Genomic Profiling of KRAS/NRAS/BRAF/PIK3CA Wild-Type Metastatic Colorectal Cancer Patients Reveals Novel Mutations in Genes Potentially Associated with Resistance to Anti-EGFR Agents.

Previous findings suggest that metastatic colorectal carcinoma (mCRC) patients with KRAS/NRAS/BRAF/PIK3CA wild-type (quadruple-wt) tumors are highly sensitive to anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (MoAbs). However, additional molecular alterations might be involved in the de novo resistance to these drugs. We performed a comprehensive molecular profiling of 21 quadruple-wt tumors from mCRC patients enrolled in the "Cetuximab After Progression in KRAS wild-type colorectal cancer patients" (CAPRI-GOIM) trial of first line FOLFIRI plus cetuximab. Tumor samples were analyzed with a targeted sequencing panel covering single nucleotide variants (SNVs), insertions/deletions (Indels), copy number variations (CNVs), and gene fusions in 143 cancer-related genes. The analysis revealed in all 21 patients the presence of at least one SNV/Indel and in 10/21 cases (48%) the presence of at least one CNV. Furthermore, 17/21 (81%) patients had co-existing SNVs/Indels in different genes. Quadruple-wt mCRC from patients with the shorter progression free survival (PFS) were enriched with peculiar genetic alterations in KRAS, FBXW7, MAP2K1, and NF1 genes as compared with patients with longer PFS. These data suggest that a wide genetic profiling of quadruple-wt mCRC patients might help to identify novel markers of de novo resistance to anti-EGFR MoAbs.

1. Introduction

The median overall survival (mOS) of patients affected by metastatic colorectal carcinoma (mCRC) has notably increased in the past 20 years, from 12 months using 5-fluorouracil-based chemotherapy to around 20–30 months with combination therapies including target-based agents [1]. In particular, agents that block the epidermal growth factor receptor (EGFR), such as the anti-EGFR monoclonal antibodies (MoAbs) cetuximab or panitumumab, are an effective therapeutic option in combination with chemotherapy in mCRC patients [2,3].

Treatment with anti-EGFR agents is currently recommended only for mCRC patients with KRAS/NRAS/BRAF wild type (wt) tumors, because mutations in these genes have been shown to determine resistance to anti-EGFR therapies [4,5]. Results from different clinical trials also suggest that anti-EGFR MoAbs significantly improve survival only in patients with tumors in the left colon [6]. However, the difference in outcome between left- and right-sided CRC is likely to reflect the different molecular landscapes of these tumors. Indeed, a number of genetic alterations might play a role in the de novo resistance to anti-EGFR agents in mCRC. In particular, single nucleotide variants (SNVs), copy number variations (CNVs) and/or rearrangements in PIK3CA, PTEN, ERBB2, MAP2K1, NTRK1-3, RET, AKT1, ALK, and ROS1, have been claimed to be associated with resistance to anti-EGFR MoAbs [7,8,9,10,11]. However, most of these observations derive from retrospective analyses of patients treated with anti-EGFR agents in advanced lines of treatment.

The “Cetuximab After Progression in KRAS wild-type colorectal cancer patients” (CAPRI) study enrolled KRAS exon 2 wt mCRC patients who received first-line FOLFIRI plus cetuximab, and at progression were randomized to FOLFOX alone or FOLFOX plus cetuximab. In first-line, the subgroup of patients with KRAS/NRAS/BRAF/PIK3CA wt (quadruple-wt) tumors had a better overall response rate (ORR; 64.4%) and median progression free survival (mPFS; 11.3 months), compared with patients harboring a mutation in any of these genes (ORR 47.4% and mPFS 7.7 months) [12,13].

The CAPRI-GOIM cohort represents a unique collection of tumor samples from mCRC patients treated with first-line anti-EGFR agents within an academic clinical trial. The availability of these tumor samples with annotated clinical data offers the possibility to identify novel genetic alterations that might be associated with de novo resistance to anti-EGFR MoAbs. Starting from the hypothesis that the quadruple-wt cohort might be enriched with rare genetic alterations involved in the sensitivity/resistance to anti-EGFR MoAbs, we performed a comprehensive genomic profiling of a subgroup of quadruple-wt tumors from patients enrolled in the CAPRI trial. By using this approach, we could identify potential candidate genes involved in the resistance to anti-EGFR agents, thus suggesting that selection of mCRC patients for treatment with anti-EGFR monoclonal antibodies can be further optimized.

2. Results

2.1. Targeted Sequencing of KRAS/NRAS/BRAF/PIK3CA Wt mCRC Samples

In order to identify possible mechanisms of resistance to anti-EGFR MoAbs in CRC, we analyzed tumor samples from 21 KRAS/NRAS/BRAF/PIK3CA wt mCRC patients enrolled in the CAPRI-GOIM clinical trial by targeted sequencing (Table S1). In particular, we tested the tumor specimens with the Oncomine Comprehensive Panel that provides information on hotspot mutations of 73 oncogenes, CNVs of 49 genes, full-length sequence of 26 tumor suppressor genes, and sequence of 22 driver gene fusions (see Materials and Methods).

The analysis revealed in all 21 patients the presence of at least 1 mutation and in 10/21 (47.6%) the presence of at least one CNV. Furthermore, 17/21 patients had co-existing genetic alterations in different genes (Table S1).

Of the 54 SNVs and insertions/deletions (Indels) identified, 35% and 41% were APC and TP53 variants, respectively (Figure 1). Nineteen patients (90.47%) had at least one TP53 SNV or Indel, whereas 15/21 (71.43%) patients carried APC mutations. All cases with APC mutations had also TP53 variants. Four tumors carried two APC variants, one tumor had two TP53 mutations and one tumor showed three co-existing TP53 mutations. Two different variants in TP53 (c.275_276insGGCC and c.837_838InsG) and three in APC (c.4467_4468insCATTTTG, c.4098_4099delTCinsAT, and c.589_590insGAGTT) have not been reported in any other sample in public databases to date (www.cbioportal.org; http://cancer.sanger.ac.uk/ cosmic, last accessed 03/14/2019). Mutations were also detected in FBXW7 (n. 3), NF1 (n. 2), MAP2K1 (n. 1), KRAS (n. 1), PTPN11 (n. 1), ATM (n. 1), CTNNB1 (n. 1), PIK3R1 (n. 1), PTEN (n. 1), and CDKN2A (n. 1). All genetic variants were confirmed by Sanger sequencing or droplet digital PCR (ddPCR). The relative frequency of the SNVs/Indels is shown in Figure 1.

Figure 1

Percentage distribution of the 54 single nucleotide variants (SNVs) and Indels identified in the quadruple-wt mCRC patients.

The presence of at least one CNV in APC, TP53, PIK3R1, BCL2L1, GAS6, MYC, ZNF217, FLT3, ERBB2, and APEX1 was observed in 10/21 (47.6%) cases. In particular, one case showed deletions of both APC and PIK3R1 (P6), two had deletions of either APC (P15) or TP53 (P14). The other genes showed copy number gains ranging between 4.67 and 78.99. Three tumors (30%) had several amplified or deleted genes (Table S1 and Figure 2).

Figure 2

Molecular profile of quadruple-wt mCRC tumors. single nucleotide variants (SNVs), Indels and copy number variations (CNVs) of mutated genes for each patient are represented. Patients’ IDs are shown at the top. Green rectangles represent SNVs. Light blue rectangles represent Indels. Red rectangles represent amplifications. Purple rectangles represent deletions. In the lower panels, progression free survival (PFS) and tumor localization of our cohort of patients are displayed.

No gene fusions were detected in 19 tumors. The analysis failed in two cases (P9 and P18).

2.2. Correlation of Genetic Landascape with Patients’ Outcome

The median PFS of the 21 patients included in this analysis was 10.7 months (95% CI 6.25–14.87) and the median OS was 32.6 months (95% CI 24.97–41.28), comparable to those observed in the whole cohort of quadruple-wt patients of the CAPRI-GOIM trial [12].

Interestingly, we observed that patients with the shorter PFS (MEK and mTOR pathways that might be associated with resistance to anti-EGFR drugs. In contrast, only one FBXW7 variant was observed among patients with a PFS ≥ median PFS (Figure 2).

All variants were at an allelic frequency >5% with the exception of a KRAS variant (c.183A>T; p.Gln61His) that was identified in the tumor tissue from patient P7 (PFS 3.93 months) at an allelic frequency of 0.4%. This variant was at an allelic frequency below the 2% sensitivity of the targeted sequencing panel used for tumor molecular profiling in the CAPRI-GOIM trial [12]. The KRAS mutation was confirmed by ddPCR analysis of tumor tissue. In addition, the same variant was detected with BEAMing in the cell-free DNA (cfDNA) from the same patient, thus confirming the specificity of the NGS analysis (data not shown).

Patient P3 (PFS 6.63 months) carried the variant c.169A>G in the MAP2K1 gene coding for the MEK1 protein. This variant has been already reported in the cBioPortal database. It results in the substitution of an amino acid residue (p.Lys57Glu) in the MEK1 negative regulatory domain and it has been associated with a gain of function of the protein [14,15].

Two patients (P20 and P21) had variants in NF1, a negative regulator of RAS, inactivated by mutation in various cancers. Specifically, we found an insertion (c.638_639insA; p.Asn214Lys fs*2) in the tumor from patient P20 (PFS 2.83 months) and a SNV (c.5101A>T; p.Lys1701Ter) in the tumor from patient P21 (PFS 3.73 months). These mutations have not been reported in both COSMIC and cBioPortal databases. Both NF1 mutations lead to the formation of a premature stop codon with consequent loss of function and increased activation of the RAS signaling pathway. Patient P21 carried also a GAS6 amplification (copy number gain 6.04).

Of the three missense mutations detected in FBXW7, two were found in patients with a PFS shorter than median PFS. Patient P14 (PFS 8.07 months) carried the c.1798G>A variant (p.Asp600Asn) and patient P18 (PFS 1.73 months) the c.1513C>T SNV (p.Arg505Cys). The biological effect of the variant p.Asp600Asn is still unknown. In contrast, the FBXW7 p.Arg505Cys mutation has been reported in several cancer types and leads to loss of function of the protein [16].

In 4/10 cases with a PFS TP53 and/or APC mutations were found. Two of these cases were right-sided colon tumors.

The CNVs were much more frequent among patients with longer PFS. Within this cohort, patient P16 had a significant copy number gain of ERBB2 (78.99) that was confirmed by FISH analysis (data not shown). Patient P16 had a partial response to cetuximab-based first-line therapy with a PFS of 12.8 months. Patient P4 (PFS 17.93 months), carrying both GAS6 copy gain (5.59) and a FBXW7 variant (c.1268G>T; p.Gly423Val), had a complete response to first-line therapy.

The tumor from patient P17 carried several genetic alterations, including an Indel in PTEN. Loss of PTEN expression has been previously associated with resistance to anti-EGFR MoAbs [17,18,19]. However, this patient had a first-line PFS of 15.1 months.

2.3. Frequency of Identified Genetic Alterations in CRC

Although we identified MAP2K1, FBXW7, and NF1 variants in patients with relatively short PFS, this finding could be due to a prognostic rather than a predictive value. Therefore, we interrogated public databases and data available at our biobank to assess the frequency in CRC of variants in MAP2K1, FBXW7, and NF1 and the correlation with clinical-pathological features. In particular, we investigated whether these variants are found in left-sided tumors, in which the use of anti-EGFR monoclonal antibodies is highly recommended, as well as their prognostic significance.

In the cBioPortal database, variants of the MAP2K1 gene are reported at frequencies of 1.7% in CRC patients (Table 1) and correlated with worse disease/progression-free survival (Logrank Test P-Value: 1.815e-3), but not with overall survival. Although MAP2K1 mutations were more frequent in right-sided tumors, they were also detected in left colon tumors (Table 1). MAP2K1 variants were also more frequent among KRAS/NRAS/BRAF wt patients as compared with unselected CRC (Table 1). The MAP2K1 mutations previously reported to be associated with de novo and acquired resistance to anti-EGFR MoAbs reside in the negative regulatory domain of the MEK1 protein and are associated with a gain of function of the protein [11,14]. We interrogated our database for these specific mutations. Among 939 CRC cases tested at our laboratory for MAP2K1 mutations within clinical practice and clinical research, only 2 (0.2%) showed MEK1 gain of function variants (c.199G>A, p.Asp67Asn; c.169A>G, p.Lys57Glu), thus confirming the rarity of these specific genetic alterations in CRC. Importantly, both variants were found in patients with left-sided CRC.

Table 1

Frequency of MAP2K1, FBXW7, and NF1 mutations in CRC and correlation with sidedness based on cBioPortal database.

	Unselected CRC			KRAS/NRAS/BRAF Wild-Type CRC
Genes	All	Left-Sided	Right-Sided	All	Left-Sided	Right-Sided
MAP2K1	1.7% (61/3473)	1.1% (10/878)	3.1% (13/416)	2.7% (27/1011)	1.6% (8/497)	6% (7/117)
NF1	4.9% (169/3473)	3.9% (34/878)	7.2% (30/416)	5% (51/1011)	4.2% (21/497)	7.7% (9/117)
FBXW7	12.5% (433/3473)	13.3% (117/878)	15.6% (65/416)	8.5% (86/1011)	10.3% (51/497)	10.3% (12/117)

Alterations in NF-1 are described in 4.9% of CRC (Table 1) and do not correlate with survival, based on cBioPortal data. The frequency of these mutations is higher in right-sided tumors, without any significant difference between unselected CRC and KRAS/NRAS/BRAF wt carcinomas (Table 1).

Finally, we interrogated the cBioPortal database for the frequency of FBXW7 variants in CRC. Mutations in this gene are described in 12.5% of CRC patients and do not show correlation with survival. The frequency of FBXW7 variants is slightly higher in right-sided tumors (Table 1). These mutations also showed a slightly lower frequency in tumors that did not carry mutations in KRAS, NRAS, and BRAF genes (Table 1).

3. Discussion

Despite treatment with anti-EGFR MoAbs significantly improves the outcome of KRAS/NRAS/BRAF wt mCRC patients, additional mechanisms of resistance might limit their activity. In this respect, several previous reports hypothesized that different genetic alterations might play a role in the de novo resistance to anti-EGFR agents [7,9,10]. However, this study is the first to address this question in patients treated with first-line anti-EGFR MoAbs within a prospective clinical study. Although we could analyze a limited number of patients for which tumor samples were available, we identified variants in several genes that might be potentially involved in the resistance to anti-EGFR agents.

Among patients with the shorter PFS, we detected variants in genes that have been already associated with resistance to anti-EGFR MoAbs in CRC, such as KRAS, MAP2K1, and FBXW7, as well as in the new candidate gene NF1. We must acknowledge that the lack of a control arm prevents from the possibility to define whether these variants are predictive or prognostic. However, the mutations that we identified are mechanistically linked to EGFR-signaling, suggesting that they are good candidates as possible drivers of resistance to anti-EGFR agents. In addition, data from public database suggest that FBXW7 and NF1 mutations are not associated with worse prognosis in CRC.

We found that a patient with KRAS p.Gln61 mutation at a very low allelic frequency in the tumor tissue and a liquid biopsy positive for the same KRAS variant had a quite short PFS. Sub-clonal KRAS mutations have been reported to occur in CRC [20,21]. KRAS variants at low allelic frequency are unlikely to determine resistance to anti-EGFR MoAbs in mCRC patients [22]. However, we and other groups described that some RAS wt mCRC patients with clinical resistance to anti-EGFR agents had a liquid biopsy positive for KRAS mutations and carried the same variant at very low allelic frequency in the primary tumor [13,23]. Liquid biopsy is not expected to be positive for mutations present at very low allelic frequency in the tumor tissue due to the limit of sensitivity of this technique [24]. Therefore, we hypothesize that minor tumor clones carrying KRAS variants might be enriched during tumor progression in the metastatic sites, thus determining resistance to anti-EGFR MoAbs and positivity of liquid biopsy. These findings suggest that analysis of tumor tissue and liquid biopsy can provide complementary information on sensitivity to anti-EGFR agents in patients with metastatic disease.

Mutations in p.Lys57 of MEK1 have been previously found to be associated with de novo and acquired resistance to anti-EGFR agents [11,14]. Mechanistically, these variants lead to constitutive activation of MEK1 and increased downstream signaling. Although mutations in this site are quite rare in CRC, their identification might lead to a better identification of patients with primary resistance to anti-EGFR MoAbs. In addition, combinations of anti-EGFR MoAbs, BRAF, and MEK inhibitors, that are highly active in patients with BRAF mutations, might be effective also in patients carrying MAP2K1 activating variants [25].

The role of FBXW7 in the resistance to anti-EGFR MoAbs is more controversial. FBXW7 is a tumor suppressor gene that encodes the substrate recognition component of SKP1–Cullin1–F-box protein ubiquitin E3 ligase complexes, which in turn negatively regulate the intracellular abundance of several key oncogenic proteins [26]. In particular, its loss of function leads to increased levels of total and activated mTOR. Variants in FBXW7 have been described in 6% to 10% of CRC [27,28]. In patients with mCRC, FBXW7 missense mutations are associated with PIK3CA mutations and with a shorter overall survival (OS) [28]. By using gene expression data, loss of FBXW7 was also correlated with a gene expression profile of RAS activation and resistance to anti-EGFR MoAbs in CRC [29]. In agreement with these data, FBXW7 variants were identified in cases with resistance to anti-EGFR MoAbs in a retrospective study of 67 mCRC patients treated with different anti-EGFR MoAbs and chemotherapy regimens [30]. Interestingly, in this study the majority of the FBXW7 mutations correlating with patients’ outcome were in the WD40 domain, which is involved in FBXW7 binding to its substrates [16]. All the FBXW7 mutations identified in our study occurred in the WD40 domain. A FBXW7 variant was found in our study in a patient with a good response to cetuximab-based therapy. The tumor of this patient carried also an amplification of GAS6, whose elevated expression has been previously associated with a favorable prognosis in CRC [31]. These findings suggest that the complexity of the genetic landscape of CRC rather than the single alteration might affect the outcome of CRC patients and their sensitivity to anti-EGFR agents.

Our data also point out to NF1 variants as a possible new biomarker of resistance to EGFR MoAbs. NF1 mutations are reported in 4.9% of KRAS/NRAS/BRAF wt CRC in the cBioPortal database (Table 1). Interestingly, both variants identified in our study have not been previously described, underlying the need to use technologies that cover the full-length gene for the analysis of NF1 mutations. In a recent study of cetuximab-based therapy in a small cohort of Chinese mCRC patients (n. 33), the presence of NF1 mutations was associated with the shortest PFS [32]. Importantly, reduced NF1 expression has been also demonstrated to confer resistance to EGFR inhibition in lung cancer [33]. Collectively, these preliminary observations suggest the possible role of NF1 in the resistance to anti-EGFR MoAbs in mCRC.

We observed that a patient with ERBB2 copy number gain had a very good response to first line cetuximab-based therapy. This observation contrasts with findings suggesting a role of ERBB2 gene amplification in the resistance to anti-EGFR MoAbs in patients with mCRC [34,35]. However, these studies assessed the correlation between ERBB2 amplification and sensitivity to anti-EGFR MoAbs in patients receiving these drugs exclusively as second- or third-line treatment. Previous studies have shown activity of anti-EGFR agents in CRC patients with partial ERBB2 amplification [36]. In addition, a recent editorial highlighted a good PFS in selected patients with ERBB2 amplified tumors in the HERACLES trial [37]. Although our data deriving from a single patient cannot be generalized, our observation highlights the relevance to assess biomarkers in the first-line setting before making conclusions on their predictive role.

In 4 out of 10 tumors from patients with shorter PFS we were not able to detect genetic alterations that might be associated with resistance to anti-EGFR agents. A whole exome sequencing approach might be able to discover genetic alterations that are not covered by targeting sequencing panels. However, more complex mechanisms involving the interaction of CRC cells with tumor microenvironment might also play a relevant role in determining the sensitivity/resistance of CRC to anti-EGFR MoAbs [38].

Recent findings suggest that anti-EGFR MoAbs are highly active in patients with left-sided tumors, whereas they have little activity in right-sided tumors [6]. In agreement with this hypothesis, two out of three patients with right-sided tumors included in this analysis had a short PFS. Importantly, the possible mechanisms of resistance that we identified in this study were found in patients with left-sided tumors, who are usually treated with anti-EGFR agents in the clinical practice. Therefore, these biomarkers might help to define better the population of patients with high sensitivity to EGFR blockade.

Finally, patients with longer PFS in our series carried more CNVs as compared with patients with shorter PFS. This might be due to the different genetic background of these tumors. In fact, CNVs are more frequent in tumors related to the chromosomal instability pathway that have been suggested to be more sensitive to anti-EGFR agents [39].

4. Materials and Methods

4.1. Patients

The CAPRI-GOIM clinical trial is a nonprofit academic, open-label, multicenter study carried out by the GOIM cooperative group (EudraCT number: 2009-014041-81). Patients with KRAS exon 2 wild-type mCRC, as assessed by local pathology laboratories, received first-line treatment with FOLFIRI plus cetuximab until progression or unacceptable toxicity or patient refusal. After progression, patients were randomized (1:1) to receive FOLFOX or FOLFOX plus cetuximab as second line therapy [12,21]. The primary end point was PFS. Secondary end points included overall response rate (ORR), defined as the proportion of patients with confirmed complete responses (CR) plus partial responses (PR), and overall survival (OS). Responses were evaluated by local radiologist in each participating center according to RECIST criteria. Inclusion criteria were: age of 18 years or older, histologically confirmed adenocarcinoma of the colon or rectum, first occurrence of metastatic disease, Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1, and adequate hematologic, hepatic, and renal function. Exclusion criteria were: previous exposure to an anti-EGFR therapy or to irinotecan-based chemotherapy, previous chemotherapy for metastatic colorectal cancer, or any investigational drug in the 30-day period before the start of treatment in the study. In the first-line treatment, about 600 patients were screened for KRAS mutations to identify 340 eligible patients. Patients were evaluated every 8 weeks to assess the response to treatment. The protocol was approved by the Ethical Committee of the Istituto Tumori Giovanni Paolo II Bari on July 23, 2009 (N. 303) and it was next approved in each center by local independent Ethics Committee.

The CAPRI-GOIM clinical trial is a nonprofit academic, open-label, multicenter study carried out by the GOIM cooperative group (EudraCT number: 2009-014041-81). Patients with KRAS exon 2 wild-type mCRC, as assessed by local pathology laboratories, received first-line treatment with FOLFIRI plus cetuximab until progression or unacceptable toxicity or patient refusal. After progression, patients were randomized (1:1) to receive FOLFOX or FOLFOX plus cetuximab as second line therapy [12,21]. The primary end point was PFS. Secondary end points included overall response rate (ORR), defined as the proportion of patients with confirmed complete responses (CR) plus partial responses (PR), and overall survival (OS). Responses were evaluated by local radiologist in each participating center according to RECIST criteria. Inclusion criteria were: age of 18 years or older, histologically confirmed adenocarcinoma of the colon or rectum, first occurrence of metastatic disease, Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1, and adequate hematologic, hepatic, and renal function. Exclusion criteria were: previous exposure to an anti-EGFR therapy or to irinotecan-based chemotherapy, previous chemotherapy for metastatic colorectal cancer, or any investigational drug in the 30-day period before the start of treatment in the study. In the first-line treatment, about 600 patients were screened for KRAS mutations to identify 340 eligible patients. Patients were evaluated every 8 weeks to assess the response to treatment. The protocol was approved by the Ethical Committee of the Istituto Tumori Giovanni Paolo II Bari on July 23, 2009 (N. 303) and it was next approved in each center by local independent Ethics Committee.

Baseline CRC tumor samples (182/340, 53.5%) were retrospectively analyzed with a targeted sequencing panel covering hotspot mutations in 22 genes [12]. Tumor tissue for further genetic analysis was available for 21 KRAS/NRAS/BRAF/PIK3CA wt mCRC patients.

4.2. Targeted Sequencing

Formalin-fixed, paraffin-embedded (FFPE) tumor samples were obtained before first-line treatment with cetuximab-based therapy. Tumor tissues were analyzed with the Oncomine Comprehensive Assay v1 (Thermo Fisher Scientific, Milan, Italy) using the Ion Torrent semiconductor sequencing. Libraries were prepared starting from 10 ng of genomic DNA or RNA according to the manufacturer’s instructions. For each sample the DNA and RNA libraries were combined and clonally amplified on Ion sphere particles (ISPs) by emulsion PCR performed on the Ion One Touch 2 instrument with the Ion PGM template OT2 200 Kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. Then, ISPs were enriched, loaded on an Ion 318 chip and sequenced on a PGM sequencer with the Ion PGM sequencing 200 kit v2 according to the manufacturer’s instructions. The raw data were analyzed using the Torrent Suite Software v5.0 (Thermo Fisher Scientific). Mutations were detected using the Ion Reporter Software v5.0 with low stringency settings. Each mutation was verified in the Integrative genome viewer (IGV) from the Broad Institute (http://www.broadinstitute.org/igv/). All genetic variants were confirmed by Sanger sequencing or Droplet Digital PCR. The QX200 Droplet Digital PCR (ddPCR) System (Bio-Rad, Milan, Italy) was used to perform digital PCR and data were analyzed using the QuantaSoft analytical software v1.7.4 (Bio-Rad, Milan, Italy).

5. Conclusions

Our data suggest that a wide genetic profiling of KRAS/NRAS/BRAF/PIK3CA wt mCRC patients might improve the ability to select patients who are highly sensitive to anti-EGFR MoAbs and provide the rationale for the development of therapeutic approaches with agents targeting different signaling pathways, alone or in combination with anti-EGFR drugs. Further studies are required to confirm the role of the identified genetic alterations as biomarkers predictive of response to anti-EGFR MoAbs.