Skip to main content
Erschienen in: Gastric Cancer 6/2022

Open Access 07.08.2022 | Original Article

Survival trends in gastric cancer patients between 1987 and 2016: a population-based cohort study in Finland

verfasst von: Urgena Maharjan, Joonas H. Kauppila

Erschienen in: Gastric Cancer | Ausgabe 6/2022

Abstract

Background

Gastric cancer is the fourth leading cause of cancer-related deaths globally. There is a paucity of national studies examining gastric cancer mortality in relation to treatment status. This study evaluated the survival trends in gastric adenocarcinoma and all gastric cancers stratified by treatment in Finland during 1987–2016.

Methods

This population-based, nationwide, retrospective cohort study included all gastric cancer patients registered in the Finnish Cancer Registry and Patient Registry. The survival rates were calculated for 1, 3, and 5 years, stratified by treatment. Prognostic factors were determined using Cox regression.

Results

A total of 18,713 non-cardia gastric adenocarcinoma, and 3617 cardia adenocarcinoma patients were included. Surgical treatment decreased for non-cardia adenocarcinoma and remained constant for cardia adenocarcinoma. In non-cardia adenocarcinoma, the 5-year survival declined from 17% to 16% from 1987–1991 to 2012–2016. In surgically treated patients, survival increased from 29% to 38%, while an increase from 4% to 7% in those undergoing chemotherapy and decrease from 6% to 3% in those not receiving any treatment were observed. In cardia adenocarcinoma, the 5-year survival increased from 10% to 18% in all patients, 16% to 40% in surgical patients, 0% to 5% in patients receiving chemotherapy, and from 5% to 9% in patients receiving no treatment. Earlier calendar periods, older age, male sex, and higher comorbidity were risk factors for poor prognosis.

Conclusions

Gastric non-cardia adenocarcinoma survival declined, limited to advanced stage patients not receiving any treatment. Gastric cardia cancer survival seems to have improved over time in Finland.

Mini abstract

This study evaluated survival trends of gastric cancer in Finland during 1987–2016 and established that the 5-year survival is declining in non-cardia adenocarcinoma but improving in all gastric cancers.
Hinweise

Supplementary Information

The online version contains supplementary material available at https://​doi.​org/​10.​1007/​s10120-022-01326-5.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Introduction

Gastric cancer is the fifth most common cancer and the fourth leading cause of cancer-related death around the world [1]. Gastric cancers can be divided anatomically into non-cardia and cardia cancer, and histologically into intestinal and diffuse types [2]. Gastric non-cardia and cardia cancers exhibit differences in their etiology, incidence, and prognosis [24]. The incidence of gastric cardia cancer is increasing along with increasing obesity and reflux, while non-cardia cancer incidence is decreasing due to the lower prevalence of Helicobacter pylori infection [57]. Prevention of colonization of H. pylori has shown a potential to reduce incidences of gastric cancer [3, 8], but the best curative treatment for gastric cancer patients includes early diagnosis and surgical resection [9].
Although gastric cancer incidence is declining and survival is improving in most countries, the survival of patients after curative surgery is poor. In Europe, despite the decline in incidence and improvement in survival, gastric cancer remains a highly fatal disease with a poor prognosis. The 5-year survival rate of gastric cancer in Europe fluctuates between 10% and 30% [1012]. In Sweden, the survival after non-cardia gastric cancer diagnosis did not improve over 20 years [13]. The survival trends of gastric cancer in Finland are not known. Therefore, this study aimed to evaluate the survival trends of gastric cancer stratified by location and treatment in Finland during 1987–2016.

Materials and methods

Study design

This study was a population-based, nationwide, retrospective cohort study of all gastric cancer patients identified in Finland during the period 1987–2016, based on Finnish national registries. The study was approved by the Northern Ostrobothnia ethical committee (EETMK 115/2016) and relevant governmental bodies. Informed consent was not required for registry research [14, 15].

Data sources

All patients with gastric cancer were identified from the Finnish Cancer registry (FCR) and the Finnish Patient Registry (HILMO) using respective ICD-9 (151) and ICD-10 (C16) codes. Personal identification numbers assigned to all residents in Finland were used to combine registry data. The FCR provided data on incident cancers, date of diagnosis, cancer histology type, location, cancer stage, as well as the age of patients at diagnosis and sex of patients. FCR also provides data on whether patients had chemotherapy. HILMO was used to identify incident cancers and patients undergoing surgical resection and to calculate comorbidity in all identified gastric cancer patients, as previously defined. Surgical codes from the patient registry helped identify surgical procedure types which included gastrectomy, esophagectomy, esophagogastrectomy, endoscopic mucosal resection (EMR), and endoscopic submucosal dissection (ESD). Both open and laparoscopic surgery was included [14, 15]. FCR and HILMO are comprehensive registries in Finland, since physicians are mandated to report all incident cancers to FCR, and all healthcare units are obligated to report diagnosis and operations codes to HILMO. Thus, these operation codes serve as the basis for reimbursement [16, 17]. The Finnish death registry provided dates of death (until December 31, 2019) and cause of death (until December 31, 2018). The data in the Finnish death registry are 100% complete for vital status [18].

Data analysis

All analyses were based on a prior study protocol. Data on all patients diagnosed with gastric cancer from 1987 to 2016 were retrieved from FCR and HILMO registries. The patients were then grouped according to 5-year periods (1987–1991, 1992–1996…), age groups (< 50, 50–59, 60–69, 70–79, 80–89 and > 90), sex, Charlson Comorbidity Index score (0, 1, 2, 3 +), surgery status (yes and no), chemotherapy (no, yes, and missing), and stage (local, locally advanced, and advanced). For survival analysis, 1-year, 3-year, and 5-year survival rates were calculated for both non-cardia and cardia gastric adenocarcinoma separately, as well as stratified further by treatment: surgery, or no surgery; surgery, chemotherapy only, or no treatment; as well as by cancer stage: local, locally advanced, or advanced. Survival analysis was conducted using the life table method and plotted using Kaplan–Meier curves. Cox regression was used to calculate hazard ratios (HR) of mortality with 95% confidence intervals (95% CI) for each stratified variable (calendar year, age group, sex, and comorbidity score) which are considered prognostic factors associated with gastric cancer mortality. Finally, a separate analysis for all gastric cancer types was done to evaluate whether the survival trends were similar to trends of gastric adenocarcinoma. Analyses were carried out using IBM SPSS 26 (Armonk, NY, USA).

Results

Patients

Of the total 22,330 gastric cancer patients, 18,713 (83.8%) had non-cardia cancer and 3617 (16.2%) had cardia cancer during 1987–2016. After exclusion of 797 neuroendocrine tumors, 518 other types of tumors such as squamous cell carcinoma, melanoma, mesenchymal cancer, and gastrointestinal stromal tumor, and 3275 patients without any information on histology available, there were 18,713 histologically confirmed gastric non-cardia adenocarcinomas, and 3617 gastric cardia adenocarcinomas included in the analysis. The number of both cardia and non-cardia adenocarcinoma patients decreased over time. Most gastric adenocarcinomas occurred at the age of 70–79 years. There were more men with gastric non-cardia (52.6%) and cardia adenocarcinoma (70.0%) than women. Most gastric adenocarcinoma patients did not undergo chemotherapy and the majority had advanced cancer stages (Table 1). The demographics in all gastric cancer types were highly similar to histologically confirmed gastric adenocarcinomas. The number of gastric cardia cancer of any histology, however, remained constant over time (Supplementary Table 1).
Table 1
Histologically confirmed gastric non-cardia and cardia adenocarcinoma patients stratified by calendar period, age, sex, CCI, surgical treatment, chemotherapy, and cancer stage
Variable
Gastric non-cardia adenocarcinoma n (%)
Gastric cardia adenocarcinoma n (%)
Total n (%)
Total
18,713 (83.8)
3617 (16.2)
22,330 (100)
Calendar period
 1987–1991
4486 (24.0)
677 (18.7)
5163 (23.1)
 1992–1996
3720 (19.9)
676 (18.7)
4396 (19.7)
 1997–2001
3135 (16.8)
657 (18.2)
3792 (17.0)
 2002–2006
2928 (15.6)
551 (15.2)
3479 (15.6)
 2007–2011
2552 (13.6)
612 (16.9)
3164 (14.2)
 2012–2016
1892 (10.1)
444 (12.3)
2336 (10.5)
Age
 > 50
1325 (7.1)
265 (7.3)
1590 (7.1)
 50–59
2243 (12.0)
523 (14.5)
2766 (12.4)
 60–69
4197 (22.4)
929 (25.7)
5126 (23.0)
 70–79
5910 (31.6)
1126 (31.1)
7036 (31.5)
 80–89
4398 (23.5)
678 (18.7)
5076 (22.7)
 90 + 
640 (3.4)
96 (2.7)
736 (3.3)
Sex
 Female
8864 (47.4)
1085 (30.0)
9949 (44.6)
 Male
9849 (52.6)
2532 (70.0)
12,381 (55.4)
CCI
 0
12,007 (64.2)
2222 (61.4)
14,229 (63.7)
 1
4058 (21.7)
817 (22.6)
4875 (21.8)
 2
1717 (9.2)
375 (10.4)
2092 (9.4)
 3 + 
931 (5.0)
203 (5.6)
1134 (5.1)
Surgery
 Yes
8293 (44.3)
1320 (36.5)
9613 (43.0)
 No
10,420 (55.7)
2297 (63.5)
12,717 (57.0)
Chemotherapy
 No
12,909 (69.0)
2255 (62.3)
15,164 (67.9)
 Yes
2758 (14.7)
694 (19.2)
3452 (15.5)
 Missing
3046 (16.3)
668 (18.5)
3714 (16.6)
Stage
 Local
3608 (19.3)
599 (16.6)
4207 (18.8)
 Locally advanced
2226 (11.9)
469 (13.0)
2695 (12.1)
 Advanced
7610 (40.7)
1452 (40.1)
9062 (40.6)
 Unclear or missing
5269 (28.2)
1097 (30.3)
6366 (28.5)
CCI Charlson Comorbidity Index

Surgery

A total of 9613 (43.0%) gastric adenocarcinoma patients underwent surgical treatment. For gastric non-cardia adenocarcinoma, the proportion of surgical treatment was larger 8293 (44.3%) than for gastric cardia adenocarcinoma (1320, 36.5%, Table 1). The proportion of patients who had undergone surgery decreased from 45.0% to 34.0% for gastric non-cardia adenocarcinoma (Fig. 1a), but remained constant for gastric cardia adenocarcinoma between 1987 and 2016 (Fig. 1b). In the separate analysis of gastric cancers of any histology, the proportion of patients who underwent surgery declined in both gastric cardia and non-cardia cancers (Supplementary Fig. 1).

All patients

In all patients with gastric non-cardia adenocarcinoma, the 5-year survival rate decreased from 17% during 1987–1991 to 16% in 2012–2016 (Table 2; Fig. 2a). For gastric cancer patients of any histology, the 5-year survival rate increased from 19% during 1987–1991 to 24% during 2012–2016 (Supplementary Table 2, Supplementary Fig. 2a).
Table 2
One- year-, 3-year-, and 5-year survival in histologically confirmed gastric adenocarcinoma (non-cardia and cardia) stratified by treatment during 1987–2016
 
Gastric non- cardia adenocarcinoma
Gastric cardia adenocarcinoma
Patients
Survival in %
Patients
Survival in %
Calendar period
Number (%)
1 year
3 years
5 years
Number (%)
1 year
3 years
5 years
All patients
 1987–1991
4486 (24.0)
38
21
17
677 (18.7)
34
14
10
 1992–1996
3720 (19.9)
40
20
18
676 (18.7)
36
16
12
 1997–2001
3135 (16.8)
41
23
19
657 (18.2)
40
18
13
 2002–2006
2928 (15.6)
41
22
17
551 (15.2)
40
16
12
 2007–2011
2552 (13.6)
42
23
17
612 (16.9)
44
20
14
 2012–2016
1892 (10.1)
40
23
16
444 (12.3)
50
24
18
Surgery
 1987–1991
2051 (24.7)
62
37
29
270 (20.5)
54
23
16
 1992–1996
1817 (21.9)
66
40
31
280 (21.2)
58
31
24
 1997–2001
1505 (18.1)
69
43
35
271 (20.5)
68
37
28
 2002–2006
1293 (15.6)
71
43
35
171 (13.0)
76
44
36
 2007–2011
995 (12.0)
77
49
37
176 (13.3)
90
57
43
 2012–2016
632 (7.6)
77
49
38
152 (11.5)
86
52
40
No surgery
 1987–1991
2435 (23.4)
18
8
7
407 (17.7)
20
7
5
 1992–1996
1903 (18.3)
16
7
6
396 (17.2)
20
4
4
 1997–2001
1630 (15.6)
16
5
4
386 (16.8)
20
4
2
 2002–2006
1635 (15.7)
17
5
3
380 (16.5)
23
3
2
 2007–2011
1557 (14.9)
20
6
4
436 (19.0)
26
5
3
 2012–2016
1260 (12.1)
22
6
4
292 (12.7)
32
9
7

Surgical patients

The 5-year survival rate in patients who underwent surgical treatment for gastric non-cardia adenocarcinoma improved from 29% during 1987–1991 to 38% during 2012–2016 (Table 2, Fig. 2c). Similarly, increasing survival (31% to 44%) was observed for gastric cancers of any histology (Supplementary Table 2, Supplementary Fig. 2c).

Non-surgical patients

Among the patients without surgical treatment for gastric non-cardia adenocarcinoma, the 5-year survival declined from 7% during 1987–1991 to 4% during 2012–2016 (Table 2, Fig. 2e). The 5-year survival rate increased from 4% during 1987–1991 to 7% during 2012–2016 in those patients undergoing chemotherapy only, whereas the survival rate declined from 6% to 3% in those not going through any treatment (Supplementary Table 3, Supplementary Fig. 3c, 3e). In the analysis of all gastric histological gastric cancer types, the 5-year survival of patients not undergoing surgery increased from 11% during 1987–1991 to 15% during 2012–2016 (Supplementary Table 2, Supplementary Fig. 2e).

Cancer stage

The 5-year survival increased in gastric non-cardia adenocarcinoma patients from 45% to 57% in those with local cancer stage, from 17% to 26% in those with locally advanced cancer stage, and only slightly from 2% to 3% in those with advanced cancer stage between 1987–1991 and 2012–2016 (Table 3, Supplementary Fig. 4a, 4c, 4e).
Table 3
One-year-, 3-year-, and 5-year survival in histologically confirmed gastric adenocarcinoma (non-cardia and cardia) stratified by cancer stage during 1987–2016
 
Gastric non-cardia adenocarcinoma
Gastric cardia adenocarcinoma
Patients
Survival in %
Patients
Survival in %
Calendar period
Number (%)
1 year
3 years
5 years
Number (%)
1 year
3 years
5 years
Local
 1987–1991
1092 (30.3)
74
55
45
147 (24.5)
64
32
26
 1992–1996
960 (26.6)
79
59
48
150 (25.0)
62
42
33
 1997–2001
609 (16.9)
78
60
52
107 (17.9)
68
43
35
 2002–2006
488 (13.5)
78
60
50
85 (14.2)
71
49
37
 2007–2011
351 (9.7)
74
58
50
88 (14.7)
62
48
34
 2012–2016
108 (3.0)
79
62
57
22 (3.7)
73
54
55
Locally advanced
 1987–1991
505 (22.7)
61
26
17
83 (17.7)
46
11
5
 1992–1996
447 (20.1)
62
28
20
91 (19.4)
57
19
12
 1997–2001
459 (20.6)
68
34
23
116 (24.7)
68
32
23
 2002–2006
350 (15.7)
72
40
31
61 (13.0)
74
33
26
 2007–2011
267 (12.0)
80
44
28
80 (17.1)
82
46
28
 2012–2016
198 (8.9)
66
35
26
38 (8.1)
76
37
24
Advanced
 1987–1991
1892 (24.9)
16
3
2
290 (20.0)
14
2
1
 1992–1996
1472 (19.3)
15
2
2
278 (19.1)
18
4
3
 1997–2001
1203 (15.8)
16
4
3
258 (17.8)
18
3
1
 2002–2006
1286 (16.9)
23
6
3
263 (18.1)
24
5
3
 2007–2011
1243 (16.3)
30
12
7
273 (18.8)
34
8
6
 2012–2016
514 (6.8)
18
4
3
90 (6.2)
20
6
4

All patients

The 5- year survival rate in all patients with gastric cardia adenocarcinoma improved from 10% to 18% between the first and last calendar period (Table 2; Fig. 2b). In the analysis of all gastric cancers, the 5-year survival improved from 11% to 22% (Supplementary Table 2, Supplementary Fig. 2b).

Surgical patients

In patients who underwent surgical treatment for gastric cardia adenocarcinoma, the 5-year survival rate increased from 16% during 1987–1991 to 40% during 2012–2016 (Table 2; Fig. 2d). Similarly, increasing survival over time (18%–45%) was observed in all gastric cancers (Supplementary Table 2, Supplementary Fig. 2d).

Non-surgical patients

Among those who had not undergone surgical treatment for gastric cardia adenocarcinoma, the 5-year survival rate increased from 5% during 1987–1991 to 7% during 2012–2016 (Table 2; Fig. 2f). Similarly, an increase from 6% to 12% was observed in all gastric cancers (Supplementary Table 2, Supplementary Fig. 2f). Among non-surgical patients, the 5-year survival increased from 0% during 1987–1991 to 5% during 2012–2016 in those who underwent chemotherapy only, and from 5% to 9% between 1987–1991 and 2012–2016 in patients who received no treatment (Supplementary Table 3, Supplementary Fig. 3d, 3f).

Cancer stage

The 5-year survival increased in gastric cardia adenocarcinoma patients from 26% to 55% in those with local cancer stage, from 5% to 24% in those with locally advanced cancer stage, and from 1% to 4% in those with advanced cancer stage between 1987–1991 and 2012–2016 (Table 3, Supplementary Fig. 4b, 4d, 4f).

Risk factors for 5-year mortality in gastric non-cardia cancer

In the multivariable cox-regression analysis of all patients with gastric non-cardia adenocarcinoma, earlier calendar periods (HR 1.08, 95% CI 1.02–1.15 in 1987–1991 vs 2012–2016), older age groups (HR 2.92, 95% CI 2.64–3.24, age 90 + vs age > 50), higher comorbidity score (HR 1.22, 95% CI 1.14–1.32, CCI 3 + vs 0), and male sex (HR 1.07, 95% CI 1.03–1.10, male vs female) were observed to be associated with an increased risk of mortality. The risk factors were similar in patients undergoing surgery and not undergoing surgery, with the exception that comorbidity was not a risk factor for mortality in those not undergoing surgery (Table 4). In the analysis of all gastric cancers, the risk factors were the same as in gastric adenocarcinoma, with comorbidity in addition in those not undergoing surgery (Supplementary Table 4).
Table 4
Multivariable cox-regression analysis of risk of mortality during 5-year follow-up in all histologically confirmed gastric non-cardia adenocarcinoma patients and stratified by surgical treatment
Covariate
Category
Gastric non- cardia adenocarcinoma
 
Number of patients (%)
HR (95% CI)
All patients
 Calendar period
1987–1991
4486 (24.0)
1.08 (1.02–1.15)
1992–1996
3720 (19.9)
1.02 (0.96–1.08)
1997–2001
3135 (16.8)
0.97 (0.91–1.03)
2002–2006
2928 (15.6)
1.02 (0.95–1.08)
2007–2011
2552 (13.6)
0.97 (0.91–1.04)
2012–2016
1892 (10.1)
1 (Reference)
Age
 > 50
1325 (7.1)
1 (Reference)
50–59
2243 (12.0)
1.03 (0.95–1.12)
60–69
4197 (22.4)
1.14 (1.06–1.22)
70–79
5910 (31.6)
1.37 (1.28–1.47)
80–89
4398 (23.5)
1.90 (1.77–2.04)
90 + 
640 (3.4)
2.92 (2.64–3.24)
Sex
Female
8864 (47.4)
1 (Reference)
Male
9849 (52.6)
1.07 (1.03–1.10)
CCI
0
12,007 (64.2)
1 (Reference)
1
4058 (21.7)
1.01 (0.97–1.05)
2
1717 (9.2)
1.12 (1.06–1.18)
3 + 
931 (5.0)
1.22 (1.14–1.32)
Surgery
 Calendar period
1987–1991
2051 (24.7)
1.58 (1.41–1.77)
1992–1996
1817 (21.9)
1.40 (1.24–1.56)
1997–2001
1505 (18.1)
1.21 (1.07–1.36)
2002–2006
1293 (15.6)
1.19 (1.06–1.35)
2007–2011
995 (12.0)
1.03 (0.90–1.16)
2012–2016
632 (7.6)
1 (Reference)
 Age
 > 50
728 (8.8)
1 (Reference)
50–59
1186 (14.3)
1.01 (0.89–1.14)
60–69
2129 (25.7))
1.11 (1.00–1.24)
70–79
2777 (33.5)
1.37 (1.23–1.52)
80–89
1410 (17.0)
1.83 (1.63–2.05)
90 + 
63 (0.8)
2.94 (2.22–3.88)
 Sex
Female
3865 (46.6)
1 (Reference)
Male
4428 (53.4)
1.10 (1.05–1.16)
 CCI
0
5515 (66.5)
1 (Reference)
1
1805 (21.8)
1.13 (1.06–1.21)
2
653 (7.9)
1.25 (1.13–1.38)
3 + 
320 (3.9)
1.55 (1.36–1.77)
No surgery
 Calendar period
1987–1991
2435 (23.4)
1.05 (0.98–1.13)
1992–1996
1903 (18.3)
1.13 (1.05–1.22)
1997- 2001
1630 (15.6)
1.13 (1.05–1.22)
2002–2006
1635 (15.7)
1.16 (1.08–1.25)
2007–2011
1557 (14.9)
1.07 (0.99–1.15)
2012–2016
1260 (12.1)
1 (Reference)
 Age
 > 50
597 (5.7)
1 (Reference)
50–59
1057 (10.1)
1.03 (0.93–1.15)
60–69
2068 (19.8)
1.13 (1.02 -1.24)
70–79
3133 (30.1)
1.28 (1.17–1.40)
80–89
2988 (28.7)
1.44 (1.33–1.58)
90 + 
577 (5.5)
1.65 (1.47–1.86)
 Sex
Female
4999 (48.0)
1 (Reference)
Male
5421 (52.0)
1.03 (0.99–1.08)
 CCI
0
6492 (62.3)
1 (Reference)
1
2253 (21.6)
0.95 (0.91–1.00)
2
1064 (10.2)
0.99 (0.93–1.06)
3 + 
611 (5.9)
0.97 (0.89–1.05)
CCI Charlson Comorbidity Index

Risk factors for 5-year mortality in gastric cardia cancer

In the multivariable cox-regression analysis of all patients with gastric cardia adenocarcinoma, the risk factors of mortality were earlier calendar periods (HR 1.49, 95% CI 1.30–1.71 in 1987–1991 vs 2012–2016), older age groups (HR 2.03, 95% CI 1.59–2.60, age 90 + vs > 50), male sex (HR 1.05, 95% CI 0.97–1.14, male vs female), and high comorbidity score (HR 1.33, 95% 1.14–1.55, CCI 3 + vs 0) (Table 5). The risk factors were similar in patients undergoing surgery and not undergoing surgery, with the exception that male sex was not a risk factor for mortality in those not undergoing surgery. The results were similar in all gastric cancers with the male sex being associated with poor survival in both non-surgical and surgical groups (Supplementary Table 5).
Table 5
Multivariable cox-regression analysis of risk of mortality during 5-year follow-up in all histologically confirmed gastric cardia adenocarcinoma patients and stratified by surgical treatment
Covariate
Category
Gastric cardia adenocarcinoma
 
Number of patients (%)
HR (95% CI)
All patients
 Calendar period
1987–1991
677 (18.7)
1.49 (1.30–1.71)
1992–1996
676 (18.7)
1.36 (1.19–1.55)
1997–2001
657 (18.2)
1.27 (1.11–1.45)
2002–2006
551 (15.2)
1.24 (1.08–1.43)
2007–2011
612 (16.9)
1.13 (0.98–1.29)
2012–2016
444 (12.3)
1 (Reference)
 Age
 > 50
265 (7.3)
1 (Reference)
50–59
523 (14.5)
0.91 (0.78–1.07)
60–69
929 (25.7)
0.98 (0.84–1.14)
70–79
1126 (31.1)
1.13 (0.97–1.30)
80–89
678 (18.7)
1.59 (1.36–1.87)
90 + 
96 (2.7)
2.03 (1.59–2.60)
 Sex
Female
1085 (30.0)
1 (Reference)
Male
2532 (70.0)
1.05 (0.97–1.14)
 CCI
0
2222 (61.4)
1 (Reference)
1
817 (22.6)
1.07 (0.98–1.17)
2
375 (10.4)
1.26 (1.12–1.42)
3 + 
203 (5.6)
1.33 (1.14–1.55)
Surgery
 Calendar period
1987–1991
270 (20.5)
2.22 (1.72–2.86)
1992–1996
280 (21.2)
1.82 (1.42–2.35)
1997–2001
271 (20.5)
1.48 (1.14–1.90)
2002–2006
171 (13.0)
1.17 (0.88–1.54)
2007–2011
176 (13.3)
0.86 (0.65–1.15)
2012–2016
152 (11.5)
1 (Reference)
 Age
 > 50
117 (8.9)
1 (Reference)
50–59
225 (17.0)
0.84 (0.63–1.10)
60–69
409 (31.0)
1.00 (0.78–1.29)
70–79
445 (33.7)
1.19 (0.92–1.52)
80–89
118 (8.9)
1.45 (1.06–1.97)
90 + 
6 (0.5)
2.50 (1.09–5.77)
 Sex
Female
361 (27.3)
1 (Reference)
Male
959 (72.7)
1.22 (1.05–1.42)
 CCI
0
905 (68.6)
1 (Reference)
1
283 (21.4)
1.01 (0.85–1.19)
2
94 (7.1)
1.13 (0.87–1.46)
3 +
38 (2.9)
1.30 (0.85–1.85)
No surgery
 Calendar period
1987–1991
407 (17.7)
1.34 (1.14–1.57)
1992–1996
396 (17.2)
1.36 (1.16–1.59)
1997–2001
386 (16.8)
1.42 (1.21–1.66)
2002–2006
380 (16.5)
1.28 (1.09–1.50)
2007–2011
436 (19.0)
1.20 (1.03–1.40)
2012–2016
292 (12.7)
1 (Reference)
 Age
 > 50
148 (6.4)
1 (Reference)
50–59
298 (13.0)
0.90 (0.73–1.10)
60–69
520 (22.6)
0.96 (0.80–1.16)
70–79
681 (29.6)
1.02 (0.85–1.23)
80–89
560 (24.4)
1.12 (0.93–1.36)
90 + 
90 (3.9)
1.24 (0.95–1.64)
 Sex
Female
724 (31.5)
1 (Reference)
Male
1573 (68.5)
0.98 (0.90–1.08)
 CCI
0
1317 (57.3)
1 (Reference)
1
534 (23.2)
1.07 (0.96–1.19)
2
281 (12.2)
1.14 (1.00–1.31)
3 + 
165 (7.2)
1.11 (0.94–1.32)
CCI Charlson Comorbidity Index

Discussion

This study indicates a declining survival in histologically confirmed gastric non-cardia adenocarcinoma but an improved overall survival for gastric cardia cancer during the last 3 decades in Finland. Significant improvement in 5-year survival was observed particularly among surgically treated patients as well as patients undergoing chemotherapy. Declining survival was seen among those non-cardia adenocarcinoma patients who did not receive any treatment. Earlier calendar period, older age, male sex, and higher comorbidity score were associated with poor prognosis in both gastric non-cardia and cardia cancers.
The main strength of this study is its population-based design, which reduced selection bias. The large cohort size allowed robust and reliable estimates, and the 100% complete follow-up of all patients based on national vital registration ensures that no misclassification occurred for the outcome variables. However, missing histology records for some patients led to their exclusion from the analysis of confirmed adenocarcinoma cases, and therefore, some selection bias is present in analyses of patients with adenocarcinoma. Another strength includes the highly accurate data retrieved from two independent and complete nationwide registries (FCR and HILMO) [19], which were combined using the immutable Finnish personal identity numbers assigned to all citizens, ensuring that all cases are captured. There were some missing values for oncological treatment status and tumor stage, and therefore, the estimates concerning chemotherapy patients and stage-specific analyses should be interpreted cautiously. Weaknesses include lack of TNM stage and more granular histological data, such as Laurén or WHO classification concerning adenocarcinoma patients.
The survival patterns of gastric adenocarcinoma prognosis in several European countries have been assessed previously. A Dutch study on gastric adenocarcinomas showed that 5-year survival for gastric non-cardia adenocarcinoma decreased from 22% to 14% [20]. A Swedish study suggested that the 5-year prognosis of gastric non-cardia adenocarcinoma was stable at 18% between 1990–1994 and 2012–2014 [13]. In the present study, the 5-year survival for confirmed gastric non-cardia adenocarcinomas decreased from 17% to 16% between 1987–1991 and 2012–2016. However, significant improvements in 5-year survival were observed in patients undergoing surgery or chemotherapy, as well as those with local or locally advanced disease, while those not receiving any treatment or advanced disease had worsening prognosis over time. Some of the improvements in prognosis can be explained by increased patient awareness and developments in surgical techniques [21]. Centralization of surgery might have improved treatment results [22], but gastric cancer surgery was formally centralized in Finland after the study period. As the proportion of surgically treated patients has declined over time, it is questionable whether surgical selection of patients has become even too strict. More accurate diagnostic imaging leads to better preoperative staging, and therefore, metastatic diseases are not operated on so often. It could be speculated that the worsening prognosis in no treatment group is due to the selection of the heathier patients for palliative chemotherapy. However, it remains unclear why the prognosis in no surgery group declined over time.
The recent trends of cardia adenocarcinoma prognosis have been previously studied in the Netherlands (stable at 10% from 1990 to 2005) [20] and Sweden (increased from 12% in 1990–1994 to 18% in 2012–2014) [13]. The present study suggests improved prognosis for cardia adenocarcinoma from 10% to 18% between 1987–1991 and 2012–2016, which is uplifting and in line with the Swedish mortality figures. Similar to non-cardia adenocarcinomas, their treatment has been centralized and neoadjuvant therapies have become more commonplace, improved prognosis in those undergoing surgery and oncological treatment. Opposed to non-cardia adenocarcinomas, the prognosis of those with advanced disease and receiving no treatment has also improved over time. While there are no clear explanations for this discrepancy, these findings may indicate differences in presenting symptoms or differences in cancer biology between non-cardia and cardia adenocarcinomas.
In a larger context, the prognosis of non-cardia gastric cancer of any histology has improved from 19% in 1987–1991 to 24% in 2012–2016, and from 11% in 1987–1991 to 24% in 2012–2016 for gastric cardia cancer. This is in line with registry studies from the United States (improvement from 26% to 29% during 2000s) [23], Europe (23% in 1999 to 25% in 2007) [10], and South Korea (43% in 1993–1995 to 74% in 2010–2014) [24]. While this overall improving survival in both gastric non-cardia and cardia is encouraging, these numbers include all histology of gastric cancer, such as neuroendocrine and gastrointestinal stromal tumors, which have a much better prognosis than adenocarcinomas [25, 26]. Increasing use of abdominal computed tomography might also have led to the more frequent discovery of gastric incidentalomas, which often include asymptomatic non-adenocarcinoma tumors with better prognosis and some of these might only be followed up clinically [27]. Therefore, some of the global improvement in gastric cancer survival might not completely reflect improved survival of gastric adenocarcinomas, but might also be related to increased detection of non-adenocarcinoma cancers of other histological types, thereby, increasing incidence and improving prognosis [4].
In addition to earlier calendar periods, older age groups, comorbidity, and male sex were observed to be risk factors for poor prognosis of both gastric non-cardia and cardia cancers. While the other factors are largely in line with the previous studies, the finding on the association of sex difference in poor prognosis of gastric cancer was rather unexpected. In the subgroup analyses, sex was associated with prognosis in only surgical gastric non-cardia and cardia adenocarcinoma. In Sweden, which is a relatively similar population compared to Finland, there was no difference in prognosis between male and female gastric non-cardia adenocarcinoma patients [13]. The higher incidence of gastric cancer in men results from genetic, environmental, and behavioral factors, including alcohol and tobacco consumption, differences in healthcare-seeking patterns, and utilization of health resources between men and women. Prevalence of H. pylori is, however, the most detrimental risk factor associated with poor prognosis in both sexes [2831]. Estrogen in women might protect against H. pylori infection resulting in a lower incidence of gastric cancer in women [3234]. These factors might explain the disparity observed in survival between the two sexes.
This study has several research and clinical implications. First, the declining prognosis in gastric non-cardia adenocarcinomas highlights the need for actions, such as further centralization of gastric cancer care, and evaluation and research of treatment options such as immunotherapies or cytoreductive surgery to further improve the prognosis of the disseminated disease. Second, the discrepancy in survival trend patterns between non-cardia and cardia cancers need further studies to understand the reasons these two cancer types are behaving differently. Finally, the differences in prognostic trends between gastric adenocarcinomas and all gastric cancers may indicate that optimistic estimates of survival trends may be obtained by studying gastric cancers without taking into account cancer histology.
In conclusion, this population-based, nationwide study on survival trends of gastric cancer in Finland indicates that the 5-year survival in patients with gastric non-cardia adenocarcinoma is declining but improving for cardia adenocarcinomas. However, the overall survival in all gastric cancers has improved during the last 3 decades in Finland. Earlier calendar period, older age, male sex, and higher comorbidity scores were poor prognostic factors for both gastric non-cardia and cardia cancer.

Acknowledgements

We thank the Sigrid Jusélius Foundation (Sigrid Juséliuksen Säätiö), The Finnish Cancer Foundation (Syöpäsäätiö), and Päivikki and Sakari Sohlberg Foundation for financially supporting this work.

Declarations

Ethical approval

The study was conducted in accordance with the ethical standards approved by the ethical committee in Northern Ostrobothnia (EETMK 115/2016), The National Institute for Health and Welfare (THL/169/5.05.00), Statistics Finland (TK-53-1478-17), the Office of the Data Protection Ombudsman (Dnro 506/402/17), Finland and with the Helsinki Declaration. Individual informed consent from patients was not required, as obtaining the informed consent was waived by Finnish law.

Conflict of interest

The authors declare that they have no conflict of interest.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Unsere Produktempfehlungen

e.Med Interdisziplinär

Kombi-Abonnement

Für Ihren Erfolg in Klinik und Praxis - Die beste Hilfe in Ihrem Arbeitsalltag

Mit e.Med Interdisziplinär erhalten Sie Zugang zu allen CME-Fortbildungen und Fachzeitschriften auf SpringerMedizin.de.

e.Med Innere Medizin

Kombi-Abonnement

Mit e.Med Innere Medizin erhalten Sie Zugang zu CME-Fortbildungen des Fachgebietes Innere Medizin, den Premium-Inhalten der internistischen Fachzeitschriften, inklusive einer gedruckten internistischen Zeitschrift Ihrer Wahl.

Anhänge

Supplementary Information

Below is the link to the electronic supplementary material.
Literatur
1.
Zurück zum Zitat Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA A Cancer J Clin. 2021;71(3):209–49.CrossRef Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA A Cancer J Clin. 2021;71(3):209–49.CrossRef
2.
Zurück zum Zitat Hu B, El Hajj N, Sittler S, Lammert N, Barnes R, Meloni-Ehrig A. Gastric cancer: classification, histology and application of molecular pathology. J Gastrointest Oncol. 2012;3(3):251–61.PubMedPubMedCentral Hu B, El Hajj N, Sittler S, Lammert N, Barnes R, Meloni-Ehrig A. Gastric cancer: classification, histology and application of molecular pathology. J Gastrointest Oncol. 2012;3(3):251–61.PubMedPubMedCentral
3.
Zurück zum Zitat Colquhoun A, Arnold M, Ferlay J, Goodman KJ, Forman D, Soerjomataram I. Global patterns of cardia and non-cardia gastric cancer incidence in 2012. Gut. 2015;64(12):1881.CrossRef Colquhoun A, Arnold M, Ferlay J, Goodman KJ, Forman D, Soerjomataram I. Global patterns of cardia and non-cardia gastric cancer incidence in 2012. Gut. 2015;64(12):1881.CrossRef
4.
Zurück zum Zitat Smyth EC, Verheij M, Allum W, Cunningham D, Cervantes A, Arnold D, et al. Gastric cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2016;27(suppl 5):v38–49.CrossRef Smyth EC, Verheij M, Allum W, Cunningham D, Cervantes A, Arnold D, et al. Gastric cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2016;27(suppl 5):v38–49.CrossRef
5.
Zurück zum Zitat den Hoed CM, Kuipers EJ. Gastric cancer: how can we reduce the incidence of this disease? Curr Gastroenterol Rep. 2016;18(7):34.CrossRef den Hoed CM, Kuipers EJ. Gastric cancer: how can we reduce the incidence of this disease? Curr Gastroenterol Rep. 2016;18(7):34.CrossRef
6.
Zurück zum Zitat Crew KD, Neugut AI. Epidemiology of gastric cancer. World J Gastroenterol. 2006;12(3):354–62.CrossRef Crew KD, Neugut AI. Epidemiology of gastric cancer. World J Gastroenterol. 2006;12(3):354–62.CrossRef
7.
Zurück zum Zitat Lv L, Liang X, Wu D, Wang F, Zhang Y, Cang H, et al. Is cardia cancer a special type of gastric cancer? A differential analysis of early cardia cancer and non-cardia cancer. J Cancer. 2021;12(8):2385–94.CrossRef Lv L, Liang X, Wu D, Wang F, Zhang Y, Cang H, et al. Is cardia cancer a special type of gastric cancer? A differential analysis of early cardia cancer and non-cardia cancer. J Cancer. 2021;12(8):2385–94.CrossRef
8.
Zurück zum Zitat Bornschein J, Selgrad M, Warnecke M, Kuester D, Wex T, Malfertheiner PH. pylori infection is a key risk factor for proximal gastric cancer. Dig Dis Sci. 2010;55(11):3124–31.CrossRef Bornschein J, Selgrad M, Warnecke M, Kuester D, Wex T, Malfertheiner PH. pylori infection is a key risk factor for proximal gastric cancer. Dig Dis Sci. 2010;55(11):3124–31.CrossRef
9.
Zurück zum Zitat Maeda H, Okabayashi T, Nishimori I, Sugimoto T, Namikawa T, Dabanaka K, et al. Clinicopathologic features of adenocarcinoma at the gastric cardia: is it different from distal cancer of the stomach? J Am Coll Surg. 2008;206(2):306–10.CrossRef Maeda H, Okabayashi T, Nishimori I, Sugimoto T, Namikawa T, Dabanaka K, et al. Clinicopathologic features of adenocarcinoma at the gastric cardia: is it different from distal cancer of the stomach? J Am Coll Surg. 2008;206(2):306–10.CrossRef
10.
Zurück zum Zitat Anderson LA, Tavilla A, Brenner H, Luttmann S, Navarro C, Gavin AT, et al. Survival for oesophageal, stomach and small intestine cancers in Europe 1999–2007: results from EUROCARE-5. Eur J Cancer. 2015;51(15):2144–57.CrossRef Anderson LA, Tavilla A, Brenner H, Luttmann S, Navarro C, Gavin AT, et al. Survival for oesophageal, stomach and small intestine cancers in Europe 1999–2007: results from EUROCARE-5. Eur J Cancer. 2015;51(15):2144–57.CrossRef
11.
Zurück zum Zitat Verdecchia A, Guzzinati S, Francisci S, De Angelis R, Bray F, Allemani C, et al. Survival trends in European cancer patients diagnosed from 1988 to 1999. Eur J Cancer. 2009;45(6):1042–66.CrossRef Verdecchia A, Guzzinati S, Francisci S, De Angelis R, Bray F, Allemani C, et al. Survival trends in European cancer patients diagnosed from 1988 to 1999. Eur J Cancer. 2009;45(6):1042–66.CrossRef
12.
Zurück zum Zitat Matsuda T, Saika K. The 5-year relative survival rate of stomach cancer in the USA, Europe and Japan. Jpn J Clin Oncol. 2013;43(11):1157–8.CrossRef Matsuda T, Saika K. The 5-year relative survival rate of stomach cancer in the USA, Europe and Japan. Jpn J Clin Oncol. 2013;43(11):1157–8.CrossRef
13.
Zurück zum Zitat Asplund J, Kauppila JH, Mattsson F, Lagergren J. Survival trends in gastric adenocarcinoma: a population-based study in Sweden. Ann Surg Oncol. 2018;25(9):2693–702.CrossRef Asplund J, Kauppila JH, Mattsson F, Lagergren J. Survival trends in gastric adenocarcinoma: a population-based study in Sweden. Ann Surg Oncol. 2018;25(9):2693–702.CrossRef
14.
Zurück zum Zitat Kauppila JH, Ohtonen P, Rantanen T, Tyrväinen T, Toikkanen V, Pääaho M, et al. Cohort profile: gastric cancer in the population-based, Finnish National Esophago-Gastric Cancer Cohort (FINEGO) Study. BMJ Open. 2020;10(10): e039574.CrossRef Kauppila JH, Ohtonen P, Rantanen T, Tyrväinen T, Toikkanen V, Pääaho M, et al. Cohort profile: gastric cancer in the population-based, Finnish National Esophago-Gastric Cancer Cohort (FINEGO) Study. BMJ Open. 2020;10(10): e039574.CrossRef
15.
Zurück zum Zitat Kauppila JH, Ohtonen P, Karttunen TJ, Kokkola A, Laine S, Rantanen T, et al. Finnish National Esophago-Gastric Cancer Cohort (FINEGO) for studying outcomes after oesophageal and gastric cancer surgery: a protocol for a retrospective, population-based, nationwide cohort study in Finland. BMJ Open. 2019;9(1): e024094.CrossRef Kauppila JH, Ohtonen P, Karttunen TJ, Kokkola A, Laine S, Rantanen T, et al. Finnish National Esophago-Gastric Cancer Cohort (FINEGO) for studying outcomes after oesophageal and gastric cancer surgery: a protocol for a retrospective, population-based, nationwide cohort study in Finland. BMJ Open. 2019;9(1): e024094.CrossRef
16.
Zurück zum Zitat Leinonen MK, Miettinen J, Heikkinen S, Pitkäniemi J, Malila N. Quality measures of the population-based Finnish Cancer Registry indicate sound data quality for solid malignant tumours. Eur J Cancer. 2017;77:31–9.CrossRef Leinonen MK, Miettinen J, Heikkinen S, Pitkäniemi J, Malila N. Quality measures of the population-based Finnish Cancer Registry indicate sound data quality for solid malignant tumours. Eur J Cancer. 2017;77:31–9.CrossRef
17.
Zurück zum Zitat Sund R. Quality of the Finnish hospital discharge register: a systematic review. Scand J Public Health. 2012;40(6):505–15.CrossRef Sund R. Quality of the Finnish hospital discharge register: a systematic review. Scand J Public Health. 2012;40(6):505–15.CrossRef
19.
Zurück zum Zitat Maharjan U, Kauppila JH. Gastric cancer completeness in Finnish Cancer Registry and Finnish Patient Registry: a population-based nationwide retrospective cohort study. BMJ Open. 2022;12(4):e056320 (Published 2022 Apr 19).CrossRef Maharjan U, Kauppila JH. Gastric cancer completeness in Finnish Cancer Registry and Finnish Patient Registry: a population-based nationwide retrospective cohort study. BMJ Open. 2022;12(4):e056320 (Published 2022 Apr 19).CrossRef
20.
Zurück zum Zitat Dassen AE, Lemmens VE, van de Poll-Franse LV, Creemers GJ, Brenninkmeijer SJ, Lips DJ, et al. Trends in incidence, treatment and survival of gastric adenocarcinoma between 1990 and 2007: a population-based study in The Netherlands. Eur J Cancer. 2010;46(6):1101–10.CrossRef Dassen AE, Lemmens VE, van de Poll-Franse LV, Creemers GJ, Brenninkmeijer SJ, Lips DJ, et al. Trends in incidence, treatment and survival of gastric adenocarcinoma between 1990 and 2007: a population-based study in The Netherlands. Eur J Cancer. 2010;46(6):1101–10.CrossRef
21.
Zurück zum Zitat Young JA, Shimi SM, Kerr L, McPhillips G, Thompson AM. Reduction in gastric cancer surgical mortality over 10 years: an adverse events analysis. Ann Med Surg (Lond). 2014;3(2):26–30.CrossRef Young JA, Shimi SM, Kerr L, McPhillips G, Thompson AM. Reduction in gastric cancer surgical mortality over 10 years: an adverse events analysis. Ann Med Surg (Lond). 2014;3(2):26–30.CrossRef
22.
Zurück zum Zitat Nelen SD, Heuthorst L, Verhoeven RHA, Polat F, Kruyt PM, Reijnders K, et al. Impact of centralizing gastric cancer surgery on treatment, morbidity, and mortality. J Gastrointest Surg. 2017;21(12):2000–8.CrossRef Nelen SD, Heuthorst L, Verhoeven RHA, Polat F, Kruyt PM, Reijnders K, et al. Impact of centralizing gastric cancer surgery on treatment, morbidity, and mortality. J Gastrointest Surg. 2017;21(12):2000–8.CrossRef
23.
Zurück zum Zitat Jim MA, Pinheiro PS, Carreira H, Espey DK, Wiggins CL, Weir HK. Stomach cancer survival in the United States by race and stage (2001–2009): findings from the CONCORD-2 study. Cancer. 2017;123(Suppl 24):4994–5013.CrossRef Jim MA, Pinheiro PS, Carreira H, Espey DK, Wiggins CL, Weir HK. Stomach cancer survival in the United States by race and stage (2001–2009): findings from the CONCORD-2 study. Cancer. 2017;123(Suppl 24):4994–5013.CrossRef
24.
Zurück zum Zitat Hong S, Won Y, Park YR, Jung K, Kong H, Lee ES, et al. Cancer Statistics in Korea: incidence, mortality, survival, and prevalence in 2017. Cancer Res Treat. 2020;52(2):335–50.CrossRef Hong S, Won Y, Park YR, Jung K, Kong H, Lee ES, et al. Cancer Statistics in Korea: incidence, mortality, survival, and prevalence in 2017. Cancer Res Treat. 2020;52(2):335–50.CrossRef
25.
Zurück zum Zitat Zhang H, Liu Q. Prognostic indicators for gastrointestinal stromal tumors: a review. Transl Oncol. 2020;13(10): 100812.CrossRef Zhang H, Liu Q. Prognostic indicators for gastrointestinal stromal tumors: a review. Transl Oncol. 2020;13(10): 100812.CrossRef
26.
Zurück zum Zitat Kargwal N, Panda V, Jha A, Singh CB. Gastric neuroendocrine tumor. Surg J (N Y). 2021;7(3):e142–6.CrossRef Kargwal N, Panda V, Jha A, Singh CB. Gastric neuroendocrine tumor. Surg J (N Y). 2021;7(3):e142–6.CrossRef
27.
Zurück zum Zitat Lumbreras B, Donat L, Hernández-Aguado I. Incidental findings in imaging diagnostic tests: a systematic review. Br J Radiol. 2010;83(988):276–89.CrossRef Lumbreras B, Donat L, Hernández-Aguado I. Incidental findings in imaging diagnostic tests: a systematic review. Br J Radiol. 2010;83(988):276–89.CrossRef
28.
Zurück zum Zitat Lou L, Wang L, Zhang Y, Chen G, Lin L, Jin X, et al. Sex difference in incidence of gastric cancer: an international comparative study based on the Global Burden of Disease Study 2017. BMJ Open. 2020;10(1): e033323.CrossRef Lou L, Wang L, Zhang Y, Chen G, Lin L, Jin X, et al. Sex difference in incidence of gastric cancer: an international comparative study based on the Global Burden of Disease Study 2017. BMJ Open. 2020;10(1): e033323.CrossRef
29.
Zurück zum Zitat Blanc-Lapierre A, Rousseau M, Weiss D, El-Zein M, Siemiatycki J, Parent M. Lifetime report of perceived stress at work and cancer among men: a case–control study in Montreal, Canada. Prev Med. 2017;96:28–35.CrossRef Blanc-Lapierre A, Rousseau M, Weiss D, El-Zein M, Siemiatycki J, Parent M. Lifetime report of perceived stress at work and cancer among men: a case–control study in Montreal, Canada. Prev Med. 2017;96:28–35.CrossRef
30.
Zurück zum Zitat Edgren G, Liang L, Adami HO, Chang ET. Enigmatic sex disparities in cancer incidence. Eur J Epidemiol. 2012;27(3):187–96.CrossRef Edgren G, Liang L, Adami HO, Chang ET. Enigmatic sex disparities in cancer incidence. Eur J Epidemiol. 2012;27(3):187–96.CrossRef
31.
Zurück zum Zitat McQueen A, Vernon SW, Meissner HI, Rakowski W. Risk perceptions and worry about cancer: does gender make a difference? J Health Commun. 2008;13(1):56–79.CrossRef McQueen A, Vernon SW, Meissner HI, Rakowski W. Risk perceptions and worry about cancer: does gender make a difference? J Health Commun. 2008;13(1):56–79.CrossRef
32.
Zurück zum Zitat Camargo MC, Goto Y, Zabaleta J, Morgan DR, Correa P, Rabkin CS. Sex hormones, hormonal interventions, and gastric cancer risk: a meta-analysis. Cancer Epidemiol Biomarkers Prev. 2012;21(1):20.CrossRef Camargo MC, Goto Y, Zabaleta J, Morgan DR, Correa P, Rabkin CS. Sex hormones, hormonal interventions, and gastric cancer risk: a meta-analysis. Cancer Epidemiol Biomarkers Prev. 2012;21(1):20.CrossRef
33.
Zurück zum Zitat Chandanos E, Lagergren J. Oestrogen and the enigmatic male predominance of gastric cancer. Eur J Cancer. 2008;44(16):2397–403.CrossRef Chandanos E, Lagergren J. Oestrogen and the enigmatic male predominance of gastric cancer. Eur J Cancer. 2008;44(16):2397–403.CrossRef
34.
Zurück zum Zitat Sheh A, Ge Z, Parry NMA, Muthupalani S, Rager JE, Raczynski AR, et al. 17β-Estradiol and tamoxifen prevent gastric cancer by modulating leukocyte recruitment and oncogenic pathways in Helicobacter pylori-infected INS-GAS male mice. Cancer Prev Res (Phila). 2011;4(9):1426.CrossRef Sheh A, Ge Z, Parry NMA, Muthupalani S, Rager JE, Raczynski AR, et al. 17β-Estradiol and tamoxifen prevent gastric cancer by modulating leukocyte recruitment and oncogenic pathways in Helicobacter pylori-infected INS-GAS male mice. Cancer Prev Res (Phila). 2011;4(9):1426.CrossRef
Metadaten
Titel
Survival trends in gastric cancer patients between 1987 and 2016: a population-based cohort study in Finland
verfasst von
Urgena Maharjan
Joonas H. Kauppila
Publikationsdatum
07.08.2022
Verlag
Springer Nature Singapore
Erschienen in
Gastric Cancer / Ausgabe 6/2022
Print ISSN: 1436-3291
Elektronische ISSN: 1436-3305
DOI
https://doi.org/10.1007/s10120-022-01326-5

Weitere Artikel der Ausgabe 6/2022

Gastric Cancer 6/2022 Zur Ausgabe

Vorsicht, erhöhte Blutungsgefahr nach PCI!

10.05.2024 Koronare Herzerkrankung Nachrichten

Nach PCI besteht ein erhöhtes Blutungsrisiko, wenn die Behandelten eine verminderte linksventrikuläre Ejektionsfraktion aufweisen. Das Risiko ist umso höher, je stärker die Pumpfunktion eingeschränkt ist.

Darf man die Behandlung eines Neonazis ablehnen?

08.05.2024 Gesellschaft Nachrichten

In einer Leseranfrage in der Zeitschrift Journal of the American Academy of Dermatology möchte ein anonymer Dermatologe bzw. eine anonyme Dermatologin wissen, ob er oder sie einen Patienten behandeln muss, der eine rassistische Tätowierung trägt.

Deutlich weniger Infektionen: Wundprotektoren schützen!

08.05.2024 Postoperative Wundinfektion Nachrichten

Der Einsatz von Wundprotektoren bei offenen Eingriffen am unteren Gastrointestinaltrakt schützt vor Infektionen im Op.-Gebiet – und dient darüber hinaus der besseren Sicht. Das bestätigt mit großer Robustheit eine randomisierte Studie im Fachblatt JAMA Surgery.

Chirurginnen und Chirurgen sind stark suizidgefährdet

07.05.2024 Suizid Nachrichten

Der belastende Arbeitsalltag wirkt sich negativ auf die psychische Gesundheit der Angehörigen ärztlicher Berufsgruppen aus. Chirurginnen und Chirurgen bilden da keine Ausnahme, im Gegenteil.

Update Chirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

S3-Leitlinie „Diagnostik und Therapie des Karpaltunnelsyndroms“

Karpaltunnelsyndrom BDC Leitlinien Webinare
CME: 2 Punkte

Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

Radiusfraktur BDC Leitlinien Webinare
CME: 2 Punkte

Das Webinar beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

Appendizitis BDC Leitlinien Webinare
CME: 2 Punkte

Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.