Introduction

Non-small cell lung cancer (NSCLC) cases account for approximately 85% of all the lung cancer instances, with pulmonary carcinomas representing worldwide the leading death cause derived from cancer (Jemal et al. 2010). The uncovering of the epidermal growth factor receptor (EGFR) responsible for cell proliferation and survival (Baselga 2002) as being constitutively over-expressed in the majority of these tumour types, prompted the development of a number of anti-EGFR agents for NSCLC treatment. The best known anti-EGFR agents comprise the EGFR tyrosine kinase inhibitors (TKIs), such as gefitinib or ZD1839 (Iressa®, 2005), else erlotinib or OSI-774 (Tarceva®, 2009), all of these agents functioning through the inhibition of the EGFR phosphorylation and tyrosine kinase activities as mediated by competitive binding processes (Ciardiello and Tortora 2008).

Initial clinical trials concluded that some clinical and pathological features (Asian ethnicity, never-smokers, female gender and adenocarcinoma histology) all benefited by displaying longer survival responses to EGFR-TKI therapy (Shepherd et al. 2005; Kim et al. 2008; Cappuzzo et al. 2007; Tokumo et al. 2005). Nowadays, it has been clearly established that the EGFR gene mutational status comprises a powerful predictor of the tumour responses to EGFR-TKI treatments (Lynch et al. 2004; Janne et al. 2005; Cappuzzo et al. 2005, Takano et al. 2005; Hirsch et al. 2006; van Zandwijk et al. 2007; Mitsudomi et al. 2010), in consequence being widely used to select patients likely to respond to the medication. Findings derived from the EURTAC (Rosell et al. 2012) and OPTIMAL studies (Zhou et al. 2011) have strengthened the rationale to apply prognostic mutation status checking in the case of NSCLC patients.

Nevertheless, inclusive among EGFR mutated patients, not all individuals respond to EGFR-TKI treatment in the same manner, as a result the objective positive response to EGFR-TKI treatment has ranged 62% to 75% (Mitsudomi et al. 2010; Tamura et al. 2008; Maemondo et al. 2010). On the other hand, no EGFR mutations were identified in 10-20% of patients with partial responses to EGFR-TKI application (Pao et al. 2004; Lynch et al. 2004; Cappuzzo et al. 2005; Bell et al. 2005; Han et al. 2005). This evidence strongly suggests that other mechanisms besides of the EGFR mutation status determine the TKI treatment responsiveness (Chang et al. 2011; Cappuzzo et al. 2005; Engelman et al. 2005). Several other predictive biomarkers have also been investigated in relation to NSCLC in order to assess TKI responsiveness. Cappuzzo et al. (2005) reported on EGFR amplification and high EGFR protein expression levels associated to gefitinib responsiveness. Likewise, Takano et al. (2005) respective to recurrent NSCLC patients and Hirsch et al. (2006) considering a phase III study of advanced NSCLC subjects determined that an increased EGFR gene copy number encompasses a favourable gefitinib sensitivity marker. In addition, significant ErbB-3 over-expression levels have also been associated with gefitinib sensitivity (Engelman et al. 2005).

Furthermore, tumour specimens are required in order to efficiently select patients based on EGFR mutation profiles, yet sometimes insufficient primary tumour tissue is available or else circumstances dictate that samples are difficult to obtain having led to EGFR gene mutation detection failures (Mitsudomi et al. 2010; Costa et al. 2007).

In this study we have investigated amongst TKI erlotinib treated non-small cell lung cancer (NSCLC) patients the potential predictive outcome of three clinical practice applied serum biomarkers (CEA, CYFRA 21–1, SCC) together with the soluble form of EGFR (sEGFR) and its constituting ligands: epidermal growth factor (EGF), transforming growth factor-alpha (TGF-α) and heparin binding epidermal growth factor (HB-EGF).

Results

Patient characteristics

The characteristics of the patients included in this study are displayed in Table 1. The patients’ mean age amounted to 60.81 years (ranging 38–86) and the group consisted mostly of men (67.24%). Never-smokers comprised 24.1% of the patients. Regarding histological types, adenocarcinomas were mainly reported (70.7%) and most tumours were classified into advanced (20.7% stage IIIb) and metastatic (67.2% stage IV) states. Performance status (PS) could only be established for half of the patients: 39.7% encompassed PS 0–1 and 8.6% manifested PS 2–3.

Table 1 Patient and tumour characteristics
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In relation to the previous treatments, patients who had received one previous chemotherapy line (48.3%) had undergone a cisplatin-based doublet chemotherapy pre-treatment. Patients with two different therapies previous to the erlotinib treatment initiation (25.9%) had received cisplatin-based chemotherapy as the first line (except for one patient) and different second line therapies: 7 patients platinum, 5 patients taxane and 3 patients gemcitabine or vinorelbine. A total of three treatments were administered to only 3.4% of the patients: first and second lines consisted of platinum derivatives and with regard to the third line one patient had received gemcitabine while another had been assigned taxane. Only in one case had a patient received more than three treatments whereas the remaining 12 patients had not received any treatment before commencing the erlotinib therapy (Table 1).

Serum marker concentrations

Table 2 provides the seven serum marker levels providing their average levels together with ranges. The pre-treatment levels of the markers sEGFR, EGF, TGF-α and HB-EGF displayed Gaussian distributions, whilst the levels of CEA, CYFRA 21–1 and SCC entailed skewed distributions.

Table 2 CEA, CYFRA 21–1, SCC, sEGFR, EGF, TGF-α and HB-EGF serum marker concentrations
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Treatment outcome

The mean erlotinib treatment duration amounted to 6.37 months (spanning from 1–12.0 months). Overall, erlotinib treatment was well tolerated by the majority of the individuals. Following to the erlotinib therapy, clinical responses were assessed giving the following results: no patients exhibited a complete response (CR) to the therapy; the disease control rate covered 47.4%, of which a partial response (PR) was observed in 21.1% of the patients while a stable disease development (SD) was witnessed in 26.3%; whereas disease progression (PD) cases accounted for 52.6% of the patients.

Survival analysis stratified by patient and tumour characteristics

Patients’ follow-up was performed during a period of approximately 27 months in order to estimate the progression-free survival (PFS) along with the overall survival (OS). During that time period, altogether 51 patients suffered tumour progression of which 48 finally died as a consequence of the lung cancer. The median PFS and OS extents equalled respectively 3.1 (IC 95%: 2.2–4) and 6.97 months (IC 95%: 4.56–9.37). Univariate survival analysis was further carried out in order to assess influences of gender, age, smoking, performance status, histology, tumour stage, previous treatment administration and therapy toxicity on the PFS and OS occurrences of the NSCLC patients (Table 3).

Table 3 Univariate analysis of the clinical and pathological factors in relation to PFS and OS
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Positive smoking histories presented significantly lower PFS (p = 0.042) for active smokers and a hazard ratio (HR) value of 2 of suffering disease progression (p = 0.046). Improved performance status at the beginning of the erlotinib treatment (p = 0.007) and adenocarcinoma histology (p = 0.045) were significantly associated to longer overall survival; however, only a poor performance status remained a significant death predictor as detected by the Cox analysis, exhibiting a 3.88 times higher hazard ratio (p = 0.012).

The erlotinib-derived toxicity encompassed a significant prognostic factor with respect to both the progression-free survival (p < 0.001) and the overall survival (p = 0.009), although with more remarkable differences in the case of the overall survival. Risk assessment confirmed that the toxicity represented a protection factor, with hazard ratios of 0.44 respective to the progression-free survival (p = 0.013) and 0.35 regarding the overall survival (p = 0.031).

Patient survival analysis stratified by tumour markers

Table 4 reports the median progression-free survival (PFS) and overall survival (OS) periods of those patients having been classified as holding pre-treatment marker levels below or above of the defined cut-off levels (see Methods), in addition to the results derived from the Cox analysis in order to establish progression and death risks. The patient or sample number disparities compared to Table 2 are due to censored or missing data.

Table 4 Univariate analysis of the serum marker concentrations in relation to PFS and OS
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Two of the serum markers, namely CEA and sEGFR, were significantly related to an overall survival (OS) prolongation when patients manifested elevated levels. CEA levels above 5 ng/mL had a median OS of 10.2 months, superior to the 4.4 months of patients exhibiting inferior levels (p < 0.001). The Cox analysis established a death hazard ratio (HR) of 0.23 with respect to patients with an elevated level of CEA (p = 0.001).

As concerned sEGFR, a cut-off value of 56.87 ng/mL clearly differentiated among patients expressing lower levels and experiencing lower median overall survival periods of 4.2 months in contrast to patients displaying levels well above of the cut-off value who presented median overall survival intervals of 9.5 months (p = 0.016); progression-free survival differences were nearly significant (p = 0.051). The Cox analysis revealed that elevated sEGFR levels implied a diminished death hazard ratio corresponding to 0.43 (p = 0.019).

Relationship between EGFR mutation analysis and treatment response

Mutation analysis of the EGFR gene TK domain exons 18–21 was carried out on tumour specimens drawn from 33 patients of the study. One patient carried an unspecified mutation type, therefore this individual was further excluded from the subsequent analyses.

EGFR gene related mutations were detected in 11 out of the resulting 32 patients (34.4%), while the remaining 21 individuals held the wild type EGFR genotype. All the variants detected in this study were located on exons 18, 19 and 21; the most frequent mutation consisted of a deletion in exon 19 (del19) affecting a total of 8 individuals (72.7%), another two cases were detected in exon 21 (L858R and L861Q) and only one mutation case was identified in exon 18 (G719X).

Treatment responsiveness was recorded for 31 patients out of the 32 EGFR mutational status appraised cases. Gene mutations were detected in 9 out of 17 (52.9%) cases presenting partial responses (PR) or stable disease (SD) states after undergoing erlotinib administration; however, only 2 mutations were present in the 14 (14.3%) cases of disease progression (PD). Furthermore, EGFR mutations were not significantly associated with an improved response (p = 0.057, Fisher’s exact Test).

Patient survival analysis stratified by EGFR mutational status

Progression-free survival (PFS) and overall survival (OS) were assessed among the 32 patients characterized by EGFR mutations. The median PFS corresponded to 3.47 months (95% CI: 2.59 – 4.34) while the median OS was amounted to 6.53 months (95% CI: 3.99 – 9.07). The Kaplan-Meier analysis and the Log-Rank test detected that the EGFR gene mutations conferred significant survival advantages versus the wild type patients, both with respect to the PFS (8.6 versus 2.8 months, p = 0.012) and also to the OS (12.6 versus 5.4 months, p = 0.033). Univariate hazard ratios of the mutated EGFR genotypes corroborated that those patients bearing mutations held minor progression and death probabilities (HR of 0.36 and 0.39, respectively). Results are displayed in Table 5.

Table 5 Univariate analysis of serum markers in patients with EGFR mutation status analysed for survival
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Survival analysis of EGFR mutational status characterized patients stratified by tumour markers (sEGFR and CEA)

The tumour markers sEGFR and CEA, which had probed significant survival predictors as identified by the univariate analysis presented in Table 4, were made use of to repeat the survival analysis with respect to the EGFR mutational status characterized patients. As had occurred when all of the patients had been analysed, neither the sEGFR nor the CEA tumour markers affected significantly the progression-free survival (PFS). Despite of the statistical power loss, higher sEGFR (p = 0.013) and CEA (p = 0.004) levels were again associated with a significant overall survival (OS) improvement (Table 5). Survival medians of mutational status characterized patients were practically identical to those that had been obtained for all of the patients assessed in the study. The Cox hazard model also corroborated that these markers encompassed prognostic factors for a lower death risk.

Patient survival analysis stratified by EGFR mutational status combined with CEA and sEGFR marker levels

The mutational EGFR status together with the serum CEA and sEGFR marker levels were assayed together in order to quantify a better survival prediction (Table 6). It was possible to only assay pair combinations in relation to survival and risk owing to the low patient number recording simultaneously data with respect to these three variables when all of the three markers bore positive states (mutated EGFR, sEGFR and CEA levels above of the cut-off values; 3 patients) or negative (2 patients).

Table 6 Univariate analysis of the combination of EGFR mutational status, CEA and sEGFR for PFS and OS
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Only the EGFR mutational status and the sEGFR level associated together significantly with a longer progression-free survival (PFS) embracing a median of 23.5 months when the EGFR gene was mutated and the protein serum levels displayed increased values, compared to the 3.5 months in the case of patients with the non-mutated gene also exhibiting inferior sEGFR levels (p = 0.018) altogether enclosing a risk of progression of 4.37 (p = 0.026). Conversely, the EGFR mutation type did not maintain a high significance with respect to the PFS when combined with the CEA marker level, nor did the combination of the high sEGFR and CEA levels affect favourably the PFS.

On the contrary, concerning all three combinations taken together better survival times were exhibited when at least one of the markers had elevated levels or else the EGFR gene was mutated, although in the case of the sEGFR level and the EGFR gene mutational status the significance threshold was not reached. The univariate Cox analysis in relation to the overall-survival (OS) revealed similar propensity-death hazard ratios in the case of low sEGFR levels when combined with either the non-mutated EGFR genotype or low CEA levels, 7.89 (p = 0.011) and 7.43 (p = 0.016) respectively. The combination of the low CEA levels together with the non-mutated EGFR status implied an increased death risk of 4.39 (p = 0.050).

Figure 1 presents according to the combination of the sEGFR and CEA serum marker levels in conjunction with the EGFR mutational gene status the Kaplan Meier curves of the progression-free survival (PFS) and of the overall survival (OS).

Figure 1
figure 1

PFS and OS according to combination of sEGFR and CEA concentrations and EGFR mutational status. Groups consisted of the following: (0) patients with sEGFR levels < 56.87 ng/mL or CEA < 5 ng/mL and a negative EGFR gene mutational status, (1) only one positive marker, (2) patients with sEGFR > 56.87 ng/mL or CEA > 5 ng/mL and a positive EGFR gene mutational status. (A) and (B) Kaplan-Meier curves respectively of PFS and OS according to the combination of the sEGFR serum marker levels and the EGFR gene mutational status. PFS (C) and OS (D) curves in relation to the combination of the CEA serum levels and the EGFR gene mutational status. PFS (E) and OS (F) curves corresponding to the combination of the CEA and sEGFR serum marker levels.

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Progression-free survival and overall survival multivariate analysis

A multivariate Cox analysis was performed in order to assess which variables would be independent survival predictors of erlotinib treated NSCLC patients (Table 7). Data regarding Performance status (PS) and CEA serum marker levels were excluded from the multivariate model, thus remaining a total of 25 patients for further analysis.

Table 7 Multivariate models corresponding to progression-free survival and overall survival
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Patients with mutated EGFR genotypes, sEGFR serum marker levels above of the cut-off value of 56.87 ng/mL and displaying toxicity symptoms presented diminished progression and death risks compared to the patients who exhibited the opposed characteristics. Nevertheless, only sEGFR serum marker levels and erlotinib toxicity resulted significant independent predictors of overall survival (OS), whereas only the erlotinib toxicity was also significant in the case of the progression-free survival (PFS).

The death risk of patients with elevated sEGFR serum marker levels comprised 0.27 (p = 0.013). Furthermore, patients suffering from erlotinib toxicity exhibited a much better prognosis, with poor progression (HR = 0.201, p = 0.030) and death (HR = 0.088, p = 0.002) risks.

Discussion

Serum biomarkers to predict the survival of NSCLC patients treated with erlotinib (Tarceva®) were investigated in this study. Dating back to the development of the EURTAC (Rosell et al. 2012) and OPTIMAL studies (Zhou et al. 2011), the EGFR gene mutation status has been widely applied to select patients most likely to respond to the EGFR-TKI treatments. Nonetheless, it needs to be indicated that not all patients carrying EGFR gene mutations respond receptively to EGFR-TKI treatments (Mitsudomi et al. 2010; Tamura et al. 2008; Maemondo et al. 2010) and also, on the other hand, that no mutations are identified in 10-20% of patients with partial responses to EGFR-TKIs (Pao et al. 2004; Lynch et al. 2004; Cappuzzo et al. 2005; Bell et al. 2005; Han et al. 2005). Therefore, the quest of different sensitivity prediction methods to TKI based therapy in lung cancer remains an issue of interest.

In this study we have tested in pre-treatment serum several markers − such as sEGFR together with its associated ligands TGF-α, EGF and HB-EGF − in relationship to survival of NSCLC patients treated with the EGFR-TKI erlotinib. Routine clinical markers were also assessed: CEA, CYFRA 21–1 and SCC.

Globally, our median overall survival-OS and progression free-survival-PFS outcomes are coincident to those described in the main erlotinib drug evaluation studies (Shepherd et al. 2005). The Kaplan-Meier analysis revealed that only the performance status-PS, tumour histology and toxicity had a substantial impact on the OS of the erlotinib treated patients. The univariate analysis corroborated that PS 2–3 in addition to no toxicity development were significantly associated with a poor prognosis. In coincidence with other previous studies (Petrelli et al. 2012; Emery et al. 2009), toxicity has represented a protection factor indicative of a good clinical response. In the case of adenocarcinoma histology, our results are also in line with those of preceding works (Tsao et al. 2011; Jung et al. 2012).

In our study patients with pre-treatment sEGFR levels higher than 56.87 ng/mL evidenced longer progression free-survival (PFS) while especially overall survival (OS) phases compared to patients containing lower serum levels. Previously, Gregorc et al. (2004) and also Kappers et al. (2010) had already obtained similar results observing that patients embracing higher pre-treatment sEGFR serum levels were more likely to respond receptively. Nonetheless, other authors have described the opposite scenario disclosing discrepant sEGFR levels compared to most of the information available (Kasahara et al. 2010; Lemos-González et al. 2007), probably owing to the different methodology employed.

Of the different EGFR-specific ligands tested, none showed a significant association with patient survival. In the case of the serum marker HB-EGF a cut-off value equal to 171.07 pg/mL separated those patients comprising higher levels while presenting more extended progression free-survival-PFS and overall survival-OS episodes, although statistical significance was not reached. These results are in direct contradiction to those of other authors who have described high TGF-α and HB-EGF levels to be associated with a progressive disease and a shorter overall survival-OS lapse after NSCLC patients had been treated with gefitinib (Masago et al. 2008).

Among the diverse clinical markers analysed in our study, only the serum marker CEA revealed a statistical significant relation with the treated patients’ survival. Our finding establishing that high CEA levels constituted good predictors of survival regardless of the histology was a highly surprising and unexpected fact, as previously in other studies regarding patients with more advanced cancer stages who had been receiving chemotherapy these had displayed high CEA levels which had been associated with a poor prognosis (Lin et al. 2012). Nevertheless, other authors have made similar observations to ours in advanced NSCLC patients undergoing TKI based treatments (Jung et al. 2012; Okamoto et al. 2005). In the first study (Jung et al. 2012), high pre-treatment CEA levels were significantly associated with longer progression-free survival interludes. Similarly, Okamoto et al. (2005) reported that EGFR TKI treated patients with high pre-treatment CEA levels bestowed longer survival terms and displayed better responses than those patients encompassing lower CEA levels.

In relation to the serum marker CYFRA 21–1, levels above of the cut-off limit showed lower overall survival-OS rates, although the statistical significance threshold was not surpassed. These results are very similar to those described by Chen et al. (2010), who determined that this marker’s pre-treatment levels might provide prognostic information in the case of gefitinib treatments.

So far few reports exist regarding the relationship between serological marker levels and the curative effect of erlotinib. The associated shortcomings of these studies include an EGFR mutation test lack, the very low patient number (Ishikawa et al. 2005), or else only wild-type patient analysis (Chang et al. 2011).

We have included in our study data pertaining to the EGFR mutational status of 32 characterised patients (tumour tissue was not available for the remaining subjects). Mutations were detected among 11 patients with a resulting EGFR gene mutation rate of 34%. This percentage is markedly superior to the EGFR gene mutation frequency reported for European Caucasians covering 9.8% in the case of German NSCLC patients (Gahr et al. 2013) and amounting to 16.6% with respect to a Spanish population of advanced NSCLC patients (Rosell et al. 2009). The EGFR gene mutation frequency discrepancies are best explained on the basis of the selection criteria employed in this study restricting the eligible NSCLC patients to those receiving an erlotinib treatment, in spite of including all of the NSCLC patients, together with some patient’s non-availability of tumour tissue which precluded an accurate EGFR gene mutation estimate.

Our results related to the EGFR mutational status indicated a strong association (Fisher analysis close to significance) between the EGFR mutations present and the response to the erlotinib treatment. Furthermore, the mutational status holds a prognostic value as the mutated EGFR gene patients displayed higher overall-survival (OS) and progression free-survival (PFS) episodes in comparison to patients lacking mutations, also corroborated by the univariate Cox analysis which revealed that progression and death are less prone to occur in patients bearing mutations. Our data agrees with that of previous studies (Inoue et al. 2006; Rosell et al. 2012; Tamura et al. 2008; Sequist et al. 2008).

As was also observed in the case of Chang et al. (2011), some patients responded positively to erlotinib medication although they presented the wild type EGFR genotype: 4.8% manifested partial responses (PR), 57.1% exhibited stable disease development (SD) while 33.3% incurred in disease progression (PD).

Death predictive markers disclosed by the univariate analysis, the EGFR gene mutational status in addition to the serum CEA and sEGFR marker levels, were further assayed in combination in order to assess better survival predictions. Marker combinations were evaluated among three categories: (2) both positive markers (above of the cut-off threshold or else a mutated EGFR genotype), (1) only one marker positive and (0) both markers negative (below of the cut-off threshold or else a wild type EGFR genotype). The combination of the sEGFR level together with the EGFR gene mutational status did not have a significant impact on the overall survival (OS) as revealed by the Kaplan-Meier analysis, even though the median survival time was the highest for elevated sEGFR levels and mutated EGFR genes, while the Cox analysis indicated that possessing wild type EGFR tumours together with low receptor levels present in the pre-treatment serum entailed a death risk factor, holding those patients a hazard ratio (HR) 7.89 times higher in contrast to patients with tumours bearing a mutated EGFR gene and expressing high sEGFR levels. Accordingly, we do not consider the sEGFR level in conjunction with the EGFR gene mutational status a worthy combination.

Noticeably, sEGFR and CEA levels combined together significantly determined overall survival (OS), thus having represented a more useful combination that achieves longer survival in erlotinib-treated patients. Combined high pre-treatment serum CEA and sEGFR levels clearly indicated a better prognosis granted that these patients showed higher OS (12.6 months) time frames weighed against those individuals displaying only one marker with an elevated level (5.2 months), whilst particularly in contrast to those patients with both markers expressing low levels (3.5 months), all confirmed by the Cox analysis disclosing that group 0 patients sustained a hazard ratio (HR) 8.36 times higher than that of the group 2 patients. Almost the same results could be observed when only the patients with a known mutational status were considered. Compared to the single EGFR mutational status determination, it remains worthy to highlight that the combined CEA and sEGFR use allowed to discern 14 patients (41%) with a prolonged OS, whereas the mutational status analysis permitted to distinguish 11 patients (34.3%); moreover, the OS benefit of both the positive sEGFR and CEA levels combined was at least as good as the survival increase of patients with the mutated EGFR gene, in both cases spanning 12.6 months. Nonetheless, it should be kept in mind that the prognostic value incremental evaluation of the sEGFR and CEA levels combined to that of the EGFR gene mutational status standing alone was not performed due to insufficient available data, as has already been explained elsewhere. The before mentioned results suggest that the combined CEA and sEGFR usage may provide an equivalent prognostic information to that of the EGFR gene mutational status with regard to determining NSCLC erlotinib treated patient prognosis.

Using a multivariate Cox regression model only the pre-treatment sEGFR level together with erlotinib toxicity remained significant survival predictors. Although all of the variables with a significant death risk impact should have been included in the univariate analysis: performance status (PS), erlotinib toxicity, EGFR gene mutational status and pre-treatment serum levels of the sEGFR and CEA markers, we could not include in the multivariate analysis the marker CEA or the performance status due to an insufficient amount of data. Reinforcing our results, Gregorc et al. (2004) had previously studied the sEGFR levels of patients with advanced NSCLC stages observing that high sEGFR levels were significant with respect to the three multivariate analyses performed.

Our study presents some weaknesses; in this line our main concern contemplates the limited number of recruited individuals owing to the peculiarities of the selected subjects, in addition to an insufficient serum volume, which precluded the whole population determination of all of the markers. In the future, larger studies to corroborate the preliminary prognosis conclusions of the erlotinib-treated patients based on combined sEGFR and CEA data are needed that, in addition, could also confirm the potential of other biomarkers that might have been underestimated, such as could be the case of the HB-EGF and CYFRA 21.1 serum markers, whose levels showed survival and risk relations close to significance. Despite of these shortcomings, the high CEA and sEGFR prognostic value similarity displayed for the whole population survival analysis as compared to the subgroup analyzed for the EGFR gene mutational status indicates that the limited sample size has not affected the results.

Secondly, as our patient cohort was heterogeneous in relation to the previous treatment, caution should be exercised in drawing any firm conclusions. Our analyses have all been based on erlotinib-treated patient outcomes, given that our study lacked a control group (patients who had not received erlotinib treatment), thus, results do not allow to differentiate whether the survival benefit was due to a prognostic or predictive value of the serum markers sEGFR and CEA to identify patients who would respond positively to erlotinib therapy (Coate et al. 2009).

Conclusions

The present study has indicated that pre-treatment levels above 5 ng/mL of CEA or above 56.87 ng/mL of sEGFR comprise survival markers designed for NSCLC patients treated with erlotinib. The combined assessment of sEGFR and CEA serum marker levels could be of value in order to pre-select patients to undergo EGFR-TKI treatments. This is in particular relevant in circumstances when tumour tissues are insufficient or else the hospital lacks the appropriate facilities, in view of the fact that sEGFR and CEA level determinations are routinely feasible whilst relatively non-invasive and inexpensive procedures.

Methods

Patients and treatment assessment response

A total of 58 patients were included in this study diagnosed with NSCLC who had been treated with the TKI erlotinib at the Complejo Hospitalario Universitario de Vigo (Spain) from July 2009 to June 2011. The inclusion criterion comprised all patients who had received erlotinib medication during the study period as first or second-line treatment, these patients had failed to respond to conventional intravenous chemotherapy or had been unable to receive chemotherapy. Patients were treated with daily doses of 150 mg and dose reductions of 50 mg were undertaken in cases of observing unacceptable toxicity.

Performance status (PS) and the treatments received prior to the erlotinib therapy were recorded. PS refers to the manner in which the patient’s disease progresses affecting the daily vital capabilities, thus being applied to determine an appropriate treatment and prognosis. PS data was collected following the Eastern Cooperative Oncology Group scale (Oken et al. 1982). Erlotinib-derived toxicity data was also collected denoting any toxicity type experienced by patients due to the treatment received.

The objective tumour response was assessed every 3 months after the beginning of the treatment by means of a computerized tomography according to the Response Evaluation Criteria of Solid Tumors (Eisenhauer et al. 2009). Each patient’s response was then classified into one of the following categories: responders, including cases of complete response (CR), partial response (PR) and stable disease development (SD); and non responders, including cases of disease progression (PD).

All of the patients provided an informed consent before of the enrolment in the study and marker determination was accomplished without interrupting the normal clinical practices. The study followed all of the guidelines set up to undertake experimental investigation as required by the authors’ institutions and complied fully with the Helsinki Declaration.

Serum marker level determinations

Blood samples were collected before of the EGFR-TKI treatment initiation. Separated serums were stored at −25°C until further use.

CEA and CYFRA 21–1 measurements were carried out by electrochemiluminescence immunoassays (ECLIA, Roche Diagnostics, Germany) using an Elecsys® 2010 analyzer. The SCC antigen determination was accomplished by means of the TRACE technology (Time-Resolved Amplified Cryptate Emission) making use of a KRIPTOR BRAHMS-ATOM® apparatus.

The DuoSet® ELISA Development System human (R&D Systems Minneapolis, MN) kits were used in order to determine the sEGFR, EGF, HB-EGF and TGF-α concentrations present in the serums, performed according to manufacturer’s instructions. Optical densities were read by way of an EnVision Multilabel Plate Reader (Perkin Elmer). Final sample sizes to determine marker concentrations depended on the patient’s available serum quantities.

EGFR gene mutation analysis

Tumour tissue samples for EGFR mutation testing were available only for 33 patients (12 women, 20 men, one patient was excluded due to an unspecified mutation type). The Cobas EGFR Mutation Test kit (Roche Molecular Systems, Inc., Branchburg, USA) entailing a CE-IVD-marked allele-specific PCR test designed to detect the presence of 41 mutations within exons 18, 19, 20 and 21 of the TK domain was applied to paraffin-embedded tissue blocks. Data analysis and interpretation was implemented through the computer software Cobas z 480 (Roche Molecular Systems, Inc., Branchburg, USA).

Statistical analysis

Normality of the continuous variable distributions was assessed using the Kolmogorov-Smirnov test. Variable distribution differences between and among groups regarding the EGFR mutational status were compared using Fisher’s exact test. Receiver operating characteristic curves (ROC) were drawn for the novel tumour markers (sEGFR, EGF, HB-EGF and TGF-α) in order to assess their discerning value to tell apart the non-progressive from progressive patients and also to establish the survival analysis cut-off values: 56.87 ng/mL in the case of sEGFR, 713.59 pg/mL with respect to EGF, 171.07 pg/mL regarding HB-EGF and 21.81 pg/mL concerning TGF-α. The pertinent cut-off values of CEA, CYFRA 21–1 and SCC were respectively established at 5 ng/mL, 3.3 ng/mL and 1.5 ng/mL.

The progression-free survival (PFS), the overall survival (OS) and the 95% confidence intervals (95% CI) were assessed through the Kaplan-Meier method while survival differences between patients’ groups were compared by means of the Log-Rank test. PFS values were calculated starting the date of erlotinib treatment initiation up to the date of the first PD appearance or else up to the date of the last contact. The OS values were estimated from the date of therapy initiation up to the death date arising from any cause or else up to the date of the last contact. The association of risk factors with survival was evaluated according to the Cox proportional hazards regression model. The multivariate analysis was performed using a logistic regression model in order to identify those variables associating independently with survival. Statistical significances were defined at the p < 0.05 probability level. The statistical analysis was carried out using the software package SPSS V15 run under Windows (Copyright© SPSS Inc. 1989–2002, Chicago, IL).