114P - Prognostic biomarkers in locally advanced cervical cancer (Cx Ca) treated with chemoradiation (CRT)

Date 10 October 2016
Event ESMO 2016 Congress
Session Poster display
Topics Cervical Cancer
Translational Research
Surgical Oncology
Basic Principles in the Management and Treatment (of cancer)
Radiation Oncology
Presenter Yada Kanjanapan
Citation Annals of Oncology (2016) 27 (6): 15-42. 10.1093/annonc/mdw363
Authors Y. Kanjanapan1, S. Deb2, R. Young3, M. Bressel4, L. Mileshkin1, D. Rischin1, M. Hofman5, K. Narayan6, S. Siva6
  • 1Medical Oncology, Peter MacCallum Cancer Center, 3002 - Melbourne/AU
  • 2Anatomical Pathology, Peter MacCallum Cancer Center, Melbourne/AU
  • 3Translational Research Laboratory, Peter MacCallum Cancer Center, Melbourne/AU
  • 4Centre For Biostatistics And Clinical Trials, Peter MacCallum Cancer Center, Melbourne/AU
  • 5Cancer Imaging, Peter MacCallum Cancer Center, Melbourne/AU
  • 6Radiation Oncology, Peter MacCallum Cancer Center, Melbourne/AU



Definitive chemoradiation (CRT) is standard therapy for locally advanced cervical cancer (Cx Ca). However, there is a lack of biomarkers to identify patients at increased risk of relapse. Post-therapy 18F-fluoro-deoxyglucose positron emission tomography (PET) response correlates with outcome, but cannot inform treatment planning. We tested metabolic (glucose transporter [Glut-1]), hypoxic (hypoxia inducible factor [HIF-1a] and carbonic anhydrase [CA-9]) and proliferative (Ki-67) markers for prognostic utility in Cx Ca.


60 FIGO stage Ib to IVa Cx Ca patients treated with CRT had formalin-fixed paraffin-embedded tumour tissue from pre treatment biopsies. Immunohistochemistry was performed for Glut-1, HIF-1a and CA-9, to generate a histoscore (0-12) by multiplying intensity (0 absent, 1 mild, 2 moderate and 3 intense staining) by a categorical percentage score (0 for none, 1 for 1-24%, 2 for 25-49%, 3 for 50-74% and 4 for ≥75% of cells staining), for each biomarker in each tumour sample. Ki-67 was scored by percentage of positive cells amongst 1000 representative tumour cells. For each biomarker, the cohort was dichotomized and survival estimated by the Kaplan-Meier method and compared using logrank testing.


High Glut-1 expression was associated with inferior progression-free survival (PFS), (hazard ratio [HR] 2.8, 95% confidence interval [CI] 1.0 – 7.9, p = 0.049) and overall survival (OS), (HR 5.0, 95% CI 1.3 – 19.2, p = 0.011) on multifactor analysis adjusting for stage, node positivity, tumour volume and uterine corpus invasion. High Glut-1 correlated with increased risk of distant failure (HR 14.6, 95% CI 1.9 - 112.9, p = 0.001) but not with local failure (HR 2.1, 95% CI 0.5 - 8.9, p = 0.48). Low Glut-1 was associated with higher complete metabolic response rate on post-therapy PET scan (odds ratio 3.4, 95% CI 1.0 – 12.3, p = 0.048). Ki-67 was significantly associated with PFS only (HR 1.19 per 10 units increase, 95% CI 1.01 – 1.41, p = 0.033). Biomarkers for hypoxia were not associated with outcome.


High Glut-1 expression in pre-treatment Cx Ca biopsies is associated with worse outcome post CRT. If prospectively validated, Glut-1 may be used to select Cx Ca patients who may benefit from a more intensive treatment regimen.

Clinical trial identification

Legal entity responsible for the study

Division of Medical Oncology, Peter MacCallum Cancer Centre


Funding for statistical support from the Division of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia


All authors have declared no conflicts of interest.