Skip to main content
Top
Published in: Annals of Surgical Oncology 4/2011

01-04-2011 | Thoracic Oncology

Glasgow Prognostic Score is a Predictor of Perioperative and Long-term Outcome in Patients with only Surgically Treated Esophageal Cancer

Authors: Yogesh K. Vashist, Julian Loos, Josephine Dedow, Michael Tachezy, Guentac Uzunoglu, Asad Kutup, Emre F. Yekebas, Jakob R. Izbicki

Published in: Annals of Surgical Oncology | Issue 4/2011

Login to get access

Abstract

Background

Systemic inflammation (SI) plays a pivotal role in cancer. C-reactive protein (CRP) and albumin as parameters of SI form the Glasgow Prognostic Score (GPS). The purpose of the study was to evaluate the potential prognostic role of GPS in a homogeneous population of esophageal cancer (EC) patients undergoing only resection.

Methods

GPS was evaluated on the basis of admission blood sample taken before surgery. Patients with a CRP < 10 mg/L and albumin > 35 g/L were allocated to GPS0 group. If only CRP was increased or albumin decreased patients were allocated to the GPS1 and patients in whom CRP was ≥10 mg/L and albumin level ≤35 g/L were classified as GPS2. GPS was correlated to clinicopathological parameters and clinical outcome.

Results

Increasing GPS significantly correlated with more aggressive tumor biology in terms of tumor size (P < 0.001), presence of regional (P = 0.01) and nonregional lymph node metastasis (P = 0.02), and higher tumor recurrence rate (P < 0.001). Furthermore, GPS was identified as an independent prognosticator of perioperative morbidity (odds ratio 1.9; P = 0.03). In addition, a gradual decrease in disease-free and overall survival was evident between the three GPS subgroups. Survival differences between the GPS groups remained apparent even after stratification of the study population to underlying tumor type and nodal status. GPS was identified as a strong prognosticator of tumor recurrence (hazard ratio 2.5; P < 0.001) and survival (hazard ratio 3.0; P < 0.001) in EC.

Conclusions

GPS represents a strong prognosticator of perioperative morbidity and long-term outcome in resected EC patients without neoadjuvant or adjuvant treatment.
Literature
1.
go back to reference Boffetta P. Exploring a cancer biomarker: the example of C-reactive protein. J Natl Cancer Inst. 2010;102(3):142–3.PubMedCrossRef Boffetta P. Exploring a cancer biomarker: the example of C-reactive protein. J Natl Cancer Inst. 2010;102(3):142–3.PubMedCrossRef
2.
go back to reference Zhang SM, et al. C-reactive protein and risk of breast cancer. J Natl Cancer Inst. 2007;99(11):890–4.PubMedCrossRef Zhang SM, et al. C-reactive protein and risk of breast cancer. J Natl Cancer Inst. 2007;99(11):890–4.PubMedCrossRef
3.
go back to reference Sgambato A, Cittadini A. Inflammation and cancer: a multifaceted link. Eur Rev Med Pharmacol Sci. 2010;14(4):263–8.PubMed Sgambato A, Cittadini A. Inflammation and cancer: a multifaceted link. Eur Rev Med Pharmacol Sci. 2010;14(4):263–8.PubMed
4.
go back to reference Terzić J, Grivennikov S, Karin E, Karin M. Inflammation and colon cancer. Gastroenterology. 2010;138(6):2101–14.e5.PubMedCrossRef Terzić J, Grivennikov S, Karin E, Karin M. Inflammation and colon cancer. Gastroenterology. 2010;138(6):2101–14.e5.PubMedCrossRef
5.
go back to reference Kelsen DP, et al. Chemotherapy followed by surgery compared with surgery alone for localized esophageal cancer. N Engl J Med. 1998;339(27):1979–84.PubMedCrossRef Kelsen DP, et al. Chemotherapy followed by surgery compared with surgery alone for localized esophageal cancer. N Engl J Med. 1998;339(27):1979–84.PubMedCrossRef
6.
go back to reference Nixon DW, et al. Protein-calorie undernutrition in hospitalized cancer patients. Am J Med. 1980;68(5):683–90.PubMedCrossRef Nixon DW, et al. Protein-calorie undernutrition in hospitalized cancer patients. Am J Med. 1980;68(5):683–90.PubMedCrossRef
7.
go back to reference Lecleire S, et al. Undernutrition is predictive of early mortality after palliative self-expanding metal stent insertion in patients with inoperable or recurrent esophageal cancer. Gastrointest Endosc. 2006;64(4):479–84.PubMedCrossRef Lecleire S, et al. Undernutrition is predictive of early mortality after palliative self-expanding metal stent insertion in patients with inoperable or recurrent esophageal cancer. Gastrointest Endosc. 2006;64(4):479–84.PubMedCrossRef
8.
go back to reference Deans DA, et al. The influence of systemic inflammation, dietary intake and stage of disease on rate of weight loss in patients with gastro-oesophageal cancer. Br J Cancer. 2009;100(1):63-9.PubMedCrossRef Deans DA, et al. The influence of systemic inflammation, dietary intake and stage of disease on rate of weight loss in patients with gastro-oesophageal cancer. Br J Cancer. 2009;100(1):63-9.PubMedCrossRef
9.
go back to reference Scott HR, et al. The systemic inflammatory response, weight loss, performance status and survival in patients with inoperable non-small cell lung cancer. Br J Cancer. 2002;87(3):264–7.PubMedCrossRef Scott HR, et al. The systemic inflammatory response, weight loss, performance status and survival in patients with inoperable non-small cell lung cancer. Br J Cancer. 2002;87(3):264–7.PubMedCrossRef
10.
go back to reference O’Gorman P, McMillan DC, McArdle CS. Longitudinal study of weight, appetite, performance status, and inflammation in advanced gastrointestinal cancer. Nutr Cancer. 1999;35(2):127–9.PubMedCrossRef O’Gorman P, McMillan DC, McArdle CS. Longitudinal study of weight, appetite, performance status, and inflammation in advanced gastrointestinal cancer. Nutr Cancer. 1999;35(2):127–9.PubMedCrossRef
11.
go back to reference O’Gorman P, McMillan DC, McArdle CS. Prognostic factors in advanced gastrointestinal cancer patients with weight loss. Nutr Cancer. 2000;37(1):36-40.PubMedCrossRef O’Gorman P, McMillan DC, McArdle CS. Prognostic factors in advanced gastrointestinal cancer patients with weight loss. Nutr Cancer. 2000;37(1):36-40.PubMedCrossRef
12.
go back to reference McMillan DC. Systemic inflammation, nutritional status and survival in patients with cancer. Curr Opin Clin Nutr Metab Care. 2009;12(3):223–6.PubMedCrossRef McMillan DC. Systemic inflammation, nutritional status and survival in patients with cancer. Curr Opin Clin Nutr Metab Care. 2009;12(3):223–6.PubMedCrossRef
13.
go back to reference Brown DJ, et al. The relationship between an inflammation-based prognostic score (Glasgow Prognostic Score) and changes in serum biochemical variables in patients with advanced lung and gastrointestinal cancer. J Clin Pathol. 2007;60(6):705–8.PubMedCrossRef Brown DJ, et al. The relationship between an inflammation-based prognostic score (Glasgow Prognostic Score) and changes in serum biochemical variables in patients with advanced lung and gastrointestinal cancer. J Clin Pathol. 2007;60(6):705–8.PubMedCrossRef
14.
go back to reference Ishizuka M, et al. Inflammation-based prognostic score is a novel predictor of postoperative outcome in patients with colorectal cancer. Ann Surg. 2007;246(6):1047–51.PubMedCrossRef Ishizuka M, et al. Inflammation-based prognostic score is a novel predictor of postoperative outcome in patients with colorectal cancer. Ann Surg. 2007;246(6):1047–51.PubMedCrossRef
15.
go back to reference Ishizuka M, et al. Influence of inflammation-based prognostic score on mortality of patients undergoing chemotherapy for far advanced or recurrent unresectable colorectal cancer. Ann Surg. 2009;250(2):268–72.PubMedCrossRef Ishizuka M, et al. Influence of inflammation-based prognostic score on mortality of patients undergoing chemotherapy for far advanced or recurrent unresectable colorectal cancer. Ann Surg. 2009;250(2):268–72.PubMedCrossRef
16.
go back to reference Kobayashi T, et al. Inflammation-based prognostic score, prior to neoadjuvant chemoradiotherapy, predicts postoperative outcome in patients with esophageal squamous cell carcinoma. Surgery. 2008;144(5):729–35.PubMedCrossRef Kobayashi T, et al. Inflammation-based prognostic score, prior to neoadjuvant chemoradiotherapy, predicts postoperative outcome in patients with esophageal squamous cell carcinoma. Surgery. 2008;144(5):729–35.PubMedCrossRef
17.
go back to reference Roxburgh CS, et al. Comparison of tumour-based (Petersen Index) and inflammation-based (Glasgow Prognostic Score) scoring systems in patients undergoing curative resection for colon cancer. Br J Cancer. 2009;100(5):701–6.PubMedCrossRef Roxburgh CS, et al. Comparison of tumour-based (Petersen Index) and inflammation-based (Glasgow Prognostic Score) scoring systems in patients undergoing curative resection for colon cancer. Br J Cancer. 2009;100(5):701–6.PubMedCrossRef
18.
go back to reference Sharma R, et al. Evaluation of an inflammation-based prognostic score in patients with advanced ovarian cancer. Eur J Cancer. 2008;44(2):251–6.PubMedCrossRef Sharma R, et al. Evaluation of an inflammation-based prognostic score in patients with advanced ovarian cancer. Eur J Cancer. 2008;44(2):251–6.PubMedCrossRef
19.
go back to reference Tomimaru Y, et al. Factors affecting the prognosis of patients with esophageal cancer undergoing salvage surgery after definitive chemoradiotherapy. J Surg Oncol. 2006;93(5):422–8.PubMedCrossRef Tomimaru Y, et al. Factors affecting the prognosis of patients with esophageal cancer undergoing salvage surgery after definitive chemoradiotherapy. J Surg Oncol. 2006;93(5):422–8.PubMedCrossRef
20.
go back to reference Tsujimoto H, et al. Preoperative chemoradiotherapy for esophageal cancer enhances the postoperative systemic inflammatory response. Jpn J Clin Oncol. 2006;36(10):632–7.PubMedCrossRef Tsujimoto H, et al. Preoperative chemoradiotherapy for esophageal cancer enhances the postoperative systemic inflammatory response. Jpn J Clin Oncol. 2006;36(10):632–7.PubMedCrossRef
21.
go back to reference Peyre CG, et al. Predicting systemic disease in patients with esophageal cancer after esophagectomy: a multinational study on the significance of the number of involved lymph nodes. Ann Surg. 2008;248(6):979–85.PubMedCrossRef Peyre CG, et al. Predicting systemic disease in patients with esophageal cancer after esophagectomy: a multinational study on the significance of the number of involved lymph nodes. Ann Surg. 2008;248(6):979–85.PubMedCrossRef
22.
go back to reference Mariette C, Piessen G, Triboulet JP. Therapeutic strategies in oesophageal carcinoma: role of surgery and other modalities. Lancet Oncol. 2007;8(6):545–53.PubMedCrossRef Mariette C, Piessen G, Triboulet JP. Therapeutic strategies in oesophageal carcinoma: role of surgery and other modalities. Lancet Oncol. 2007;8(6):545–53.PubMedCrossRef
23.
go back to reference Orringer MB, et al. Two thousand transhiatal esophagectomies: changing trends, lessons learned. Ann Surg, 2007;246(3):363-72; discussion 372-4.PubMedCrossRef Orringer MB, et al. Two thousand transhiatal esophagectomies: changing trends, lessons learned. Ann Surg, 2007;246(3):363-72; discussion 372-4.PubMedCrossRef
24.
go back to reference Gockel I, Exner C, Junginger T. Morbidity and mortality after esophagectomy for esophageal carcinoma: a risk analysis. World J Surg Oncol. 2005;3:37.PubMedCrossRef Gockel I, Exner C, Junginger T. Morbidity and mortality after esophagectomy for esophageal carcinoma: a risk analysis. World J Surg Oncol. 2005;3:37.PubMedCrossRef
25.
go back to reference McCulloch P, Ward J, Tekkis PP. Mortality and morbidity in gastro-oesophageal cancer surgery: initial results of ASCOT multicentre prospective cohort study. BMJ. 2003;327(7425):1192–7.PubMedCrossRef McCulloch P, Ward J, Tekkis PP. Mortality and morbidity in gastro-oesophageal cancer surgery: initial results of ASCOT multicentre prospective cohort study. BMJ. 2003;327(7425):1192–7.PubMedCrossRef
26.
go back to reference Atkins BZ, et al. Reducing hospital morbidity and mortality following esophagectomy. Ann Thorac Surg. 2004;78(4):1170–6.PubMedCrossRef Atkins BZ, et al. Reducing hospital morbidity and mortality following esophagectomy. Ann Thorac Surg. 2004;78(4):1170–6.PubMedCrossRef
27.
go back to reference Ruol A, et al. Trends in management and prognosis for esophageal cancer surgery: twenty-five years of experience at a single institution. Arch Surg. 2009;144(3):247–54; discussion 254.PubMedCrossRef Ruol A, et al. Trends in management and prognosis for esophageal cancer surgery: twenty-five years of experience at a single institution. Arch Surg. 2009;144(3):247–54; discussion 254.PubMedCrossRef
28.
go back to reference Moyes LH, et al. Preoperative systemic inflammation predicts postoperative infectious complications in patients undergoing curative resection for colorectal cancer. Br J Cancer. 2009;100(8):1236–9.PubMedCrossRef Moyes LH, et al. Preoperative systemic inflammation predicts postoperative infectious complications in patients undergoing curative resection for colorectal cancer. Br J Cancer. 2009;100(8):1236–9.PubMedCrossRef
29.
go back to reference Cook EJ, et al. Postoperative neutrophil-lymphocyte ratio predicts complications following colorectal surgery. Int J Surg. 2007;5(1):27–30.PubMedCrossRef Cook EJ, et al. Postoperative neutrophil-lymphocyte ratio predicts complications following colorectal surgery. Int J Surg. 2007;5(1):27–30.PubMedCrossRef
30.
go back to reference Krzystek-Korpacka M, et al. Acute-phase response proteins are related to cachexia and accelerated angiogenesis in gastroesophageal cancers. Clin Chem Lab Med. 2008;46(3):359–64.PubMedCrossRef Krzystek-Korpacka M, et al. Acute-phase response proteins are related to cachexia and accelerated angiogenesis in gastroesophageal cancers. Clin Chem Lab Med. 2008;46(3):359–64.PubMedCrossRef
31.
go back to reference Jain RK, et al. Biomarkers of response and resistance to antiangiogenic therapy. Nat Rev Clin Oncol. 2009;6(6):327–38.PubMedCrossRef Jain RK, et al. Biomarkers of response and resistance to antiangiogenic therapy. Nat Rev Clin Oncol. 2009;6(6):327–38.PubMedCrossRef
32.
go back to reference Mumm JB, Oft M. Cytokine-based transformation of immune surveillance into tumor-promoting inflammation. Oncogene. 2008;27(45):5913–9.PubMedCrossRef Mumm JB, Oft M. Cytokine-based transformation of immune surveillance into tumor-promoting inflammation. Oncogene. 2008;27(45):5913–9.PubMedCrossRef
33.
go back to reference Germano G, Allavena P, Mantovani A. Cytokines as a key component of cancer-related inflammation. Cytokine. 2008;43(3):374–9.PubMedCrossRef Germano G, Allavena P, Mantovani A. Cytokines as a key component of cancer-related inflammation. Cytokine. 2008;43(3):374–9.PubMedCrossRef
34.
go back to reference Seliger B, Ruiz-Cabello F, Garrido F. IFN inducibility of major histocompatibility antigens in tumors. Adv Cancer Res. 2008;101:249–76.PubMedCrossRef Seliger B, Ruiz-Cabello F, Garrido F. IFN inducibility of major histocompatibility antigens in tumors. Adv Cancer Res. 2008;101:249–76.PubMedCrossRef
35.
go back to reference Critchley-Thorne RJ, et al. Impaired interferon signaling is a common immune defect in human cancer. Proc Natl Acad Sci USA. 2009;106(22):9010–5.PubMedCrossRef Critchley-Thorne RJ, et al. Impaired interferon signaling is a common immune defect in human cancer. Proc Natl Acad Sci USA. 2009;106(22):9010–5.PubMedCrossRef
36.
go back to reference Shevde LA, et al. Impaired T lymphocyte function and differential cytokine response pattern in members from cancer families. Nat Immun. 1998;16(4):146–56.PubMedCrossRef Shevde LA, et al. Impaired T lymphocyte function and differential cytokine response pattern in members from cancer families. Nat Immun. 1998;16(4):146–56.PubMedCrossRef
37.
go back to reference Marsik C, et al. C-reactive protein and all-cause mortality in a large hospital-based cohort. Clin Chem. 2008;54(2):343–9.PubMedCrossRef Marsik C, et al. C-reactive protein and all-cause mortality in a large hospital-based cohort. Clin Chem. 2008;54(2):343–9.PubMedCrossRef
38.
go back to reference Ramsey S, et al. Evaluation of an inflammation-based prognostic score in patients with metastatic renal cancer. Cancer. 2007;109(2):205–12.PubMedCrossRef Ramsey S, et al. Evaluation of an inflammation-based prognostic score in patients with metastatic renal cancer. Cancer. 2007;109(2):205–12.PubMedCrossRef
39.
go back to reference McMillan DC, et al. Evaluation of an inflammation-based prognostic score (GPS) in patients undergoing resection for colon and rectal cancer. Int J Colorectal Dis. 2007;22(8):881–6.PubMedCrossRef McMillan DC, et al. Evaluation of an inflammation-based prognostic score (GPS) in patients undergoing resection for colon and rectal cancer. Int J Colorectal Dis. 2007;22(8):881–6.PubMedCrossRef
40.
go back to reference Glen P, et al. Evaluation of an inflammation-based prognostic score in patients with inoperable pancreatic cancer. Pancreatology. 2006;6(5):450–3.PubMedCrossRef Glen P, et al. Evaluation of an inflammation-based prognostic score in patients with inoperable pancreatic cancer. Pancreatology. 2006;6(5):450–3.PubMedCrossRef
41.
go back to reference Forrest LM, et al. Comparison of an inflammation-based prognostic score (GPS) with performance status (ECOG) in patients receiving platinum-based chemotherapy for inoperable non-small-cell lung cancer. Br J Cancer. 2004;90(9):1704–6.PubMed Forrest LM, et al. Comparison of an inflammation-based prognostic score (GPS) with performance status (ECOG) in patients receiving platinum-based chemotherapy for inoperable non-small-cell lung cancer. Br J Cancer. 2004;90(9):1704–6.PubMed
42.
go back to reference Crumley AB, et al. Evaluation of an inflammation-based prognostic score in patients with inoperable gastro-oesophageal cancer. Br J Cancer. 2006;94(5):637–41.PubMed Crumley AB, et al. Evaluation of an inflammation-based prognostic score in patients with inoperable gastro-oesophageal cancer. Br J Cancer. 2006;94(5):637–41.PubMed
43.
go back to reference Al Murri AM, et al. Evaluation of an inflammation-based prognostic score (GPS) in patients with metastatic breast cancer. Br J Cancer. 2006;94(2):227–30.PubMedCrossRef Al Murri AM, et al. Evaluation of an inflammation-based prognostic score (GPS) in patients with metastatic breast cancer. Br J Cancer. 2006;94(2):227–30.PubMedCrossRef
44.
go back to reference McMillan DC. An inflammation-based prognostic score and its role in the nutrition-based management of patients with cancer. Proc Nutr Soc. 2008;67(3):257-62.PubMedCrossRef McMillan DC. An inflammation-based prognostic score and its role in the nutrition-based management of patients with cancer. Proc Nutr Soc. 2008;67(3):257-62.PubMedCrossRef
45.
go back to reference Forrest LM, et al. Evaluation of cumulative prognostic scores based on the systemic inflammatory response in patients with inoperable non-small-cell lung cancer. Br J Cancer. 2003;89(6):1028–30.PubMedCrossRef Forrest LM, et al. Evaluation of cumulative prognostic scores based on the systemic inflammatory response in patients with inoperable non-small-cell lung cancer. Br J Cancer. 2003;89(6):1028–30.PubMedCrossRef
46.
go back to reference Gupta R, Ihmaidat H. Nutritional effects of oesophageal, gastric and pancreatic carcinoma. Eur J Surg Oncol. 2003;29(8):634–43.PubMedCrossRef Gupta R, Ihmaidat H. Nutritional effects of oesophageal, gastric and pancreatic carcinoma. Eur J Surg Oncol. 2003;29(8):634–43.PubMedCrossRef
47.
go back to reference Walsh S.R, et al. Neutrophil-lymphocyte ratio as a prognostic factor in colorectal cancer. J Surg Oncol. 2005;91(3):181–4.PubMedCrossRef Walsh S.R, et al. Neutrophil-lymphocyte ratio as a prognostic factor in colorectal cancer. J Surg Oncol. 2005;91(3):181–4.PubMedCrossRef
48.
go back to reference Yamanaka T, et al. The baseline ratio of neutrophils to lymphocytes is associated with patient prognosis in advanced gastric cancer. Oncology. 2007;73(3-4):215-20.PubMedCrossRef Yamanaka T, et al. The baseline ratio of neutrophils to lymphocytes is associated with patient prognosis in advanced gastric cancer. Oncology. 2007;73(3-4):215-20.PubMedCrossRef
49.
go back to reference Malik HZ, et al. Preoperative prognostic score for predicting survival after hepatic resection for colorectal liver metastases. Ann Surg. 2007;246(5):806–14.PubMedCrossRef Malik HZ, et al. Preoperative prognostic score for predicting survival after hepatic resection for colorectal liver metastases. Ann Surg. 2007;246(5):806–14.PubMedCrossRef
50.
go back to reference Smith RA, et al. Preoperative platelet-lymphocyte ratio is an independent significant prognostic marker in resected pancreatic ductal adenocarcinoma. Am J Surg. 2009;197(4):466–72.PubMedCrossRef Smith RA, et al. Preoperative platelet-lymphocyte ratio is an independent significant prognostic marker in resected pancreatic ductal adenocarcinoma. Am J Surg. 2009;197(4):466–72.PubMedCrossRef
51.
go back to reference Roxburgh CS, et al. Comparison of the prognostic value of inflammation-based pathologic and biochemical criteria in patients undergoing potentially curative resection for colorectal cancer. Ann Surg. 2009;249(5):788–93.PubMedCrossRef Roxburgh CS, et al. Comparison of the prognostic value of inflammation-based pathologic and biochemical criteria in patients undergoing potentially curative resection for colorectal cancer. Ann Surg. 2009;249(5):788–93.PubMedCrossRef
Metadata
Title
Glasgow Prognostic Score is a Predictor of Perioperative and Long-term Outcome in Patients with only Surgically Treated Esophageal Cancer
Authors
Yogesh K. Vashist
Julian Loos
Josephine Dedow
Michael Tachezy
Guentac Uzunoglu
Asad Kutup
Emre F. Yekebas
Jakob R. Izbicki
Publication date
01-04-2011
Publisher
Springer-Verlag
Published in
Annals of Surgical Oncology / Issue 4/2011
Print ISSN: 1068-9265
Electronic ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-010-1383-7

Other articles of this Issue 4/2011

Annals of Surgical Oncology 4/2011 Go to the issue