Predictive value of epidermal growth factor receptor expression for first-line chemotherapy plus cetuximab in patients with head and neck and colorectal cancer: Analysis of data from the EXTREME and CRYSTAL studies

被引:118
作者
Licitra, Lisa [1 ]
Stoerkel, Stephan [2 ,3 ]
Kerr, Keith M. [4 ]
Van Cutsem, Eric [5 ]
Pirker, Robert [6 ]
Hirsch, Fred R. [7 ,8 ]
Vermorken, Jan B. [9 ]
von Heydebreck, Anja [10 ]
Esser, Regina [10 ]
Celik, Ilhan [10 ]
Ciardiello, Fortunato [11 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Head & Neck Med Oncol Unit, Milan, Italy
[2] Univ Witten Herdecke, Inst Pathol, Wuppertal, Germany
[3] HELIOS Hosp Wuppertal, Wuppertal, Germany
[4] Aberdeen Royal Infirm, Dept Pathol, Aberdeen, Scotland
[5] Univ Hosp Gasthuisberg, Digest Oncol Unit, B-3000 Louvain, Belgium
[6] Med Univ Vienna, Dept Med 1, Vienna, Austria
[7] Univ Colorado, Ctr Canc, Dept Med, Aurora, CO USA
[8] Univ Colorado, Ctr Canc, Dept Pathol, Aurora, CO USA
[9] Univ Antwerp Hosp, Dept Med Oncol, Edegem, Belgium
[10] Merck KGaA, Darmstadt, Germany
[11] Univ Naples 2, Div Med Oncol, Dept Expt & Clin Med & Surg F Magrassi & A Lanzar, I-80131 Naples, Italy
关键词
EXTREME; CRYSTAL; Cetuximab; Epidermal growth factor receptor; First-line chemotherapy; Biomarker; CELL LUNG-CANCER; GENE COPY NUMBER; EGFR EXPRESSION; CARCINOMA; COMBINATION; IRINOTECAN; BIOMARKER; SURVIVAL; EFFICACY; MUTATION;
D O I
10.1016/j.ejca.2012.11.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The phase III EXTREME and CRYSTAL studies demonstrated that the addition of cetuximab to chemotherapy significantly improved survival in the first-line treatment of recurrent/metastatic squamous cell carcinoma of the head and neck (SCCHN) and KRAS wild-type metastatic colorectal cancer (mCRC). In advanced non-small-cell lung cancer (NSCLC), high EGFR expression was identified as a tumour biomarker that can predict survival benefit associated with the addition of cetuximab to first-line chemotherapy. We investigated whether tumour EGFR expression level was predictive of cetuximab benefit in EXTREME and CRYSTAL study patients. Methods: Prospectively collected tumour immunohistochemistry data were used to generate an EGFR immunohistochemistry score (scale 1-300) for patients in the EXTREME and CRYSTAL studies. For each study, the association between tumour immunohistochemistry score and cetuximab benefit was investigated. The EXTREME and CRYSTAL studies are registered with Clinical Trials.gov, numbers NCT00122460 and NCT00154102, respectively. Findings: Tumour EGFR immunohistochemistry data were available for 411 of 442 (93%) patients from the EXTREME study intention-to-treat (ITT) population and 664 of 666 (100%) patients from the ITT population of the CRYSTAL study with EGFR-expressing, KRAS wild-type disease. The distribution of immunohistochemistry scores was similar between the treatment arms of each study, but differed between studies. A clinically relevant benefit for progression-free and overall survival associated with the addition of cetuximab to chemotherapy was seen across the full score range in EXTREME study patients. Similarly, CRYSTAL study patients derived a clinical benefit across the full score range, with no meaningful association between EGFR expression level and benefit. Interpretation: The addition of cetuximab to chemotherapy improved survival in the first-line treatment of recurrent/metastatic SCCHN and KRAS wild-type mCRC regardless of tumour EGFR expression level, indicating that in contrast to findings in NSCLC, EGFR expression level is not a clinically useful predictive biomarker in these settings. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1161 / 1168
页数:8
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