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Erschienen in: Journal of Gastrointestinal Cancer 4/2022

Open Access 14.09.2021 | Original Research

The Glasgow Prognostic Score Before Curative Resection May Predict Postoperative Complications in Patients with Gastric Cancer

verfasst von: Yota Shimoda, Hirohito Fujikawa, Keisuke Komori, Hayato Watanabe, Kosuke Takahashi, Kazuki Kano, Takanobu Yamada, Manabu Shiozawa, Soichiro Morinaga, Kenji Katsumata, Akihiko Tsuchida, Takashi Ogata, Takashi Oshima

Erschienen in: Journal of Gastrointestinal Cancer | Ausgabe 4/2022

Abstract

Purpose

Despite improvements in surgical techniques and devices and perioperative care of gastric cancer (GC), the rate of postoperative complications still has not decreased. If patients at high risk for postoperative complications could be identified early using biomarkers, these complications might be reduced. In this study, we investigated usefulness of the preoperative Glasgow Prognostic Score (GPS) as a predictive factor for complications after surgery in patients with stage II/III GC.

Methods

This study retrospectively analyzed the outcomes of 424 patients who underwent curative surgery for pathological stage II/III GC from February 2007 to July 2019 at a single center. The GPS was assessed within 4 days before surgery. To identify independent risk factors for postoperative complications, univariate and multivariate analyses were performed using a Cox proportional hazards model.

Results

The numbers of patients with a GPS of 0, 1, and 2 were 357, 55, and 12, respectively. The rate of complications after surgery was significantly higher among patients with a GPS of 1 or 2 than among patients with a GPS of 0 (p = 0.008). Multivariate analysis identified a GPS of 1 or 2 as an independent predictive factor for postoperative complications (p = 0.037).

Conclusion

The preoperative GPS may be a useful predictive factor for postoperative complications in patients with stage II/III GC. Being aware of the risk of complications after surgery as indicated by the GPS before surgery may promote safe and minimally invasive surgery that we expect will improve outcomes in patients with a GPS of 1 or 2.
Hinweise

Publisher's Note

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Introduction

Gastric cancer (GC) is the fifth most prevalent carcinoma in the world, with 1,089,103 new cases in 2020, and the fourth leading cause of death from cancer, with 768,793 deaths globally [1]. The standard treatment for pathological (p)stage II/III GC is curative surgery and adjuvant chemotherapy [2].
Despite improvements in surgical techniques and devices and perioperative care, the rate of postoperative complications still has not decreased. Recent studies reported that postoperative complication rates after GC resection were 17.4–24.5% [35]. Postoperative complications may significantly impact both long-term and short-term outcomes because they can sometimes lead to the production of cytokines that are growth factors for GC micrometastases. Complications prolong hospital stays, reduce the quality of life of patients, and increase health care costs [6, 7]. Additionally, postoperative complications often delay the initiation of adjuvant chemotherapy and decrease patients’ tolerance of chemotherapy [8]. Furthermore, a postoperative systemic inflammatory response is related to poor cancer-specific survival independent of the tumor stage [9]. Postoperative complications contribute to poor cancer-specific survival in various types of cancer including GC [1012]. Therefore, if patients at high risk for postoperative complications could be identified early using biomarkers, these complications might be reduced by selecting risk-adapted procedures and perioperative management. Such biomarkers must be easy-to-use, low-cost, rapid, and objective measures accessible to all patients and hospitals.
The Glasgow Prognostic Score (GPS) has been reported as a parameter that elevated serum C-reactive protein (CRP) levels reflect a progression cancer stage, and decreased serum albumin levels are an indicator of malnutrition [1318]. Therefore, we hypothesized that the GPS might be a useful predictor of postoperative complications. In this study, we investigated the usefulness of the GPS before surgery in predicting complications after surgery in patients with stage II/III GC.

Patients and Methods

Patients

The study was approved by the Research Ethics Committee of the Kanagawa Cancer Center in Yokohama, Japan, before the study started (approval number: Epidemiological Study, 2019 − 113). A total of 623 patients who underwent gastrectomy with D2 lymph node dissection for pstage II/III GC from February 2007 to July 2019 at the Kanagawa Cancer Center measured serum albumin and CRP levels before surgery and documented in their medical record were eligible for this study. Of those patients, patients who underwent preoperative treatment including neoadjuvant chemotherapy, those with remnant GC, those with stage IV GC, and those with non-curative (R1 or R2) resection were excluded. Finally, a total of 424 patients were analyzed.

Definition of GPS

The GPS was calculated using the serum CRP and serum albumin levels extracted from the medical records. Serum albumin and CRP levels before surgery were assessed within 4 days before surgery. The GPS was scored by allocating one point each for hypoalbuminemia (< 3.5 mg/dL) and elevated CRP (> 1.0 mg/dL). Patients with a hypoalbuminemia (< 3.5 mg/dL) and elevated CRP (> 1.0 mg/dL) were assigned a score of 2. Those with a hypoalbuminemia alone or elevated CRP alone were assigned a score of 1. Those with normal albumin (≥ 3.5 mg/dL) and CRP (CRP ≤ 1.0 mg/dL) levels were assigned a score of 0 [19].

Surgical Procedure and Perioperative Care

Patient with cstage IB GC underwent laparoscopy-assisted gastrectomy with D1 + lymphadenectomy, and those with cstage II/III GC underwent open gastrectomy with D2 lymphadenectomy according to the TNM classification (8th edition).
Our center uses the “enhanced recovery after surgery” protocol, which has been described in a previous study [20]. Oral intake was initiated on postoperative day (POD) 1, beginning with water. Patients began to eat on POD 2, starting with rice gruel and advancing in three steps to regular food intake on POD 6.

Data Collection

All variables, including patient age, sex, body mass index (kg/m2), type of surgery, operative time, blood loss, depth of invasion, and lymph node metastasis, were collected from the clinicopathological database in Kanagawa Cancer Center. All resected specimens had been examined and histopathologically staged according to UICC TNM 8th edition [21]. Complications after surgery were defined as those observed within 1 month after surgery that were grade 2 or higher according to the Clavien-Dindo classification [22].

Evaluations and Statistical Analysis

Patients were divided into a GPS 0 group and a GPS 1 or 2 group based on their preoperative GPS. We used the Mann–Whitney U test for comparison of age, body mass index, operation time, and intraoperative blood loss between two groups. Categorical variables were analyzed using Pearson’s χ2 test. To identify independent risk factors for postoperative complications, univariate and multivariate analyses were performed using a Cox proportional hazards model. All statistical analyses were performed using IBM SPSS Statistics for Windows, version 24.0 (IBM Corp., Armonk, NY, USA). Statistical significance was defined at a p-value < 0.05.

Results

Comparison of Clinicopathological Characteristics Between the GPS 0 and GPS 1 or 2 Groups

In this study, a total of 424 patients were examined. A flow diagram of the patient selection is shown in Fig. 1. The numbers of patients with a GPS of 0, 1, and 2 were 357, 55, and 12, respectively. The clinicopathological characteristics of the GPS 0 and GPS 1 or 2 groups are shown in Table 1. Age, operative time, blood loss during surgery, and pathological lymph node metastasis were significantly higher in the GPS 1 or 2 group than in the GPS 0 group. The body mass index was significantly lower in the GPS 1or 2 group than in the GPS 0 group.
Table 1
Clinicopathological characteristics of patients in the GPS 0 and GPS 1 or 2 groups
 
GPS
 
Variables/categories
0
(n = 357)
1 or 2
(n = 67)
p-Value
Age, years (mean ± SD)
66.7 ± 11.0
72.2 ± 8.8
 < 0.001
Sex, n (%)
Male
239 (67)
43 (64)
0.66
Female
118 (33)
24 (36)
Body mass index, kg/m2
(mean ± SD)
22.7 ± 3.1
21.8 ± 3.1
0.035
Type of surgery, n (%)
Distal gastrectomy
199 (56)
30 (45)
0.098
Total gastrectomy
158 (44)
37 (55)
Operation time, min (mean ± SD)
214.6 ± 63.6
238.8 ± 71.5
0.005
Blood loss, mL (mean ± SD)
335.6 ± 334.9
497.4 ± 404.5
0.001
Pathological tumor depth, n (%)
T2
98 (27)
12 (18)
0.157
T3
104 (29)
26 (39)
T4
155 (44)
29 (43)
Pathological lymph node metastasis, n (%)
  
N0
135 (38)
14 (21)
0.038
N1
71 (20)
13 (19)
N2
65 (18)
17 (25)
N3
86 (24)
23 (34)
GPS Glasgow Prognostic Score, SD standard deviation

Comparison of Postoperative Complications Between the GPS 0 and GPS 1 or 2 Groups

Sixty-six postoperative complications (18%) were observed in the GPS 0 group and 22 (33%) in the GPS 1 or 2 group. The rate of postoperative complications was significantly higher in the GPS 1 or 2 group than in the GPS 0 group (p = 0.008). The postoperative complications in the two groups are shown in Table 2. The rate of infectious complications, such as pancreatic fistula, anastomotic leakage, pneumonia, intraabdominal abscess, and wound infection, was significantly higher in the GPS 1 or 2 group than in the GPS 0 group (p = 0.008).
Table 2
Comparison of postoperative complications between the GPS 0 and GPS 1 or 2 groups
 
GPS
 
Variables/categories, n (%)
0
(n = 357)
1 or 2
(n = 67)
p-Value
All postoperative complications
66 (18)
22 (33)
0.008
Pancreatic fistula
21 (6)
6 (9)
0.345
Anastomotic leakage
12 (3)
4 (6)
0.304
Ileus
7 (2)
3 (4)
0.213
Pneumonia
5 (1)
4 (6)
0.017
Intraabdominal abscess
5 (1)
1 (1)
0.953
Postoperative bleeding
4 (1)
1 (1)
0.796
Wound infection
3 (1)
0 (0)
0.451
Delayed gastric emptying
2 (1)
0 (0)
0.539
Others
9 (3)
2 (2)
0.826
Infectious complication
45 (13)
16 (24)
0.016
Noninfectious complication
21 (6)
6 (9)
0.345
GPS Glasgow Prognostic Score

Risk Factors of Postoperative Complication

Table 3 shows the results of the univariate analysis of postoperative complications. The types of the surgical procedure, operative time, blood loss, and GPS were significantly associated with postoperative complications. Table 4 shows the results of the multivariate logistic regression analysis. An operation time ≥ 200 min (hazard ratio [HR] 1.947, 95% confidence interval [CI] 1.080 − 3.512, p = 0.027), and a GPS of 1 or 2 (HR 1.877, 95% CI 1.039 − 3.388, p = 0.037) was identified as independent risk factors for postoperative complications.
Table 3
Univariate analysis of variables and their potential relation to the occurrence of postoperative complications
Variables/categories
Patients
(n)
Complications
n (%)
p-Value
Age, years
 < 75
306
60 (20)
0.348
 ≥ 75
118
28 (24)
Sex
 Male
282
66 (23)
0.058
 Female
142
22 (15)
Body mass index, kg/m2
 < 25
345
71 (21)
0.853
 ≥ 25
79
17 (22)
Surgical procedure
 Distal gastrectomy
229
36 (16)
0.006
 Total gastrectomy
195
52 (27)
Operation time, min
 < 200
179
23 (13)
0.001
 ≥ 200
245
65 (27)
Blood loss, mL
 < 250
202
32 (16)
0.017
 ≥ 250
222
56 (25)
Pathological tumor depth
 2 and 3
241
55 (23)
0.228
 4
183
33 (18)
Pathological lymph node metastasis
 ( −)
149
33 (22)
0.175
 ( +)
275
55 (20)
Glasgow Prognostic Score
 0
357
66 (18)
0.008
 1 and 2
67
22 (33)
GPS Glasgow Prognostic Score
Table 4
Multivariate analysis of selected variables and their relation to the occurrence of postoperative complications
 
OR
95% CI
p-Value
Surgical procedure
Distal gastrectomy
   
Total gastrectomy
1.579
0.958–2.601
0.073
Operation time, min
 < 200
   
 ≥ 200
1.947
1.080–3.512
0.027
Blood loss, mL
 < 250
   
 ≥ 250
1.947
1.080–3.512
0.584
GPS
0
   
1 and 2
1.877
1.039–3.388
0.037
OR odds ratio, CI confidence interval, GPS Glasgow Prognostic Score

Discussion

In the present study, we investigated the usefulness of the GPS calculated using the serum CRP and serum albumin levels before surgery in predicting postoperative complications in patients with stage II/III GC who underwent curative surgery. Our results confirm our hypothesis that the preoperative GPS is an independent predictive marker of postoperative complications.
Today, the most commonly used clinical biomarker of systemic inflammation is the serum CRP level. There is an association between systemic inflammation and complications after oncologic surgery [23, 24]. It has been reported that proinflammatory cytokines such as interleukin-1, interleukin-6, and tumor necrosis factor-α induce an increase in serum CRP levels [25]. Those cytokines produced by various cancers and lymphocytes sensitized to cancer cause systemic inflammatory responses and cancer cachexia [26]. Preoperatively elevated serum CRP levels are associated with an increased incidence of postoperative complications in cancer patients [27], while serum albumin is produced in the liver and is the most abundant serum protein [28]. Low albumin is an indicator of malnutrition, and preoperative hypoalbuminemia is often seen in patients with advanced GC. Serum albumin levels decline in patients with poor nutritional status, loss of skeletal muscle, and systemic inflammatory response [29]. In cancer, the progression of the disease is associated with increasing systemic inflammation, leading to hyper catabolism and decreased serum albumin levels [30]. Several studies have demonstrated that hypoalbuminemia increases the incidence of postoperative complications in cancer patients [3133].
We hypothesized that the GPS could be a useful predictor of postoperative complications in patients with GC because it is calculated based on serum CRP and albumin levels. However, until now, few studies have examined the association between the GPS and postoperative complications. As for previous reports, Fujiwara et al. [34] showed that the GPS was related to blood transfusion requirements and postoperative complications in patients with hepatocellular carcinoma undergoing resection. Moyes et al. [35] reported that a preoperative elevated modified GPS was independently associated with an increased risk of postoperative infectious complications in patients undergoing resection of colorectal cancer. As for the study in patients with GC, Kubota et al. [36] did not find an association between the preoperative GPS and the occurrence of postoperative complications after curative resection of GC. While, in our study, the preoperative GPS was identified as a predictor of postoperative complications in patients with GC. The rate of total gastrectomy in the GPS 1 or 2 group in our study was 55%, which was more than twice that in their study. In general, because complications of total gastrectomy, such as anastomotic insufficiency, are higher than those of subtotal gastrectomy, this difference might be explained by the different proportions of total gastrectomy to subtotal gastrectomy in the two studies.
As for possible clinical application of the preoperative GPS, because the preoperative GPS may identify patients with a high risk of postoperative complications, it may assist surgeons in assessing the risk of postoperative complications and choosing an approach that is as safe and minimally invasive as possible. Furthermore, recent studies have shown the efficacy of perioperative immune-nutritional support according to the condition of each cancer patient in reducing the incidence of postoperative complications [37, 38]. In patients with GPS 1, those with low serum albumin and CRP levels may be undernutrition related with cancer, while those with high serum albumin and CRP levels may be pre-cachexic. Patients of GPS 2 with low serum albumin and high CRP levels may be cancer cachexia. It was reported that supportive nutritional interventions in patients with preoperative cancer cachexia and pre-cachexic may be ineffective and early supportive nutritional interventions for patients with undernutrition related with cancer can be effective for improvement of preoperative nutritional status [37, 38].
Our study had a limitation. Our study was retrospective study in a single affiliation. Prospective and multicenter studies in larger cohorts are necessary to clarify the predictive value of preoperative GPS for postoperative complications in GC patients.
In conclusion, the GPS before surgery may be a useful predictive marker for complications after surgery in patients with stage II/III GC who underwent curative resection. Being aware of the risk of complications after surgery as indicated by the GPS before surgery may promote safe and minimally invasive surgery that we expect will improve outcomes in these patients.

Acknowledgements

The authors thank the patients, their families, and the staff at the center for their participation in this study.

Declarations

Ethics Approval

This study was approved prior to initiation by the Research Ethics Committee of the Kanagawa Cancer Center (approval number: Epidemiological Study − 2019 − 113).
All study participants provided informed consent.
All study participants provided consent for publication.

Conflict of Interest

The authors declare no competing interests.
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/​.

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Literatur
2.
3.
Zurück zum Zitat Kurita N, Miyata H, Gotoh M, Shimada M, Imura S, Kimura W, Tomita N, Baba H, Kitagawa Y, Sugihara K, Mori M. Risk model for distal gastrectomy when treating gastric cancer on the basis of data from 33,917 Japanese patients collected using a nationwide web-based data entry system. Ann Surg. 2015;262:295–303. https://doi.org/10.1097/SLA.0000000000001127.CrossRefPubMed Kurita N, Miyata H, Gotoh M, Shimada M, Imura S, Kimura W, Tomita N, Baba H, Kitagawa Y, Sugihara K, Mori M. Risk model for distal gastrectomy when treating gastric cancer on the basis of data from 33,917 Japanese patients collected using a nationwide web-based data entry system. Ann Surg. 2015;262:295–303. https://​doi.​org/​10.​1097/​SLA.​0000000000001127​.CrossRefPubMed
4.
Zurück zum Zitat Katai H, Sasako M, Fukuda H, Nakamura K, Hiki N, Saka M, Yamaue H, Yoshikawa T, Kojima K, Takagane A, Fukushima N, Katai H, Saka M, Kojima K, Inokuchi M, Yamada H, Hiki N, Fukunaga T, Yoshiba H, Tokunaga M, Yoshikawa T, Cho H, Mochizuki Y, Misawa K, Uyama I, Kanaya S, Taniguchi K, Imamoto H, Miyashiro I, Tanigawa N, Iwahashi M, Takifuji K, Nishizaki M, Kitanov S, Shiraishi N, Eto T. Safety and feasibility of laparoscopy-assisted distal gastrectomy with suprapancreatic nodal dissection for clinical stage I gastric cancer: a multicenter phase II trial (JCOG 0703). Gastric Cancer. 2010;13:238–44. https://doi.org/10.1007/s10120-010-0565-0.CrossRefPubMed Katai H, Sasako M, Fukuda H, Nakamura K, Hiki N, Saka M, Yamaue H, Yoshikawa T, Kojima K, Takagane A, Fukushima N, Katai H, Saka M, Kojima K, Inokuchi M, Yamada H, Hiki N, Fukunaga T, Yoshiba H, Tokunaga M, Yoshikawa T, Cho H, Mochizuki Y, Misawa K, Uyama I, Kanaya S, Taniguchi K, Imamoto H, Miyashiro I, Tanigawa N, Iwahashi M, Takifuji K, Nishizaki M, Kitanov S, Shiraishi N, Eto T. Safety and feasibility of laparoscopy-assisted distal gastrectomy with suprapancreatic nodal dissection for clinical stage I gastric cancer: a multicenter phase II trial (JCOG 0703). Gastric Cancer. 2010;13:238–44. https://​doi.​org/​10.​1007/​s10120-010-0565-0.CrossRefPubMed
5.
8.
Zurück zum Zitat Jin LX, Sanford DE, Squires MH, Moses LE, Yan Y, Poultsides GA, Votanopoulos KI, Weber SM, Bloomston M, Pawlik TM, Hawkins WG, Linehan DC, Schmidt C, Worhunsky DJ, Acher AW, Cardona K, Cho CS, Kooby DA, Levine EA, Winslow E, Saunders N, Spolverato G, Colditz GA, Maithel SK, Fields RC. Interaction of postoperative morbidity and receipt of adjuvant therapy on long-term survival after resection for gastric adenocarcinoma: results from the U.S. Gastric Cancer Collaborative Ann Surg Oncol. 2016;23:2398–408. https://doi.org/10.1245/s10434-016-5121-7.CrossRefPubMed Jin LX, Sanford DE, Squires MH, Moses LE, Yan Y, Poultsides GA, Votanopoulos KI, Weber SM, Bloomston M, Pawlik TM, Hawkins WG, Linehan DC, Schmidt C, Worhunsky DJ, Acher AW, Cardona K, Cho CS, Kooby DA, Levine EA, Winslow E, Saunders N, Spolverato G, Colditz GA, Maithel SK, Fields RC. Interaction of postoperative morbidity and receipt of adjuvant therapy on long-term survival after resection for gastric adenocarcinoma: results from the U.S. Gastric Cancer Collaborative Ann Surg Oncol. 2016;23:2398–408. https://​doi.​org/​10.​1245/​s10434-016-5121-7.CrossRefPubMed
10.
Zurück zum Zitat Khuri SF, Henderson WG, DePalma RG, Mosca C, Healey NA, Kumbhani DJ, Participants in the VA National Surgical Quality Improvement Program. Determinants of long-term survival after major surgery and the adverse effect of postoperative complications. Ann Surg. 2005;242:326–41; discussion 341–3. https://doi.org/10.1097/01.sla.0000179621.33268.83 Khuri SF, Henderson WG, DePalma RG, Mosca C, Healey NA, Kumbhani DJ, Participants in the VA National Surgical Quality Improvement Program. Determinants of long-term survival after major surgery and the adverse effect of postoperative complications. Ann Surg. 2005;242:326–41; discussion 341–3. https://​doi.​org/​10.​1097/​01.​sla.​0000179621.​33268.​83
12.
Zurück zum Zitat Watanabe H, Hayashi T, Komori K, Hara K, Maezawa Y, Kano K, Shimoda Y, Fujikawa H, Aoyama T, Yamada T, Yamamoto N, Cho H, Ito H, Shiozawa M, Yukawa N, Morinaga S, Yoshikawa T, Rino Y, Masuda M, Ogata T, Oshima T. Impact of postoperative complications on recurrence in patients with stage II/III gastric cancer who received adjuvant chemotherapy with S-1. Anticancer Res. 2020;40:1683–1690. https://doi.org/10.21873/anticanres.14120 Watanabe H, Hayashi T, Komori K, Hara K, Maezawa Y, Kano K, Shimoda Y, Fujikawa H, Aoyama T, Yamada T, Yamamoto N, Cho H, Ito H, Shiozawa M, Yukawa N, Morinaga S, Yoshikawa T, Rino Y, Masuda M, Ogata T, Oshima T. Impact of postoperative complications on recurrence in patients with stage II/III gastric cancer who received adjuvant chemotherapy with S-1. Anticancer Res. 2020;40:1683–1690. https://​doi.​org/​10.​21873/​anticanres.​14120
13.
Zurück zum Zitat Kasahara N, Sunaga N, Tsukagoshi Y, Miura Y, Sakurai R, Kitahara S, Yokobori T, Kaira K, Mogi A, Maeno T, Asao T, Hisada T. Post-treatment Glasgow Prognostic Score predicts efficacy in advanced non-small-cell lung cancer treated with anti-PD1. Anticancer Res. 2019;39:1455–1461. https://doi.org/10.21873/anticanres.13262 Kasahara N, Sunaga N, Tsukagoshi Y, Miura Y, Sakurai R, Kitahara S, Yokobori T, Kaira K, Mogi A, Maeno T, Asao T, Hisada T. Post-treatment Glasgow Prognostic Score predicts efficacy in advanced non-small-cell lung cancer treated with anti-PD1. Anticancer Res. 2019;39:1455–1461. https://​doi.​org/​10.​21873/​anticanres.​13262
14.
Zurück zum Zitat Shiba H, Misawa T, Fujiwara Y, Futagawa Y, Furukawa K, Haruki K, Iwase R, Wakiyama S, Ishida Y, Yanaga K. Glasgow prognostic score predicts therapeutic outcome after pancreaticoduodenectomy for carcinoma of the ampulla of Vater. Anticancer Res. 2013;33:2715–21.PubMed Shiba H, Misawa T, Fujiwara Y, Futagawa Y, Furukawa K, Haruki K, Iwase R, Wakiyama S, Ishida Y, Yanaga K. Glasgow prognostic score predicts therapeutic outcome after pancreaticoduodenectomy for carcinoma of the ampulla of Vater. Anticancer Res. 2013;33:2715–21.PubMed
15.
Zurück zum Zitat Yamada S, Fujii T, Yabusaki N, Murotani K, Iwata N, Kanda M, Tanaka C, Nakayama G, Sugimoto H, Koike M, Fujiwara M, Kodera Y. Clinical implication of inflammation-based prognostic score in pancreatic cancer: Glasgow prognostic score is the most reliable parameter. Medicine (Baltimore). 2016;95: e3582. https://doi.org/10.1097/MD.0000000000003582.CrossRef Yamada S, Fujii T, Yabusaki N, Murotani K, Iwata N, Kanda M, Tanaka C, Nakayama G, Sugimoto H, Koike M, Fujiwara M, Kodera Y. Clinical implication of inflammation-based prognostic score in pancreatic cancer: Glasgow prognostic score is the most reliable parameter. Medicine (Baltimore). 2016;95: e3582. https://​doi.​org/​10.​1097/​MD.​0000000000003582​.CrossRef
18.
Zurück zum Zitat Inamoto T, Matsuyama H, Sakano S, Ibuki N, Takahara K, Komura K, Takai T, Tsujino T, Yoshikawa Y, Minami K, Nagao K, Inoue R, Azuma H. The systemic inflammation-based Glasgow Prognostic Score as a powerful prognostic factor in patients with upper tract urothelial carcinoma. Oncotarget. 2017;8:113248–113257. https://doi.org/10.18632/oncotarget.22641 Inamoto T, Matsuyama H, Sakano S, Ibuki N, Takahara K, Komura K, Takai T, Tsujino T, Yoshikawa Y, Minami K, Nagao K, Inoue R, Azuma H. The systemic inflammation-based Glasgow Prognostic Score as a powerful prognostic factor in patients with upper tract urothelial carcinoma. Oncotarget. 2017;8:113248–113257. https://​doi.​org/​10.​18632/​oncotarget.​22641
21.
Zurück zum Zitat Brierley JD, Gospodarowicz MK, Wittekind C, Editors. TNM Classification of Malignant Tumors. 2017;8th ed. ISBN:978–1–119–26357–9, West Sussex: Wiley-Blackwell. Brierley JD, Gospodarowicz MK, Wittekind C, Editors. TNM Classification of Malignant Tumors. 2017;8th ed. ISBN:978–1–119–26357–9, West Sussex: Wiley-Blackwell.
34.
Zurück zum Zitat Fujiwara Y, Shiba H, Furukawa K, Iida T, Haruki K, Gocho T, Wakiyama S, Hirohara S, Ishida Y, Misawa T, Ohashi T, Yanaga K. Glasgow Prognostic Score is related to blood transfusion requirements and post-operative complications in hepatic resection for hepatocellular carcinoma. Anticancer Res. 2010;30:5129–36.PubMed Fujiwara Y, Shiba H, Furukawa K, Iida T, Haruki K, Gocho T, Wakiyama S, Hirohara S, Ishida Y, Misawa T, Ohashi T, Yanaga K. Glasgow Prognostic Score is related to blood transfusion requirements and post-operative complications in hepatic resection for hepatocellular carcinoma. Anticancer Res. 2010;30:5129–36.PubMed
Metadaten
Titel
The Glasgow Prognostic Score Before Curative Resection May Predict Postoperative Complications in Patients with Gastric Cancer
verfasst von
Yota Shimoda
Hirohito Fujikawa
Keisuke Komori
Hayato Watanabe
Kosuke Takahashi
Kazuki Kano
Takanobu Yamada
Manabu Shiozawa
Soichiro Morinaga
Kenji Katsumata
Akihiko Tsuchida
Takashi Ogata
Takashi Oshima
Publikationsdatum
14.09.2021
Verlag
Springer US
Erschienen in
Journal of Gastrointestinal Cancer / Ausgabe 4/2022
Print ISSN: 1941-6628
Elektronische ISSN: 1941-6636
DOI
https://doi.org/10.1007/s12029-021-00689-9

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Auch für Trägerinnen von BRCA-Varianten gilt: Erkranken sie fünf bis zehn Jahre nach der letzten Schwangerschaft an Brustkrebs, ist das Sterberisiko besonders hoch.

Hypertherme Chemotherapie bietet Chance auf Blasenerhalt

07.05.2024 Harnblasenkarzinom Nachrichten

Eine hypertherme intravesikale Chemotherapie mit Mitomycin kann für Patienten mit hochriskantem nicht muskelinvasivem Blasenkrebs eine Alternative zur radikalen Zystektomie darstellen. Kölner Urologen berichten über ihre Erfahrungen.

Ein Drittel der jungen Ärztinnen und Ärzte erwägt abzuwandern

07.05.2024 Klinik aktuell Nachrichten

Extreme Arbeitsverdichtung und kaum Supervision: Dr. Andrea Martini, Sprecherin des Bündnisses Junge Ärztinnen und Ärzte (BJÄ) über den Frust des ärztlichen Nachwuchses und die Vorteile des Rucksack-Modells.

Update Onkologie

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