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Development and validation of insulin-like growth factor-1 score to assess hepatic reserve in hepatocellular carcinoma.

Publication ,  Journal Article
Kaseb, AO; Xiao, L; Hassan, MM; Chae, YK; Lee, JS; Vauthey, JN; Krishnan, S; Cheung, S; Hassabo, HM; Aloia, T; Conrad, C; Curley, SA ...
Published in: Journal of the National Cancer Institute
January 1, 2014

Child-Turcotte-Pugh (CTP) score is the standard tool to assess hepatic reserve in hepatocellular carcinoma (HCC), and CTP-A is the classic group for active therapy. However, CTP stratification accuracy has been questioned. We hypothesized that plasma insulin-like growth factor 1 (IGF-1) is a valid surrogate for hepatic reserve to replace the subjective parameters in CTP score to improve its prognostic accuracy. We retrospectively tested plasma IGF-1 levels in the training set (n = 310) from MD Anderson Cancer Center. Recursive partitioning identified three optimal IGF-1 ranges that correlated with overall survival (OS): greater than 50 ng/mL = 1 point; 26 to 50 ng/mL = 2 points; and less than 26 ng/mL = 3 points. We modified the CTP score by replacing ascites and encephalopathy grading with plasma IGF-1 value (IGF-CTP) and subjected both scores to log-rank analysis. Harrell's C-index and U-statistics were used to compare the prognostic performance of both scores in both the training and validation cohorts (n = 155). All statistical tests were two-sided. Patients' stratification was statistically significantly stronger for IGF-CTP than CTP score for the training (P = .003) and the validation cohort (P = .005). Patients reclassified by IGF-CTP relative to their original CTP score were better stratified by their new risk groups. Most important, patients classified as A by CTP but B by IGF-CTP had statistically significantly worse OS than those who remained under class A by IGF-CTP in both cohorts (P = .03 and P < .001, respectively, from Cox regression models). AB patients had a worse OS than AA patients in both the training and validation set (hazard ratio [HR] = 1.45, 95% confidence interval [CI] = 1.03 to 2.04, P = .03; HR = 2.83, 95% CI = 1.65 to 4.85, P < .001, respectively). The IGF-CTP score is simple, blood-based, and cost-effective, stratified HCC better than CTP score, and validated well on two independent cohorts. International validation studies are warranted. © The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Duke Scholars

Published In

Journal of the National Cancer Institute

EISSN

1460-2105

Publication Date

January 1, 2014

Volume

106

Issue

5

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis
 

Citation

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Kaseb, A. O., Xiao, L., Hassan, M. M., Chae, Y. K., Lee, J. S., Vauthey, J. N., … Morris, J. S. (2014). Development and validation of insulin-like growth factor-1 score to assess hepatic reserve in hepatocellular carcinoma. Journal of the National Cancer Institute, 106(5).
Kaseb, A. O., L. Xiao, M. M. Hassan, Y. K. Chae, J. S. Lee, J. N. Vauthey, S. Krishnan, et al. “Development and validation of insulin-like growth factor-1 score to assess hepatic reserve in hepatocellular carcinoma.Journal of the National Cancer Institute 106, no. 5 (January 1, 2014).
Kaseb AO, Xiao L, Hassan MM, Chae YK, Lee JS, Vauthey JN, et al. Development and validation of insulin-like growth factor-1 score to assess hepatic reserve in hepatocellular carcinoma. Journal of the National Cancer Institute. 2014 Jan 1;106(5).
Kaseb, A. O., et al. “Development and validation of insulin-like growth factor-1 score to assess hepatic reserve in hepatocellular carcinoma.Journal of the National Cancer Institute, vol. 106, no. 5, Jan. 2014.
Kaseb AO, Xiao L, Hassan MM, Chae YK, Lee JS, Vauthey JN, Krishnan S, Cheung S, Hassabo HM, Aloia T, Conrad C, Curley SA, Vierling JM, Jalal P, Raghav K, Wallace M, Rashid A, Abbruzzese JL, Wolff RA, Morris JS. Development and validation of insulin-like growth factor-1 score to assess hepatic reserve in hepatocellular carcinoma. Journal of the National Cancer Institute. 2014 Jan 1;106(5).
Journal cover image

Published In

Journal of the National Cancer Institute

EISSN

1460-2105

Publication Date

January 1, 2014

Volume

106

Issue

5

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis