Genitourinary (Nonprostate) Cancer
Personalized Management of Advanced Kidney Cancer
The treatment of renal cell carcinoma represents one of the great success stories in translational cancer research, with the development of novel therapies targeting key oncogenic pathways. These include drugs that target the VEGF and mTOR pathways, as well as novel immuno-oncology agents. Despite the therapeutic advancements, there is a paucity of well-validated prognostic and predictive biomarkers in advanced kidney cancer. With a number of highly effective therapies available across multiple lines, it will become increasingly important to develop a more tailored approach to treatment selection. Prognostic clinical models, such the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model, are routinely used for prognostication in clinical practice. The IMDC model has demonstrated a predictive capability in the context of these treatments including immune checkpoint inhibition. A number of promising molecular markers and gene expression signatures are being explored as prognostic and predictive biomarkers, but none are ready to be widely used for treatment selection. In this review, we will explore the current landscape of personalized care in metastatic renal cell carcinoma. This will include a focus on both prognostic and predictive factors as well as clinical applications of biology in kidney cancer.
As the number of therapeutic options in metastatic renal cell carcinoma increases, it will be critical to develop a more personalized strategy to treatment, taking into consideration both tumor and patient characteristics to develop a tailored treatment plan.
Clinical prognostic models like the IMDC in advanced renal cell carcinoma are important tools for both clinical decision making and risk stratification in clinical trials.
More robust predictors of response to novel immuno-oncology agents, including immune checkpoint inhibitors, are an unmet need in metastatic renal cell carcinoma.
Modern genomic profiling in renal cell carcinoma is uncovering a number of promising predictive and prognostic molecular biomarkers.
Enrollment of patients with advanced kidney cancer in biomarker-directed clinical trials is encouraged.
The treatment of renal cell carcinoma (RCC) has undergone a dramatic evolution over the last decade. The improvements in treatment are secondary to a better understanding of the biologic factors driving cancer growth. The elucidation of the importance of the VEGF and mTOR pathways led to the introduction of several novel agents in the treatment of metastatic renal cell carcinoma (mRCC). More recently, several new immuno-oncology agents have shown impressive activity in advanced kidney cancer and are currently being explored in combination with targeted therapy.1 The evolution of targeted therapy as the mainstay of management in RCC has been a dominant part of the advances.
Despite these impressive successes in exploiting molecular targets, there has been a paucity of biomarkers in RCC that can predict response or clinical outcomes with the novel agents. As the number of therapeutic options increases, it is critical to develop a personalized strategy to treatment, taking into consideration both tumor and patient characteristics to develop a tailored treatment plan. In a disease such as RCC where the spectrum of overall survival (OS) ranges from a few months to many years even without administration of any systemic therapy, the risk prognostication of the patients is of paramount importance in therapeutic decision making. Individualized care using predictive biomarkers is central to the treatment of other advanced malignancies. This includes the anti-HER2 antibody in HER2-amplified breast cancer, anti-EGFR therapies in KRAS wild-type colorectal cancer, and BRAF inhibitors in BRAF mutant melanomas.2 Thus, the elucidation of predictive factors is an unmet need in mRCC and an area of active research.3
In this review, we will explore the current landscape of personalized care in mRCC. This will include a focus on both prognostic and predictive factors as well as clinical applications of biology in kidney cancer. We will provide examples of a personalized approach to systemic therapy and explore future directions in the individualized treatment of advanced kidney cancer.
A personalized approach to the treatment of cancer necessitates an understanding of the variables influencing prognosis. Prior to the advent of targeted agents, a commonly used prognostic risk index was the Memorial Sloan Kettering Cancer Center model. This model was developed and validated in the era of interferon therapy, and it incorporated a number of clinical and biochemical variables. The Memorial Sloan Kettering Cancer Center model integrated five adverse factors: Karnofsky performance status of less than 80%, elevated lactate dehydrogenase, high corrected serum calcium, low hemoglobin, and interval from diagnosis to treatment of less than 1 year. Based on the number of pretreatment factors, three prognostic groups were identified: favorable (zero risk factors), intermediate (one to two risk factors), and poor risk (more than two risk factors).4
The IMDC prognostic model was developed in the more modern era of VEGF-targeted therapy. In total, six variables were identified as having prognostic significance in this population.5 These included two clinical factors (a Karnofsky performance status of less than 80% and time from diagnosis to initiation of therapy of less than 1 year) as well as four laboratory factors (hemoglobin below the lower limit of normal and elevated corrected calcium, neutrophil count, and platelet counts greater than the upper limit of normal). The final IMDC model was able to successfully stratify real-world patients into three distinct prognostic groups: favorable (zero risk factors), intermediate (one to two risk factors), and poor risk (more than two risk factors). Table 1 summarizes the Memorial Sloan Kettering Cancer Center and IMDC prognostic models.
The IMDC model was externally validated using a cohort of 1,028 real-world patients from 13 international cancer centers. In this analysis, the median OS associated with each prognostic group was 43 months, 23 months, and 8 months in the favorable, intermediate, and poor risk groups, respectively.6 The IMDC model continues to be widely used to stratify patients in contemporary clinical trials and to provide personalized, risk-directed treatment selection in everyday clinical practice. The recent trials of nivolumab, cabozantinib, and ipilimumab and nivolumab as well as lenvatinib and everolimus have used the IMDC criteria, as they were specifically applicable to anti-VEGF therapy with sunitinib.
Since the initial validation of the IMDC model, it has been studied in a number of other populations of patients with RCC. Similar to the first-line setting, the IMDC model has been demonstrated to provide prognostic stratification in both the second and third-line settings.7,8 Because the original IMDC model included predominately clear cell renal cell carcinoma (ccRCC), Kroeger et al9 examined the applicability of the IMDC prognostic model in advanced non–clear cell renal cell carcinoma (nccRCC). In this population, patients with nccRCC had inferior OS (12.8 vs. 22.3 months) compared with patients with ccRCC. Similar to the clear cell population, the IMDC model was able to reliably stratify the nccRCC cohort into three distinct prognostic groups.9 More recently, the IMDC was shown to provide prognostic stratification among patients receiving second-line immunotherapy agents, including the immune checkpoint inhibitor nivolumab.10
Given that the IMDC prognostic model did not include patients receiving pazopanib, Perez-Valderrama et al11 conducted a retrospective observational study to validate the model in this population. The study included 278 patients treated with first-line pazopanib for mRCC in 34 centers in Europe. Within this cohort, 19.4% had favorable risk, 57.2% had intermediate risk, and 23.4% had poor risk. As with first-line sunitinib, the IMDC model was able to estimate the prognosis of patients treated with first-line pazopanib. The median OS was not reached in the favorable risk group and was 21.6 months and 7.1 months in the intermediate and poor risk groups, respectively.
Beyond the aforementioned variables included in the IMDC model, there have been a number of other clinical factors demonstrated to have prognostic significance in advanced kidney cancer. These include the baseline neutrophil-to-lymphocyte ratio (NLR) and the presence of bone and liver metastases. McKay et al12 examined the prognostic impact of bone and liver metastases in a retrospective analysis of 2,027 patients with mRCC treated with first-line targeted therapy. Both of these factors were associated with inferior outcomes, with hazard ratios (HR) of 1.38 and 1.37 (p < .0001) for the presence of bone and liver metastases, respectively. Elevated markers of systemic host inflammation, such as NLR, have been shown to be associated with a poor prognosis in several solid tumors. Templeton et al13 explored the impact of baseline NLR on survival in advanced RCC. In this analysis, higher NLR at baseline was associated with shorter OS (adjusted HR per 1-unit increase in lnNLR, 1.69; 95% CI, 1.46–1.95; p < .001).13
Although uncovering variables associated with poor prognosis is important in developing personalized treatment strategies, identifying factors that do not influence clinical outcomes is also helpful. As the overall life expectancy of our population increases, understanding the impact of age on cancer outcomes will become increasingly important. Khambati et al14 explored the use of first-line targeted therapy in elderly patients (older than age 75) with mRCC. In this analysis, outcomes were found to be similar between the older and younger subgroups, even when adjusted for known poor prognostic factors. These findings suggest that age alone should not be used as an absolute contraindication to targeted therapy.
mRCC is a heterogeneous disease and one that is characterized by a variable natural history. There appears to be a certain subset of patients with mRCC who may display a less aggressive and more indolent pattern of progression. Given these observations, there has been ongoing interest in the idea of deferred systemic therapy with active surveillance, in contrast to the more standard approach of starting therapy immediately at the onset of metastatic disease. This deferred approach has been examined in a number of retrospective analyses as well as prospectively in a large observational registry, the Metastatic Renal Cell Cancer Registry.15,16 Park et al17 performed a retrospective analysis of 58 patients undergoing active surveillance for mRCC. In this series, the median time to disease progression was 12.4 months. Multivariable analysis revealed that Karnofsky performance status of less than 100%, liver metastases, and time from diagnosis to the start of surveillance of less than 1 year were associated with a shorter time to progression. Importantly, the response rate and OS for the subsequent systemic treatment after surveillance were comparable with those of previous reports.
Rini et al18 conducted a prospective phase II trial designed to examine the feasibility and safety of an initial active surveillance approach in the era of modern targeted therapy. They included patients with asymptomatic mRCC, measurable disease, and no prior systemic therapy. In total, 52 patients were enrolled into the study. Patients were radiographically assessed at baseline and then every 3 months for year 1, every 4 months for year 2, then every 6 months thereafter. The decision to initiate systemic therapy was at the discretion of the treating physician and patient. The median surveillance time until initiation of systemic therapy was 14.9 months. Multivariate analysis showed that a higher number of IMDC risk factors (p = .0403) and a greater number of metastatic sites (p = .0414) were associated with a shorter surveillance period. Based on this, the authors identified a favorable subgroup, defined as patients with zero to one IMDC risk factor and fewer than two organs with metastatic disease, who had an estimated median surveillance time of 22.2 months. These findings suggest that deferred initiation of systemic therapy using an active surveillance protocol may be appropriate for carefully selected patients with low-risk disease.
Despite improvements in systemic therapy options, local therapy to sites of metastatic disease remains an important component in the personalized management of mRCC. These therapies can include surgical resection (metastasectomy), definitive radiotherapy, and other ablative procedures. The most common sites of metastatic disease in RCC are the lung (45%), bone (30%), lymph nodes (20%), liver (20%), adrenal gland (9%), and brain (8%).19 For each of these sites, there is evidence that local therapies may be effective, particularly in the setting of a limited number of metastases. In a series of 141 patients treated with metastasectomy in the pretargeted therapy era, curative intent resection was associated with a 44% 5-year OS rate.20 A disease-free interval greater than 12 months from the time of nephrectomy, solitary site (vs. multiple sites) of metastasis, and age younger than 60 were associated with improved survival.
With regard to resection of pulmonary metastases, Pfannschmidt et al21 retrospectively analyzed 191 patients with pulmonary metastases from RCC who underwent surgical resection. The 5-year survival rate after complete metastasectomy was 41.5%. Favorable prognostic factors included having fewer than seven metastatic lesions and a disease-free interval of greater than 23 months. Pancreatic metastases also tend to have a favorable outcome after resection.22 Solitary bone and soft tissue metastases should also be considered for local therapy. Embolization of metastases, especially bone metastasis, prior to resection is strongly advised to reduce the risk of hemorrhage and complications.
The role of local therapy in the management of RCC is rapidly increasing. Noninvasive techniques such as stereotactic radiation therapy or cryotherapy are increasingly being applied for oligometastatic disease and for consolidative control of residual masses after systemic therapy.23 Aoun et al24 reported on cryoablation of more than 2,000 tumor masses including metastatic sites and renal masses and established efficacy of the procedure. The successful experience with a series of patients specifically with advanced kidney cancer treated with cryotherapy has helped establish the safety, feasibility, and efficacy of this procedure. Wang et al23 evaluated stereotactic ablative radiation therapy for extracranial RCC metastases and reported results on 175 metastatic foci, where they observed 1-year local control rates in excess of 90%. There are also emerging data on abscopal effects and of synergy between immunotherapy and ablative techniques as a result of the release of neoantigens.25 Currently, clinical trials evaluating the direct and abscopal clinical effects and immune changes with a combination of radiation or cryotherapy and immune checkpoint inhibition are in development.
The role of systemic therapy following complete resection of metastatic disease is unclear. The ECOG 2810 phase III trial is comparing adjuvant pazopanib with placebo after metastasectomy and may help clarify the use of targeted agents in resected mRCC. Other trials exploring immune checkpoint inhibitors also allow the inclusion of patients with completely resected metastatic disease, such as KEYNOTE-564, which compares pembrolizumab with placebo in the adjuvant setting, or IMmotion010, which evaluates atezolizumab.
In the first-line setting, there are a number of established therapeutic options in mRCC. These include VEGF-targeted drugs (e.g., sunitinib, pazopanib, and cabozantinib), mTOR inhibitors, high-dose interleukin (IL)-2, and more recently, immuno-oncology agents.1 One of the cornerstones of personalized care in oncology is the discovery and validation of factors that can predict response to various therapeutic agents. These can include clinical or patient-specific factors as well as tumor-specific biomarkers. In this section, we will review clinical factors that may be used to help establish a more personalized approach to the treatment of advanced RCC.
Prognostic clinical factors are important in guiding treatment decisions in mRCC. In 2007, Hudes et al26 conducted a phase III randomized trial exploring the role of the mTOR inhibitor temsirolimus in previously untreated, poor-risk, advanced RCC. In this trial, 626 patients were randomly assigned to temsirolimus, temsirolimus plus interferon-alfa, or interferon-alfa monotherapy. Inclusion criteria necessitated that patients have at least three of the following six predictors of poor prognosis: elevated lactate dehydrogenase, elevated serum calcium, low hemoglobin, time from diagnosis to randomization of less than 1 year, Karnofsky performance status of 60 or 70, and metastases in multiple organs. In this poor-risk population, temsirolimus significantly prolonged the median OS compared with interferon-alfa as a single agent (10.9 vs. 7.3 months; HR for mortality, 0.73; 95% CI, 0.58–0.92). These results led the U.S. Food and Drug Administration to approve temsirolimus in the first-line setting for patients with a poor prognosis. Although this trial did not directly compare the use of an mTOR inhibitor among patients with good-intermediate versus poor risk, it did provide a risk-directed approach to treatment selection. It is important to note that the prognostic index used in this trial is different from the IMDC model. In real-world practice, the use of temsirolimus in this setting is limited as a result of intravenous administration.
Risk profiling has also been used in studies using VEGF-targeted agents. In the recently reported phase II CABOSUN trial, 157 patients with intermediate or poor risk mRCC based on IMDC criteria were randomly assigned to cabozantinib or sunitinib.27 Cabozantinib is a VEGF, MET, and AXL inhibitor. Patients were stratified by IMDC risk category (intermediate or poor) and presence of bone metastases. The response rate for cabozantinib was 46%, with a significantly increased median progression-free survival (PFS; 8.2 vs. 5.6 months; HR 0.66; 95% CI, 0.46–0.95; p = .012) compared with sunitinib. OS was also increased with cabozantinib, (26.6 vs. 21.2 months), but the difference was not statistically significant (HR 0.79; 95% CI, 0.53–1.20). A PFS benefit with cabozantinib was also observed in subgroup analyses, including among those with poor IMDC risk and bone metastases. The results of the independent review of response and PFS in the CABOSUN trial led the U.S. Food and Drug Administration to approve cabozantinib in the frontline setting of RCC. Table 2 summarizes the key results of the CABOSUN trial.
More recently, the predictive capability of the IMDC model was demonstrated in the CheckMate 214 clinical trial.28 This was a large phase III randomized controlled trial evaluating the combination of two immune checkpoint inhibitors, nivolumab and ipilimumab, compared with standard sunitinib alone in previously untreated advanced RCC or mRCC. This trial stratified patients by IMDC prognostic group and sample size was powered for overall analysis and for the intermediate and poor risk groups. In the IMDC intermediate and poor risk groups, combination immunotherapy was associated with superior OS compared with sunitinib (HR 0.63; p < .0001). In contrast, the IMDC favorable group appeared to have superior outcomes with sunitinib alone in terms of response rate and PFS. In the favorable risk group, the objective response rate (ORR) was 52% versus 29% (p = .0002) and PFS was 25.2 versus 15.3 months (HR 2.18; p < .0001) in the sunitinib and immunotherapy arms, respectively. These data suggest that favorable risk tumors may have a distinct biology, which is characterized by greater dependence on VEGF signaling.
The investigators also performed an exploratory analysis looking at PD-L1 expression. Patients with a tumor PD-L1 of 1% or greater demonstrated a higher response rate and improved PFS with nivolumab and ipilimumab compared with sunitinib, but those with less than 1% expression demonstrated a response rate of 37%. This suggests that PD-L1 expression may increase the likelihood or response but cannot accurately predict which patients will not respond. With regard to toxicity, an increased incidence of high-grade treatment-related adverse events was observed with sunitinib. This may have been influenced by the early introduction of steroids, which were required for 60% of patients with combination immunotherapy. Health-related quality of life data were also collected, with patients reporting better symptom control with immunotherapy versus sunitinib. It is unclear why the intermediate and poor risk groups appeared to benefit more from immunotherapy. This may be attributable to higher levels of neoantigen exposure and immune stimulation or secondary to unidentified biomarkers common to this group. Tumors in the intermediate and poor risk groups may also be more inflamed, which may account for increased neutrophil or platelet counts as well as anemia and possibly a worse performance status. The results of this pivotal trial have the potential to transform the treatment landscape of mRCC, and they provide clinicians with a more personalized approach to upfront systemic therapy. Table 3 summarizes the key results of the CheckMate 214 trial.
Other regimens that are currently in ongoing phase III trials consist of a common theme of comparing combinations of anti-VEGF therapy and immunotherapy, using sunitinib as the control arm. One of the combinations, bevacizumab and atezolizumab, has shown favorable outcomes in the PD-L1–positive population in a randomized trial (IMmotion 151) compared with the control arm of sunitinib.
Selecting patients with advanced kidney cancer that may benefit from a cytoreductive nephrectomy (CN) is another important decision in the personalized treatment of this population. In the pretargeted therapy era, a combined analysis of two prospective randomized clinical trials revealed that CN followed by interferon treatment was associated with a 5.8-month increase in OS versus interferon alone (13.6 vs. 7.8 months).29 Unfortunately, there has been a lack of randomized trials exploring the role of CN for patients with mRCC being treated with molecularly targeted therapy. To investigate this further, a retrospective analysis was performed to address the survival benefit of CN for patients with mRCC treated with targeted therapy.30 The median OS for patients with CN versus without CN was 20.6 versus 9.5 months (p < .0001). When adjusted for IMDC risk criteria to correct for imbalances, the HR of death was 0.60 (95% CI, 0.52–0.69; p < .0001). Importantly, patients who possessed four or more of the IMDC prognostic factors did not appear to benefit from CN. Thus, not all patients should be offered this procedure and the decision should be individualized based on prognosis. In the real world, other considerations include bulk of tumor burden outside of the kidney, brain/liver metastases, symptoms from the primary tumor, and surgical feasibility.
In the recently reported SURTIME trial, investigators attempted to determine whether the sequence of CN among patients who receive sunitinib has an effect on patient outcomes.31 In this trial, patients with metastatic ccRCC were randomly assigned to immediate CN followed by sunitinib versus three cycles of sunitinib followed by CN plus sunitinib (deferred CN). As a result of poor accrual, the investigators decided to report the progression-free rate at week 28 as the primary endpoint. No significant difference between the two groups was observed; the progression-free rate was 42.0% (95% CI, 28.2–56.8) versus 42.9% (95% CI, 28.8–57.8) in the immediate and deferred arms, respectively (p > .99). Although the study was not adequately powered, an OS improvement was seen for deferred CN. The authors concluded that the deferred approach initiates therapy quickly, does not lead to the inability to perform CN, and CN after sunitinib appears to be safe.
Given the relative lack of well-validated predictive biomarkers, there has been interest in examining the use of on-treatment predictors of response. Most of these rely on mechanism-based adverse events that may act as a surrogate for clinical efficacy, focusing mainly on VEGF-targeted therapies. This class of drugs has specific toxicities, many of which have been analyzed as potential surrogate biomarkers. These include hypertension, hypothyroidism, neutropenia, thrombocytopenia, and hand-foot syndrome.32
The most well established of these adverse events is treatment-related hypertension.33 This side effect is common with sunitinib, occurring in approximately one-third of patients.34 Rini et al35 examined the association between sunitinib-induced hypertension and antitumor efficacy in a large retrospective, pooled analysis of four studies that included 544 patients with mRCC. In this study, hypertension was defined as a systolic blood pressure of at least 140 mmHg or a diastolic blood pressure of at least 90 mmHg. Systolic hypertension was associated with an ORR of 54.8% compared with an ORR of 8.7% for patients without systolic hypertension (p < .001). PFS (12.5 vs. 2.5 months; p < .001) and OS (30.9 vs. 7.2 months; p < .001) were also significantly longer for patients with systolic hypertension than for those without. Importantly, the incidence of hypertension-associated end organ dysfunction, such as cardiovascular events, was low. Although retrospective in nature, these findings suggest that treatment-induced hypertension may be a viable predictive biomarker of efficacy in mRCC. Other studies suggest that the phenomenon is generalizable to other anti-VEGF receptor therapies. Inasmuch as the hypertension is likely related to the magnitude of systemic VEGF receptor blockade, higher rates of hypertension may reflect higher effective drug levels.
In the second-line setting, there are again a number of potential treatment options. These include targeted drugs such as axitinib, cabozantinib, lenvatinib plus everolimus, and the checkpoint inhibitor nivolumab. The optimal sequence of therapy is still an area of active research. Al-Marrawi et al36 used the IMDC data set to retrospectively investigate the association of clinical outcome between two lines of targeted therapy. In this study, 464 patients who received both a first- and second-line VEGF inhibitor were included. In this analysis, there was no correlation between first- and second-line responses, in terms of both ORR and PFS. For the entire group, the ORR for first-line therapy was 22% compared with 11% for the second-line therapy. These results suggest that in clinical practice, a patient’s response, or lack thereof, should not necessarily influence the choice of second-line targeted therapy.
The phase III METEOR trial helped establish cabozantinib as an effective second-line option in mRCC.37 In this trial, 658 previously treated patients were randomly assigned to receive cabozantinib (60 mg/day) or everolimus (10 mg/day). All patients had progressed after receiving prior VEGF tyrosine kinase inhibitor therapy; 69% of patients had received only one prior course of systemic therapy, whereas 31% had been treated with two or more prior regimens. Patients progressing while treated with immune checkpoint inhibitors were also included. Randomization was stratified according to the number of previous VEGF tyrosine kinase inhibitors and prognostic risk category. Cabozantinib was associated with an improved PFS compared with everolimus (7.4 vs. 3.8 months), with a corresponding HR of 0.58 (95% CI, 0.45–0.75; p < .001). This PFS benefit was consistently observed in prespecified subgroups defined according to the number of prior VEGF tyrosine kinase inhibitors and prognostic risk category. A dedicated subset analysis of patients with bone metastases also revealed improved outcomes with cabozantinib.38 In this subgroup, the PFS was 7.4 months for cabozantinib versus 2.7 months for everolimus (HR 0.33; 95% CI, 0.21–0.51). Median OS was also longer with cabozantinib (20.1 vs. 12.1 months; HR 0.54; 95% CI, 0.34–0.84). These results are consistent with those from the previously discussed CABOSUN trial and suggest that cabozantinib is an effective treatment option for this specific patient population.
Another recently approved second-line option in mRCC is the immune checkpoint inhibitor nivolumab. In the CheckMate 025 trial, 821 patients were randomly assigned to nivolumab (3 mg/kg every 2 weeks) or everolimus (10 mg/day), with all patients having received one or two prior antiangiogenic therapies.39 Randomization was stratified by the prognostic risk group and the number of previous antiangiogenic therapy regimens. Nivolumab was associated with a significant improvement in OS (25.0 vs. 19.6 months; HR 0.73). The ORR was also greater with nivolumab compared with everolimus (25% vs. 5%). Expression of PD-L1 on tumor cells was not associated with a survival benefit to nivolumab, because those with 1% or greater expression and those with less than 1% expression had a similar survival benefit compared with everolimus. Among patients with 1% or greater PD-L1 expression, the median OS was 21.8 months (95% CI, 16.5–28.1) in the nivolumab group and 18.8 months (95% CI, 11.9–19.9) in the everolimus group (HR 0.79; 95% CI, 0.53–1.17). Higher levels of PD-L1 expression appeared to be associated with shorter OS irrespective of treatment arm. A substantial improvement in quality of life was also observed over the 2-year study period during nivolumab treatment. A dedicated subgroup analysis of this trial has also been reported. This has confirmed a benefit to nivolumab across a number of key baseline factors, including risk groups, age, number and sites of metastases, and type and duration of prior therapy.40 Duration of response to prior anti-VEGF therapy and NLR (cutoff greater than or less than three) were noted to be independent predictors of benefit from nivolumab therapy in pretreated RCC.41 In the context of immune therapy, no clear predictive or prognostic factors have emerged that have been correlated in large populations. Exploration of the IMDC database to evaluate prognostic criteria with immunotherapy treatment is ongoing.
The treatment of RCC represents one of the great success stories in translational cancer research, with the development of novel therapies targeting key oncogenic pathways. Despite these advancements, there is a relative lack of well-validated prognostic and predictive molecular biomarkers in advanced kidney cancer.
Broadly speaking, RCC represents a diverse collection of distinct histologic subtypes, with ccRCC comprising more than 75% of cases.42 Molecular heterogeneity within these subtypes is likely playing an important role in the diversity of responses and resistance to targeted therapies and has complicated biomarker discovery.2 The elucidation and subsequent clinical validation of these molecular markers will be critical in the development of a more personalized approach to treatment. In this section, we will highlight the contemporary clinical applications of biology in RCC. We will focus on potential molecular prognostic biomarkers as well as predictive factors related to VEGF-targeted therapy and immune checkpoint inhibitors.
Advancements in modern genomic techniques, including next-generation sequencing, have revealed the diverse spectrum of both genetic and epigenetic changes in kidney cancer. The most commonly mutated gene in ccRCC is von Hippel Lindau (VHL), which in inactivated in more than 50% of patients with ccRCC.43 This gene resides on chromosome 3p25 and is essential to the regulation of hypoxia-inducible factor α and angiogenesis. Three other tumor suppressor genes (PBRM1, SETD2, and BAP1) are also located on chromosome 3p and together constitute the most frequently mutated genes after VHL.44 All three of these genes appear to be involved in regulating epigenetic processes such as chromatin and histone modification.2 Interestingly, whereas mutations in PBRM1 and BAP1 tend to be mutually exclusive, mutations in PBRM1 and SETD2 appear to synergize.45
The prognostic significance of many of these genes has been an area of active research. Kapur et al46 performed a retrospective analysis of 145 patients with ccRCC at The University of Texas Southwestern Medical Center, the majority of whom had localized or locoregional disease. Their results demonstrated that patients with tumors harboring BAP1 mutations had significantly reduced median OS compared with those who had tumors containing PBRM1 mutations (4.6 vs. 10.6 years, respectively; HR 2.7; p = .04).46 They observed similar results in analysis of a second cohort (with 327 patients) from The Cancer Genome Atlas (TCGA).46 Hakimi et al47 performed a similar study looking at 188 patients who underwent resection of primary ccRCC at the Memorial Sloan Kettering Cancer Center, as well as an independent cohort of 421 patients from the TCGA. BAP1 mutations were associated with worse cancer-specific survival, with an HR of 7.71 (p = .002). PBRM1 mutations appeared to have no impact on cancer-specific survival, whereas SETD2 mutations were associated with worse cancer-specific survival only in the TCGA cohort (HR 1.68; p = .036).
Beyond single gene mutations, other studies have explored the use of gene expression profiling in the prognostication of RCC. Brannon et al48 obtained gene expression data from 48 ccRCC samples and identified two distinct molecular subtypes, which they defined as clear cell type A and clear cell type B. Using a validation data set of 177 samples, patients with clear cell type A tumors had significantly better cancer-specific survival than those with clear cell type B tumors (median survival, 8.6 vs. 2.0 years, respectively; p = .002). This signature was subsequently validated in a meta-analysis of six ccRCC gene expression data sets encompassing a total of 480 patients.49 Similarly, an analysis of the TCGA data set revealed four distinct molecular subgroups, designated m1 to m4. Similar to the study by Brannon et al,49 postnephrectomy survival was related to these ccRCC subtypes. Interestingly, this study identified changes in key metabolic pathways within these subtypes. This included a more aggressive phenotype that was associated with increased expression of enzymes associated with the pentose phosphate shunt, glutamine transport, and fatty acid synthesis.43
As alluded to previously, the use of molecular classifications to predict response to therapy is a crucial step toward a more personalized approach to the treatment of kidney cancer. With regard to VEGF-targeted therapy, a number of tumor-specific factors have been studied as potential biomarkers, including VHL mutations and hypoxia-inducible factor levels. None of these are currently used in clinical practice and require further prospective validation.50 Interestingly, however, expression of the particular hypoxia-inducible factor α isoform may predict responsiveness to a new class of agents targeting hypoxia-inducible factor 2α.51
Beuselinck et al52 performed an integrated genomic analysis of primary ccRCCs to identify subgroups that may be more sensitive or resistant to anti-VEGF treatment. They collected primary tumor samples from 121 patients with metastatic ccRCC who were receiving first-line sunitinib. Using gene expression profiling, they identified four robust ccRCC subtypes (ccRCC1–ccRCC4). These groups showed a high correlation with the prognostic groups previously described by Brannon et al.48 These four molecular subtypes were associated with different responses to sunitinib treatment: ccRCC1/ccRCC4 tumors had a lower response rate (p = .005) and a shorter PFS and OS compared with the ccRCC2/ccRCC3 subtypes (p = .001 and .0003, respectively). The ccRCC4 subtype was associated with the poorest sunitinib response.
The poor-responder ccRCC1/ccRCC4 subtypes appeared to share a number of common molecular characteristics such as upregulation of MYC targets or a hypermethylated status strongly correlated with a polycomb stem-cell phenotype. The ccRCC3 tumors revealed a gene expression profile similar to that of the normal kidney and appeared to have an indolent disease course. The ccRCC4 tumors showed specific pathologic features such as a more inflammatory and sarcomatoid phenotype as well as an upregulation of cellular immune pathways. These findings suggest that the ccRCC4 subtype may be more susceptible to immune-based therapies. The authors have subsequently shown that these four molecular subtypes are also associated with outcome among patients receiving pazopanib as first-line therapy.53 Although intriguing, the results must be further validated in a larger, independent patient cohort before they are used in routine clinical practice for treatment selection.
There have also been a number of studies examining potential predictive biomarkers to mTOR-directed therapy. Kucejova et al54 identified mutations in the mTOR-negative regulator TSC1 in ccRCC and proposed that such mutations may identify tumors most likely to respond to mTOR inhibitors. Kwiatkowski et al55 retrospectively analyzed a cohort of 79 patients with mRCC treated with mTOR inhibitors. They performed molecular genetic analysis on both responders and nonresponders to identify mutations associated with response. Mutations in MTOR, TSC1, or TSC2 were more common for patients who experienced clinical benefit than for those who progressed. However, a substantial fraction of responders (31 of 43; 72%) had no mTOR pathway mutation identified. Thus, more research is needed before promising biomarkers such as these are used for treatment selection in clinical practice.
With regard to immune-based therapies, the use of high-dose IL-2 remains a first-line option for a select group of patients. Early evidence suggested that certain tumor characteristics such as carbonic anhydrase IX expression may predict for response. Unfortunately, the phase II SELECT trial (with 120 patients) failed to demonstrate the predictive value of carbonic anhydrase IX expression on overall response rate.56 The identification of reliable predictive biomarkers for immune checkpoint inhibitors is another area of active research in many tumor types, including RCC. The immune checkpoints most commonly targeted in cancer are the PD-1/PD-L1 pathway and the CTLA-4 pathway. In mRCC, the PD-1 inhibitor nivolumab has shown activity in the second-line setting, as well as in the first-line setting in combination with the CTLA-4 inhibitor, ipilimumab.28,39
One of the most studied potential biomarkers for immunotherapy is PD-L1 expression. Unlike in other tumors, PD-L1 has not been shown to be a reliable predictor of response to anti–PD-1 therapy in RCC. In the CheckMate 025 trial exploring nivolumab in the second-line setting, a benefit was observed with nivolumab irrespective of PD-L1 expression.39 In a subgroup analysis of the previously discussed CheckMate 214 trial, patients with tumor PD-L1 of 1% or greater demonstrated a higher response rate and improved PFS with nivolumab and ipilimumab compared with sunitinib, but those with less than 1% expression still had a response rate of 37%.28 IMmotion 151 is a recently reported randomized trial that compared bevacizumab and atezolizumab therapy to sunitinib, specifically in PD-L1 positive (> 1% expression on tumor infiltrating cells; SP142 assay) patients with metastatic renal cancer.57 The primary endpoint of the study was investigator assessed PFS in PD-L1 positive patients with untreated metastatic RCC and OS in all patients by intent to treat. The results revealed that PFS was significantly improved with the combination in PD-L1 positive patients (HR 0.74; 95% CI, 0.57–0.96; p = .0217). Median PFS was 7.7 months with sunitinib and 11.2 months with atezolizumab and bevacizumab combination. The OS results are not mature at the time of present report. In general, there are several key limitations with the use of PD-L1 expression as a potential biomarker. These include heterogeneity between the primary and metastatic sites as well as intratumor heterogeneity. PD-L1 is also a dynamic biomarker, which may change based on prior VEGF-targeted therapy. Other limitations involve the technical methods used, including the choice of antibody, the selected cutoffs to define positivity, and the types of cells analyzed.57
To explore genomic alterations in ccRCC that may correlate with response to anti–PD-1 therapy, Miao et al58 performed whole exome sequencing of metastatic ccRCC from 35 patients treated with nivolumab. In this analysis, they found that loss-of-function mutations in the PBRM1 gene appeared to be associated with increased clinical benefit to immune checkpoint therapy. Those with PBRM1 loss had significantly prolonged OS and PFS compared with patients without PBRM1 loss (log-rank p = .0074 and p = .029, respectively). These findings were confirmed in an independent validation cohort of 63 patients with ccRCC treated with checkpoint inhibitors. It is speculated that PBRM1 loss may alter global expression profiles to influence responsiveness to immune-based therapies. The use of genomic analysis to predict response to immunotherapy represents an exciting step forward in the personalized care of mRCC. These findings will need further prospective validation before they are used in clinical practice.
nccRCC represents approximately 20% of diagnoses and comprises a number of distinct histologies, each of which appears to have unique biology. The most common of the non–clear cell variants is papillary RCC. Durinck et al59 performed integrated genomic analyses of 167 non–clear cell tumors, including 67 papillary RCCs. The authors identified 10 significantly mutated genes, including MET, NF2, SLC5A3, PNKD, and CPQ.59 The TCGA Network recently performed a comprehensive molecular characterization of papillary RCC from 161 samples and confirmed two clinically and biologically distinct subtypes.60 Type I disease was noted to bear a higher frequency of alterations in the MET proto-oncogene, whereas type II tumors had CDKN2A silencing and SETD2 mutations. Data from the French RCC Network further support MET as an oncogenic driver across papillary RCC subtypes. In their analysis of 220 samples, 81% and 46% of type I and type II cases, respectively, demonstrated alterations in the MET gene.61
These findings have led to interest in exploring the use of MET-directed therapies in papillary RCC. The predictive ability of MET mutational status was demonstrated in a phase II trial looking at the MET inhibitor foretinib in metastatic papillary RCC. In this trial, the presence of a germline MET mutation was highly predictive of a response to this novel targeted therapy.62 Another phase II study evaluated the safety and efficacy of the MET inhibitor savolitinib for patients with papillary RCC according to MET status.63 In this trial, ORR was significantly higher for patients with MET-driven disease (18% vs. none; p = .002). Median PFS for patients with MET-driven and MET-independent disease was 6.2 and 1.4 months, respectively (HR 0.33; p < .001). Given these findings, an international, randomized, phase II study led by the Southwest Oncology Group (SWOG 1500) is further exploring this approach. This trial is randomly assigning patients with metastatic papillary RCC to receive either sunitinib or one of three MET-directed therapies: savolitinib, cabozantinib, and crizotinib. There will be an additional exploratory evaluation of MET mutational status and expression. The results of this trial could help change the treatment paradigm of nccRCC and further promote a more personalized approach to therapy.
RCC is characterized by a high degree of intratumor heterogeneity. Analyses of RCC samples have shown that a single tumor biopsy may reveal only a minority of the genetic alterations within the entire tumor and that differences in genetic alterations are seen between the primary and metastatic sites.64,65 This degree of heterogeneity and clonal evolution complicates biomarker development and the delivery of precision medicine. Given these limitations, there has been increasing interest in the use ctDNA in kidney cancer.
Pal et al66 conducted the largest patient series of ctDNA evaluation in mRCC to date. In this study, they obtained ctDNA profiles from a cohort of 220 consecutive patients with mRCC.66 Genomic alterations were detected for 79% of patients. The most frequent alterations included TP53 (35%), VHL (23%), EGFR (17%), NF1 (16%), and ARID1A (12%). They also attempted to define differences in the ctDNA profile across lines of targeted therapy. When looking at post first-line VEGF-therapy versus first-line VEGF-therapy profiles, they identified differences in genomic alterations: TP53 (64% vs. 31%; p = .04), NF1 (29% vs. 4%; p = .02), and PIK3CA (29% vs. 8%; p = .07). These changes may suggest a selective pressure from therapy and could imply a role in therapeutic resistance. Although it is not without a number of important limitations, this study illustrates the potential of ctDNA in further evaluating the genomic diversity of RCC. In the future, the use of ctDNA may expedite biomarker discovery and facilitate the selection of novel targeted therapies.
In summary, the treatment of advanced RCC has undergone an impressive transformation over the last decade. With a number of highly effective therapies available across multiple lines, it will become increasingly important to develop a more tailored approach to treatment selection. Clinical prognostic models like the IMDC have shown a predictive ability in the context of immune checkpoint inhibition in the first-line setting and will likely be used in clinical practice for patient selection. In Figure 1, we present a proposed plan based on current available information to help determine frontline therapy of ccRCC. As our understanding of the genomic landscape of RCC improves, a number of molecular markers are being explored as biomarkers. These include robust gene expression profiles that will hopefully further improve our ability to predict who will and will not respond to targeted therapy. Novel platforms such as ctDNA analysis may also provide a less-invasive avenue toward personalized medicine. In the end, given the complexity of cancer treatment, it will likely require a combination of clinical and biologic approaches to fully realize the potential of precision oncology.
The following represents disclosure information provided by authors of this manuscript. All relationships are considered compensated. Relationships are self-held unless noted. I = Immediate Family Member, Inst = My Institution. Relationships may not relate to the subject matter of this manuscript. For more information about ASCO's conflict of interest policy, please refer to www.asco.org/rwc.
Honoraria: Bayer, Bristol-Myers Squibb, Exelixis, Genentech, Janssen, Novartis, Pfizer, Sanofi
Consulting or Advisory Role: Astellas Pharma, Bayer, Bristol-Myers Squibb, Exelixis, Genentech/Roche, Pfizer
Speakers' Bureau: Bayer, Bristol-Myers Squibb, Exelixis, Genentech/Roche, Pfizer, Sanofi
Research Funding: Astellas Pharma, Bristol-Myers Squibb, Exelixis, Novartis, Pfizer
Consulting or Advisory Role: Astellas Pharma, Bristol-Myers Squibb, Janssen, Novartis, Pfizer
Research Funding: Bristol-Myers Squibb (Inst), Exelixis (Inst), Novartis (Inst), Pfizer (Inst)
Consulting or Advisory Role: Nektar
Research Funding: Genentech/Roche
Patents, Royalties, Other Intellectual Property: #Patent of HIF-2 biomarker (Inst)
Other Relationship: Nektar
No relationship to disclose
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