Dabrafenib for treatment of BRAF-mutant melanoma

Abstract

Melanoma has the highest mortality of all the skin cancer subtypes. Historically, chemotherapy and immunologic therapies have yielded only modest results in the treatment of metastatic melanoma. The discovery of prevalent V600 BRAF mutations driving proliferation makes this oncogenic protein an ideal target for therapy. Dabrafenib, a reversible inhibitor of mutant BRAF kinase, improved response rates and median progression-free survival in patients with V600E BRAF-mutant metastatic melanoma, including those with brain metastases. With a well-tolerated toxicity profile, dabrafenib is effective as a monotherapy; however, resistance eventually develops in almost all patients. As a result, current research is exploring the role of combination therapies with dabrafenib to overcome resistance.

Keywords:

• dabrafenib
• metastatic melanoma
• V600E BRAF mutation

Introduction to melanoma and personalized medicine

Skin cancer is the most common cancer in the US, and melanoma has the highest mortality rate of all the skin cancer subtypes.¹ The incidence and prevalence of cutaneous melanoma have increased over the last 30 years, and one in 50 Americans will be diagnosed with melanoma at some point in their lifetime.² Although more than 80% of patients have localized disease at the time of diagnosis and a 5-year survival of more than 90%, metastatic melanoma continues to carry a poor prognosis, with a median overall survival of 9–11 months and one-year and 5-year survivals of about 33% and 15%, respectively.^2,3

Until recently, standard treatments for metastatic melanoma have yielded only modest response rates and significant toxicities. Dacarbazine, an alkylating agent, was one of the first chemotherapies approved for metastatic melanoma, with a response rate of about 20% and a median response duration of 5–6 months.⁴ However, multiple studies have failed to demonstrate a survival benefit with dacarbazine.⁴ Similarly, highdose interleukin (IL)-2 has a response rate of about 6%–16%, and responders have a progression-free survival of 13.1 months.^5,6 For those with brain metastasis, the response rate with IL-2 is only 5%.⁷ Addition of the peptide vaccine gp-100 to high-dose IL-2 therapy slightly improved response rates and progression-free survival, but unfortunately the significant toxicity profile associated with high-dose IL-2, which includes capillary leak syndrome, arrhythmias, hypotension, and neurologic changes, makes the treatment difficult to tolerate in many patients.^5,6 In spite of its modest response rates, significant toxicity profile, and lack of overall survival advantage, IL-2 continues to be a treatment option for metastatic melanoma because of the prolonged median progression-free survival of several years in patients who experience a complete response.⁵ Temozolomide, an oral alkylating agent that crosses the blood–brain barrier and has the same chemical active species that causes cell death as dacarbazine, has a response rate of approximately 7% and a median progression-free survival of about 1.2 months in patients with brain metastasis and no prior treatment.⁸ In addition to single-agent therapies, combination chemotherapy regimens have been explored but have also yielded relatively modest response rates.⁹ Strategies that combine cytotoxic chemotherapies with immune-modulating agents, such as biochemotherapy, have also been investigated.^10,11 One biochemotherapy regimen combining cisplatin, vinblastine, dacarbazine, interferon, and IL-2 has demonstrated modest improvement in progression-free survival but not overall survival in Phase III trials.^11,12 Although some combination regimens have slightly improved response rates, none have demonstrated improved overall survival when compared with dacarbazine monotherapy, and many regimens are associated with toxicities that are poorly tolerated by patients.^4,10,11

Recent research efforts have explored the potential role of targeted therapy for metastatic melanoma. Understanding the driver mutations which contribute to the uncontrolled proliferation of cancer cells has been crucial for the development of drugs that specifically target the underlying cellular defect. In metastatic melanoma, oncogenic mutations in multiple cellular pathways have been identified, including BRAF and NRAS mutations in the mitogen-activated protein kinase (MAPK) pathway, p53 mutations, and PTEN mutations.^13–15 Inhibitors have been developed that target specific proteins, such as BRAF and MEK, in unregulated proliferation cascades. Likewise, immune-modifying agents, such as anti-CTLA-4 and anti-PD-1 antibodies, have been developed to control melanoma growth by activating cytotoxic T-lymphocytes.^16,17 Ipilimumab, an anti-CTLA-4 antibody, has a response rate of 10.9%, with a complete response rate of 1.5% and a median progression-free survival of 2.86 months.¹⁸ Importantly, ipilimumab was the first drug to demonstrate improved overall survival in patients with metastatic melanoma, with one-year and 2-year survival rates of 45.6% and 23.5%, respectively.¹⁸ Although severe immune-related adverse events are observed in about 10%– 15% of patients, algorithmic management of the adverse events can significantly mitigate these serious toxicities.¹⁸ Additionally, combining ipilimumab with nivolumab, an anti-PD-1 antibody, in a Phase I study of patients with metastatic melanoma led to an objective response in 53% of patients, with all responding patients demonstrating tumor reductions of 80% or more. Although grade 3 and 4 adverse events occurred in 53% of patients, most side effects were reversible and manageable.¹⁹ Further, lambrolizumab, an anti-PD-1 antibody, had a response rate of about 38%, with a median progression-free survival of over 7 months and a fairly well-tolerated toxicity profile.²⁰ The goal of molecular-targeted research has been to identify relevant molecular aberrations in individual patients and use this knowledge to guide treatment decisions.

Introduction to BRAF

The MAPK cascade plays an important role in cellular proliferation and differentiation.^21,22 Mutations in the MAPK signaling pathway have been identified in patients with malignant melanoma.^13–15,22 Growth factors activate a small GTP binding protein (RAS) on cell membranes, which triggers intracellular signaling (Figure 1).²¹ Downstream activation of RAF, a serine/threonine kinase protein, leads to phosphorylation of MEK proteins and eventual activation of the protein kinase ERK, which translocates into the nucleus and stimulates progrowth signals.^21,22 Unregulated activation of the MAPK pathway can therefore lead to malignancy.^21–23

Figure 1 Redundancy of the MAPK signaling cascade and targeted inhibitors. Single arrows signify direct pathways. Double arrows reflect a culmination of multiple steps in the signaling cascade.

Note: Adapted from Cancer Discov, copyright 2013, 3(5), 487–490, Girotti MR, Marais R, Déjà vu: EGF receptors drive resistance to BRAF inhibitors, with permission from AACR.⁵⁹
Abbreviations: HGF, human growth factor; IGF-IR, insulin-like growth factor 1 receptor; PDGFR-β, platelet-derived growth factor-β; Pi3K, phosphoinositide 3-kinase; ERK, extracellular signal-regulated kinase; MAPK, mitogen-activated protein kinase.

The RAF protein kinases have been extensively studied for their role in oncogenesis. Specifically, BRAF mutations have been identified in many malignancies, including cutaneous melanoma, colorectal cancer, and papillary thyroid carcinoma.^24–27 In each tumor type, the presence of a BRAF mutation has been associated with a more aggressive disease course and worse overall prognosis.^24–26

BRAF mutational status in malignant melanoma

BRAF mutations have been identified in 50%–60% of all metastatic melanomas, and 80%–90% of all BRAF mutations consist of an exchange of glutamine for valine at amino acid 600 (V600E).^13,26,27 This alteration locks the kinase into a 500-fold more active conformation than wild-type BRAF and leads to oncogenesis via unregulated MAPK signaling.²⁸ Substitution of lysine for valine (V600K) is another transformation observed in about 20% of BRAF mutations in metastatic melanoma.²⁶ Historically, the prognosis of BRAF-mutant melanoma has been worse than melanomas with wild-type BRAF because untreated patients have a median overall survival of 11.1 months versus 46.1 months, respectively.²⁶

The frequency of BRAF mutations in metastatic melanoma has driven the development of agents to disrupt the pathway signaling associated with these activating oncogenic mutations. Vemurafenib, an inhibitor that is ten times more selective for mutant BRAF than wild-type, induces potent cell cycle arrest, inhibits proliferation, and initiates apoptosis exclusively in V600E-mutant cells in a variety of experimental in vitro systems.^29,30 Xenograft studies similarly demonstrated sensitivity and activity against melanomas with V600E BRAF mutations.³⁰

Meanwhile, dabrafenib was developed separately as an ATP-competitive, reversible inhibitor of mutant BRAF kinase. Like vemurafenib, dabrafenib decreases phosphorylated ERK and causes cell cycle arrest.³¹ In preclinical studies, dabrafenib was almost 20 times more selective at inhibiting V600E BRAF-mutants than wild-type BRAF in multiple cancer cell lines.³¹ Additionally, dabrafenib has inhibitory effects on cell lines containing other activating BRAF mutations, including Val600Lys (V600K) and Val600Asp (V600D).³¹ Dabrafenib achieved a half maximal inhibitory concentration (IC₅₀) with 0.6 nM, 0.5 nM, 1.9 nM, and 12 nM in V600E, V600K, V600D, and wild-type BRAF cell lines, respectively.³¹

Dabrafenib targeting mutated BRAF in metastatic melanoma

Clinical trials

The first-in-human Phase I trial of dabrafenib showed promising results. The treatment was well-tolerated with no maximum tolerated dose identified despite dose escalation that achieved pharmacokinetic concentrations well above the levels predicted to have adequate target inhibition.³² A recommended Phase II dose (RP2D) of 150 mg by mouth twice a day was selected for future studies.³² Patients with V600E BRAF-mutant melanoma were more responsive to treatment, with a confirmed response rate of 57% compared with 37% in patients with V600K mutations.³² Patients with either V600E or V600K had similar median progression-free survival of 5.5 and 5.6 months, respectively (Table 1).³² The most serious side effects with a grade 2 or higher at the RP2D were well differentiated cutaneous squamous cell carcinoma (7%), fever (6%), and fatigue (4%).³² Pyrexia was an unusual dose-limiting toxicity observed; however, almost all cases could be managed with antipyretics, low-dose steroids, or dose reduction. No patient required discontinuation of treatment secondary to side effects, and no deaths occurred from the treatment.³²

Table 1 Comparison of endpoints among dabrafenib clinical trials

	# of patients enrolled*	Response rate (confirmed CR and PR)	Stable disease	Progression-free survival
Dabrafenib: Phase I/II^Citation32
All patients	36	19 (53%)	Not reported	5.5 months
V600E	28	16 (57%)		5.5 months
V600K	8	3 (37%)		5.6 months
Dabrafenib vs dacarbazine: Phase III^Citation33
Dabrafenib	187	93 (50%)	78 (42%)	6.9 months^Citation34
Dacarbazine	63	4 (6%)	30 (48%)	2.7 months
Dabrafenib for brain metastasis: Phase II^Citation35
Initial treatment
V600E	74	29 (39%)	31 (42%)	16.1 weeks
V600K	15	1 (7%)	4 (27%)	8.1 weeks
Previously treated
V600E	65	20 (31%)	38 (58%)	16.6 weeks
V600K	18	4 (22%)	5 (28%)	15.9 weeks
Dabrafenib with trametinib: Phase I/II^Citation43
Dabrafenib monotherapy	54	29 (54%)	22 (41%)	5.8 months
Dabrafenib + trametinib	54	41 (76%)	13 (24%)	9.4 months

Note:

* At the recommended Phase II dose.

Abbreviations: CR, complete response: PR, partial response.

Following the promising preliminary results of the Phase I trial, a randomized Phase III trial compared dabrafenib with dacarbazine in patients with V600E BRAF-mutant metastatic melanoma.³³ Eligible patients had excellent performance status, with an Eastern Cooperative Oncology Group score of 0 (fully active and able to carry out all performance without restrictions) or 1 (restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature) and no other prior treatments except high-dose IL-2.³³ All patients with active central nervous system metastases were excluded.³³ The confirmed response rate for dabrafenib was 50% compared with 6% for dacarbazine per the study’s independent review committee (Table 1).³³ In those treated with dabrafenib, 47% had a partial response while 3% showed a complete response.³³ The median progression-free survival in patients receiving dabrafenib was 6.9 months compared with 2.7 months in patients who received dacarbazine therapy.³⁴ The most common side effects with dabrafenib were dermatologie, and included hyperkeratosis (39%) and squamous cell carcinoma (10%). Other common side effects observed were pyrexia (32%), headache (35%), and arthralgia (35%).³⁴ The occurrence of pyrexia of at least grade 2 was higher in the Phase III study than in the Phase I study (11% versus 6%, respectively) but was manageable in most cases.^32,33 Grade 3 and 4 adverse events were uncommon, and 28% of patients needed dose reductions secondary to toxicity.^33,34 Overall, dabrafenib has markedly higher response rates and progression-free survival along with a well-tolerated toxicity profile compared with dacarbazine in patients with V600E BRAF-mutated metastatic melanoma.³³

BRAF-mutant melanoma with brain metastasis

A small subset of ten patients with untreated brain metastases were enrolled at the RP2D in the first-in-human Phase I trial of dabrafenib.³² Nine patients responded to treatment, with four having complete resolution of brain lesions and a median progression-free survival of 4.2 months.³²

Because of these encouraging preliminary results, a multicenter, open-label, Phase II trial compared dabrafenib treatment in V600E and V600K BRAF-mutant melanoma with metastases to the brain in patients with and without previous local treatment, including brain surgery, whole-brain radiation, or stereotactic radiosurgery (Table 1).³⁵ In V600E mutants with no prior treatment, 39% had an intracranial response, with 3% having a complete reponse.³⁵ Median progression-free survival was 16.1 weeks.³⁵ In participants with V600E-BRAF and disease progression following prior local treatment, 31% demonstrated a partial response to dabrafenib, with a median progression-free survival of 16.6 weeks.³⁵

Conversely, V600K BRAF mutants were less responsive, with an intracranial partial response of 7% and 22% in previously untreated and treated patients, respectively (Table 1).³⁵ None had a complete response. Median progression-free survival in those with no prior treatment was 8.1 weeks versus 15.9 weeks in previously treated participants.³⁵ The most common side effects in all groups were pyrexia (7% in untreated and 12% in previously treated patients) and cutaneous squamous cell carcinoma or keratoacanthoma (6% in previously untreated patients and 7% in those with prior local treatment).³⁵ The results suggest that dabrafenib is a possible treatment option in patients with V600E or V600K BRAF-mutant melanoma metastatic to the brain regardless of history of prior local treatment.

Dabrafenib resistance and alternative combination strategies

Although dabrafenib has a high specificity and response rate in patients with V600E BRAF-mutated melanoma, resistance develops in almost all patients.^31,33 Disease progression is observed in about 50% of patients on monotherapy within 6 months of treatment initiation.^33,36 Multiple acquired mechanisms of resistance to BRAF inhibition have been investigated. Using sustained exposure to a specific V600E BRAF inhibitor, previously susceptible cell lines developed strong resistance.^37,38 In vitro and in vivo analyses of melanoma cell lines and tumor biopsies with acquired resistance demonstrated intact V600E BRAF with no secondary mutation to account for the evasion of inhibition.^37–39 Monitoring of MEK and ERK activation revealed distinct mechanisms of resistance, with elevated downstream phosphorylation in the setting of BRAF inhibition suggesting alternative MAPK pathway activation (Figure 1).^37,40 Although multiple mechanisms appear to account for continued downstream signaling, utilization of different RAF isoforms, ie, ARAF or CRAF, to circumvent BRAF inhibition has been identified.^38,40 Specifically, development of activating mutations of N-RAS kinase proteins, which tend to phosphorylate CRAF instead of BRAF, continue uncontrolled MAPK signaling.^37,39,41 Another mechanism of resistance is acquisition of alternative splicing of BRAF (p61 BRAF), resulting in dimerization of RAF kinase and continued downstream ERK phosphorylation in the presence of RAF inhibitors.⁴² In addition, RAF-independent mechanisms have been identified with increased COT, a different serine/threonine MAP kinase, driving persistent MAPK cascade activation in the presence of BRAF inhibition.⁴⁰ Alternatively, upregulation of receptor tyrosine kinases, such as platelet-derived growth factor receptor-β and insulin-like growth factor-1 receptor, confirms acquired MAPK-independent resistance.^37,38 Ultimately, the mechanism of acquired BRAF inhibitor resistance appears to be complex, with multiple diverse pathways circumventing inhibition to cause disease progression after initial treatment response. Understanding resistance allows for combination treatment strategies to not only increase median progression-free survival but also potentially also improve complete response rates.

Combined BRAF and MEK inhibition

With evidence of persistent MAPK signaling through continued downstream MEK phosphorylation despite BRAF inhibition in vitro and in vivo, dabrafenib has been combined with trametinib, a MEK inhibitor, in both preclinical studies and clinical trials.^39,43 In in vitro studies, cells having acquired resistance to dabrafenib with continued ERK phosphorylation in the presence of the BRAF inhibitor demonstrated restoration of inhibition similar to sensitive parental cell lines when treated with both dabrafenib and trametinib.³⁹ These promising preclinical observations provided the rationale for a Phase I trial and a randomized Phase II clinical trial to determine the effects of this combination on response rates and median progression-free survivial.⁴³ Enrolled participants had metastatic melanoma with confirmed V600E or V600K BRAF mutations but no prior treatment. Those with treated brain metastases and stable brain lesions for greater than 3 months were also eligible for enrollment.⁴³ The recommended Phase II dose was 150 mg dabrafenib twice daily and 2 mg trametinib once daily, which are the recommended monotherapy doses for each agent.⁴³

The response rate for combination therapy was improved at 76% compared with dabrafenib monotherapy, which was 54% (Table 1).⁴³ The cohort treated with the recommended Phase II combination dose had a partial response rate of 67% and a complete response rate of 9%.⁴³ Similar to previous studies, those treated with dabrafenib monotherapy had a partial response rate of 50% and complete response rate of 4%.^33,43 The median progression-free survival in the group receiving combination dabrafenib and trametinib was 9.4 months, which was significantly better than the 5.8 months observed in those receiving dabrafenib monotherapy.⁴³ Combination therapy was also generally tolerated well. The most frequent side effect of pyrexia, which was worse on combination therapy than on monotherapy (71% versus 26%), was the most common reason for dose reduction.⁴³ Neutropenia was the most frequent grade 3 or 4 (11%) adverse effect with combination treatment.⁴³ Surprisingly, the incidence of cutaneous squamous cell carcinoma was decreased on combination therapy compared with monotherapy using dabrafenib (7% versus 19%), possibly because MEK inhibition by trametinib attenuates dabrafenib-induced paradoxical activation of the MAPK pathway in normal keratinocytes.⁴³ However, the dual therapy cohort experienced MEK inhibitor-associated toxic effects not seen with dabrafenib monotherapy, including decreased ejection fraction (9%) and chorioretinopathy (2%), although none were grade 3 or higher.⁴³ Overall, combining dabrafenib with the MEK inhibitor trametinib led to improved response rates and median progression-free survival compared with treatment using dabrafenib alone and had a well tolerated toxicity profile.⁴³

Combined BRAF, MEK, and PI3K/mTOR inhibition

BRAF and MEK inhibition vertically target two distinct proteins in the MAPK pathway; however, activation of alternative proliferative pathways can continue to drive oncogenesis (Figure 1). Mutations in both the MAPK and phosphoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) pathways can coexist, with PI3K/mTOR activating mutations contributing to unregulated proliferation.^44,45 An interaction between the MAPK and PI3K/mTOR signaling cascades has also been established, with increased AKT and mTOR phosphorylation occurring in the setting of BRAF inhibition.^46,47 An in vitro study showed decreased cell proliferation in dabrafenib-resistant cells treated with both dabrafenib and trametinib; however, S6P, a protein activated by both the MAPK and PI3K/mTOR pathways, continued to be phosphorylated downstream.³⁹ The addition of a dual PI3K/mTOR inhibitor to either dabrafenib or trametinib led to decreased S6P activation when compared with combination dabrafenib and trametinib therapy.³⁹ The combination of dabrafenib with the PI3K/mTOR inhibitor decreased cell proliferation in both parental and resistant cell lines and offers a potential alternative treatment strategy in patients with acquired dabrafenib resistance.³⁹ Clinical trials using a combination of dabrafenib, trametinib, and a PI3K/mTOR inhibitor are planned. Few overlapping toxicities are expected, given the individual mechanisms of action associated with each drug.

Combined dabrafenib and immune modulator strategies

BRAF activation induces downstream cytokine production that suppresses the immune system; therefore, dabrafenib-induced inhibition of the MAPK pathway could enable the immune system to play a vital role in clearing tumor cells and preventing recurrence.^48,49 However, many immune cells, such as cytotoxic T-lymphocytes, use the MAPK pathway to function, and some MAPK pathway inhibitors negatively affect systemic immunity.^50,51 To determine the effect of dabrafenib on the immune system, the peripheral blood of patients with metastatic melanoma treated with dabrafenib was analyzed using cytokine and immunologic assays along with flow cytometric analysis.⁴⁹ Dabrafenib did not exhibit immunosuppression, likely secondary to its specificity for tumor cells containing V600 BRAF mutations, and spared the wild-type BRAF present in immune cells.⁴⁹ In another study, biopsies obtained from patients before and after dabrafenib treatment were examined to determine the effect on tumor-infiltrating lymphocytes.⁵² Post-treatment tumor samples generally had high concentrations of both intratumoral and peritumoral CD4⁺ and CD8⁺ cells compared with samples before exposure to dabrafenib.⁵² Tumors with increased intratumoral CD8⁺ cells correlated with decreased tumor size and increased tumor necrosis.⁵² The initial increase in CD8+ cells found immediately post-treatment was reduced in biopsies taken from tumors following disease progression.⁵² These results suggest that dabrafenib combined with an immune stimulator, such as IL-2 or an anti-CTLA-4 antibody, could work synergistically. A recent Phase I study combining vemurafenib with ipilimumab was limited by grade 3 hepatotoxicity that was reversible with discontinuation of the drugs or use of glucocorticoids.⁵³ Therefore, such combinations should be explored with caution in the future. Additional clinical trials are needed to assess the efficacy and safety of combining dabrafenib with immune modulators.

Combination BRAF and HGF/MET inhibition

In addition to acquired intracellular mechanisms of resistance, the tumor microenvironment can confer resistance to BRAF inhibition in cells containing V600E BRAF mutations.⁵⁴ In vitro studies demonstrated that tumor cells initially sensitive to RAF inhibitors can become resistant when cultured with stromal cells that simulate the tumor microenvironment.⁵⁴

Investigation of fibroblast-conditioned media using antibody array-based analysis identified hepatocyte growth factor (HGF) as the factor inducing resistance.⁵⁴ When added to media containing a BRAF inhibitor, recombinant HGF caused growth of BRAF-inhibited cell lines and correlated with increased MET expression, whereas in other cell lines, HGF exposure resulted in undetectable MET expression with continued growth supression.^54,55 HGF is a ligand to the receptor tyrosine kinase MET, which has been implicated in progression of melanoma (Figure 1).⁵⁶ MET can initiate the MAPK cascade and bypass BRAF inhibition via phosphorylation of CRAF.⁵⁶ MET also activates the PI3K-AKT pathway.⁵⁴ In vitro studies demonstrated that dual inhibition of RAF and either HGF or MET resulted in reversal of resistance in cells with V600E BRAF mutations.⁵⁴ Similarly, small molecules that inhibit MET eliminated resistance attributed to HGF secretion from surrounding fibroblast cells.⁵⁴ These findings suggest that combining HGF/MET-specific inhibitors with BRAF inhibitors could possibly reduce some of the resistance conferred through the tumor microenvironment and ultimately improve both response rates and progression-free survival.

Place of dabrafenib in therapy

As a monotherapy, dabrafenib has been demonstrated in clinical trials to be an effective targeted agent in the treatment of metastatic melanoma with V600 BRAF mutations, especially in V600E and V600K mutants. Along with high response rates and a well tolerated toxicity profile, dabrafenib demonstrates durable activity against brain metastases. Taken by mouth twice daily, dabrafenib can be conveniently administered as an outpatient treatment. In May 2013, the US Food and Drug Administration approved dabrafenib for the treatment of unresectable or metastatic melanoma with V600E BRAF mutations.⁵⁷

Although dabrafenib is effective as a single-agent treatment, resistance eventually develops in most patients. Preliminary studies examining combination strategies suggest enhanced response rates when dabrafenib is combined with a variety of inhibitors targeting proteins, not only in the MAPK cascade but also in alternative pathways conferring redundancy to oncogenesis. To improve overall response rates and survival outcome, more studies are needed to understand the interplay among the tumor microenvironment, systemic immune system, and intracellular signaling driving tumor progression. With recent approval from the US Food and Drug Administration, the role of dabrafenib as a single agent has been established, and combination therapy strategies to overcome resistance will be explored in future and ongoing clinical trials (Table 2).

Table 2 Active and recruiting clinical trials involving dabrafenib use in patients with melanoma

NCT#	Trial	Status
01677741	The study to determine safety, tolerability, and pharmacokinetics of oral dabrafenib in pediatric subjects	Recruiting
01584648	A Phase III study comparing trametinib and dabrafenib combination therapy to dabrafenib monotherapy in subjects with BRAF-mutant melanoma	Active, not recruiting
01767454	Phase I study of dabrafenib ± trametinib in combination with ipilimumab for V600E/K mutation positive metastatic or unresectable melanoma	Recruiting
01682083	A study of the BRAF inhibitor dabrafenib in combination with the MEK inhibitor trametinib in the adjuvant treatment of high-risk BRAF mutation-positive melanoma after surgical resection	Recruiting
01682213	Adjuvant dabrafenib in patients with surgically resected AJCC stage IIIC melanoma characterized by a BRAFV600E/K mutation	Recruiting
01726738	Open label Phase II trial of dabrafenib and trametinib in unresectable stage III and stage IV BRAF mutant melanoma; correlation of resistance with the kinome and functional mutations	Recruiting
01721603	A Phase II prospective trial of dabrafenib with stereotactic radiosurgery in BRAFV600E melanoma brain metastases	Recruiting
01597908	Dabrafenib plus trametinib vs vemurafenib alone in unresectable or metastatic BRAF V600E/K cutaneous melanoma	Recruiting
01940809	Ipilimumab with and without dabrafenib, and/or trametinib in treating patients with melanoma that is metastatic or cannot be removed by surgery	Recruiting
01701037	Dabrafenib alone and in combination with trametinib before surgery in treating patients with locally or regionally advanced melanoma that can be removed by surgery	Recruiting

Note: Trial information obtained from http://www.clinicaltrials.gov/.⁵⁸

Abbreviation: NCT#, National Clinical Trial number.

Disclosure

KBK is a member of the GlaxoSmithKline (GSK) advisory board and has received research funding from GSK. GSF has received research funding and travel reimbursement from GSK. RK has no conflicts of interest to declare.