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Significance of Co-expression of Epidermal Growth Factor Receptor and Ki67 on Clinical Outcome in Patients With Anal Cancer Treated With Chemoradiotherapy: An Analysis of NRG Oncology RTOG 9811.
Doll, Corinne M; Moughan, Jennifer; Klimowicz, Alexander; Ho, Clement K; Kornaga, Elizabeth N; Lees-Miller, Susan P; Ajani, Jaffer A; Crane, Christopher H; Kachnic, Lisa A; Okawara, Gordon S; Berk, Lawrence B; Roof, Kevin S; Becker, Mark J; Grisell, David L; Ellis, Robert J; Sperduto, Paul W; Marsa, Gerald W; Guha, Chandan; Magliocco, Anthony M.
Affiliation
  • Doll CM; Tom Baker Cancer Centre, Calgary, Alberta, Canada. Electronic address: Corinne.Doll@albertahealthservices.ca.
  • Moughan J; NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania.
  • Klimowicz A; Tom Baker Cancer Centre, Calgary, Alberta, Canada.
  • Ho CK; Tom Baker Cancer Centre, Calgary, Alberta, Canada.
  • Kornaga EN; Tom Baker Cancer Centre, Calgary, Alberta, Canada.
  • Lees-Miller SP; University of Calgary, Calgary, Alberta, Canada.
  • Ajani JA; University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Crane CH; University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Kachnic LA; Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee.
  • Okawara GS; McMaster University Juravinski Cancer Center, Hamilton Health Sciences, Hamilton, Ontario, Canada.
  • Berk LB; Mount Sinai Comprehensive Cancer Center Community Clinical Oncology Program (CCOP), Miami Beach, Florida.
  • Roof KS; Southeast Cancer Control Consortium, Inc, CCOP, Winston-Salem, North Carolina.
  • Becker MJ; Columbus CCOP, Columbus, Ohio.
  • Grisell DL; Greenville CCOP, Greenville, South Carolina.
  • Ellis RJ; Cancer Research of the Ozarks, Springfield, Missouri.
  • Sperduto PW; Metro-MN CCOP, St. Louis Park, Minnesota.
  • Marsa GW; Toledo Community Hospital Oncology Program CCOP, Toledo, Ohio.
  • Guha C; Montefiore Medical Center, Bronx, New York.
  • Magliocco AM; H. Lee Moffitt Cancer Center, Tampa, Florida.
Int J Radiat Oncol Biol Phys ; 97(3): 554-562, 2017 03 01.
Article in En | MEDLINE | ID: mdl-28126304
PURPOSE: To measure co-expression of EGFR and Ki67 proteins in pretreatment tumor biopsies of anal cancer patients enrolled on NRG Oncology RTOG 9811, a phase III trial comparing 5-fluorouracil/mitomycin-C/radiation therapy (Arm A) versus 5-fluorouracil/cisplatin/radiation therapy (Arm B), and to correlate expression with clinical outcome. METHODS AND MATERIALS: EGFR and Ki67 co-expression was measured after constructing a tissue microarray using fluorescence immunohistochemistry and automated quantitative image analysis. The Ki67 score within EGFR high versus low areas (Ki67ratio in EGFRhigh:low) in each tumor core was analyzed at the median, quartiles, and as a continuous variable. Associations between the tumor markers and clinical endpoints (overall and disease-free survival, locoregional and colostomy failure, and distant metastases) were explored. RESULTS: A total of 282 pretreatment tumors were analyzed from NRG Oncology RTOG 9811. Of evaluated specimens, 183 (65%, n=89, Arm A; n=94, Arm B) were eligible and analyzable. There were no significant differences in baseline characteristics or outcomes between analyzable and unanalyzable patient cases. Median follow-up was 6.0 years. On multivariate analysis, after adjusting for gender, patients with Ki67ratio in EGFRhigh:low ≥median had worse overall survival (hazard ratio 2.41, 95% confidence interval 1.38-4.19, P=.0019). After adjusting for N stage and largest tumor dimension, patients with Ki67ratio in EGFRhigh:low ≥ median had a higher risk of a disease-free failure (hazard ratio 1.85, 95% confidence interval 1.18-2.92, P=.0078). Technical validation with an independent anal cancer patient cohort was performed and shows a very similar biomarker score distribution. CONCLUSIONS: High Ki67ratio in EGFRhigh:low is associated with worse clinical outcome in this subset of patients with anal cancer treated with chemoradiation on NRG Oncology RTOG 9811. Evaluation within a clinical trial will be required to determine whether patients with these tumor characteristics may specifically benefit from an EGFR-targeted therapeutic agent.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Anus Neoplasms / Antineoplastic Combined Chemotherapy Protocols / Ki-67 Antigen / Chemoradiotherapy / ErbB Receptors / Neoplasm Proteins Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Int J Radiat Oncol Biol Phys Year: 2017 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Anus Neoplasms / Antineoplastic Combined Chemotherapy Protocols / Ki-67 Antigen / Chemoradiotherapy / ErbB Receptors / Neoplasm Proteins Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Int J Radiat Oncol Biol Phys Year: 2017 Document type: Article Country of publication: United States