Introduction
Among patients with solid tumors, lung cancer, melanoma, breast cancer, and renal cell carcinoma are most likely to spread to the CNS [1]. For example, over one-quarter of patients with locally advanced or advanced NSCLC will be diagnosed with brain metastases over time [1, 2]. In patients with metastatic HER2-positive breast cancer, the likelihood of eventual CNS involvement is as high as 50 % [3, 4•]. Historically, survival after a diagnosis of CNS metastasis was quite poor [5]. However, recent data indicate favorable trends in survival among some patient subsets [6]. As patients live longer, the need for effective treatments in the upfront and salvage settings has significantly increased as well.
Guidelines for the management of patients with brain metastases have been formulated by several groups, including the European Federation of Neurological Societies (EFNS), National Comprehensive Cancer Network (NCCN), American Society for Radiation Oncology (ASTRO), and the American Association of Neurological Surgeons (AANS)/Congress of Neurological Surgeons [7, 8, 9•, 10]. The choice of therapy depends on a number of factors, including performance status, expected prognosis, number, location, and size of brain metastases, the presence or absence of symptoms and/or mass effect, suitability for surgical resection, and availability (or not) of options to control extracranial disease. A detailed discussion of current management paradigms is outside of the scope of this article. However, the sections below summarize treatment options that are commonly offered today, and provide context for the discussion of targeted systemic therapies to follow.
Anzeige
Initial management of patients with a single brain metastasis
Patients who present with a single brain lesion should be assessed for their suitability for surgical resection or SRS. Three randomized studies have tested the role of surgical resection followed by WBRT in such patients, compared with WBRT alone. Two of the three studies demonstrated a survival advantage in favor of the surgical arm [11, 12]. A third study was negative, but has been criticized for a relatively high rate of nonadherence to the assigned treatment, as well as enrollment of a patient population with poorer performance status and more active extracranial disease [13]. RTOG 9508 tested the addition of SRS to WBRT in patients with one to three brain metastases [14]. A survival advantage was observed in the subset of patients with a single brain metastasis. Randomized trials directly comparing surgical resection with SRS limited to patients with a single brain metastasis have not been conducted. In the absence of such data, either option may be acceptable in good prognosis patients, though surgical resection is strongly favored when a histological diagnosis is needed, and in the case of large lesions and/or those with significant mass effect. As will be discussed further below, whether or not WBRT should be routinely offered in addition to surgery or SRS is a matter of ongoing debate.
Initial management of patients with limited brain metastases
Patients who present with limited (ie, two-four) brain metastases may be offered SRS alone, SRS and WBRT, or WBRT alone [9•]. Whether certain histologies should preferentially receive SRS is controversial. Most prospective trials evaluating radiotherapy-based approaches for the treatment of brain metastases have enrolled predominantly patients with NSCLC, with relatively smaller proportions of patients with other tumor types, thus constraining the ability of such trials to answer histology-focused questions [14, 15, 16••]. In a single arm, phase 2 trial of SRS for “radioresistant” histologies (eg, renal cell carcinoma, melanoma, and sarcoma); intracranial failure rates were 25.8 % at 3 months and 48.3 % at 6 months [17].
Several randomized trials have tested the effects of routine WBRT after surgery or SRS on overall survival and cognition, compared with surgery or SRS alone [18]. Aoyama and colleagues randomized patients with one-four brain metastases to SRS alone or SRS plus WBRT [15]. Patients who received SRS alone could later receive WBRT as salvage therapy. Though there was a difference in intracranial control favoring WBRT + SRS, no differences in overall survival were observed, nor were there differences in the likelihood of death due to neurological causes. In terms of neurocognitive outcomes as measured by the Mini-Mental Status Examination (MMSE), the 12-month time point favored WBRT + SRS, likely due to improved intracranial tumor control, though in the small number of patients with extended survival, the 36-month time point showed numerically fewer patients with MMSE decline in the SRS alone arm [19]. The EORTC 22952-26001 trial included patients with one-three brain metastases who could undergo either surgery or radiosurgery, and who were randomized to WBRT or not [16••]. Again, no overall survival improvement was observed with the routine addition of WBRT. Notably, patients who received WBRT experienced worse health related quality of life (HRQOL), particularly during the early follow-up period, relative to patients treated with surgery or SRS alone [20]. Finally, a small study from M.D. Anderson Cancer Center examined the effects of treatment on neurocognitive function [21••]. In this study, patients assigned WBRT + SRS more commonly experienced declines in memory and learning at 4 months, as assessed by the Hopkins Verbal Learning Test, compared with patients who received SRS alone. Curiously, the study also demonstrated a survival advantage for SRS alone. Given that this result was not seen in the much larger randomized trials referenced above, the weight of the evidence does not favor a survival advantage for either strategy.
Given the reproducible reduction in intracranial failure rates, yet the lack of difference in overall survival, individualized discussions with patients are required in making treatment recommendations. In addition, nomograms to predict the risk and timing of subsequent intracranial events would be highly valuable.
Anzeige
Initial management of patients with multiple brain metastases
For patients who present with multiple brain metastases, WBRT remains the mainstay of therapy [9•, 18]. Best supportive care alone is also an option, particularly in patients with poor performance status. The ongoing QUARTZ trial is a randomized, noninferiority trial investigating whether WBRT adds to best supportive care alone in terms of quality-adjusted life years in patients with inoperable brain metastases from NSCLC. Interim analysis after 151 of 534 planned patients were enrolled demonstrated no decrement in overall survival or quality of life with the omission of WBRT in such patients [22]. At the same time, among patients with breast cancer brain metastases, the number of brain metastases did not appear to be a significant prognostic factor in the analyses leading to the diagnosis-specific graded prognostic assessment (DS-GPA) [23•]. Indeed, in patients with good performance status, and HER2-positive breast cancer, median survival after a brain metastasis diagnosis now approaches 2 years in some series [23•]. These contrasting data highlight some of the disease- and patient-specific considerations in managing patients with brain metastases from solid tumors.
Management of patients with recurrent/progressive brain metastases
The vast majority of data from high quality, prospective, randomized clinical trials focus on the initial management of patients with brain metastases. There are little to no randomized data to support the choice of one treatment strategy over another in the case of recurrent/progressive CNS disease. The 2013 NCCN guidelines suggest that for patients with one-three metastatic lesions, surgery, SRS, WBRT, or chemotherapy could all be options [8]. For patients with multiple brain metastases who have stable systemic disease or “reasonable” systemic treatment options at the time of CNS progression, the NCCN guidelines state that surgery, re-irradiation, or chemotherapy could all be considered, whereas best supportive care or re-irradiation be considered in patients with systemic disease progression and limited systemic treatment options [8].
Role of systemic therapy
The role of systemic therapy, either chemotherapy or targeted therapy, in the management of patients with brain metastases is not well-defined. To date, no systemic therapies have gained regulatory approval in the United States for the treatment of brain metastases from solid tumors. However, data supporting the efficacy of systemic therapies is available from prospective clinical trials as well as small experiences in the context of case series or case reports, and significant opportunities exist for drug development in this space [24]. The following section will highlight some of the targeted agents, which have been studied in settings of solid tumor brain metastases.
Treatment
-
The role of systemic therapy in the treatment of patients with solid tumor brain metastases is not well-defined. In particular, the use of systemic therapy in lieu of standard surgical/radiotherapy approaches in newly diagnosed patients is controversial. There are no class I data comparing systemic therapy with localized (ie, surgery/radiotherapy) approaches in this patient population.
-
Consideration of systemic therapy should generally occur as part of a multidisciplinary approach, taking into account surgical and radiotherapy options that may also be available.
-
Systemic therapy may be an appropriate option in patients who have progressed through standard initial options, such as surgical resection, WBRT, and/or SRS.
-
When choosing systemic therapy, the general principles are to prioritize agents with known activity against a specific tumor type, those with evidence of CNS activity, and those with the potential to reach therapeutic levels in brain metastases.
-
When available, patients should be considered for clinical trials.
-
A comprehensive review of all targeted agents with postulated CNS activity is outside of the scope of this article. However, details of selected agents, prioritizing those with data from prospective clinical trials, are provided below.
-
A number of prospective clinical trials of targeted agents are ongoing. Table 1 provides a summary of representative studies.Table 1Ongoing trials of targeted therapy in patients with solid tumor brain metastasesAgentPhase of trialTargetPatient populationClinicalTrials.gov identifierEverolimus + trastuzumab + vinorelbineIImTORHER2+ breast cancerNCT01305941BKM120 + trastuzumabIPI3KHER2+ breast cancerNCT01132664Lapatinib + WBRTIIHER2HER2+ breast cancerNCT01622868NeratinibIIHER2HER2+ breast cancerNCT01494662AfatinibIIHER2HER2+ breast cancerNCT01441596ARRY-380 + trastuzumabIHER2HER2+ breast cancerNCT01921335WBRT +/- erlotinibIIEGFRNSCLCNCT01518621WBRT + bevacizumabIVEGFSolid tumorsNCT01332929BevacizumabIIVEGFSolid tumorsNCT01898130Sunitinib + SRSIVEGFRSolid tumorsNCT00981890Sorafenib + SRSIVEGFRSolid tumorsNCT01276210Dabrafenib + SRSIIBRAFMelanomaNCT01721603VemurafenibIIBRAFMelanomaNCT01781026Ipilumumab + WBRT or SRSICLTA-4MelanomaNCT01703507Veliparib + WBRTIIPARPNSCLCNCT01657799
Lapatinib
Lapatinib is an orally bioavailable, dual inhibitor of EGFR and HER2, which is indicated for use in combination with capecitabine for the treatment of patients with advanced or metastatic breast cancer whose tumors overexpress HER2 and who have received prior therapy including an anthracycline, taxane, and trastuzumab. The approval was based on a randomized phase III trial comparing capecitabine vs capecitabine plus lapatinib, and which showed a significant prolongation in time to progression (4.4 months vs 8.4 months; hazard ratio [HR] 0.49 [95 % confidence interval 0.34–0.71], P < 0.001) favoring the combination [25]. Of note, patients with active CNS metastases were excluded from the trial, though patients could have been included if their CNS metastases were clinically stable for at least 3 months prior to study entry.
Although lapatinib does not cross the intact blood-brain barrier to a significant degree, it can reach therapeutic levels in brain tumors and brain metastases [26‐28]. Data for the use of lapatinib in patients with active brain metastases comes from several prospective clinical trials [29, 30•, 31•, 32]. However, there are not randomized data comparing lapatinib against radiotherapy. EGF105084 was a phase 2, single-arm study evaluating lapatinib monotherapy in 242 patients with HER2-positive breast cancer and progressive brain metastases after WBRT and/or SRS [30•]. The CNS response rate was 6 %. Patients who progressed were allowed to enter an extension arm to receive the combination of lapatinib and capecitabine. Among the 50 evaluable patients who did so, 20 % achieved a CNS objective response. The LANDSCAPE study was a single-arm, phase 2 study, which evaluated the combination of lapatinib and capecitabine in lieu of radiotherapy, in HER2-positive patients with newly diagnosed brain metastases [31•]. The CNS response rate was 65.9 %, and responses were durable. Median TTP in the intent-to-treat population was 5.5 months and 1-year survival exceeded 70 %. Based on the strength of these data, a randomized trial comparing lapatinib and capecitabine vs WBRT is in its planning stages. In addition, trials of other HER2-directed tyrosine kinase inhibitors, including neratinib, afatinib, and ARRY-380 for the treatment of breast cancer brain metastases are currently in progress.
Standard dosage
Initiate lapatinib 1,250 mg orally once daily for 21 days in combination with capecitaine 2,000 mg/m2/day (administered orally in two doses approximately 12 hours apart) on days 1–14 of a 21–day cycle. Lapatinib should be taken at least 1 hour before or 1 hour after meals. Capecitabine should be taken with food or within 30 minutes after food.
Contraindication
Inability to tolerate or absorb oral medications. Known severe hypersensitivity to either drug or its components. Impaired left ventricular ejection fraction.
Complications
Diarrhea, palmar-plantar erythrodysesthesia, acneiform rash, fatigue, hepatic impairment, nausea/vomiting. There is also a small risk of pneumonitis and cardiac impairment [25].
Special points
Concomitant use of strong CYP3A4 inhibitors (eg, clarithromycin, ketoconazole) should be avoided. Grapefruit may also increase lapatinib absorption and should be avoided. Patients with baseline severe hepatic dysfunction (Child-Pugh Class C) should begin at a reduced dose of lapatinib.
Cost/cost-effectiveness
Expensive.
Erlotinib
Erlotinib is an orally bioavailable EGFR inhibitor, which is indicated for first-line treatment of patients with metastatic NSCLC whose tumors have EGFR exon 19 deletions or exon 21 (L858R) substitution mutations [33•]. The drug is also approved as maintenance therapy in patients whose disease has not progressed after four cycles of platinum-containing first-line therapy.
Evaluation of the efficacy of EGFR inhibitors, including erlotinib and gefitinib, in patients with brain metastases from NSCLC comes from case reports, case series, and small prospective clinical trials [34]. A prospective study of gefitinib in 41 NSCLC patients unselected for mutations status reported an objective response rate of 10 % in the brain [35]. Studies of EGFR inhibitors in patients with known EGFR mutations have demonstrated much higher response rates [36•, 37]. For example, in an open-label phase II study of 28 patients with newly diagnosed NSCLC, measurable brain metastases and a known EGFR mutation, treatment with erlotinib or gefitinib at standard doses resulted in a partial response rate of 83 % and disease control rate of 93 % [36•]. Median progression-free survival (PFS) was 6.6 months and median overall survival was 15.9 months. Of interest, in a nonrandomized retrospective experience, the 1- and 2-year actuarial risk of CNS progression in patients with stage IIIB/IV NSCLC treated with first-line gefitinib or erolotinib was 7 % and 19 %, which is lower than the rate of 40 % expected from historical data [38].
Anzeige
Erlotinib has also been studied in combination with WBRT. In a single-arm phase II trial, forty patients unselected for mutation status received erlotinib 150 mg daily for 1 week, then concurrently with WBRT followed by maintenance [39]. The overall response rate was 86 %. As expected, median survival time was longer among patients with a known EGFR mutation. The Radiation Therapy Oncology Group (RTOG) attempted a phase 3 trial to test the role of temozolomide or erlotinib in addition to WBRT + SRS in patients with NSCLC and up to three brain metastases [40]. The studied closed early after 126 patients were enrolled due to slow accrual. At the time of analysis, there were not significant differences in survival seen between arms, and if anything, the numerical trends favored the WBRT + SRS only arm, possibly due to increased toxicity in the combination arm. Thus, at this time, concurrent erlotinib with radiotherapy is not recommended outside of a clinical trial. Indeed, the data in EGFR-mutant patients treated with erlotinib alone, as detailed above, raise the question of whether it should be the preferred front-line approach, in lieu of radiotherapy, with radiotherapy reserved for salvage, particularly in patients presenting with asymptomatic brain metastases.
Pulsatile dosing of EGFR tyrosine kinase inhibitors has also been explored as a way to improve the CNS penetration of the drug [41, 42]. In nine patients who had developed parenchymal or leptomeningeal metastases on standard dose erlotinib or other EGFR tyrosine kinase inhibitors, six (67 %, including two patients with leptomeningeal disease) responded to erlotinib when given at a dose of 1,500 mg once weekly.
Standard dosage
150 mg orally once daily, taken at least 1 hour before or 2 hours after a meal.
Contraindication
Inability to tolerate or absorb oral medications.
Complications
Diarrhea, acneiform rash, anorexia, fatigue, dyspnea, cough, nausea, vomiting. Interstitial lung disease in about 1 % of patients.
Special points
Concomitant use of strong CYP3A4 inhibitors (eg, clarithromycin, ketoconazole) should be avoided. Grapefruit may also increase erlotinib absorption and should be avoided.
Cost/cost-effectiveness
Expensive.
Vemurafenib
Vemurafenib is an oral BRAF inhibitor indicated in patients with unresectable or metastatic melanoma whose tumors contain the BRAF V600E mutation. Approval was based on a randomized trial comparing vemurafenib with dacarbazine, which showed a statistically significant improvement in progression-free and overall survival [43••].Of note, patients with CNS metastases were excluded from the pivotal trial, unless the CNS disease had been definitively treated more than 3 months previously with no evidence of progression and no requirement for ongoing glucocorticoid treatment.
Preliminary results have been reported from a single-arm pilot study evaluating vemurafenib in 24 patients with V600E-mutated melanoma and nonresectable brain metastases pretreated with radiotherapy and/or chemotherapy [44]. Partial responses in both body and brain have been noted. At the same time, there have also been case reports of isolated CNS progression in the setting of extracranial disease response, raising questions about CNS penetration and relative CNS response compared with extracranial response [45]. Vemurafenib has not been directly compared with radiotherapy-based approaches for the treatment of melanoma brain metastases.
Standard dosage
960 mg orally twice daily, administered approximately 12 hours apart, with or without a meal.
Contraindication
None.
Complications
The most common adverse reactions are arthralgia, rash, alopecia, fatigue, photosensitivity reaction, nausea, pruritus, and skin papilloma.
Special points
Cutaneous squamous cell carcinomas occur in about one-quarter of patients. Baseline and follow-up skin examinations should be performed for patients receiving vemurafenib. QT prolongation has also been reported and drug should be held if the QTc exceeds 500 ms. Uveitis and iritis can occur. Patients should be monitored for visual symptoms.
Cost/cost-effectiveness
Expensive.
Anzeige
Dabrafenib
Dabrafenib is an oral BRAF inhibitor indicated in patients with unresectable or metastatic melanoma whose tumors contain the BRAF V600E mutation. Approval was based on a randomized trial comparing dabrafenib with dacarbazine, which showed a statistically significant improvement in objective response rate and progression-free survival [46••].
Dabrafenib has been studied in a phase 1 dose-escalation trial, which included ten patients with untreated melanoma brain metastases [47]. In this study, nine of ten patients experienced a reduction in the size of their brain lesions. A subsequent multicenter phase 2 trial enrolled 172 patients with V600E or V600K BRAF-mutant melanoma and either untreated (Cohort A) or previously treated (Cohort B) asymptomatic brain metastases [48]. Intracranial responses by modified RECIST criteria were noted in both cohorts (for V600E, 39.2 % in Cohort A and 30.8 % in Cohort B; for V600K, 6.7 % in Cohort A and 22.2 % in Cohort B). Intracranial hemorrhage was reported in 6 % of patients enrolled on the study. As with vemurafenib, trials directly comparing dabrafenib against radiotherapy have not been conducted.
Standard dosage
150 mg orally twice daily, at least 1 hour before or 2 hours after a meal.
Contraindication
None.
Complications
The most common adverse reactions are hyperkeratosis, headache, pyrexia, arthralgia, papilloma, alopecia, and palmar-plantar erythrodysesthesia.
Special points
Cutaneous squamous cell carcinomas occur in about one-quarter of patients. Baseline and follow-up skin examinations should be performed for patients receiving dabrafenib. Uveitis and iritis can occur. Patients should be monitored for visual symptoms. Febrile drug reactions can occur and may necessitate drug hold or discontinuation.
Cost/cost-effectiveness
Expensive.
Ipilumumab
Ipilumumab is a monoclonal antibody directed against cytotoxic T-lymphocyte antigen-4 (CTLA-4). It is indicated for the treatment of unresectable or metastatic melanoma based on results of a randomized trial demonstrating an overall survival advantage compared with a tumor vaccine or vaccine placebo in patients who had previously received at least one prior systemic treatment [49].
Ipilumumab has also been studied in an open-label phase 2 trial in patients with melanoma brain metastases [50]. Among 51 patients with asymptomatic brain metastases on study entry, nine patients (18 %) exhibited disease control in both brain and body. Among 21 patients who were symptomatic and on corticosteroids, one patient (5 %) exhibited disease control in all sites. Whether ipilumumab administration after SRS provides clinical benefit is unclear. One small retrospective study including 25 patients treated with ipilumumab found no difference in the rate of freedom from new brain metastases or overall survival compared with patients who received SRS alone [51]. However, another retrospective study did appear to support a possible improvement in survival [52]. Whether newer immunomodulatory approaches, such as PD-1 and PD-L1 inhibitors will have CNS activity remains to be seen.
Standard dosage
Three mg/kg as an intravenous infusion every 3 weeks for a total of four doses.
Contraindication
None.
Complications
The most common adverse events are immune-mediated reactions, such as diarrhea, pruritus, rash, and colitis.
Special points
Ipilumumab can result in severe and fatal immune-mediated adverse reactions, which can involve any organ system. These can include enterocolitis, hepatitis, dermatitis, neuropathy, and endocrinopathy. Patients should be assessed at baseline and before each dose. Ipilumumab should be permanently discontinued for severe immune-mediated reactions.
Cost/cost-effectiveness
Expensive.
Anzeige
Bevacizumab
Bevacizumab is a humanized monoclonal antibody directed against vascular endothelial growth factor (VEGF)-A. It is currently approved by the United States Food and Drug Administration (FDA) for the treatment of several malignancies, including metastatic colorectal cancer, metastatic renal cell carcinoma, and NSCLC. The breast cancer approval was revoked in 2011.
In the majority of the initial trials of bevacizumab, patients with brain metastases, whether stable or active, were excluded out of a concern for intracranial hemorrhage. More recent data supports the safety of bevacizumab in patients with both treated and untreated brain metastases. A retrospective exploratory analysis from 13 randomized controlled trials included 131 patients with treated CNS metastases who went on to receive bevacizumab. Only one patient (0.8 %) developed grade 2 cerebral hemorrhage [53]. The PASSPORT trial enrolled 115 patients with treated brain metastases and reported no episodes of grade 2 or higher CNS hemorrhage [54].
Data supporting the potential for clinical activity of bevacizumab in patients with active brain metastases comes from case series and small prospective trials. In breast cancer, a small series (n = 4) of patients were treated with the combination of bevacizumab and paclitaxel. All patients responded (1 CR, 3 PR) with duration of response 6 to 11 months [55]. Combinations of bevacizumab and platinum agents have been studied in two prospective trials, both of which are available in abstract form [56, 57]. The larger of the two studies reported a CNS response rate of 63 % (95 % CI 46 %–78 %) among 38 patients with either HER2-negative or HER2-positive breast cancer [57]. A randomized trial (with an overall survival endpoint) to test the role of bevacizumab in breast cancer patients is being considered. Anecdotal evidence of CNS activity has also been reported in NSCLC [58]. As in breast cancer, randomized data are not available to fully assess its clinical impact.
Standard dosage
Dose and schedule vary by indication. Please refer to package insert for details.
Contraindication
Do not initiate bevacizumab for 28 days following major surgery and until surgical wound is fully healed. Do not administer bevacizumab to patients with serious hemorrhage or recent hemoptysis.
Complications
The most common adverse reactions include epistaxis, headache, hypertension, rhinitis, and proteinuria. The incidence of gastrointestinal perforation is 0.3 %–2.5 %. Bevacizumab increases the risk for both bleeding as well as thromboembolic events. Rarely, reversible posterior leukoencephalopathy (RPLS) may occur.
Special points
None.
Cost/cost-effectiveness
Expensive.
Sunitinib
Sunitinib is an oral inhibitor of VEGFR, PDGFR, and c-kit indicated for the treatment of advanced renal cell carcinoma (RCC). Approval was based on an improvement in PFS compared with interferon-α when given in the first-line setting [59]. Notably, patients with brain metastases were excluded from the pivotal trial.
Subsequently, 321 patients with brain metastases were treated as part of an expanded access program [60]. In this experience, objective responses were observed in 26/213 (12 %) of evaluable patients. Median PFS was 5.6 months. The toxicity profile was comparable with that of the general metastatic RCC population. Only one patient experienced a grade 1/2 cerebral hemorrhage. No grade 3 or 4 CNS hemorrhage events were observed. Other groups have since corroborated these findings, albeit with small numbers of treated patients [61, 62].
Standard dosage
For RCC, 50 mg orally once daily, with or without food, in a 6-week cycle (4 weeks on-treatment / 2 weeks off)
Contraindication
None.
Complications
The most common adverse reactions are fatigue, asthenia, fever, diarrhea, nausea, mucositis/stomatitis, vomiting, dyspepsia, abdominal pain, constipation, hypertension, peripheral edema, rash, palmar-plantar erythrodysesthesia, skin discoloration, dry skin, hair color changes, altered taste, headache, back pain, arthralgia, extremity pain, cough, dyspnea, anorexia, and bleeding.
Special points
Hepatotoxicity has been observed in clinical trials and postmarketing experience. This hepatotoxicity may be severe, and deaths have been reported. Liver function tests should be checked at baseline and monitored during each cycle of treatment. Cardiac toxicity has been observed. Prolonged QT intervals have been observed. Thyroid dysfunction may occur. Consider dose reduction when administered with strong CYP3A4 inhibitors.
Cost/cost-effectiveness
Expensive.
Sorafenib
Sorafenib is an oral VEGF receptor and Raf kinase inhibitor indicated for the treatment of patients with advanced RCC. Approval was based on a randomized phase III study demonstrating a PFS benefit compared with placebo in patients who had received at least one prior systemic treatment [63]. Patients with brain metastases were not eligible for trial participation.
In the expanded access program, patients with brain metastases were allowed. In the brain metastasis subset (n = 70), two patients (4 %) achieved a partial response, and 34 patients (68 %) experienced stable disease for at least 8 weeks [64]. Among the program as a whole (n = 2,504), CNS hemorrhage occurred in less than 1 % of patients; no cases of CNS hemorrhage were noted in the brain metastasis subset. The effect of sorafenib on the incidence of brain metastases has also been studied. In a post-hoc analysis of patients enrolled on the Treatment Approaches in Renal Cancer Global Evaluation Trial (TARGET), the incidence of brain metastases was lower in patients who received sorafenib compared with patients who received placebo (3 % vs 12 %, P < 0.05), raising the question of whether targeted agents might be used as chemoprevention [65]. Studies directly comparing radiotherapy vs sorafenib have not been reported.
Standard dosage
400 mg orally twice daily taken either 1 hour before or 2 hours after meals.
Contraindication
Known severe hypersensitivity to sorafenib or any other component of sorafenib.
Complications
Adverse events include fatigue, weight loss, rash, palmar-plantar erythrodysesthesia, diarrhea, anorexia, and hypertension. There is an increase in the risk of cardiac ischemic events (2.9 % vs 0.4 % in the placebo group). Asymptomatic hypophosphatemia and elevated serum lipase are common.
Special points
Hypertension is common and usually occurs early in the course of treatment. Blood pressure should be monitored weekly during the first cycle and periodically thereafter. Sorafenib should be held in patients undergoing major surgical procedures.
Cost/cost-effectiveness
Expensive.
Acknowledgment
The author wishes to acknowledge support from the Breast Cancer Research Foundation.
Compliance with Ethics Guidelines
Conflict of Interest
Nancy U. Lin has served as a consultant for Novartis and GlaxoSmithKline and has received research funding from Genentech, GlaxoSmithKline, Novartis, and Array BioPharma.
Human and Animal Rights and Informed Consent
This article does not contain any studies with animal subjects performed by the author. With regard to the author’s research cited in this paper, all procedures were followed in accordance with the ethical standards of the responsible committee on human experimentation and with the Helsinki Declaration of 1975, as revised in 2000 and 2008.
Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.