EGF and EGFR genetic polymorphisms predict prognosis in locally advanced pharyngolaryngeal squamous cell carcinoma patients receiving postoperative concurrent chemoradiotherapy
Received 28 June 2014
Accepted for publication 8 September 2014
Published 28 November 2014 Volume 2014:7 Pages 2197—2204
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 3
Editor who approved publication: Dr Jianmin Xu
Nai-Wen Su,1 Yi-Shing Leu,2 Jehn-Chuan Lee,2 Chung-Ji Liu,3 Chieh-Yuan Cheng,3 Jiun-Sheng Lin,3 Yu-Jen Chen,4 Chi-Kuan Chen,5 I-Chih Fang,6 Ruey-Kuen Hsieh,1 Yi-Fang Chang1,6
1Division of Medical Oncology and Hematology, Department of Internal Medicine, 2Department of Otorhinolaryngology, 3Department of Oral and Maxillofacial Surgery, 4Department of Radiation Oncology, 5Department of Pathology, 6Good Clinical Research Center, Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan
Background: Epidermal growth factor (EGF) and its receptor (EGFR) are part of an important signaling pathway that is involved in the pathogenesis of squamous cell carcinoma of the head and neck (SCCHN). We hypothesized that EGF/EGFR genetic polymorphisms might have a prognostic impact on disease-free survival and overall survival (OS) in locally advanced SCCHN.
Materials and methods: The patient group included a consecutive cohort of 180 patients with locally advanced SCCHN who underwent postoperative concurrent chemoradiotherapy between 2002 and 2010. DNA from formalin-fixed, paraffin-embedded tumor tissues was genotyped for the single nucleotide polymorphism (SNP) of EGF A61G A>G, EGFR R521K G>A and G-216T. The log-rank test was applied to evaluate the impact of SNPs on the outcomes. Survival was estimated using the Kaplan–Meier statistical method.
Results: We demonstrated that EGF/EGFR SNPs might predict prognosis in patients with primary pharyngolaryngeal tumors, but not in those with oral cavity tumors. In pharyngolaryngeal tumor subgroup, EGF61 G/G genotype led to worse 5 year OS rate when compared to G/A or A/A genotypes (13.3% versus 34.3% versus 50.0%, P=0.017). The 5 year OS of patients with EGFR R521K G/G (11.1%) and G/A (15.9%) were lower than the A/A (62.5%) genotype (P=0.054). Patients carrying one or two unfavorable alleles had worse 5 year OS than those without unfavorable allele (not available versus 20% versus 71.4%, P=0.002). Multivariate analysis revealed that the highest risk of death was associated with the coexistence of two unfavorable genotypes (hazard ratio 25.7, 95% confidence interval =3.4–193.4; P=0.002).
Conclusion: In this study, we were able to demonstrate that the EGF A61G and EGFR R521K genetic polymorphisms might be important prognostic factors in patients with locally advanced primary pharyngolaryngeal squamous cell carcinoma who underwent postoperative concurrent chemoradiotherapy.
Keywords: polymorphisms, EGF A61G, EGFR R521K, head and neck cancer, biomarker
Squamous cell carcinoma of the head and neck (SCCHN) is the sixth most common cancer worldwide, and over 60% of the patients show locally advanced disease at presentation.1 Curative surgery followed by adjuvant concurrent chemoradiotherapy (CCRT), guided by the grading of pathologic risk features, is the standard of care for most tumors originating in the oral cavity and for part of the pharyngolaryngeal tumors.2,3 Despite recent advances, over 50% of the patients experience treatment failures.4 Meanwhile, acute and late adverse effects are of great concern while we are attempting to use more aggressive therapeutic approaches in the pursuit of better outcomes.5 In practice, prognostic biomarkers would be of great help to make more targeted decisions with respect to treatment strategies.
The epidermal growth factor receptor (EGFR) is a cell surface receptor and belongs to the ErbB receptor family. The EGFR is widely expressed on the epithelial cells in various tissue. After ligand binding, the receptor forms homo- or heterodimers and activates receptor autophosphorylation which triggers a series of intracellular signaling. Epidermal growth factor (EGF) is one of the ligands binding to ErbB receptors. In cancer cells, the EGFR signaling pathway is often deregulated which promotes their proliferation, resistance to apoptosis, ability to metastasize, and angiogenesis.6–9 The EGFR pathway activation is associated with the development of the SCCHN malignant phenotype and tumor growth.10,11 Overexpression of EGFR and of its ligand are well documented in SCCHN.12,13 Furthermore, elevated EGFR expression predicts worse disease survival.14 EGF and EGFR genetic polymorphisms have been investigated for carcinogenesis and prognosis in several cancer types.15–18 An A>G single nucleotide polymorphism (SNP) at position +61 of the EGF gene was shown to increase EGF production in cultured peripheral blood mononuclear cells.19 Patients with the EGF61 A>G (rs4444903) polymorphism have poor prognosis for different cancers.19,20 The EGFR R521K G>A (rs2227983) SNP leads to an Arg (R) to Lys (K) substitution. This EGFR variant allele shows reduced ligand binding and decreased tyrosine kinase activity as compared to the wild-type G allele.21 The other EGFR SNP of interest is the -216 G>T (rs712829) change in the sp1-binding site of the promoter region. In vitro, studies revealed that this replacement increases the promoter activity by 30%.22 Both these EGFR SNPs have prognostic implications mainly for colorectal cancer.23,24 Only one report examined EGFR polymorphisms and their prognostic association in SCCHN.25 In the current study, we investigated the three EGF/EGFR SNPs that are described above, and their correlation with prognosis, in a consecutive cohort of locally advanced SCCHN (LA-SCCHN) patients, all of whom received postoperative CCRT.
Materials and methods
Study cohort and treatment
The study protocol was approved by the hospital’s institutional review board. Retrospectively, we included patients with newly-diagnosed non-metastatic LA-SCCHN originating from the oral cavity, the oropharynx, the hypopharynx, or the larynx. All patients underwent curative surgery and received the planned radiotherapy (RT) doses with concurrent chemotherapy in our institution. Patients who received cetuximab at any step as part of their treatment were excluded. Each tumor was staged according to the 2002 American Joint Committee on Cancer staging classification. In all surviving patients, follow-up was performed for at least 2 years.
Indications for postoperative CCRT were the presence of any major pathologic risk features, positive surgical margins or extracapsular nodal extensions, or at least two co-existing minor risk factors, including T classification (T3/T4), N classification (N2-3), close surgical margins (1–5 mm), perineural invasion, or lymphovascular invasion (LVI), and a poorly differentiated tumor. RT fractionation involved five consecutive daily fractions over the course of a week, with a 1.8–2.0 Gy fraction size. The RT techniques were 2D conventional RT and intensity-modulated radiotherapy. The planned RT dose to the primary tumor bed and the affected lymph node regions was 60–66 Gy. The concurrent chemotherapy regimen involved one of the following: single agent cisplatin (30 mg/m2 weekly or 75 mg/m2 every 3 weeks), single agent tegafur-uracil (tegafur 300 mg/m2 daily), or the cisplatin/5-FU combination (cisplatin 15 mg/m2 and 5-FU 750 mg/m2 daily in a 120 hour continuous infusion, on day 1 and day 29 during RT).
DNA extraction and genotyping
Genomic DNA was extracted from formalin-fixed paraffin-embedded tissue blocks of the resected tumor, and EGF/EGFR polymorphism genotyping was carried out. A total of 180 tumor samples were analyzed as each patient correlates to one tumor sample.
forward primer: 5′-TGTCACTAAAGG AAAGGA-3′
reverse primer: 5′-TTCACAGAGTTTAACAGCCC-3
EGFR R521K G>A
forward primer: 5′-TGCTGTGA CCCACTCTGTCT-3′
reverse primer: 5′-CCAGAAGGTTGCACTTGTCC-3′
EGFR -216 G>T
forward primer: 5′-TGTCACTAAA GGAAAGGAGGT-3′
reverse primer: 5-TTCACAGAGTTTAACAGCCC-3′
PCR reactions were carried out in 20 μL reactions that contained 150 ng DNA template, 0.4 μM of each primer, 10 μL 2× GoTaq® Green Master Mix, 5% dimethyl sulfoxide, and nuclease-free water. PCR amplification involved an initial 5 minute denaturation step at 95°C, followed by 35 cycles of denaturation (95°C for 30 seconds), annealing (57°C for EGFR R521K G>A and EGF61 A>G and 60°C for EGFR-216 G>T for 60 seconds), and finally elongation (72°C for 7 minutes). The resulting PCR products were analyzed on the ABI3730 Sequencer (Thermo Fisher Scientific, Waltham, MA, USA) which is a genetic analyzer for allele determination.
Endpoints and statistical analysis
The time to events was counted from the date of surgery to the event occurrence or to the last date of the study, December 31, 2012, whichever came first. Death from any cause was incorporated when calculating overall survival (OS). Disease recurrences, the presence of a second primary tumor, and death from any cause were events considered when evaluating disease-free survival (DFS). Patients were recorded as censor if no events occurred until the last follow-up or the end of study.
Survival rates were estimated using the Kaplan–Meier statistical method. The log-rank test was used to evaluate the possible impact of EGF and EGFR genetic polymorphisms, separately and in combination, on OS and DFS. Additional clinical factors were also included in the analysis. The multivariate Cox proportional hazards model was used to estimate the adjusted hazard ratio (HR) and the 95% confidence interval (95% CI). All reported P-values were two-tailed and considered to be statistically significant for P<0.05. All statistical analyses were performed using SPSS version 12 (SPSS Inc., Chicago, IL, USA).
Patient characteristics and treatment outcomes
From January 2002 to December 2010, a total of 180 LA-SCCHN patients were included in this study. The median age of all patients was 51 years (interquartile range 45–57 years), and 176 (97.8%) were male. Primary tumors were located to the oral cavity in 140 (77.8%), the oropharynx in eight (4.4%), the hypopharynx in 22 (12.2%), and the larynx in ten (5.5%) patients. The pathologic stage distribution was: stage III 15%, stage IVa 75%, and stage IVb 10%. The median total RT dose was 6,480 cGy (interquartile range 6,300–6,600 cGy). Eighty-three (46.1%) patients received 2D conventional RT and the others were treated by intensity-modulated radiotherapy. The median RT treatment duration was 7.3 weeks (interquartile range 6.7–8.1 weeks). One hundred (55.6%) patients died and 112 patients had DFS events until the last follow-up date. After a median follow-up time of 32.0 months (interquartile range 15–68 months), the median OS and DFS were 56 and 37 months, respectively. There were 43 locoregional recurrences and 47 distant metastases. In the univariate analysis, N classification ≥ N2, the presence of LVI, and extracapsular nodal extensions were poor prognosticators for 5 year OS and DFS. Detailed patient demographics and treatment outcomes are listed in Table 1.
Table 1 Patient characteristics and treatment outcome
Genetic polymorphisms and outcome correlations
The genotype frequencies for the three SNPs are presented in Table 2. No significant associations were detected between the three genotypes and OS or DFS when the entire study population was examined. When the primary location of the tumor was considered during the analysis, the EGF61 A>G and R521K G>A EGFR polymorphisms showed a significant prognostic impact in patients with primary pharyngolaryngeal tumors but not in those with oral cavity tumors (Table 2). In this subgroup, patients with the A/A, A/G, and G/G EGF61 genotypes had 5 year OS rates of 50.0%, 34.3%, and 13.3%, respectively (P=0.017, Figure 1A). The EGF61 G/G genotype also led to a lower 5 year DFS rate when compared to the G/A or the A/A genotypes (not available versus 29.8% and 50%, P=0.026, Figure 1B). For the EGFR R521K genotype, the 5 year OS rates in patients carrying the three variants (G/G, G/A, and A/A) were 11.1%, 15.9%, and 62.5%, respectively (P=0.054, Figure 1C). The 5 year DFS was significantly worse in patients with the G/G (11.1%) and G/A (0%) genotypes than in those with the A/A (62.5%) genotype (P=0.038, Figure 1D). We did not observe any correlations between the EGFR -216 G>T genotype and OS or DFS. From these results, we identified EGF61 G/G and EGFR R521K G/G and G/A as unfavorable genotypes for the primary pharyngolaryngeal tumors. Patients harboring one or two of these unfavorable alleles had a worse 5 year OS and DFS than those without these unfavorable alleles (not available versus 20% versus 71.4%, P=0.002, Figure 1E; not available versus 10.4% versus 71.4%, P=0.003, Figure 1F).
We also investigated the correlation between the A61G EGF and the R521K EGFR genotypes and patient characteristics in the pharyngolaryngeal tumor subgroup. Patients with the G/G EGF61 genotype had significantly lower T stage (P=0.024) and more LVI (P=0.003) and perineural invasion (P=0.027). There were no associations between the R521K EGFR genotypes and any patient characteristics (data not shown).
Multivariate analysis of treatment outcome
Since the EGF A61G and EGFR R521K genotypes might be prognostic markers in pharyngolaryngeal tumors, we performed univariate analysis first in this subgroup of patients (N=40). We found that patients with higher pathologic N stage, poor tumor differentiation, LVI and one or two unfavorable genotypes correlated with poor prognosis by univariate analysis. We included the above factors into multivariate analysis and significant HR for death was observed in patients <50 years old (adjusted HR =2.6, 95% CI =1.1–6.1; P=0.03), poor tumor differentiation (adjusted HR =9.9, 95% CI =1.9–50.6; P=0.006), and one or two unfavorable genotypes (adjusted HR =5.3, 95% CI =1.1–25.3; P=0.037, and adjusted HR =25.7, 95% CI =3.4–193.4; P=0.002, respectively) (Table 3). As for DFS, patients with poor tumor differentiation and the coexistence of two unfavorable genotypes had significantly worse outcomes (Table 3).
In this study, we showed that EGF and EGFR genetic polymorphisms correlate with prognosis in patients with primary pharyngolaryngeal squamous cell carcinoma. We revealed that the EGF61 G/G and the EGFR R521K G/G and G/A genotypes are unfavorable genotypes, and the presence of one or two unfavorable alleles resulted in a worse outcome in this patient subgroup. The genotype frequencies were comparable whether they were examined overall in the entire study cohort or categorized according to the primary tumor location. The fact that the prognostic effect of the EGF/EGFR SNPs was restricted to the primary pharyngolaryngeal tumor subgroup was unexpected, and further studies are needed to confirm this finding. The genotype frequencies in our cohort were similar to the ones found in other reports of Asian populations, though different cancer types were looked at.24,27 The major limitation of the current study is its retrospective nature and the relatively small sample size. Our findings focused on an Asian population of individuals who received postoperative CCRT. These results should be tested in larger case series and in other ethnic groups.
The poor prognostic genotypes unveiled in this study also predict inferior outcomes for other cancer types.22,24,28 The only study investigating EGFR polymorphisms in SCCHN was reported by Bandres et al.25 They found that the R521K R/R or R/K EGFR genotypes, in combination with short (CA) repeats (<17), predicted survival. However, the study included stage II and metastatic patients who underwent surgery or received CCRT as the primary therapy, and this might have confounded their analysis.
With the advent of EGFR targeted therapy, we could now inhibit this important signaling pathway in SCCHN. One of the targeted agents, cetuximab, was shown to be effective and tolerated when administered concurrently with radiotherapy29 or in combination with platinum-based chemotherapy.30 Unlike metastatic colorectal cancer in which the K-RAS mutation is an established negative predictor of the response to cetuximab,31 no biomarkers have been validated for SCCHN. The copy number of the tumor EGFR gene had no predictive value.32 The p16 expression status and cetuximab-induced rash exceeding grade 2 were suggested as biomarkers that need further investigation.33,34 EGF/EGFR polymorphisms have been examined as predictive biomarkers to cetuximab treatment. Studies on metastatic colorectal cancer populations showed a trend towards better treatment outcomes in patients carrying the EGF61 G/G genotype, while the predictive value of the EGFR R521K genotype was more controversial.35–38 A similar analysis was reported in two studies of recurrent or metastatic SCCHN patients receiving cetuximab-based systemic therapies.39,40 Patients with the EGFR R521K G/G or EGF61 G/G genotypes had better outcomes in response to cetuximab. This implicates the likelihood that cetuximab might reverse the poor outcome associated with these unfavorable genotypes. However, these preliminary results were obtained in studies that enrolled limited patient numbers, and they need further verification.
In conclusion, this study demonstrates that the EGF61 G/G and the EGFR R521K G/G and G/A genotypes predict poor outcome in patients with locally advanced pharyngolaryngeal tumors receiving postoperative CCRT. The possible predictive role of EGF/EGFR polymorphisms in response to cetuximab treatment warrants further investigation in the same treatment setting.
This work was supported by the Department of Medical Research, Mackay Memorial Hospital, Project No MMH-101-104. The authors thank An-chi Lo for her dedication and great help with the statistical analysis.
The authors have declared no conflicts of interest.
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