SMAD4 and NF1 mutations as potential biomarkers for poor prognosis to cetuximab-based therapy in Chinese metastatic colorectal cancer patients

Background Cetuximab, an anti-EGFR monoclonal antibody, is used in combination with chemotherapy in clinic to enhance the outcome in metastatic colorectal cancer (mCRC) patients with only ~ 20% response rate. To date only activating mutations in KRAS and NRAS have been identified as poor prognosis biomarkers in cetuximab-based treatment, which makes an urgent need for identification of novel prognosis biomarkers to precisely predict patients’ response in order to maximize the benefit. Methods In this study, we analysed the mutation profiles of 33 Chinese mCRC patients using comprehensive next-generation sequencing (NGS) targeting 416 cancer-relevant genes before cetuximab treatment. Upon receiving cetuximab-based therapy, patients were evaluated for drug response, and the progression-free survival (PFS) was monitored. The association of specific genetic alterations and cetuximab efficacy was analyzed. Results Patients carrying SMAD4 mutations (SMAD4mut, n = 8) or NF1 mutations (NF1mut, n = 4) had significantly shorter PFS comparing to those carrying wildtype SMAD4 (SMAD4wt, n = 25) (P = 0.0081) or wildtype NF1 (NF1wt, n = 29) (P = 0.0028), respectively. None of the SMAD4mut or NF1mut patients showed response to cetuximab when assessed at 12-week post-treatment. Interestingly, two patients carrying both SMAD4mut and NF1mut showed the shortest PFS among all the patients. Conclusions Our results demonstrated that SMAD4 and NF1 mutations can serve as potential biomarkers for poor prognosis to cetuximab-based therapy in Chinese mCRC patients. Electronic supplementary material The online version of this article (10.1186/s12885-018-4298-5) contains supplementary material, which is available to authorized users.


Background
Colorectal cancer (CRC) represents a major public health issue due to its high incidence and mortality rate. In China, it is the fifth most common cancer in 2015 and causes~191,000 deaths annually [1]. Comparing to other malignant tumors, CRC has a higher intra-tumoral heterogeneity and harbours higher tumor mutation burden [2,3]. Common driver genes for CRC include TP53, APC, KRAS, NRAS, PIK3CA, and SMAD4, etc. [4,5].
Current treatment of unresectable metastatic CRC (mCRC) in advanced stage mainly relies on fluoropyrimidine-based chemotherapies alone or in combination with Bevacizumab according to the National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology (NCCN Guidelines) in Colon Cancer [6,7]. The efficacy of chemotherapy could be further increased via the addition of cetuximab or panitumumab, which are humanized monoclonal antibodies that target the extracellular ligand binding domain of the epidermal growth factor receptor (EGFR) [8,9]. However, only~20% of patients benefit from the cetuximab-based therapy [10]. To date, prognostic biomarkers for cetuximab treatment is limited to the activating mutations of KRAS and NRAS, which have been approved for poor response to cetuximab [11][12][13]. Other potential biomarkers, including mutations in BRAF (V600E), PIK3CA, SMAD4, PTEN, etc., have also been reported, albeit requiring further validation [14][15][16][17]. However, all the aforementioned biomarkers could not adequately explain the poor response rate, and thus limits patients to get maximal benefit from cetuximabbased therapy.
The aim of this study was to seek better prognosis biomarkers for cetuximab-based therapy via a comprehensive analysis of the mCRC patients' mutation profiles using next-generation sequencing (NGS) targeting 416 cancer-relevant genes. In combination with their response to cetuximab treatment, our data show that patients carrying at least one of SMAD4 or NF1 mutations had a higher possibility of a poor response to EGFR blockade with a shorter progression-free survival (PFS), suggesting that SMAD4 and NF1 mutations may play an important role in tumor progression and might function as biomarkers for poor prognosis to cetuximab-based therapy in mCRC patients.

Patients
This study was approved by the ethic committee of the First Affiliated Hospital with Nanjing Medical University. From 2009 to Nov 2015, tumor specimens or plasma samples were collected at the time of diagnosis from 33 Chinese patients with mCRC with written informed consents. All patients received at least one course of cetuximab treatment in combined with FOL-FIRI, FOLFOX or XELOX until progressive disease (PD) was observed. Disease progression was evaluated every 6 weeks during treatment according to the Response Evaluation Criteria In Solid Tumors (RECIST) version 1. 1 [18]. PFS was calculated from the first day of the administration of cetuximab-based therapy until PD. According to the Guidance for Industry Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics, partial response (PR) and complete response (CR) are considered as response to the treatment applied [19].

Clinical sample collection and DNA extraction
Specimen collection and preparation were performed following the standard protocols approved by the First Affiliated Hospital with Nanjing Medical University, China. A minimum of 20% tumor content was required for formalin-fixed paraffin-embedded (FFPE) specimens, from which genomic DNA was extracted using QIAamp DNA FFPE Tissue Kit (QIAGEN) following the manufacturer's instructions. Plasma was extracted from 5 to 10 ml peripheral blood collected in EDTA-coated tubes within 2 h from the blood withdrawn. Circulating tumor DNA (ctDNA) was extracted from the plasma using QIAamp Circulating Nucleic Acid Kit (QIAGEN). Genomic DNA of the whole blood was extracted with DNeasy Blood & Tissue Kit (QIAGEN) as germline control. The DNA quantity was measured on Qubit 3.0 with dsDNA HS Assay Kit (Life Technologies).

Library preparation and sequencing
Sequencing libraries were prepared with KAPA Hyper Prep Kit (KAPA Biosystems) as per manufacturer's instructions with optimized protocols as previously described [20]. Briefly, fragmented DNA was subjected to end-repairing, A-tailing, indexed-adapter ligation, size selection, and PCR amplification. For targeted enrichment, indexed DNA libraries were pooled together for hybridization with customized xGen lockdown probes (Integrated DNA Technologies) for 416 predefined cancer-relevant genes. Enriched libraries were amplified and subjected for NGS on Illumina Hiseq4000 platforms (Illumina) to a targeted mean coverage depth of 500× for FFPE samples or 3000× for ctDNA samples.

Data processing
After demultiplexing, FASTQ files were processed with Trimmomatic [21] for quality control. Reads were then mapped to human reference genome 19 (hg19) using Burrows-Wheeler Aligner (BWA) [22]. Local realignment and base quality score recalibration were conducted with Genome Analysis Toolkit (GATK) [23]. Mapping rate for each sample is over 99.5% with 82% on-target rate and 99.2% of uniformity (percentage of bases over 0.2× mean coverage depth). SNV and indel mutation calling was performed using VarScan (https:// dkoboldt.github.io/varscan) (< 10% minor allele frequency [MAF]) and GATK (> 10% MAF). Identified Mutations were first filtered with dbSNP and 1000 Genome data sets to remove common SNPs. Mutations identified within the whole blood controls were subtracted to exclude germline mutations where applicable. Structural variants were detected using FACTERA with default parameters [24]. ADTEx (https://adtex.sourceforge.net) was used to identify copy number variations (CNVs) with default parameters. All the genetic alterations identified were manually reviewed on Integrative Genomics Viewer (IGV) software for curation [25].

Statistical analysis
Cox proportional hazards model was applied to assess if patients' baseline characteristics show significant association to the PFS. To each gene where applicable, Wilcoxon ranked sum test was applied to compare the PFS of patients with or without mutations in the specified gene. Gehan-Breslow-Wilcoxon method was used to further assess the PFS curves of different patient groups based on their genotype. P value less than 0.05 was considered statistically significant.

Mutation profiling in Chinese mCRC patients
All patients enrolled in this study were pre-screened as KRAS G12 and G13 mutation-negative using amplification-refractory mutation system (ARMS) [26] analysis based on the NCCN guideline that patients with mutations in KRAS are not suggested for cetuximab-based therapy [6]. The clinical information of the 33 Chinese mCRC patients enrolled in this study was summarized in Table 1 and the detailed clinical characteristics of each patient were listed in Additional file 1: Table S1. Precetuximab-based treatment, tumor samples from 31 patients and plasma samples from 2 patients (Patient 4 and Patient 33) were analyzed using NGS targeting 416 cancer-relevant genes [20]. All patients received at least one course of cetuximab-based therapy until PD was observed. Drug response was evaluated at week 12 posttreatment, and PFS was calculated from the first day of the treatment until PD (Fig. 1). Other than the ECOG score (P = 0.007), no baseline characteristics are correlated to PFS according to Cox proportional hazards model (Table 1).
To further identify potential prognosis biomarkers for cetuximab-based therapy, we performed Wilcoxon ranked sum test [27] by comparing the PFS of patients divided by the mutation status in a specific gene. Of the 21 top mutated genes in Fig. 1, significant difference of PFS from the mutated group and the corresponding wildtype group was discovered to be caused by two genes, SMAD4 (P = 0.026) and NF1 (P = 0.034) (Additional file 4: Table S3). The median PFS in the SMAD4 mutated (SMAD4 mut ) or NF1 mutated (NF1 mut ) subsets was 90 days and 53.5 days compared to the 250 days and 211 days in the corresponding wildtype group, respectively ( Table 2). Of note, two patients carrying both SMAD4 and NF1 mutations had the shortest PFS in our data set (12 and 37 days, respectively, Fig. 1). Furthermore, significance was also found in PFS curves between SMAD4 mut and SMAD4 wt groups (P = 0.0081) (Fig. 2a), and that of NF1 mut and NF1 wt groups (P = 0.0028) (Fig. 2b). In addition, when combining patients carrying mutated SMAD4 and/or NF1 (SMAD4 mut or NF1 mut ), the difference was still significant comparing to patients carrying both wildtype SMAD4 and NF1 (SMAD4 wt and NF1 wt ) (P = 0.0063) (Fig. 2c), suggesting that at least one mutated SMAD4 or NF1 could serve as potential biomarker to predict poor cetuximab prognosis. Furthermore, according to the drug response evaluation at week 12 post-ceuximabbased treatment, all the SMAD4 mut or NF1 mut patients showed PD or stable disease (SD), which is considered as no response according to the Guidance for Industry Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics (Fig. 1) [19]. However, no difference in PFS was observed in the KRAS mut group comparing to the KRAS wt group in this study (Additional file 3: Figure S1). Of note, the two patients with KRAS amplification showed a trend of shorter PFS (53 days and 99 days, respectively) with no response to EGFR blockade, in accordance with the results described by a previous study [28].
In summary, analysis of the mutation profiles in the 33 mCRC patients in combination with the efficacy of their cetuximab-based therapy demonstrated that SMAD4 or NF1 mutations are promising potential biomarkers for cetuximab-based therapy in Chinese mCRC patients.

Discussion
In this study, we analyzed the mutation landscape of 33 Chinese mCRC specimens using NGS targeting 416 cancer-relevant genes. Most frequently mutated genes are TP53 (75.8%), APC (54.5%), SMAD4 (24.2%), and PIK3CA (18.2%). In comparison with data from TCGA [4], TP53 was mutated more frequently in the Chinese mCRC patients, while the mutation frequency of FBXW7 was much lower. Furthermore, we have identified SMAD4 and NF1 as candidates for potential prognosis biomarkers for cetuximab-based therapy, as patients carrying mutated SMAD4 and/or NF1 genes had significantly shorter PFS than the SMAD4 wt and NF1 wt group.
SMAD4 plays an important role as a common mediator in the transcriptional regulator complex in the TGF-β pathway [29], which is a bypass signaling pathway of EGFR-mediated signaling pathway for cell proliferation, differentiation and survival. It has been shown that loss of SMAD4 expression is associated to poor overall survival and poor prognosis of chemotherapy in CRC patients [30,31]. Furthermore, studies of SMAD4 as potential biomarkers for cetuximab prognosis have been reported previously, although insufficient and controversial. Two groups conclude that alterations in SMAD4 are associated with a poor cetuximab prognosis [17,32], while another study made the opposite conclusion that SMAD4 is a biomarker for superior cetuximab prognosis [33]. Our results are in agreement with the former two studies that SMAD4 is likely correlated to primary resistance to anti-EGFR therapy.
NF1 encodes neurofibromin 1, which functions as a negative regulator of the RAS signaling pathway downstream of EGFR [34]. To our knowledge, our study is the first report of NF1 as a biomarker for the prognosis of cetuximab-based therapy in mCRC. It is likely that deregulation of the TGF-β and RAS pathways due to mutations in SMAD4 and NF1 results in primary resistance to anti-EGFR blockade, possibly via the activation of the bypass or downstream signalling pathways of EGFR.
Although these patients were screened as KRAS G12 and G13 mutation-negative by ARMS method, we identified 9 out of 33 patients with KRAS alterations using NGS. By comparing the KRAS mut and KRAS wt patients, no difference was seen in PFS curves (P = 0.2826), which is not consistent with the current treatment guideline that patients carrying KRAS mutations, especially exon 2 mutations, present primary-resistance to anti-EGFR blockade [6]. The reason for the inconsistency might be due to the relative smaller sample size in this study. In addition, it has been reported in several studies that patients harbouring KRAS G13D mutation, comparing to other exon 2 mutations, might benefit from cetuximabbased therapy [35][36][37]. Mutations in other exons have different effects on cetuximab efficacy. Studies show that KRAS Q61 mutation has adverse effect on cetuximab prognosis while A146 seems to have little effect [16]. In our patient cohort, the KRAS mutations were evenly distributed in three exons at 6 spots (Additional file 3: Figure S1) after pre-screening for KRAS exon 2 mutation-negative, which might put bias on patient selection and thus makes the difference of PFS curves of KRAS mut and KRAS wt not significant.

Conclusion
In this study, we have depicted pan-cancer mutation profiles from 33 Chinese mCRC patients. We further identified SMAD4 and NF1 mutations as potential biomarkers for poor prognosis of cetuximab-based therapy, which needs to be further validated in a larger patient cohort.

Additional files
Additional file 1: Table S1. Clinical characteristics of the 33 Chinese mCRC patients enrolled in this study. (XLSX 12 kb) Additional file 2: Table S2. Genetic alterations detected in targeted NGS with a 416 pan-cancer gene panel from the 33 Chinese mCRC patients. (XLSX 53 kb) Additional file 3: Figure S1. Prognosis of cetuximab-based treatment between KRAS mut and KRAS wt patients. A. Mutation site and type of the 9 KRAS mutations or genetic alterations detected in this study associated with PFS and drug response to cetuximab-based therapy. KRAS wt indicates the median PFS of wildtype KRAS patients (230.5 days). The minor allele frequency (MAF) of each KRAS mutation is displayed in red. Availability of data and materials Raw NGS data cannot be made publicly available for patients' confidentiality.
Authors' contributions ZM, YWS, YS, ZF, and YG made substantial contributions to the concept and design of the study; ZM, PL, XC, BW, YX, DZ, YS, ZF and YG were involved in the acquisition of patients' sample, clinical information and patient follow-up; YD and XM performed the NGS testing; ZM, YWS, YD, XM, XW made substantial contributions to the data analysis and interpretation; ZM, YWS, and YG drafted the manuscript. All authors read and approved the final manuscript to be published.
Ethics approval and consent to participate This study was approved by the ethic committee of the First Affiliated Hospital with Nanjing Medical University. All the patients enrolled in this study have provided written informed consents for specimen collection, genetic testing, and participation in the research anonymously.

Consent for publication
Not applicable.
Competing interests Yang W. Shao, Yan Ding, Xiangyuan Ma, and Xue Wu are the shareholders or employees of Geneseeq Technology Inc.; Yewei Xia, and Dongqin Zhu are the employee of Nanjing Geneseeq Technology Inc..