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We address the prognostic and predictive value of KRAS, PIK3CA and BRAF mutations for clinical outcomes in response to active agents in the treatment of metastatic colorectal cancer (mCRC).
We determined KRAS, BRAF and PIK3CA mutations in tumours from 168 patients treated for mCRC at two institutions. All patients received 5-FU-based first-line chemotherapy and treatment outcome was analysed retrospectively.
KRAS, BRAF and PIK3CA mutations were present in 62 (37%), 13 (8%) and 26 (15%) cases, respectively. Multivariate analysis uncovered BRAF mutation as an independent prognostic factor for decreased survival (hazard ratio (HR) 4.0, 95% confidence interval (CI) 2.1–7.6). In addition, patients with BRAF-mutant tumours had significantly lower progression-free survival (PFS: HR 4.0, 95% CI 2.2–7.4) than those whose tumors that carried wild-type BRAF. Among 92 patients treated using chemotherapy and cetuximab as salvage therapy, KRAS mutation was associated with lack of response (P=0.002) and shorter PFS (P=0.09). BRAF (P=0.0005) and PIK3CA (P=0.01) mutations also predicted reduced PFS in response to cetuximab salvage therapy.
These results underscore the potential of mutational profiling to identify CRCs with different natural histories or treatment responses. The adverse significance of BRAF mutation should inform patient selection and stratification in clinical trials.
Combinatorial and sequential administration of 5-fluorouracil (5-FU), oxaliplatin and irinotecan has substantially increased the overall survival (OS) in metastatic colorectal cancer (mCRC), although treatment goals remain primarily palliative (Grothey et al, 2004). Monoclonal antibodies (mAb) bevacizumab, against the vascular endothelial growth factor (VEGF) receptor, and cetuximab or panitumumab, against the epidermal growth factor receptor (EGFR), expand treatment options and further improve progression-free (PFS) and OS (Cunningham et al, 2004; Hurwitz et al, 2004; Van et al, 2007).
The genetic underpinnings of colorectal cancer (CRC) are especially well characterized (Vogelstein and Kinzler, 2004) and include common somatic mutations in the APC, TP53 and KRAS genes, followed in frequency by PIK3CA and BRAF mutations (Wood et al, 2007). Activating mutations in the KRAS, BRAF and PIK3CA oncogenes deregulate growth-factor pathways, stimulate cell proliferation and promote metastasis (Huang et al, 2007; Schubbert et al, 2007). Presence of KRAS mutations in primary CRC portends a poor response to monotherapy and combination therapy using anti-EGFR mAB cetuximab or panitumumab (Amado et al, 2008; Karapetis et al, 2008; Lievre et al, 2008). In one study that included few patients with stage IV disease and BRAF mutations, the latter were associated with limited survival in patients with microsatellite-stable (MSS) disease (Samowitz et al, 2005); mutations in exons 9 or 20 of the PIK3CA gene are associated with lower relapse-free survival in patients with stage II or III CRC (Kato et al, 2007). These data notwithstanding, there is limited understanding of the extent to which common KRAS, BRAF and PIK3CA mutations influence clinical outcomes in patients with mCRC treated with chemotherapy and/or biological therapy. Treatments are selected largely without regard for tumour mutation profiles, although recent evidence linking KRAS mutation with poor response to EGFR mAb (Amado et al, 2008; Karapetis et al, 2008; Lievre et al, 2008) now influences decisions in the clinic.
We postulated that mutations in some of these oncogenes would correlate with overall prognosis and with treatment outcomes in patients receiving different regimens. To test these hypotheses, we first evaluated the prognostic significance of KRAS, BRAF and PIK3CA mutations in a cohort of patients with mCRC, treated using 5FU-based chemotherapy. Using a uniform catalogue of retrospective but detailed clinical information, we then tested the predictive value of these mutations on patient outcomes after treatment using the most common therapeutic regimens.
Tumour samples were collected from patients with histologically confirmed mCRC, treated at two centers, Dana-Farber/Partners Cancer Care (Boston, MA, USA) and University Hospital of Heraklion (Heraklion, Crete, Greece), between January 2004 and March 2007. All patients who gave informed consent and whose colectomy samples were available for molecular analysis were included in the analysis, without further selection. Failure to participate in the tumour registry was unusual, and the cohort essentially represents consecutive patients with mCRC who were treated at the two academic centres and gave informed consent for molecular analysis of DNA from the primary tumour. Institutional ethics committees approved the study.
First-line and salvage regimens, selected at the discretion of the treating physician, followed common practices in mCRC (summarized in Table 1). Patients were evaluated at baseline and after every four cycles of therapy, with occasional variation, as clinically indicated, during the treatment. Disease status was coded, without the knowledge of the mutational profile, after retrospective review of physician notes and reports of staging radiographs, including tumour measurements; efficacy was assessed on an intent-to-treat basis. Disease progression was defined as the appearance of any new lesion or a greater than 20% increase in the sum of the longest diameter (LD) of target lesions, extracted from radiology reports, and taking as reference the lowest value recorded in the treatment period. Response toward cetuximab was defined as the reduction, by at least 30%, in the sum of the LD of target lesions compared with the baseline sum.
Formalin-fixed, paraffin-embedded tumour sections were reviewed by pathologists to confirm the diagnosis and define tumour-enriched areas for dissection. From each paraffin block of representative tumour areas, we stained 10 serial sections of 8μm thickness with nuclear fast red (Sigma-Aldrich, St Louis, MO, USA) and isolated malignant cells by scrape dissection under a binocular microscope. Macrodissected cells were lysed in buffer containing Proteinase K (Puregene, Gentra Systems, Minneapolis, MN, USA) at 60°C for 72h, followed by DNA extraction according to the manufacturer's protocol.
Mutations were detected in the Dana-Farber sample set by Sequenom mass-spectrometric genotyping (Thomas et al, 2007) after whole-genome amplification by PCR, and in the Heraklion samples by Sanger sequencing after PCR amplification of KRAS exon 2, BRAF exon 15, and PIK3CA exons 9 and 20. PCR conditions and the primers used to amplify specific exons are listed in Supplementary Table 1. Results from the two different methods for detecting mutations were cross-confirmed on the other platform, along with positive and negative controls.
Associations between treatment response and mutation status or baseline characteristics were assessed using the Fisher's exact test for dichotomous variables, or logistic regression for continuous variables. PFS was measured from the last radiographic study before the initiation of first-line therapy to the first radiographic documentation of disease progression or death, and OS was calculated from the date of diagnosis of metastatic disease to death due to any cause. For cetuximab treatment, PFS was calculated from the date of documented progression after the previous treatment to the next documentation of disease progression or death. Kaplan–Meier curves were used to describe the proportion of patients who remained free of events over the follow-up period. Associations between prognostic factors and PFS or OS were examined using Cox proportional hazards regression models; we report hazard ratio (HR) estimates and their 95% confidence intervals (CI).
We used Cox regression models with interaction terms to assess whether mutational effects varied across treatment subgroups. For each mutation, three hypotheses were tested: (1) whether effect on first-line PFS varied according to regimen (oxaliplatin based, irinotecan based or both); (2) whether the effect on first-line PFS varied according to inclusion or exclusion of bevacizumab; and (3) whether the effect on PFS for cetuximab varied according to the line of treatment (first vs third). All reported P-values are two-sided and not adjusted for multiple testing.
We determined with confidence the mutational status for KRAS exon 2, BRAF exon 15, and PIK3CA exons 9 and 20 in 168 consecutive patients with mCRC, for whom a representative sample from the primary tumour was available for molecular analysis of DNA. Disease characteristics were typical for mCRC in North America and Europe (Table 2), and patients were treated according to prevailing practice patterns (Table 1). KRAS mutations were detected in 62 (37%), BRAF mutations in 13 (8%) and PIK3CA mutations in 26 (15%, 18 in exon 9 and 8 in exon 20) primary tumours, respectively. Seven tumours carried both KRAS and PIK3CA mutations, whereas BRAF mutations did not co-occur with the others; these frequencies closely match those in published reports (Wood et al, 2007) and were similar between the US and Greek cohorts (Supplementary Table 2). Mutations in any gene did not correlate significantly with patient gender or age, stage at diagnosis, or histological grade (all P-values >0.05). As patient characteristics, mutation frequencies and treatment regimens were all typical for CRC, the results of our analysis should serve as a useful guide for clinical practice.
The median time from initial diagnosis to diagnosis of metastatic disease was 18.4 months (95% CI 14.4–20.4) for patients with stage I–III disease at presentation and 0.6 months (95% CI 0.1–1.4) for patients classified with stage IV disease. The median time from the last radiological assessment to the initiation of first-line chemotherapy was 0.6 months (95% CI 0.4–0.8), whereas median duration from the diagnosis of metastatic disease was 1.2 months (95% CI 0.9–1.3).
OS was similar between the two participating centres (median 38.9 months, 95% CI 33.4–46.3 months) and higher than other published values (Grothey et al, 2004; Hurwitz et al, 2004). Considering that patients were not selected on the basis of performance status or other clinical criteria, one possibility for improved outcomes may be that after initial response to systemic treatment, 30 out of 50 patients with solitary metastases (representing 18% of the total cohort) had metastases resected. Response to particular agents was, however, monitored in all patients and we examined the role of metastatectomy as a variable. Univariate analysis (Table 2) showed significant associations of OS with age >65 years (P=0.03), undifferentiated (grade 3) primary tumours (P=0.02), colonic vs rectal location (P=0.02), solitary metastasis (P=0.008) and BRAF mutations (P<0.0001, Figure 1). When all factors significant in univariate analysis were subjected to multivariate analysis (Table 3), only BRAF mutation remained as an independent prognostic factor for reduced OS (HR 4.0, 95% CI 2.1–8.0).
Combination chemotherapy was administered in the first line in 161 patients (96%), with or without mAb supplementation (Table 1); 5 patients (3%) received 5-FU as the only cytotoxic agent. One hundred patients (60%) were treated with the folinic acid–fluororuracil–oxaliplatin (FOLFOX) regimen, with or without the addition of a mAb, in the first line and 97 patients (58%) received bevacizumab in addition to fluoropyrimidine-based chemotherapy; a smaller fraction, 24% (44 patients) was treated with irinotecan in the first line. Seventeen patients (10%) received both oxaliplatin and irinotecan (Table 1). In all, 106 patients (63%) received all three active chemotherapy drugs and 87 patients (52%) received all five active agents at some point in their disease course.
KRAS or PIK3CA mutations did not influence PFS after first-line therapy (Figure 2). In contrast, patients with BRAF-mutant tumours had significantly lower PFS (median 4.3 vs 12.5 months; P<0.0001) compared with patients whose primary tumours carried only wild-type (WT) BRAF alleles (Figure 2). The association between BRAF mutation and reduced PFS (HR 4.9, 95% CI 2.7–9.0) after first-line therapy (Table 3) was similar for patients receiving oxaliplatin-, irinotecan- or both (interaction test P=0.7), and similar for patients receiving a regimen with or without bevacizumab (interaction test P=0.8). Specifically, BRAF mutation predicted more rapid disease progression in patients treated with first-line oxaliplatin- (HR 6.4, 95% CI 2.6–15.6), irinotecan- (HR 4.1, 95% CI 1.5–11.3), or oxaliplatin and irinotecan (HR 7.9, 95% CI 1.3–48.2), as well as bevacizumab-containing (HR 5.1, 95% CI 2.4–11.1) regimens (Supplementary Table 3). Thus, KRAS and PIK3CA mutations did not show predictive value with respect to cytotoxic agents and our observations single out BRAF mutation in the primary tumour as an adverse factor, independent of the first-line treatment.
One hundred patients were treated with cetuximab, 8 in the first line, 37 in the second and 55 in the third or higher, always in combination with chemotherapy. All patients receiving cetuximab in the second or subsequent line were refractory to previous regimens. Restricting analysis to the 92 patients who received cetuximab combinations as salvage therapy, none of the 32 patients with a KRAS-mutant tumour responded to treatment, whereas objective responses occurred in 14 of 60 (23%) patients whose tumors harboured only WT KRAS alleles (P=0.002). This striking difference confirms the results from prospective trials of cetuximab or panitumumab monotherapy (Amado et al, 2008; Karapetis et al, 2008; Lievre et al, 2008) and validates our approach to identify associations to guide the treatment of mCRC. It should be noted that none of the 9 patients with a BRAF-mutant tumour responded to cetuximab, whereas objective responses occurred in 14 of 83 (17%) patients whose tumours carried WT BRAF alleles. Presence of PIK3CA mutations showed no correlation with objective tumour responses to cetuximab. PFS was significantly lower among patients whose tumours carried mutations in BRAF (2.0 vs 3.9 months, HR 3.6, 95% CI 1.8–7.4), PIK3CA (2.5 vs 3.9 months, HR 2.1, 95% CI 1.2–3.9) or any of the three genes (2.5 vs 6.4 months, HR 2.1, 95% CI 1.3–3.2), and marginally lower in patients with KRAS-mutant tumours (2.5 vs 4.8 months, HR 1.5, 95% CI 0.9–2.3), compared with patients whose primary tumors were wild type at each locus (Figure 3, Supplementary Table 3). Importantly, patients whose tumour had BRAF or PIK3CA mutation had shorter PFS regardless of whether cetuximab was administered in the second, or third and higher lines (interaction tests P=0.5 and 0.6, respectively). Thus, the lack of EGFR mAb response observed in the setting of mutant KRAS (Schubbert et al, 2007; Amado et al, 2008) extends to other common mutations that deregulate cellular signalling pathways, especially BRAF and probably even PIK3CA. Lower PFS did not translate into differences in OS between patients with WT or mutant KRAS and PIK3CA alleles in the primary tumour.
Among the many genetic alterations in CRC, particular point mutations in three oncogenes, KRAS, PIK3CA and BRAF, occur at sufficiently high frequencies to be implicated in disease pathogenesis and as targets for molecular therapy (Wood et al, 2007). Each of these targets is the subject of intense drug development efforts. Appreciation of the predictive significance of underlying oncogene mutations will aid in design of clinical trials of new agents, administered either alone or in combination with other drugs, and in interpreting results from new and old trials. Moreover, current treatment approaches toward mCRC rarely consider biological properties associated with individual mutations, mainly because there is a paucity of information about the influence of specific mutations on natural history or the response to particular treatments. We report the results of retrospective investigation designed to help define the role of tumour mutation profiles in the management of patients with mCRC. Even though treatment choices and staging studies were not dictated by a strict clinical trial, the results are robust and relate well to current treatment paradigms.
A principal finding was that BRAF mutation the primary tumour marks patients who carry an especially poor prognosis, regardless of specific treatment regimen. Compared with patients with BRAFWT tumours, those with BRAFMUT tumours have significantly higher likelihood of disease progression (P<0.0001) or death (P<0.0001) with any current regimen (Table 3); the BRAF V600E mutation predicted independently for early relapse on first-line therapy (HR 4.0, 95% CI 2.2–7.4) and death (HR 4.0, 95% CI 2.1–8.0). These data warrant confirmation and should provoke thoughtful consideration of the risks and benefits of administering 5-FU, oxaliplatin or irinotecan in such patients, who should probably also be considered as a distinct group by stratification in future clinical trials. The poorer PFS with first-line therapy suggests that BRAF mutation could be prognostic, predictive or both. As this association was highly significant for patients receiving oxaliplatin, irinotecan or both, as well as for patients receiving bevacizumab or not, the conservative interpretation is that BRAF mutation is a prognostic rather than a predictive marker.
Our observations have interesting implications for pathogenic mechanisms and disease subgroups. Activating mutations in both KRAS and BRAF stimulate the MEK or extracellular signal-regulated kinase–microtubule-associated protein (ERK–MAP) kinase cascade (Vogelstein and Kinzler, 2004). As the two mutations tend to be mutually exclusive (Rajagopalan et al, 2002; Yuen et al, 2002), KRAS is inferred to signal principally through BRAF in colon cancer cells, leading to an assumption that tumours with KRAS or BRAF mutations may be equally vulnerable to inhibition of BRAF. Our finding that the natural history and treatment response of BRAF-mutant tumours differ markedly from all others implies that BRAF mutation does not simply substitute for KRAS activation in a linear signalling pathway but probably confers additional or distinct properties, with ominous consequences. In cultured cells, the V600E mutation increases BRAF activity independent of KRAS and shows lower transforming activity than oncogenic KRAS (Davies et al, 2002). Likewise, small-molecule inhibition of MEK abrogated tumour growth more profoundly in BRAF-mutant than KRAS-mutant tumour xenografts (Solit et al, 2006). Such differences may in part underlie the contrast in predictive value of activating KRAS and BRAF mutations. Second, the frequency of BRAF mutation is especially high, up to 50%, in tumours with microsatellite instability (MSIhi) (Rajagopalan et al, 2002), which otherwise carry a favourable prognosis (Popat et al, 2005). If the outcome of patients with BRAF mutation is so poor, then the natural history of MSIhi tumours lacking BRAF mutation must be even more favourable; a recent study of patients with operable stage II or stage III CRC made the same suggestion (French et al, 2008). If this idea is confirmed, patients with such tumors may, in the future, be candidates for prolonged observation without treatment.
In agreement with recent reports (Bokemeyer et al, 2008; Van Cutsem et al, 2009), mutant or WT status for KRAS did not correlate with the outcomes in patients treated with front-line 5FU-based regimens. Although a previous study reported worse outcomes in patients with early (stages II–III) PIK3CA-mutant CRC (Kato et al, 2007), the aggregate data do not currently suggest that KRAS- or PIK3CA-mutant tumours have distinctive clinical profiles or differential response to currently approved chemotherapy. The lack of overall predictive significance of KRAS mutation despite its effect on cetuximab treatment hints that the adverse effect of BRAF mutation is not explained just by the limited response to cetuximab.
This study reinforces the value of mutational analysis in patients treated with EGFR mAb. Patients with KRAS-mutant tumours treated with cetuximab in any combination had lower PFS compared with those with KRASWT tumours, results that extend those reported in recent clinical trials (Bokemeyer et al, 2008; Van Cutsem et al, 2009) and suggest that KRAS mutation may bypass aberrant EGFR signalling. We observed similar trends in the likelihood of response between patients with BRAF-mutant or BRAFWT tumours (0 vs 17%). Although responses in PIK3CA-mutant cases were not clearly as worse as they were in cases with KRAS or BRAF mutation, PFS with cetuximab-based therapy was significantly lower when tumors carried mutations in any of the three examined genes, and both BRAF (HR 3.9, P=0.0005) and PIK3CA (HR 2.1, P=0.01) mutations conferred higher risk of relapse after treatment with cetuximab-containing salvage combinations. Two studies that previously considered the significance of BRAF and PIK3CA mutations in treatment response to anti-EGFR mAb (Moroni et al, 2005; Lievre et al, 2006) had small sample sizes (30 and 31 cases, fewer than three with mutations). Our study extends the current paradigm to imply that patients with KRAS-, BRAF- or PIK3CA-mutant tumours may all derive limited benefit from treatment with EGFR mAb, and that BRAF mutations in particular account for a measurable fraction of patients whose KRASWT tumours do not respond to cetuximab. Reduced PFS in PIK3CA-mutant mCRC is not simply a function of poorer prognosis because overall outcomes are unrelated to this genetic event (Figure 1). Indeed, KRAS and PIK3CA mutations were not associated with worse OS, possibly because 82% of patients received another regimen after progression on cetuximab-based treatment or because response to cetuximab impacts modestly on the natural history of mCRC. (Messersmith and Ahnen, 2008).
Colorectal tumours are typically accessible for molecular characterization and common mutations localize in specific exons. Although it is formally possible that the mutational profile of metastatic deposits differs from that in the primary tumour, recent analyses indicate that this is not the case, (Jones et al, 2008); in any event, our analysis shows certain molecular lesions in the primary tumor as markers of the clinical outcome in mCRC. As we studied a large number of unselected cases with good representation of index mutations, the results are robust and directly relevant to current management of mCRC. They advance application of CRC mutation profiles to define patient sub-groups and should influence patient selection or stratification for prospective trials. KRAS and PIK3CA mutations seem not to be useful predictors for response to current treatment regimens. If our conclusions are confirmed independently, then patients with the BRAF V600E mutation might justify foregoing approved treatments in favour of investigational therapy. It will also be instructive to confirm the idea that like KRAS mutations, those in BRAF and PIK3CA also predict for lack of clinical benefit from EGFR mAb therapy.
We thank Laura MacConnaill and Levi Garraway for assistance with tumour genotyping and Dr Robert Mayer for critical reading of the paper. The study was supported by the Dana-Farber Cancer Institute-Novartis Drug Discovery Program (RAS), SPORE grant P50CA127003 from the National Institutes of Health and a research fellowship from the Hellenic Society of Medical Oncology (JS).