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The BRAF mutant colorectal cancer subgroup is a small population with unique clinicopathological and molecular features. This subgroup has been associated with particularly poor prognosis and advanced disease. The poor response of these patients to available treatments has driven much of the effort in trialling combination targeted treatments involving BRAF and MEK inhibitors. Most recently, an observed survival benefit with intensive triplet chemotherapy agents would encourage its use as first-line treatment in suitable candidates given that few of these patients proceed to second- or third-line treatments.


Introduction
The BRAF mutant (MT) colorectal cancer (CRC) population is a small and unique subgroup noted for its association with poor prognosis and survival. BRAF mutation occurs in approximately 10% (range, 5-22%) [1,2] of the unselected CRC population and consistently has inferior median survival outcomes ranging from 8 to 14 months [3,4]. Failure to achieve good survival outcomes through standard doublet chemotherapy agents in this population has ignited efforts to combine multiple target therapies, aiming for breakthroughs. In this chapter, the BRAF gene and its signalling pathway are explored in detail. BRAF gene mutation frequency and its impact on clinical presentation as well as its prognostic and predictive significance are also discussed. Updates on the current and latest management strategies as well as novel investigational treatments in this subgroup are also presented.

BRAF and the RAS/RAF/MEK/ERK signalling pathway
V-raf murine sarcoma viral oncogene homologue (RAF) is one of the most intensively researched mammalian effectors of RAS in the RAS/RAF/MEK/ERK signalling pathway (Figure 1) [5,6]. The RAF protein itself is made up of three conserved regions: CR1, CR2, and CR3. CR1 and CR2 are situated in the N terminus. CR1 acts as the main binding domain for RAS. CR2 is the regulatory domain. CR3 is situated at the C terminus and functions as the catalytic kinase domain [7].
When GTP bound, RAS recruits RAF protein to the cell membrane and binds to it. This binding process activates RAF kinase by the phosphorylation of two amino acids (T599 and S602 of BRAF) situated in the activation segment of the kinase domain. RAF then phosphorylates its downstream effectors MEK1, MEK2, ERK1, and ERK2, leading to the activation of cellular proliferation, differentiation, and transcriptional regulation (Figure 1) [7]. B-RAF (BRAF) together with A-RAF and C-RAF are the members of the RAF kinase family [8]. These three RAF isoforms are homologous in sequence and substrate specificity but do differ in their biological functions and regulations. Of these, BRAF remains the most potent activator of MEK [9].
The BRAF gene is a proto-oncogene located on chromosome arm 7q34, composed of 18 exons. There are more than 30 different BRAF mutations [10]. The most common activating mutation, BRAF V600E (p.Val600Glu/c.1799T>A), accounts for 90% of all activating BRAF mutations and is found in exon 15 at nucleotide position 1799 [11]. The thymine-to-adenine transversion within codon 600 leads to the substitution of valine by glutamate at the amino acid level. This mutation occurs in the activating segment of the kinase domain, resulting in increased basal kinase activity. Compared to wild-type (WT) BRAF, BRAF V600E demonstrates an almost 500fold increase in endogenous kinase activity [10,12].

BRAF mutation detection methods
CRC BRAF mutations can be identified using first-and second-generation direct sequencing, immunohistochemistry (IHC), and, potentially, circulating tumour cells (CTC).
Sanger sequencing is the earliest form of first-generation direct sequencing. Sanger sequencing was developed in 1975 and relies on the chain-termination sequencing of amplified DNA by polymerase chain reaction (PCR) and detection through electrophoresis. It requires approximately 18 to 19 h to process and is also 10 times less sensitive than pyrosequencing. Sanger sequencing method also cannot detect the changes in chromosomal copy number and translocations [18].
Next-generation sequencing (NGS) differs in technology using a specific reagent wash of nucleotide triphosphates with synchronised optical detection and includes pyrosequencing, allele-specific (AS) PCR, mass spectrometry, and real-time qPCR with melt-curve analysis [19]. NGS is the new gold standard test in BRAF mutation detection given its superior detection and speed.
Pyrosequencing is referred to as sequencing by synthesis and relies on the release of pyrophosphate (PPi) by DNA polymerase. The test detects light emitted when nucleotides are added to the target DNA template by DNA polymerase releasing PPi via a chemiluminescence reaction. It is a more rapid and sensitive test in detecting BRAF V600E mutations in addition to other variants such as V600D, V600K, V600R, and K601E. It can provide the percentage of DNA that harbours the BRAF V600E mutations. However, this method is limited by the length of DNA template and is prone to error readings in homopolymer sequences (TTTTTTTT) [18].
AS-PCR enriches known mutations in samples to increase the sensitivity of detection and is particularly useful in tissue with low tumour content. Mass spectrometry-based sequencing relies on the analysis of matrix-assisted laser desorption/ionisation time-of-flight (MALDI-TOF). This process is facilitated by the addition of mass-modified bases A, C, T, and G to the primed and amplified mutational hotspots. It is this flight time difference of the generated mass-modified complex that is measured by the mass spectrometer. Mass spectrometry-based sequencing is an even more sensitive test compared to pyrosequencing, with a detection ratio of 1:10 and 1:8, respectively [18].
Melt-curve analysis involves detecting the melting temperature for WT BRAF at 61°C and the V600E MT melting at 53°C. PCR methods, on the contrary, can perform as well and has advantages in terms of reduced labour (1.25 vs 16 min), faster turnaround (4 min vs 10 h), and lower cost ($2.6 vs $10.4). The sensitivity and specificity of real-time qPCR is reported to be 100% [19].  [20,21].
The IHC detection of BRAF V600E with a mutation-specific antibody (clone VE1) was first described in metastatic melanoma and papillary thyroid carcinoma and is currently commercially available [22]. The advantage of IHC lies in the minimal amount of tissue needed and the availability of this technique in most pathological laboratories. Most studies have reported high sensitivities and specificities (98.8-100%) compared to PCR-based methods or sequencing [23][24][25]. However, there is one study that has reported sensitivity and specificity of only 71% and 74%, respectively [26]. The choice of positive control tissue and the amplification protocol is regarded to be crucial in the successful detection of BRAF mutation by IHC [27].
Recently, examination of CTC in peripheral blood has been explored as a new non-invasive means for detecting BRAF mutation in CRC [28]. Blood collected from 44 patients was enriched for CTC using a size-based microsieve technology. By incorporating the high-resolution meltcurve analysis technique, the concordance rates between CTC and tumour mutations were observed to be 90.9% (p=0.174) for BRAF mutation genotype status and 84.1% (p=0.000129) for KRAS mutation genotype status.

BRAF mutation and its frequency in CRC
A meta-analysis of 10 studies reported BRAF mutations in 4.8% to 20.8% of CRC [74].   Importantly, BRAF MT CRC is reported to be mutually exclusive to KRAS mutation [36]. BRAF mutation coexists with PIK3CA mutations in 13% and PTEN mutations in 22% of CRC [37]. Figure 2

CRC tumourigenesis pathways
The two main separate pathways observed in CRC development and progression are the chromosomal instability pathway (CIN), which accounts for 75% of the cases, and the microsatellite instability (MSI) pathway in 25% of the cases. Two processes are observed to contribute towards the MSI pathway: (1) germ-line mutations from Lynch syndrome and (2) sporadic MLH1 methylation from the serrated methylated pathway (Figure 3) [38] [100]. The CIN pathway involves a defect in replication, mitosis, or DNA repair leading to genetic abnormalities, both structural and numeric, which are acquired sequentially. As a result, oncogenes are activated or tumour suppressor gene function is lost, which contributes towards malignant growth. This pathway is also often associated with aneuploidy by karyotyping. The genetic changes found in CRC arising via the CIN pathway include APC mutations (90%), KRAS mutation (50%), TP53 mutations (70%), and allelic loss of 18q (80%) [39]. The CIN pathway has been traditionally associated with CRC arising in adenomatous polyps.
The MSI pathway is a result of defective mismatch repair (MMR) and occurs in a subset of CRC that arise from either adenomas or serrated polyps. It contributes towards tumour progression via the accumulation of tiny insertions and deletions in the repetitive sequences of microsatellites in coding genes, thereby retaining a near-diploid karyotype. This mechanism of tumourigenesis is readily recognized through a test for MSI, which categorises each tumour as MSI-high (MSI-H), MSI-low (MSI-L), or microsatellite stable (MSS), based on the proportion of microsatellites mutated. MSI-H cases usually imply an acquired or inherited defect in DNA repair.
In inherited cases of MSI-H CRC, germ-line mutation in one of the four genes that encode proteins responsible for MMR (MLH1, MSH2, PMS2, and MSH6) is responsible for a familial predisposition to cancer. This familial predisposition to CRC is known as Lynch syndrome [40], and the CRC that arise in this condition develop in adenomas.
In sporadic cases of MSI-H CRC, the serrated methylated pathway is increasingly implicated. Serrated polyps, not driven by CIN but by BRAF mutations, are observed to replace adenomas as precursor lesions in CRC. MSI-H CRC occur due to the epigenetic inactivation of MLH1 by promoter methylation, which prevents MLH1 protein expression, resulting in defective MMR and producing MSI. This pathway is also closely associated with the widespread methylation of CpG islands, causing the transcriptional silencing of tumour suppressor genes, known as the CpG island methylator phenotype (CIMP) [38,39].

BRAF testing to distinguish between sporadic versus germ-line MSI-H cases (Lynch syndrome)
Approximately 12% of MSI-H cases are sporadic in nature and BRAF mutation is implicated in nearly all (91%) of these cases [41,42]. The methylation of MLH1 is found only in 1.6% of germ-line Lynch syndrome cases [43], whereas it is typically found in sporadic tumour lacking MLH1 expression [44]. Hence, BRAF mutation testing is recommended in MSI-H CRC as a triage for Lynch syndrome. Only those lacking the BRAF mutation proceed with further workup for Lynch syndrome, as CRC harbouring the BRAF mutation are, with few exceptions, unlikely to have this condition.
MLH1 methylation testing is an alternative assay to distinguish sporadic from familial cases of CRC. However, given that methylation testing is more technically challenging than BRAF mutation testing, most would advocate BRAF testing as the more cost-effective assay to distinguish sporadic from familial MSI-H CRC [44].

Clinicopathological and molecular features of BRAF MT CRC
BRAF mutation has been reported in multiple studies to be associated with several clinicopathological parameters in CRC patients. BRAF V600E mutation is reported to increase from 10% in unselected patients to 37% in females ages >70 years [45]. BRAF mutations in the Western population tend to be more common in females and to have a more proximal location in the colorectum [27,[46][47][48][49][50][51][52]. BRAF mutations are rarely found in the left-sided colon (4%) and rectal cancers (2%) compared to the right-sided colon (22%; p<0.0001) [53]. BRAF mutation also varies by pathology. Approximately 60% of BRAF MT tumours are poorly differentiated and only up to 36% of them are well to moderately differentiated. Mucinous cancers tend to have a higher rate of BRAF mutation (22-67%) compared to non-mucinous cancers (6-21%) [39,54,55].
The relationship between BRAF mutation and these clinicopathological features was confirmed in a meta-analysis reported in 2014 [36]. Twenty-five studies of 11,955 CRC patients were included in this analysis. The mutation rate was seen to vary with the highest reported at 21.8% [2], the lowest being 5.0% [1], and the overall rate being 10 Another study [56] reported a significantly increased rate of peritoneal (46% vs 24%; p<0.001) and distant lymph node metastases (53% vs 38%; p=0.001) and a lower rate of lung metastases (35% vs 49%; p=0.049) in BRAF MT CRC compared to BRAF WT tumours that might help to explain their poor prognosis.   [29]. The pooled analysis of CRYSTAL and OPUS had also reported lower median OS in the BRAF MT group compared to the BRAF WT group (9.9 vs 21.1 months in the chemotherapy arm and 14.1 vs 24.8 months in the chemotherapy in combination with cetuximab arms) [57]. In 2013, the PLoS ONE metaanalysis analysed 21 mCRC trials of 5229 patients treated with monoclonal antibodies [58]. Fourteen of these trials were retrospective; two trials were prospective and five trials were randomised-controlled trials (RCTs In accordance with their aggressive nature, BRAF MT cancers have also been reported to have poor PFS with sequential systemic treatments. A retrospective study on 1567 patients detected a BRAF mutation rate of 8%. These BRAF MT patients had received a median of two later lines of chemotherapy, with the median PFS for the first three lines of chemotherapy being 6.3, 2.5, and 2.6 months, respectively [68]. Another smaller study had reported even shorter median PFS (4.3 months) after first-line treatment in BRAF MT [69]. This observation highlights the importance of considering early intensified treatment given the propensity for these patients to not survive long enough for second-or third-line treatments.
Recently, other rare (<1%) subtypes of BRAF MT, which harbour mutations in codon 594 or 596, were reported to have markedly longer OS compared to BRAF V600E MT (median OS=62.0 vs 12.6 months; HR=0.36; 95% CI=0.20-0.64; p=0.002). These subtypes are noted to be MSS and also differ in other molecular and clinical characteristics, being more frequently rectal in origin, non-mucinous, and with no peritoneal spread [70].

Predictive role
Given that RAS MT are negative predictors of anti-epidermal growth factor receptor (EGFR) therapies, the predictive role of BRAF MT for anti-EGFR agents has been of interest given the relationship with RAS in the EGFR/RAS/RAF/MEK/ERK pathway. BRAF MT and its associated resistance to anti-EGFR agents have been suggested by several retrospective analyses [71][72][73].
To date, the predictive role of BRAF MT on anti-EGFR agents remains unclear, in light of differing conclusions from two separate meta-analyses [74,75]. Pietrantonio et al. concluded that BRAF MT might be a negative predictor for anti-EGFR agents, supporting the metaanalysis by Yuan et al. [58]. This study included a pooled analysis of nine phase III trials and one phase II trial and shown that cetuximab-or panitumumab-based therapy did not increase the benefit of standard treatment versus best supportive care in RAS-WT/BRAF-MT CRC patients. Overall, the addition of cetuximab or panitumumab did not significantly improve the PFS (HR=0.88; p=0.33), OS (HR=0.91; p=0.63), and overall response rate [ORR; relative risk (RR)=1. 31; p=0.25] in this subgroup population [74]. However, another recent meta-analysis reviewed seven RCTs for OS and eight RCTs for PFS and concluded on insufficient evidence to justify the exclusion of anti-EGFR agents in the BRAF MT population [75]. Nevertheless, these latest findings have supported the need for BRAF mutation assessment before the initiation of treatment to study and tailor the most effective strategies to the BRAF MT population.

Triplet chemotherapy effect
BRAF MT has not been known to be a predictor of benefit from chemotherapy or anti-vascular endothelial growth factor (VEGF) agents. The Italian TRIBE study [35] compared anti-VEGF therapy, bevacizumab added to intensified triplet chemotherapy, fluorouracil, oxaliplatin, and irinotecan (FOLFOXIRI), to standard first-line doublet chemotherapy with fluorouracil and irinotecan (FOLFIRI) plus bevacizumab in 508 unresectable mCRC patients. The study reported a higher response rate of 65% vs 53% with the triplet FOLFOXIRI and bevacizumab arm. Reassuringly, there was no increase in fatal or serious adverse events.
The updated analyses of the same study reported a BRAF mutation rate of 7.5%. In the BRAF MT group, there was a significant trend for better survival in the triplet arm compared to the doublet arm (19.1 vs 10.8 months; HR=0.55). Significantly, this is the only regimen to have resulted in a median OS of more than 15 months in the BRAF MT group compared to the more often reported median of 4.4 to 14 months in most studies [29,57]. It was proposed that intensified triplet chemotherapy (FOLFOXIRI+bevaczicumab) is considered first line in the BRAF MT group, who usually have aggressive cancers with limited ability to undergo a more sequential approach to treat metastatic disease.

Maintenance treatment
A recent meta-analysis on five RCTs had failed to demonstrate a statistically significant OS benefit (HR=0.93; 95% CI=0.85-1.02; p=0.12; I 2 =5%) with administering maintenance chemotherapy versus complete treatment interruption after first-line therapy in unselected CRC [76]. The chemotherapy free interval in the group not using maintenance treatment was 3.9 months (3.6-4.3 months). Nevertheless, the author had emphasized the importance of predictive markers to guide the selection of patients who would benefit from the maintenance strategy.
Although not formally tested in the BRAF MT subgroup population, the maintenance strategy might prove more favourable than the intermittent strategy given its known aggressive nature. This is especially relevant given that the median reported PFS in BRAF MT as indicated previously ranged from 4.3 to 6.3 months after first-line treatment [68,69].
In terms of the choice for maintenance treatment, there is no current recommended standard. However, practice trends could perhaps be extrapolated from the AIO KRK 0207 trial, which confirmed the prognostic impact of mutation status [77]. In all patients (irrespective of BRAF or RAS status), at a median follow-up of 27 months, the authors reported a time to failure of strategy of 3.6, 6.2, and 4.6 months among all patients receiving no treatment, fluoropyrimidine plus bevacizumab, or bevacizumab alone, respectively (p<0.001). However, in RAS/BRAF WT patients, bevacizumab monotherapy was as effective as combination treatment (fluoropyra-midine/bevacizumab) for maintenance. In contrast, in the RAS or BRAF MT subgroup, the combination treatment was favoured, as single-agent bevacizumab was equivalent to no maintenance at all.

BRAF/MEK inhibitors
As mentioned above, RAS proteins normally activate BRAF along with A-RAF and C-RAF [78]. BRAF mutations lead to the constitutive activation of BRAF kinase activity, resulting in phosphorylation and activation of the MEK kinases (MEK1 and MEK2). Once activated, MEK kinases phosphorylate and activate ERK kinases, which phosphorylate a multitude of cellular substrates involved in cell proliferation and survival (Figure 1).
RAF inhibitors, such as vemurafenib and dabrafenib, have produced response rates of 50 to 80% in melanomas that harbour the BRAF V600 mutations [79,80]. This is disappointingly contrasting to the response rate of only 5%, and median PFS of 2.1 months achieved in BRAF MT CRC [81]. Previous observations have proposed that RAF inhibitor insensitivity in BRAF MT CRC was driven by the feedback reactivation of the RAS/RAF/MEK/ERK signalling cascade. In many BRAF MT CRC cell lines, EGFR-mediated activation of RAS and C-RAF was observed to be the culprit [82,83]. Solit et al. had also demonstrated the critical dependency of BRAF MT colorectal cell lines and xenografts on MEK-ERK signalling, which renders them highly sensitive to pharmacological MEK inhibition. Pharmacological MEK inhibition completely abrogated tumour growth in BRAF MT xenografts, whereas RAS MT tumours were only partially inhibited [84].
Many RAF inhibitor combinations were hence evaluated in clinical trials in recent years and have shown promising results. A phase I to II clinical trial of combined RAF/MEK inhibition with dabrafenib (150 mg BD) and trametenib (2 mg OD) in 43 BRAF MT CRC resistant to anti-EGFR therapy produced partial responses in 12% and complete response in 2%. One patient achieved a durable complete response exceeding 36 months. Additionally, 56% achieved stable disease as the best confirmed response [85].

Dual and triplet targeting EGFR/BRAF/MEK inhibitors
The observations above have also led to a number of studies assessing the combined blockade at other sites in the EGFR pathway in addition to RAF/MEK inhibition. It was observed that the dual inhibition of anti-EGFR therapy in combination with RAF inhibition in resistant cell lines might still produce a lower degree of mitogen-activated protein kinase (MAPK) pathway inhibition in BRAF MT CRC compared to single-agent RAF inhibitors in BRAF MT melanoma patients. Dabrafenib and panitumumab doublet was trialled with a response rate of (partial and complete response) 2/20 (10%) and stabilised disease in 16/20 (80%) as the best overall response [86]. Another study examined the combination of vemurafenib (BRAF-inhibitor) and panitumumab in 15 patients. Two (13%) patients reported partial responses lasting 40 and 24 weeks, respectively. Eight (53%) patients stable disease lasting more than 6 months [87]. A phase II study studied dual inhibition with encorafenib (BRAF inhibitor) and cetuximab with 26 patients. Encorafenib and cetuximab doublet was reported to produce an overall RR (complete and partial) of 23.1% with a median PFS of 3.7 months. The most common treatmentrelated grade 3/4 adverse events associated with this doublet regimen were fatigue and hypophosphatemia (8% each) [88].

Acquired resistance to EGFR/RAF/MEK targeted therapies
Although trials have demonstrated early efficacies of combination targeted therapies in these BRAF MT patients, attention was brought towards their eventual treatment resistance and disease progression. A group in Harvard recently compared pretreatment and postprogression BRAF MT CRC tumour biopsies by whole exome sequencing (WES) to examine the related changes that could explain treatment resistance in these cases [89]. They have identified four possible acquired molecular mechanisms that could lead to resistance to combination treatments with RAF/MEK and RAF/EGFR. These four mechanisms include (1)  Interestingly, the group also discovered an ERK inhibitor that retained the ability to suppress MAPK signalling and overcome each of these mechanisms identified [89]. In conjunction with these findings, early-phase clinical trials are currently incorporating ERK inhibitors as potential future treatment strategies for BRAF MT CRC.

Alternative target signalling pathways
Although our increasing understanding of the complexity of the EGFR/RAF pathway has led to some advances in our understanding of possible mechanisms of resistance to BRAF inhibition, additional complex interactions with related pathways are likely to be involved, including the phosphatidylinositol 3-kinase (PI3K)/AKT pathway, mammalian target of rapamycin (mTOR), and Wnt signalling.

PI3K/AKT and mTOR pathway
The PI3K/AKT pathway is an alternative resistance mechanism to BRAF inhibition in BRAF MT CRC. Approximately 40% of CRC have been shown to have alterations in one of eight PI3K pathway genes. These mutations are almost always mutually exclusive to each other [91]. In addition, BRAF mutation co-exists with PIK3CA mutations in 13% and PTEN mutations in 22% of CRC [37]. Compared to BRAF MT melanoma cell lines, BRAF MT CRC cell lines seemed to also display a higher rate of PI3K/AKT pathway activation. These cell lines were reported to be less sensitive to the BRAF inhibitor, vemurafenib [92].
Based on the above observations, the combination triplet inhibition treatment was studied with encorafenib (BRAF inhibitor), cetuximab, and PI3K inhibitor (alpelisib) in 28 patients and reported an overall RR of 32.1% with a median PFS of 4.3 months. The most common grade 3/4 adverse events reported were hyperglycemia (11%) and increased lipase (7%) [88].
Sustained PI3K/mTOR activity was demonstrated also by Corcoran et al. [82] in BRAF MT CRC cell lines upon BRAF inhibition. Pleasingly, a potent growth-inhibitory effect was recently observed in xenografts of BRAF MT CRC with the combined BRAF/PI3K/mTOR inhibition [93].

Wnt/β-catenin pathway
A study by Lemieux et al. demonstrated the Wnt/β-catenin pathway (Figure 3) as a potential novel target in MEK/ERK signalling involved in CRC tumourigenesis [94]. The Wnt/β-catenin pathway is activated via the binding of Wnt1 protein to the G-protein coupled receptor, Frizzled. After the activation by Wnt1, Dishevelled protein (Dsh) induces the dissociation of the destruction complex that usually degrades β-catenin. Without the destruction complex, β-catenin is accumulated in the cytoplasm and transported to the nucleus to act as a transcriptional coactivator of transcription factors as shown in Figure 4. The aforementioned destruction complex comprises Axin (A), adenomatous polyposis coli (APC), and glycogen synthase kinase 3 (GSK3β). In the absence of Wnt1 activation, the destruction complex phosphorylates the downstream ubiquinating process. Here, the β-transducin repeat containing protein (βTrCP) binds β-catenin, ubiquinating it and marks it for degradation by the proteasome. Although there is conflicting literature with regards to the role of MAPK signalling in activating Wnt/β-catenin pathway, this group found Wnt signalling induction in high-grade BRAF MT tumours. Their data also show that the oncogenic activation of KRAS/BRAF/MEK signalling stimulates the canonical Wnt/β-catenin pathway, which in turn promotes intestinal tumour growth and invasion. This has in turn sparked trial designs to incorporate Wnt signalling as a treatment strategy.

Other possible therapeutic mechanisms
Recently, a number of other early studies have reported additional potential mechanisms of targeted treatment, which had shown promise in BRAF MT CRC xenografts or cell line studies.
Although not effective in vitro, in vivo studies have shown the inhibition of BRAF MT xenografts tumours with dovitinib. Lee et al. proposed that this observation is secondary to its angiogenesis-suppressing effect and could be a novel approach to improve the outcome of CRC patients in whom FGFR is overexpressed or amplified [95].

Proteasome inhibitor (carfilzomib)
A novel use of proteasome inhibitors (carfilzomib, bortezomib), known more for utility in haematological malignancy, has shown promising preclinical results in BRAF MT CRC [96]. Zecchin et al. have observed increased sensitivity of BRAF MT CRC to carfilzomib, whereas WT cells were significantly less affected (p<0.05). This response seemed to be independent of the phosphatase and tensin homologue (PTEN) or retinoblastoma protein (RB1) expression status in CRC. The mechanism of this activity was explained by the higher accumulation rate of ubiquitinated proteins in MT cells with respect to WT. It was speculated that this is secondary to the non-oncogenic addiction of BRAF MT cells to the protein degradation function of proteasome to counterbalance the proteotoxic stress induced by the MT protein.
Interestingly, carfilzomib was also found to have antagonistic effects with the RAF inhibitor, vemurafenib, and was proposed as a possible alternative treatment to BRAF/MEK inhibition.

microRNA (miR-145)
miR-145, a short RNA molecule of microRNA gene, which was observed to have tumour suppressor function, was found to be down-regulated in vemurafenib-resistant BRAF MT CRC cell lines [97]. Peng et al. reported that the overexpression of miR-145 increased the sensitivity of BRAF MT CRC cell lines both in vitro and in vivo and could be used as a potential therapeutic target.

In situ cancer vaccine (Allostim)
AlloStim is an innovative design based on immunotherapy principles. It is derived from the blood of normal blood donors and is intentionally mismatched to the recipient. CD4 + T cells are initially separated from the blood and differentiated and expanded for 9 days in culture to make an intermediary called T-Stim. AlloStim is made by incubating T-Stim cells for 4 h with antibody-coated microbeads. The cells with the beads still attached are suspended in infusion media and loaded into syringes. The syringes are shipped refrigerated to the point-of-care. A phase I study was completed in May 2011 and a phase II/III study is due to recruit in 2016. It involves an in situ (in the body) cancer vaccine step that combines killing a single metastatic tumour (usually liver metastasis) lesion by the use of cryoablation to cause the release of tumour-specific markers to the immune system and then injecting bioengineered allogeneic immune cells (AlloStim) into the lesion as an adjuvant to modulate the immune response and educate the immune system to kill other tumour cells wherever they reside in the body [98].

Apoptosis regulator (BCL-2/BCL-XL) inhibitor (Navitoclax)
Apoptosis regulator (BCL-2/BCL-XL) inhibitor (Navitoclax) was explored as a novel approach in sensitising BRAF MT CRC to mTOR inhibition. The results showed that this combination strategy leads to efficient apoptosis in specifically KRAS and BRAF MT but not WT CRC cells [99]. These data showed promising results with the combination strategy of apoptosis regulator inhibitors with mTOR inhibitors in BRAF MT CRC.

Ongoing trials for BRAF MT CRC
Many phase I/II trials are currently ongoing for BRAF MT mCRC. Most of them focus on the RAS/RAF/MEK/ERK signalling pathway, trialling combination targeted treatments. Table 5 lists these available trials.

Conclusion
The BRAF V600E MT CRC typically presents with right-sided proximal high-grade mucinous tumours in older women and may arise from serrated polyps. Molecularly, they are associated with more MLH1 methylation, MSI, and CIMP. This small subset of CRC, which generally affects approximately 10% of CRC patients, remains a challenging group with poor response to both anti-EGFR and standard doublet chemotherapy. This CRC subgroup is typically aggressive, has short median PFS between sequential lines of treatments, and emphasises the need to use effective treatments early. New evidence suggests that triplet chemotherapy with FOLFOXIRI could be considered in suitable patients with or without bevacizumab as first-line treatment. Many trials are currently studying the effective combinations of targeted treatments involving BRAF and MEK inhibitors in this subgroup and ways to overcome resistance.