy alongside T represent the only significantly altered organ resection approaches applied to elderly patients. The rates of colon and liver resection as well as splenectomy are not significantly divergent compared to younger patients.

Aside from a slightly increased rate of unintended damaging of blood vessels and organs, there appears to exist no significant influence of advanced age on the immediate intraoperative course. Bleeding during surgery and the interruption of the planned procedure are not impacted. Of course, a possibly explorative intent of a surgery cannot be deduced ultimately from the presented data. Even the postoperative surgical course seems only to be influenced by three particular aspects, namely, the necessity of blood transfusions, a higher rate of bowel perforation, and anastomotic leakage after total gastrectomy, aside from an increase in ‘other complications’ (see the supplement for code definition). However, we cannot derive the actual reason for a higher rate of transfusions from the data. As intraoperative bleeding seems not to be responsible, there may be other aspects like a decreased ability for compensation in the presence of low hemoglobin values among the elderly group. As already mentioned above in terms of comorbidity, a preoperative assessment of anemia and age-appropriate management could improve the outcome and avoid the extensive use of blood transfusions (18). Regarding the increased incidence of anastomotic leakage after total gastrectomy in the elderly, nutritional aspects and comorbidity may be important factors and further research is required to overcome this life-threatening adverse event (19).

Non-surgical complications like respiratory, renal or myocardial failure, and the need for cardio pulmonary resuscitation (CPR) in case of cardiac arrest are significantly increased in the elderly. Moreover, the distinct susceptibility to postoperative infections must be taken into account. However, there are preoperative screening tools available or currently under development addressing this problem; there is an urgent need for further improvement (2023). In this sense, even an appropriate assessment of the mentioned postoperative complications and adverse events with clear recommendations would be helpful to minimize morbidity.

Regarding postoperative mortality, there was a more-than-doubled probability of in-hospital death in the elderly collective. The rates of 11%–13%, depending on the extent of resection, highlight once again the vulnerability of that group compared to younger patients and raise the question of whether less invasive surgery might be of advantage in the selected subgroups of this collective. However, a meta-analysis by Kong et al. did not show a difference regarding morbidity and mortality between T and ST without regard on age; the extent of resection seems to be relevant in elderly patients (24).

There exist several limitations in the presented study regarding data quality and the informative value. The necessity to avoid small group sizes in the query strategy for the G-DRG database to minimize the probability of indexing by the Statistical Office for secrecy reasons delimits the grade of detail, like the particular strategy of LAD in each subgroup. Furthermore, only morbidity and procedures operationalized within the ICD-10 and OPS are evaluable. For example, there exists no information about the histological subtype of a tumor if not explicitly defined in the particular code. Our intent to use the international consensus list of complications after gastrectomy could not be realized ultimately as the pieces of information cannot be derived from the DESTATIS database (10). Finally, the quality of data depends highly on the sincerity of the encoding personnel in the hospitals, and economical interests may bias the data to a certain degree. Aside from this, it may not be deducted from the data presented if patients died from aggressive or progressing tumor burden or the complication itself. This fact further limits the generalizability of the data presented.

All in all, the impact of age on the perioperative outcome of patients undergoing gastrectomy is still controversial and cannot be fully uncovered by the present data. Varying endpoints and cutoffs in recent studies further complicate a comprehensive overview of the underlying issues. For instance, a cutoff age of 45 years with the definition that patients older than 45 years are ‘elderly’ in an exemplary study by Cheng et al. in 2021 suggests that there exists no difference between young and older patients during and after gastrectomy regarding several complications contrarily to our results (25). On the other hand, there exist several publications that confirm our impression of a significant impact of age on the postoperative outcome after gastrectomy (8, 26). Many articles about elderly patients already indicate a general consideration of geriatric aspects in major gastric surgery as this group is obviously more susceptible to numerous complications. Nevertheless, further systematic investigation is mandatory as there do not exist valid and comprehensive recommendations regarding a reasonable balance between surgical extent and the oncological outcome in the western collectives of elderly patients with gastric cancer yet.

Conclusion

The presented results demonstrate that the immediate outcome of major oncological gastric surgery depends highly on age aspects. Elderly patients have a tremendously increased likelihood of in-hospital morbidity and mortality, a fact that must be considered thoroughly when planning gastric resection. Nonetheless, the present data allow a real-life evaluation of all surgical gastric cancer cases in Germany and should be respected when counseling patients to decide for further therapeutic steps. Further research and new approaches to individualized geriatric surgery for gastrectomy are urgently needed in that sense.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Author contributions

MB: Programming of the query to the Federal Statistical Office of Germany, data evaluation, statistical analysis, literature review, manuscript writing M-CW: data evaluation, statistical analysis, literature review, manuscript writing P-AN: data evaluation, statistical analysis, literature review, manuscript writing HF: data evaluation, statistical analysis, literature review, manuscript writing DR: data evaluation, statistical analysis, literature review, manuscript writing. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2022.1032443/full#supplementary-material

References

  • 1. Neumann PA, Berlet MW, Friess H. Surgical oncology in the age of multimodality therapy for cancer of the upper and lower gastrointestinal tract. Expert Rev Anticancer Ther (2021) 21(5):511–22. doi: 10.1080/14737140.2021.1868991 [DOI] [PubMed] [Google Scholar]
  • 2. Tan KK, Quek TJ, Wong N, Li KK, Lim KH. Early outcome following emergency gastrectomy. Ann Acad Medicine-Singapore (2012) 41(10):451. doi:  10.47102/annals-acadmedsg.V41N10p451 [DOI] [PubMed] [Google Scholar]
  • 3. Seo SH, Hur H, An CW, Yi X, Kim JY, Han SU, et al. Operative risk factors in gastric cancer surgery for elderly patients. J gastric cancer (2011) 11(2):116–21. doi: 10.5230/jgc.2011.11.2.116 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Katai H, Sasako M, Sano T, Maruyama K. The outcome of surgical treatment for gastric carcinoma in the elderly. Japanese J Clin Oncol (1998) 28(2):112–5. doi: 10.1093/jjco/28.2.112 [DOI] [PubMed] [Google Scholar]
  • 5. Shimada S, Sawada N, Oae S, Seki J, Takano Y, Ishiyama Y, et al. Safety and curability of laparoscopic gastrectomy in elderly patients with gastric cancer. Surg Endosc (2018) 32(10):4277–83. doi: 10.1007/s00464-018-6177-1 [DOI] [PubMed] [Google Scholar]
  • 6. Wang J-f, Zhang S-z, Zhang N-y, Wu Z-y, Feng J-y, Ying L-p, et al. Laparoscopic gastrectomy versus open gastrectomy for elderly patients with gastric cancer: a systematic review and meta-analysis. World J Surg Oncol (2016) 14(1):1–10. doi: 10.1186/s12957-016-0859-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Garbarino GM, Costa G, Frezza B, Biancafarina A, Balducci G, Mercantini P, et al. Robotic versus open oncological gastric surgery in the elderly: a propensity score-matched analysis. J Robotic Surg (2021) 15(5):741–9. doi: 10.1007/s11701-020-01168-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Hayashi T, Yoshikawa T, Aoyama T, Ogata T, Cho H, Tsuburaya A. Severity of complications after gastrectomy in elderly patients with gastric cancer. World J Surg (2012) 36(9):2139–45. doi: 10.1007/s00268-012-1653-6 [DOI] [PubMed] [Google Scholar]
  • 9. RDC of the Federal Statistical Officeand Statistical Offices of the Länder, Diagnosis-Related Group Statistics (DRG Statistics), 2008-2018, own calculations, doi:  10.21242/23141.2018.00.00.1.1.0 [DOI]
  • 10. Baiocchi GL, Giacopuzzi S, Marrelli D, Reim D, Piessen G, Matos da Costa P, et al. International consensus on a complications list after gastrectomy for cancer. Gastric Cancer (2019) 22(1):172–89. doi: 10.1007/s10120-018-0839-5 [DOI] [PubMed] [Google Scholar]
  • 11. R Core Team . R: A language and environment for statistical computing [Internet]. Vienna Austria: R Foundation for Statistical Computing; (2020). Available at: https://www.R-project.org/. [Google Scholar]
  • 12. Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis (1987) 40(5):373–83. doi: 10.1016/0021-9681(87)90171-8 [DOI] [PubMed] [Google Scholar]
  • 13. Weber MC, Berlet M, Novotny A, Friess H, Reim D. [Reconstruction following gastrectomy]. Chirurg. (2021) 92(6):506–14. doi: 10.1007/s00104-020-01350-0 [DOI] [PubMed] [Google Scholar]
  • 14. Endo S, Fujiwara Y, Higashida M, Kubota H, Matsumoto H, Tanaka H, et al. Is D2 lymphadenectomy necessary in elderly gastric cancer patients? a retrospective study. Int Surg (2022). doi:  10.9738/INTSURG-D-22-00001.1 [DOI] [Google Scholar]
  • 15. Jeong O, Park YK, Ryu SY, Kim YJ. Effect of age on surgical outcomes of extended gastrectomy with D2 lymph node dissection in gastric carcinoma: Prospective cohort study. Ann Surg Oncol (2010) 17(6):1589–96. doi: 10.1245/s10434-010-0916-4 [DOI] [PubMed] [Google Scholar]
  • 16. Back J, Sallinen V, Kokkola A, Puolakkainen P. Surgical and oncological outcomes of D1 versus D2 gastrectomy among elderly patients treated for gastric cancer. Scand J Surg (2022) 111(2):14574969221096192. doi: 10.1177/14574969221096193 [DOI] [PubMed] [Google Scholar]
  • 17. Chen ZX, Li J, Liu WB, Zhang SR, Sun H. Elemene-containing hyperthermic intraperitoneal chemotherapy combined with chemotherapy for elderly patients with peritoneal metastatic advanced gastric cancer. World J Clin Cases (2022) 10(5):1498–507. doi: 10.12998/wjcc.v10.i5.1498 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Goodnough LT, Schrier SL. Evaluation and management of anemia in the elderly. Am J Hematol (2014) 89(1):88–96. doi: 10.1002/ajh.23598 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Makuuchi R, Irino T, Tanizawa Y, Bando E, Kawamura T, Terashima M. Esophagojejunal anastomotic leakage following gastrectomy for gastric cancer. Surg Today (2019) 49(3):187–96. doi: 10.1007/s00595-018-1726-8 [DOI] [PubMed] [Google Scholar]
  • 20. Hamakawa T, Kurokawa Y, Mikami J, Miyazaki Y, Takahashi T, Yamasaki M, et al. Risk factors for postoperative complications after gastrectomy in gastric cancer patients with comorbidities. Surg Today (2016) 46(2):224–8. doi: 10.1007/s00595-015-1175-6 [DOI] [PubMed] [Google Scholar]
  • 21. Aceto P, Antonelli Incalzi R, Bettelli G, Carron M, Chiumiento F, Corcione A, et al. Perioperative management of elderly patients (PriME): recommendations from an Italian intersociety consensus. Aging Clin Exp Res (2020) 32(9):1647–73. doi: 10.1007/s40520-020-01624-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Hirahara N, Tajima Y, Fujii Y, Kaji S, Kawabata Y, Hyakudomi R, et al. Prediction of postoperative complications and survival after laparoscopic gastrectomy using preoperative geriatric nutritional risk index in elderly gastric cancer patients. Surg Endosc (2021) 35(3):1202–9. doi: 10.1007/s00464-020-07487-7 [DOI] [PubMed] [Google Scholar]
  • 23. Endo S, Yamatsuji T, Fujiwara Y, Higashida M, Kubota H, Matsumoto H, et al. Prognostic factors for elderly gastric cancer patients who underwent gastrectomy. World J Surg Onc (2022) 20(1):10. doi: 10.1186/s12957-021-02475-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Kong L, Yang N, Shi L, Zhao G, Wang M, Zhang Y. Total versus subtotal gastrectomy for distal gastric cancer: meta-analysis of randomized clinical trials. Onco Targets Ther (2016) 9:6795–800. doi: 10.2147/OTT.S110828 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Cheng YX, Tao W, Liu XY, Yuan C, Zhang B, Zhang W, et al. The outcome of young vs. old gastric cancer patients following gastrectomy: a propensity score matching analysis. BMC Surg (2021) 21(1):399. doi:  10.1186/s12893-021-01401-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Hager ES, Abdollahi H, Crawford AG, Moudgill N, Rosato EL, Chojnacki KA, et al. Is gastrectomy safe in the elderly? a single institution review. Am Surgeon (2011) 77(4):488–92. doi: 10.1177/000313481107700429 [DOI] [PubMed] [Google Scholar]

Associated Data

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Supplementary Materials

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.


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